paragraph_index int64 | sec string | p_has_citation int64 | cites string | citeids list | pmid int64 | cited_id string | sentences string | all_sent_cites list | sent_len int64 | sentence_batch_index int64 | sent_has_citation float64 | qc_fail bool | cited_sentence string | cites_in_sentence list | cln_sentence string | is_cap bool | is_alpha bool | ends_wp bool | cit_qc bool | lgtm bool | __index_level_0__ int64 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
3 | DISCUSSION | 1 | 38 | [
"B38",
"B62",
"B63"
] | 17,355,988 | pmid-1918087|pmid-7768938|pmid-1918087|pmid-8702819|pmid-7768940|pmid-12620221|pmid-14630952|pmid-14630952|pmid-12620221|pmid-16959568|pmid-16959569 | Taken together, these data suggest that a helix–loop–helix structure is induced on interaction with α, with the extended helix 6 serving as a scaffold that links the globular domain of τC14 and α. | [
"38",
"62",
"63"
] | 196 | 3,400 | 0 | false | Taken together, these data suggest that a helix–loop–helix structure is induced on interaction with α, with the extended helix 6 serving as a scaffold that links the globular domain of τC14 and α. | [] | Taken together, these data suggest that a helix–loop–helix structure is induced on interaction with α, with the extended helix 6 serving as a scaffold that links the globular domain of τC14 and α. | true | true | true | true | true | 582 |
3 | DISCUSSION | 1 | 38 | [
"B38",
"B62",
"B63"
] | 17,355,988 | pmid-1918087|pmid-7768938|pmid-1918087|pmid-8702819|pmid-7768940|pmid-12620221|pmid-14630952|pmid-14630952|pmid-12620221|pmid-16959568|pmid-16959569 | Whether the globular domain itself establishes contacts with α in either of the two proposed α–τ binding modes (38) remains to be shown. | [
"38",
"62",
"63"
] | 136 | 3,401 | 1 | false | Whether the globular domain itself establishes contacts with α in either of the two proposed α–τ binding modes remains to be shown. | [
"38"
] | Whether the globular domain itself establishes contacts with α in either of the two proposed α–τ binding modes remains to be shown. | true | true | true | true | true | 582 |
3 | DISCUSSION | 1 | 38 | [
"B38",
"B62",
"B63"
] | 17,355,988 | pmid-1918087|pmid-7768938|pmid-1918087|pmid-8702819|pmid-7768940|pmid-12620221|pmid-14630952|pmid-14630952|pmid-12620221|pmid-16959568|pmid-16959569 | NMR studies of the interaction of τC16Δ11 with α yielded a dissociation constant of ∼0.9 mM (61), indicating that additional binding residues are located within the structured portion near the end of helix 6. | [
"38",
"62",
"63"
] | 208 | 3,402 | 0 | false | NMR studies of the interaction of τC16Δ11 with α yielded a dissociation constant of ∼0.9 mM (61), indicating that additional binding residues are located within the structured portion near the end of helix 6. | [] | NMR studies of the interaction of τC16Δ11 with α yielded a dissociation constant of ∼0.9 mM (61), indicating that additional binding residues are located within the structured portion near the end of helix 6. | true | true | true | true | true | 582 |
3 | DISCUSSION | 1 | 38 | [
"B38",
"B62",
"B63"
] | 17,355,988 | pmid-1918087|pmid-7768938|pmid-1918087|pmid-8702819|pmid-7768940|pmid-12620221|pmid-14630952|pmid-14630952|pmid-12620221|pmid-16959568|pmid-16959569 | Two structures of α, from different bacteria, have recently been reported (62,63). | [
"38",
"62",
"63"
] | 82 | 3,403 | 0 | false | Two structures of α, from different bacteria, have recently been reported. | [
"62,63"
] | Two structures of α, from different bacteria, have recently been reported. | true | true | true | true | true | 582 |
3 | DISCUSSION | 1 | 38 | [
"B38",
"B62",
"B63"
] | 17,355,988 | pmid-1918087|pmid-7768938|pmid-1918087|pmid-8702819|pmid-7768940|pmid-12620221|pmid-14630952|pmid-14630952|pmid-12620221|pmid-16959568|pmid-16959569 | Since τC16 is expected to be bound close to the C-terminus of α due to its close proximity to the β2 sliding clamp that binds in this region, one could speculate that the incipient additional helix 7 binds in a C-terminal cleft in α. | [
"38",
"62",
"63"
] | 233 | 3,404 | 0 | false | Since τC16 is expected to be bound close to the C-terminus of α due to its close proximity to the β2 sliding clamp that binds in this region, one could speculate that the incipient additional helix 7 binds in a C-terminal cleft in α. | [] | Since τC16 is expected to be bound close to the C-terminus of α due to its close proximity to the β2 sliding clamp that binds in this region, one could speculate that the incipient additional helix 7 binds in a C-terminal cleft in α. | true | true | true | true | true | 582 |
4 | DISCUSSION | 0 | null | null | 17,355,988 | pmid-11078743|pmid-12620221|pmid-10748120|pmid-12620221|pmid-14630952|pmid-11078744|pmid-11078743|NA|NA|pmid-16505960|NA|pmid-8744573 | Of the remaining mutants examined, the D636G change had a modest effect on α binding (ΔΔG° = 1.9 kcal/mol) while F631I resulted in a much weaker interaction (3.8 kcal/mol). | null | 172 | 3,405 | 0 | false | null | null | Of the remaining mutants examined, the D636G change had a modest effect on α binding (ΔΔG° = 1.9 kcal/mol) while F631I resulted in a much weaker interaction (3.8 kcal/mol). | true | true | true | true | true | 583 |
4 | DISCUSSION | 0 | null | null | 17,355,988 | pmid-11078743|pmid-12620221|pmid-10748120|pmid-12620221|pmid-14630952|pmid-11078744|pmid-11078743|NA|NA|pmid-16505960|NA|pmid-8744573 | Consistent with these data, Asp636 is not highly conserved while Phe631 is, and since isoleucine is a helix-breaking residue, the F631I mutation would be expected to disrupt the proposed helical structure in this region. | null | 220 | 3,406 | 0 | false | null | null | Consistent with these data, Asp636 is not highly conserved while Phe631 is, and since isoleucine is a helix-breaking residue, the F631I mutation would be expected to disrupt the proposed helical structure in this region. | true | true | true | true | true | 583 |
5 | DISCUSSION | 1 | 40 | [
"B40",
"B43"
] | 17,355,988 | NA|NA|pmid-16505960|NA|pmid-8744573|pmid-11078743|NA | Study of the single point mutants (Table 1) revealed that no single amino acid change is sufficient to completely disrupt the α–τ interaction, presumably because the interactions at the interface involve a series of residues located in an otherwise flexible segment of τ. | [
"40",
"43"
] | 271 | 3,407 | 0 | false | Study of the single point mutants (Table 1) revealed that no single amino acid change is sufficient to completely disrupt the α–τ interaction, presumably because the interactions at the interface involve a series of residues located in an otherwise flexible segment of τ. | [] | Study of the single point mutants (Table 1) revealed that no single amino acid change is sufficient to completely disrupt the α–τ interaction, presumably because the interactions at the interface involve a series of residues located in an otherwise flexible segment of τ. | true | true | true | true | true | 584 |
5 | DISCUSSION | 1 | 40 | [
"B40",
"B43"
] | 17,355,988 | NA|NA|pmid-16505960|NA|pmid-8744573|pmid-11078743|NA | Finally, we note that although no single point mutation was identified in the last seven amino acids of τC16, complete removal of this segment (in τC16Δ7; Figure 1B) had a large effect of binding of α (ΔΔG° = 6.3 kcal/mol). | [
"40",
"43"
] | 223 | 3,408 | 0 | false | Finally, we note that although no single point mutation was identified in the last seven amino acids of τC16, complete removal of this segment (in τC16Δ7; Figure 1B) had a large effect of binding of α (ΔΔG° = 6.3 kcal/mol). | [] | Finally, we note that although no single point mutation was identified in the last seven amino acids of τC16, complete removal of this segment (in τC16Δ7; Figure 1B) had a large effect of binding of α (ΔΔG° = 6.3 kcal/mol). | true | true | true | true | true | 584 |
5 | DISCUSSION | 1 | 40 | [
"B40",
"B43"
] | 17,355,988 | NA|NA|pmid-16505960|NA|pmid-8744573|pmid-11078743|NA | There must therefore be further contacts with this region in the complex with α. | [
"40",
"43"
] | 80 | 3,409 | 0 | false | There must therefore be further contacts with this region in the complex with α. | [] | There must therefore be further contacts with this region in the complex with α. | true | true | true | true | true | 584 |
5 | DISCUSSION | 1 | 40 | [
"B40",
"B43"
] | 17,355,988 | NA|NA|pmid-16505960|NA|pmid-8744573|pmid-11078743|NA | Indeed, extension of this region in full-length τ by fusion of a biotin-tag sequence also disrupts the interaction (40). | [
"40",
"43"
] | 120 | 3,410 | 1 | false | Indeed, extension of this region in full-length τ by fusion of a biotin-tag sequence also disrupts the interaction. | [
"40"
] | Indeed, extension of this region in full-length τ by fusion of a biotin-tag sequence also disrupts the interaction. | true | true | true | true | true | 584 |
5 | DISCUSSION | 1 | 43 | [
"B40",
"B43"
] | 17,355,988 | NA|NA|pmid-16505960|NA|pmid-8744573|pmid-11078743|NA | NMR studies (43) similarly suggest that all determinants in τC16 required for binding to α likely reside towards the end of helix 6 and in the following unstructured 26-residue segment that we propose to become structured on α binding. | [
"40",
"43"
] | 235 | 3,411 | 1 | false | NMR studies similarly suggest that all determinants in τC16 required for binding to α likely reside towards the end of helix 6 and in the following unstructured 26-residue segment that we propose to become structured on α binding. | [
"43"
] | NMR studies similarly suggest that all determinants in τC16 required for binding to α likely reside towards the end of helix 6 and in the following unstructured 26-residue segment that we propose to become structured on α binding. | true | true | true | true | true | 584 |
6 | DISCUSSION | 1 | 4–7 | [
"B4 B5 B6 B7"
] | 17,355,988 | NA|NA|pmid-16505960|pmid-16036556|pmid-15952889|pmid-16421093|pmid-16857582 | The DnaB helicase interacts with Domain IV of τ, a region that immediately precedes helix 1 in the structure of τC14 (Figure 1) and an α subunit interacts with the extension of helix 6 of the τC14 domain in each of the two τ subunits in the clamp loader complex in the replisome (4–7). | [
"4–7"
] | 285 | 3,412 | 1 | false | The DnaB helicase interacts with Domain IV of τ, a region that immediately precedes helix 1 in the structure of τC14 (Figure 1) and an α subunit interacts with the extension of helix 6 of the τC14 domain in each of the two τ subunits in the clamp loader complex in the replisome. | [
"4–7"
] | The DnaB helicase interacts with Domain IV of τ, a region that immediately precedes helix 1 in the structure of τC14 (Figure 1) and an α subunit interacts with the extension of helix 6 of the τC14 domain in each of the two τ subunits in the clamp loader complex in the replisome. | true | true | true | true | true | 585 |
6 | DISCUSSION | 1 | 4–7 | [
"B4 B5 B6 B7"
] | 17,355,988 | NA|NA|pmid-16505960|pmid-16036556|pmid-15952889|pmid-16421093|pmid-16857582 | This places restraints on the α–DnaB and α–α distances that need to be considered once there is sufficient information to build models of the structure of the replisome in its various functional states. | [
"4–7"
] | 202 | 3,413 | 0 | false | This places restraints on the α–DnaB and α–α distances that need to be considered once there is sufficient information to build models of the structure of the replisome in its various functional states. | [] | This places restraints on the α–DnaB and α–α distances that need to be considered once there is sufficient information to build models of the structure of the replisome in its various functional states. | true | true | true | true | true | 585 |
7 | DISCUSSION | 1 | 6 | [
"B6",
"B7",
"B38",
"B39",
"B40",
"B43"
] | 17,355,988 | pmid-16505960|pmid-16421093|pmid-16857582|pmid-12620221|pmid-14630952|pmid-11078743|NA | The DNA-binding properties of τC24 place further structural restraints. | [
"6",
"7",
"38",
"39",
"40",
"43"
] | 71 | 3,414 | 0 | false | The DNA-binding properties of τC24 place further structural restraints. | [] | The DNA-binding properties of τC24 place further structural restraints. | true | true | true | true | true | 586 |
7 | DISCUSSION | 1 | 6 | [
"B6",
"B7",
"B38",
"B39",
"B40",
"B43"
] | 17,355,988 | pmid-16505960|pmid-16421093|pmid-16857582|pmid-12620221|pmid-14630952|pmid-11078743|NA | The τ subunit is known to house a DNA-sensing function that leads to active detachment of α from the β2 clamp when the last nucleotide of an Okazaki fragment on the lagging strand is incorporated, resulting in the processivity switch (6,7,38). | [
"6",
"7",
"38",
"39",
"40",
"43"
] | 243 | 3,415 | 0 | false | The τ subunit is known to house a DNA-sensing function that leads to active detachment of α from the β2 clamp when the last nucleotide of an Okazaki fragment on the lagging strand is incorporated, resulting in the processivity switch. | [
"6,7,38"
] | The τ subunit is known to house a DNA-sensing function that leads to active detachment of α from the β2 clamp when the last nucleotide of an Okazaki fragment on the lagging strand is incorporated, resulting in the processivity switch. | true | true | true | true | true | 586 |
7 | DISCUSSION | 1 | 6 | [
"B6",
"B7",
"B38",
"B39",
"B40",
"B43"
] | 17,355,988 | pmid-16505960|pmid-16421093|pmid-16857582|pmid-12620221|pmid-14630952|pmid-11078743|NA | Further, it was shown that Domain IVa + | [
"6",
"7",
"38",
"39",
"40",
"43"
] | 39 | 3,416 | 0 | false | Further, it was shown that Domain IVa + | [] | Further, it was shown that Domain IVa + | true | true | false | true | false | 586 |
7 | DISCUSSION | 1 | 39 | [
"B6",
"B7",
"B38",
"B39",
"B40",
"B43"
] | 17,355,988 | pmid-16505960|pmid-16421093|pmid-16857582|pmid-12620221|pmid-14630952|pmid-11078743|NA | V of τ (τC24) senses a primed template structure, resulting in lowering of its affinity for the C-terminal region of α (39). | [
"6",
"7",
"38",
"39",
"40",
"43"
] | 124 | 3,417 | 1 | false | V of τ (τC24) senses a primed template structure, resulting in lowering of its affinity for the C-terminal region of α. | [
"39"
] | V of τ (τC24) senses a primed template structure, resulting in lowering of its affinity for the C-terminal region of α. | true | true | true | true | true | 586 |
7 | DISCUSSION | 1 | 6 | [
"B6",
"B7",
"B38",
"B39",
"B40",
"B43"
] | 17,355,988 | pmid-16505960|pmid-16421093|pmid-16857582|pmid-12620221|pmid-14630952|pmid-11078743|NA | Although we have shown that the highly basic Domain IVa region of τC24 interacts with DNA, we have been unable to confirm under our experimental conditions that it binds primer-template DNA with high affinity or significant specificity. | [
"6",
"7",
"38",
"39",
"40",
"43"
] | 236 | 3,418 | 0 | false | Although we have shown that the highly basic Domain IVa region of τC24 interacts with DNA, we have been unable to confirm under our experimental conditions that it binds primer-template DNA with high affinity or significant specificity. | [] | Although we have shown that the highly basic Domain IVa region of τC24 interacts with DNA, we have been unable to confirm under our experimental conditions that it binds primer-template DNA with high affinity or significant specificity. | true | true | true | true | true | 586 |
7 | DISCUSSION | 1 | 40 | [
"B6",
"B7",
"B38",
"B39",
"B40",
"B43"
] | 17,355,988 | pmid-16505960|pmid-16421093|pmid-16857582|pmid-12620221|pmid-14630952|pmid-11078743|NA | Domain IV has previously been shown not to contribute directly to α binding (40). | [
"6",
"7",
"38",
"39",
"40",
"43"
] | 81 | 3,419 | 1 | false | Domain IV has previously been shown not to contribute directly to α binding. | [
"40"
] | Domain IV has previously been shown not to contribute directly to α binding. | true | true | true | true | true | 586 |
7 | DISCUSSION | 1 | 43 | [
"B6",
"B7",
"B38",
"B39",
"B40",
"B43"
] | 17,355,988 | pmid-16505960|pmid-16421093|pmid-16857582|pmid-12620221|pmid-14630952|pmid-11078743|NA | Considering the close proximity of the N- and C-terminal helices in the globular fold of Domain V (43), the DNA-binding Domain IV may readily interact with the α-binding site of τ to regulate the α–β2 interaction when Domain IV senses changes in DNA structure. | [
"6",
"7",
"38",
"39",
"40",
"43"
] | 260 | 3,420 | 1 | false | Considering the close proximity of the N- and C-terminal helices in the globular fold of Domain V, the DNA-binding Domain IV may readily interact with the α-binding site of τ to regulate the α–β2 interaction when Domain IV senses changes in DNA structure. | [
"43"
] | Considering the close proximity of the N- and C-terminal helices in the globular fold of Domain V, the DNA-binding Domain IV may readily interact with the α-binding site of τ to regulate the α–β2 interaction when Domain IV senses changes in DNA structure. | true | true | true | true | true | 586 |
7 | DISCUSSION | 1 | 6 | [
"B6",
"B7",
"B38",
"B39",
"B40",
"B43"
] | 17,355,988 | pmid-16505960|pmid-16421093|pmid-16857582|pmid-12620221|pmid-14630952|pmid-11078743|NA | Possibly, the affinity with the lagging strand is enhanced through interaction between Domains IV and/or V in neighboring τ subunits in the clamp loader complex. | [
"6",
"7",
"38",
"39",
"40",
"43"
] | 161 | 3,421 | 0 | false | Possibly, the affinity with the lagging strand is enhanced through interaction between Domains IV and/or V in neighboring τ subunits in the clamp loader complex. | [] | Possibly, the affinity with the lagging strand is enhanced through interaction between Domains IV and/or V in neighboring τ subunits in the clamp loader complex. | true | true | true | true | true | 586 |
7 | DISCUSSION | 1 | 6 | [
"B6",
"B7",
"B38",
"B39",
"B40",
"B43"
] | 17,355,988 | pmid-16505960|pmid-16421093|pmid-16857582|pmid-12620221|pmid-14630952|pmid-11078743|NA | This would place rather severe geometric constraints on the positions of the two Pol III cores and DnaB in the replisome. | [
"6",
"7",
"38",
"39",
"40",
"43"
] | 121 | 3,422 | 0 | false | This would place rather severe geometric constraints on the positions of the two Pol III cores and DnaB in the replisome. | [] | This would place rather severe geometric constraints on the positions of the two Pol III cores and DnaB in the replisome. | true | true | true | true | true | 586 |
0 | INTRODUCTION | 1 | 1 | [
"b1",
"b2",
"b3",
"b4",
"b6",
"b7",
"b8",
"b9",
"b12",
"b13",
"b14",
"b15",
"b16",
"b17",
"b18",
"b20",
"b21",
"b22"
] | 17,135,188 | pmid-12120257|pmid-15952901|pmid-12359866|pmid-14564000|NA|pmid-12654261|pmid-15578064|pmid-15272050|pmid-16839274|pmid-15538359|pmid-16565705|pmid-2849509|pmid-2849510|pmid-1777485|pmid-8290579|pmid-10664605|pmid-15485768|pmid-16254940|pmid-9207018|pmid-15196012|pmid-15196012 | Today there is a fast growing number of nucleic acid-based strategies to modulate a vast variety of cellular functions | [
"1",
"2",
"3",
"4",
"6",
"7",
"8",
"9",
"12",
"13",
"14",
"15",
"16",
"17",
"18",
"20",
"21",
"22"
] | 118 | 3,423 | 0 | false | Today there is a fast growing number of nucleic acid-based strategies to modulate a vast variety of cellular functions | [] | Today there is a fast growing number of nucleic acid-based strategies to modulate a vast variety of cellular functions | true | true | false | true | false | 587 |
0 | INTRODUCTION | 1 | 1 | [
"b1",
"b2",
"b3",
"b4",
"b6",
"b7",
"b8",
"b9",
"b12",
"b13",
"b14",
"b15",
"b16",
"b17",
"b18",
"b20",
"b21",
"b22"
] | 17,135,188 | pmid-12120257|pmid-15952901|pmid-12359866|pmid-14564000|NA|pmid-12654261|pmid-15578064|pmid-15272050|pmid-16839274|pmid-15538359|pmid-16565705|pmid-2849509|pmid-2849510|pmid-1777485|pmid-8290579|pmid-10664605|pmid-15485768|pmid-16254940|pmid-9207018|pmid-15196012|pmid-15196012 | [for a review see: (1)]. | [
"1",
"2",
"3",
"4",
"6",
"7",
"8",
"9",
"12",
"13",
"14",
"15",
"16",
"17",
"18",
"20",
"21",
"22"
] | 24 | 3,424 | 0 | false | . | [
"for a review see: (1)"
] | . | false | false | true | true | false | 587 |
0 | INTRODUCTION | 1 | 1 | [
"b1",
"b2",
"b3",
"b4",
"b6",
"b7",
"b8",
"b9",
"b12",
"b13",
"b14",
"b15",
"b16",
"b17",
"b18",
"b20",
"b21",
"b22"
] | 17,135,188 | pmid-12120257|pmid-15952901|pmid-12359866|pmid-14564000|NA|pmid-12654261|pmid-15578064|pmid-15272050|pmid-16839274|pmid-15538359|pmid-16565705|pmid-2849509|pmid-2849510|pmid-1777485|pmid-8290579|pmid-10664605|pmid-15485768|pmid-16254940|pmid-9207018|pmid-15196012|pmid-15196012 | Several classes of oligonucleotides like aptamers, transcription factor-binding decoy oligonucleotides, ribozymes, triplex-forming oligonucleotides, immunostimulatory CpG motifs, antisense oligonucleotides (including peptide nucleic acids), small interfering RNAs (siRNAs) and microRNAs have attained much interest as a ... | [
"1",
"2",
"3",
"4",
"6",
"7",
"8",
"9",
"12",
"13",
"14",
"15",
"16",
"17",
"18",
"20",
"21",
"22"
] | 380 | 3,425 | 0 | false | Several classes of oligonucleotides like aptamers, transcription factor-binding decoy oligonucleotides, ribozymes, triplex-forming oligonucleotides, immunostimulatory CpG motifs, antisense oligonucleotides (including peptide nucleic acids), small interfering RNAs (siRNAs) and microRNAs have attained much interest as a ... | [] | Several classes of oligonucleotides like aptamers, transcription factor-binding decoy oligonucleotides, ribozymes, triplex-forming oligonucleotides, immunostimulatory CpG motifs, antisense oligonucleotides (including peptide nucleic acids), small interfering RNAs (siRNAs) and microRNAs have attained much interest as a ... | true | true | true | true | true | 587 |
0 | INTRODUCTION | 1 | 1 | [
"b1",
"b2",
"b3",
"b4",
"b6",
"b7",
"b8",
"b9",
"b12",
"b13",
"b14",
"b15",
"b16",
"b17",
"b18",
"b20",
"b21",
"b22"
] | 17,135,188 | pmid-12120257|pmid-15952901|pmid-12359866|pmid-14564000|NA|pmid-12654261|pmid-15578064|pmid-15272050|pmid-16839274|pmid-15538359|pmid-16565705|pmid-2849509|pmid-2849510|pmid-1777485|pmid-8290579|pmid-10664605|pmid-15485768|pmid-16254940|pmid-9207018|pmid-15196012|pmid-15196012 | Even more important, these oligomeric nucleic acids do have a considerable potential to be used as therapeutics. | [
"1",
"2",
"3",
"4",
"6",
"7",
"8",
"9",
"12",
"13",
"14",
"15",
"16",
"17",
"18",
"20",
"21",
"22"
] | 112 | 3,426 | 0 | false | Even more important, these oligomeric nucleic acids do have a considerable potential to be used as therapeutics. | [] | Even more important, these oligomeric nucleic acids do have a considerable potential to be used as therapeutics. | true | true | true | true | true | 587 |
0 | INTRODUCTION | 1 | 1 | [
"b1",
"b2",
"b3",
"b4",
"b6",
"b7",
"b8",
"b9",
"b12",
"b13",
"b14",
"b15",
"b16",
"b17",
"b18",
"b20",
"b21",
"b22"
] | 17,135,188 | pmid-12120257|pmid-15952901|pmid-12359866|pmid-14564000|NA|pmid-12654261|pmid-15578064|pmid-15272050|pmid-16839274|pmid-15538359|pmid-16565705|pmid-2849509|pmid-2849510|pmid-1777485|pmid-8290579|pmid-10664605|pmid-15485768|pmid-16254940|pmid-9207018|pmid-15196012|pmid-15196012 | However, the bottleneck of any nucleic acid-based strategy remains the cellular delivery of these macromolecules. | [
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0 | INTRODUCTION | 1 | 1 | [
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0 | INTRODUCTION | 1 | 1 | [
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"b16",
"b17",
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0 | INTRODUCTION | 1 | 1 | [
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"b17",
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0 | INTRODUCTION | 1 | 1 | [
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"b8",
"b9",
"b12",
"b13",
"b14",
"b15",
"b16",
"b17",
"b18",
"b20",
"b21",
"b22"
] | 17,135,188 | pmid-12120257|pmid-15952901|pmid-12359866|pmid-14564000|NA|pmid-12654261|pmid-15578064|pmid-15272050|pmid-16839274|pmid-15538359|pmid-16565705|pmid-2849509|pmid-2849510|pmid-1777485|pmid-8290579|pmid-10664605|pmid-15485768|pmid-16254940|pmid-9207018|pmid-15196012|pmid-15196012 | There is general consent that viral vector systems are the most efficient vehicles to deliver nucleic acids into cells. | [
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] | 119 | 3,431 | 0 | false | There is general consent that viral vector systems are the most efficient vehicles to deliver nucleic acids into cells. | [] | There is general consent that viral vector systems are the most efficient vehicles to deliver nucleic acids into cells. | true | true | true | true | true | 587 |
0 | INTRODUCTION | 1 | 1 | [
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"b16",
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"for a review see: (2,3)"
] | However, despite substantial efforts over the last 15 years, up to now research has failed to develop suitable and especially safe viral systems. | true | true | true | true | true | 587 |
0 | INTRODUCTION | 1 | 1 | [
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"b16",
"b17",
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] | 17,135,188 | pmid-12120257|pmid-15952901|pmid-12359866|pmid-14564000|NA|pmid-12654261|pmid-15578064|pmid-15272050|pmid-16839274|pmid-15538359|pmid-16565705|pmid-2849509|pmid-2849510|pmid-1777485|pmid-8290579|pmid-10664605|pmid-15485768|pmid-16254940|pmid-9207018|pmid-15196012|pmid-15196012 | On the contrary, the field has experienced several setbacks causing important clinical trials to be put on hold (4–6). | [
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"4–6"
] | On the contrary, the field has experienced several setbacks causing important clinical trials to be put on hold. | true | true | true | true | true | 587 |
0 | INTRODUCTION | 1 | 1 | [
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"b13",
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"b16",
"b17",
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] | 17,135,188 | pmid-12120257|pmid-15952901|pmid-12359866|pmid-14564000|NA|pmid-12654261|pmid-15578064|pmid-15272050|pmid-16839274|pmid-15538359|pmid-16565705|pmid-2849509|pmid-2849510|pmid-1777485|pmid-8290579|pmid-10664605|pmid-15485768|pmid-16254940|pmid-9207018|pmid-15196012|pmid-15196012 | As a result of the difficulties encountered with these viral vectors (e.g. | [
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] | 74 | 3,434 | 0 | false | As a result of the difficulties encountered with these viral vectors (e.g. | [] | As a result of the difficulties encountered with these viral vectors (e.g. | true | true | true | true | true | 587 |
0 | INTRODUCTION | 1 | 1 | [
"b1",
"b2",
"b3",
"b4",
"b6",
"b7",
"b8",
"b9",
"b12",
"b13",
"b14",
"b15",
"b16",
"b17",
"b18",
"b20",
"b21",
"b22"
] | 17,135,188 | pmid-12120257|pmid-15952901|pmid-12359866|pmid-14564000|NA|pmid-12654261|pmid-15578064|pmid-15272050|pmid-16839274|pmid-15538359|pmid-16565705|pmid-2849509|pmid-2849510|pmid-1777485|pmid-8290579|pmid-10664605|pmid-15485768|pmid-16254940|pmid-9207018|pmid-15196012|pmid-15196012 | mutagenesis and immune responses) much attention was paid to the development of allegedly safer non-viral delivery systems. | [
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] | 123 | 3,435 | 0 | false | mutagenesis and immune responses) much attention was paid to the development of allegedly safer non-viral delivery systems. | [] | mutagenesis and immune responses) much attention was paid to the development of allegedly safer non-viral delivery systems. | false | true | true | true | false | 587 |
0 | INTRODUCTION | 1 | 1 | [
"b1",
"b2",
"b3",
"b4",
"b6",
"b7",
"b8",
"b9",
"b12",
"b13",
"b14",
"b15",
"b16",
"b17",
"b18",
"b20",
"b21",
"b22"
] | 17,135,188 | pmid-12120257|pmid-15952901|pmid-12359866|pmid-14564000|NA|pmid-12654261|pmid-15578064|pmid-15272050|pmid-16839274|pmid-15538359|pmid-16565705|pmid-2849509|pmid-2849510|pmid-1777485|pmid-8290579|pmid-10664605|pmid-15485768|pmid-16254940|pmid-9207018|pmid-15196012|pmid-15196012 | This conception includes an assortment of fairly unrelated approaches yielding various degrees of enhanced cellular uptake of nucleic acids. | [
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] | 140 | 3,436 | 0 | false | This conception includes an assortment of fairly unrelated approaches yielding various degrees of enhanced cellular uptake of nucleic acids. | [] | This conception includes an assortment of fairly unrelated approaches yielding various degrees of enhanced cellular uptake of nucleic acids. | true | true | true | true | true | 587 |
0 | INTRODUCTION | 1 | 1 | [
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"b3",
"b4",
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"b7",
"b8",
"b9",
"b12",
"b13",
"b14",
"b15",
"b16",
"b17",
"b18",
"b20",
"b21",
"b22"
] | 17,135,188 | pmid-12120257|pmid-15952901|pmid-12359866|pmid-14564000|NA|pmid-12654261|pmid-15578064|pmid-15272050|pmid-16839274|pmid-15538359|pmid-16565705|pmid-2849509|pmid-2849510|pmid-1777485|pmid-8290579|pmid-10664605|pmid-15485768|pmid-16254940|pmid-9207018|pmid-15196012|pmid-15196012 | Currently, cationic lipids and polymers are used as a standard tool to transfect cells in vitro. | [
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] | 96 | 3,437 | 0 | false | Currently, cationic lipids and polymers are used as a standard tool to transfect cells in vitro. | [] | Currently, cationic lipids and polymers are used as a standard tool to transfect cells in vitro. | true | true | true | true | true | 587 |
0 | INTRODUCTION | 1 | 1 | [
"b1",
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"b7",
"b8",
"b9",
"b12",
"b13",
"b14",
"b15",
"b16",
"b17",
"b18",
"b20",
"b21",
"b22"
] | 17,135,188 | pmid-12120257|pmid-15952901|pmid-12359866|pmid-14564000|NA|pmid-12654261|pmid-15578064|pmid-15272050|pmid-16839274|pmid-15538359|pmid-16565705|pmid-2849509|pmid-2849510|pmid-1777485|pmid-8290579|pmid-10664605|pmid-15485768|pmid-16254940|pmid-9207018|pmid-15196012|pmid-15196012 | However, these approaches are commonly characterised by a significant lack of efficiency accompanied by a high level of toxicity and thus rendering them mostly inadequate for in vivo applications. | [
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] | 196 | 3,438 | 0 | false | However, these approaches are commonly characterised by a significant lack of efficiency accompanied by a high level of toxicity and thus rendering them mostly inadequate for in vivo applications. | [] | However, these approaches are commonly characterised by a significant lack of efficiency accompanied by a high level of toxicity and thus rendering them mostly inadequate for in vivo applications. | true | true | true | true | true | 587 |
0 | INTRODUCTION | 1 | 1 | [
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"b12",
"b13",
"b14",
"b15",
"b16",
"b17",
"b18",
"b20",
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"b22"
] | 17,135,188 | pmid-12120257|pmid-15952901|pmid-12359866|pmid-14564000|NA|pmid-12654261|pmid-15578064|pmid-15272050|pmid-16839274|pmid-15538359|pmid-16565705|pmid-2849509|pmid-2849510|pmid-1777485|pmid-8290579|pmid-10664605|pmid-15485768|pmid-16254940|pmid-9207018|pmid-15196012|pmid-15196012 | Nonetheless, there are a few studies reporting a successful delivery of siRNA in vivo applying cationic liposomes (7,8), atelocollagen- or PEI-complexed siRNAs (9–12) as well as cholesterol-conjugated siRNAs (13,14). | [
"1",
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"9",
"12",
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"15",
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] | 216 | 3,439 | 0 | false | Nonetheless, there are a few studies reporting a successful delivery of siRNA in vivo applying cationic liposomes, atelocollagen- or PEI-complexed siRNAs as well as cholesterol-conjugated siRNAs. | [
"7,8",
"9–12",
"13,14"
] | Nonetheless, there are a few studies reporting a successful delivery of siRNA in vivo applying cationic liposomes, atelocollagen- or PEI-complexed siRNAs as well as cholesterol-conjugated siRNAs. | true | true | true | true | true | 587 |
0 | INTRODUCTION | 1 | 1 | [
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"b2",
"b3",
"b4",
"b6",
"b7",
"b8",
"b9",
"b12",
"b13",
"b14",
"b15",
"b16",
"b17",
"b18",
"b20",
"b21",
"b22"
] | 17,135,188 | pmid-12120257|pmid-15952901|pmid-12359866|pmid-14564000|NA|pmid-12654261|pmid-15578064|pmid-15272050|pmid-16839274|pmid-15538359|pmid-16565705|pmid-2849509|pmid-2849510|pmid-1777485|pmid-8290579|pmid-10664605|pmid-15485768|pmid-16254940|pmid-9207018|pmid-15196012|pmid-15196012 | Peptides, on the other hand, acting as shuttles for a controlled cellular delivery of nucleic acids, represent a new and innovative concept to bypass the problem of poor bio-availability of these macromolecules. | [
"1",
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] | 211 | 3,440 | 0 | false | Peptides, on the other hand, acting as shuttles for a controlled cellular delivery of nucleic acids, represent a new and innovative concept to bypass the problem of poor bio-availability of these macromolecules. | [] | Peptides, on the other hand, acting as shuttles for a controlled cellular delivery of nucleic acids, represent a new and innovative concept to bypass the problem of poor bio-availability of these macromolecules. | true | true | true | true | true | 587 |
0 | INTRODUCTION | 1 | 1 | [
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"b2",
"b3",
"b4",
"b6",
"b7",
"b8",
"b9",
"b12",
"b13",
"b14",
"b15",
"b16",
"b17",
"b18",
"b20",
"b21",
"b22"
] | 17,135,188 | pmid-12120257|pmid-15952901|pmid-12359866|pmid-14564000|NA|pmid-12654261|pmid-15578064|pmid-15272050|pmid-16839274|pmid-15538359|pmid-16565705|pmid-2849509|pmid-2849510|pmid-1777485|pmid-8290579|pmid-10664605|pmid-15485768|pmid-16254940|pmid-9207018|pmid-15196012|pmid-15196012 | The idea of using peptides as carriers goes back some 18 years, when two groups discovered by chance that the HIV-1 transactivating protein Tat is taken up by mammalian cells (15,16). | [
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"8",
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"15",
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"21",
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] | 183 | 3,441 | 0 | false | The idea of using peptides as carriers goes back some 18 years, when two groups discovered by chance that the HIV-1 transactivating protein Tat is taken up by mammalian cells. | [
"15,16"
] | The idea of using peptides as carriers goes back some 18 years, when two groups discovered by chance that the HIV-1 transactivating protein Tat is taken up by mammalian cells. | true | true | true | true | true | 587 |
0 | INTRODUCTION | 1 | 17 | [
"b1",
"b2",
"b3",
"b4",
"b6",
"b7",
"b8",
"b9",
"b12",
"b13",
"b14",
"b15",
"b16",
"b17",
"b18",
"b20",
"b21",
"b22"
] | 17,135,188 | pmid-12120257|pmid-15952901|pmid-12359866|pmid-14564000|NA|pmid-12654261|pmid-15578064|pmid-15272050|pmid-16839274|pmid-15538359|pmid-16565705|pmid-2849509|pmid-2849510|pmid-1777485|pmid-8290579|pmid-10664605|pmid-15485768|pmid-16254940|pmid-9207018|pmid-15196012|pmid-15196012 | Just a few years later, the Antennapedia homeodomain of Drosophila melanogaster was shown to act similarly (17). | [
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"8",
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"12",
"13",
"14",
"15",
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"17",
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"21",
"22"
] | 112 | 3,442 | 1 | false | Just a few years later, the Antennapedia homeodomain of Drosophila melanogaster was shown to act similarly. | [
"17"
] | Just a few years later, the Antennapedia homeodomain of Drosophila melanogaster was shown to act similarly. | true | true | true | true | true | 587 |
0 | INTRODUCTION | 1 | 1 | [
"b1",
"b2",
"b3",
"b4",
"b6",
"b7",
"b8",
"b9",
"b12",
"b13",
"b14",
"b15",
"b16",
"b17",
"b18",
"b20",
"b21",
"b22"
] | 17,135,188 | pmid-12120257|pmid-15952901|pmid-12359866|pmid-14564000|NA|pmid-12654261|pmid-15578064|pmid-15272050|pmid-16839274|pmid-15538359|pmid-16565705|pmid-2849509|pmid-2849510|pmid-1777485|pmid-8290579|pmid-10664605|pmid-15485768|pmid-16254940|pmid-9207018|pmid-15196012|pmid-15196012 | Further on, it could be shown that peptides derived from Tat and Antennapedia as well as other proteins are capable of transporting macromolecular cargo molecules into cells (18–20). | [
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] | 182 | 3,443 | 0 | false | Further on, it could be shown that peptides derived from Tat and Antennapedia as well as other proteins are capable of transporting macromolecular cargo molecules into cells. | [
"18–20"
] | Further on, it could be shown that peptides derived from Tat and Antennapedia as well as other proteins are capable of transporting macromolecular cargo molecules into cells. | true | true | true | true | true | 587 |
0 | INTRODUCTION | 1 | 1 | [
"b1",
"b2",
"b3",
"b4",
"b6",
"b7",
"b8",
"b9",
"b12",
"b13",
"b14",
"b15",
"b16",
"b17",
"b18",
"b20",
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] | 17,135,188 | pmid-12120257|pmid-15952901|pmid-12359866|pmid-14564000|NA|pmid-12654261|pmid-15578064|pmid-15272050|pmid-16839274|pmid-15538359|pmid-16565705|pmid-2849509|pmid-2849510|pmid-1777485|pmid-8290579|pmid-10664605|pmid-15485768|pmid-16254940|pmid-9207018|pmid-15196012|pmid-15196012 | Based on such promising results, a rapidly expanding field focusing on the so-called cell-penetrating peptides (CPPs) began to develop. | [
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] | 135 | 3,444 | 0 | false | Based on such promising results, a rapidly expanding field focusing on the so-called cell-penetrating peptides (CPPs) began to develop. | [] | Based on such promising results, a rapidly expanding field focusing on the so-called cell-penetrating peptides (CPPs) began to develop. | true | true | true | true | true | 587 |
0 | INTRODUCTION | 1 | 1 | [
"b1",
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"1",
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] | 195 | 3,445 | 0 | false | Up to now numerous additional peptides have been reported to show cell-penetrating properties and many of them have been used to successfully deliver a variety of macromolecular cargos into cells | [] | Up to now numerous additional peptides have been reported to show cell-penetrating properties and many of them have been used to successfully deliver a variety of macromolecular cargos into cells | true | true | false | true | false | 587 |
0 | INTRODUCTION | 1 | 1 | [
"b1",
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"b8",
"b9",
"b12",
"b13",
"b14",
"b15",
"b16",
"b17",
"b18",
"b20",
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] | 17,135,188 | pmid-12120257|pmid-15952901|pmid-12359866|pmid-14564000|NA|pmid-12654261|pmid-15578064|pmid-15272050|pmid-16839274|pmid-15538359|pmid-16565705|pmid-2849509|pmid-2849510|pmid-1777485|pmid-8290579|pmid-10664605|pmid-15485768|pmid-16254940|pmid-9207018|pmid-15196012|pmid-15196012 | [for a review see: (21,22)]. | [
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] | 28 | 3,446 | 0 | false | . | [
"for a review see: (21,22)"
] | . | false | false | true | true | false | 587 |
1 | INTRODUCTION | 1 | 23 | [
"b23",
"b24",
"b26"
] | 17,135,188 | pmid-16305500|pmid-9207018|pmid-11024364|pmid-12888501|pmid-12054897|NA|pmid-15386618|pmid-15576677 | For all the sequence diversity, CPPs share some common features beside their ability to cross biological membranes: (i) a high content of basic amino acids, and (ii) a length of 10–30 residues. | [
"23",
"24",
"26"
] | 193 | 3,447 | 0 | false | For all the sequence diversity, CPPs share some common features beside their ability to cross biological membranes: (i) a high content of basic amino acids, and (ii) a length of 10–30 residues. | [] | For all the sequence diversity, CPPs share some common features beside their ability to cross biological membranes: (i) a high content of basic amino acids, and (ii) a length of 10–30 residues. | true | true | true | true | true | 588 |
1 | INTRODUCTION | 1 | 23 | [
"b23",
"b24",
"b26"
] | 17,135,188 | pmid-16305500|pmid-9207018|pmid-11024364|pmid-12888501|pmid-12054897|NA|pmid-15386618|pmid-15576677 | Two strategies are utilised for the attachment of cargo molecules. | [
"23",
"24",
"26"
] | 66 | 3,448 | 0 | false | Two strategies are utilised for the attachment of cargo molecules. | [] | Two strategies are utilised for the attachment of cargo molecules. | true | true | true | true | true | 588 |
1 | INTRODUCTION | 1 | 23 | [
"b23",
"b24",
"b26"
] | 17,135,188 | pmid-16305500|pmid-9207018|pmid-11024364|pmid-12888501|pmid-12054897|NA|pmid-15386618|pmid-15576677 | By far the majority of studies include a covalent attachment of carrier and cargo | [
"23",
"24",
"26"
] | 81 | 3,449 | 0 | false | By far the majority of studies include a covalent attachment of carrier and cargo | [] | By far the majority of studies include a covalent attachment of carrier and cargo | true | true | false | true | false | 588 |
1 | INTRODUCTION | 1 | 23 | [
"b23",
"b24",
"b26"
] | 17,135,188 | pmid-16305500|pmid-9207018|pmid-11024364|pmid-12888501|pmid-12054897|NA|pmid-15386618|pmid-15576677 | [for a review see: (23)]. | [
"23",
"24",
"26"
] | 25 | 3,450 | 0 | false | . | [
"for a review see: (23)"
] | . | false | false | true | true | false | 588 |
1 | INTRODUCTION | 1 | 23 | [
"b23",
"b24",
"b26"
] | 17,135,188 | pmid-16305500|pmid-9207018|pmid-11024364|pmid-12888501|pmid-12054897|NA|pmid-15386618|pmid-15576677 | This approach might be effective for a specific application (e.g. | [
"23",
"24",
"26"
] | 65 | 3,451 | 0 | false | This approach might be effective for a specific application (e.g. | [] | This approach might be effective for a specific application (e.g. | true | true | true | true | true | 588 |
1 | INTRODUCTION | 1 | 23 | [
"b23",
"b24",
"b26"
] | 17,135,188 | pmid-16305500|pmid-9207018|pmid-11024364|pmid-12888501|pmid-12054897|NA|pmid-15386618|pmid-15576677 | a particular nucleic acid cargo), but it is fairly limited in terms of flexibility, as a new construct has to be generated for any given nucleic acid cargo. | [
"23",
"24",
"26"
] | 156 | 3,452 | 0 | false | a particular nucleic acid cargo), but it is fairly limited in terms of flexibility, as a new construct has to be generated for any given nucleic acid cargo. | [] | a particular nucleic acid cargo), but it is fairly limited in terms of flexibility, as a new construct has to be generated for any given nucleic acid cargo. | false | true | true | true | false | 588 |
1 | INTRODUCTION | 1 | 23 | [
"b23",
"b24",
"b26"
] | 17,135,188 | pmid-16305500|pmid-9207018|pmid-11024364|pmid-12888501|pmid-12054897|NA|pmid-15386618|pmid-15576677 | Alternatively, the positive charges of certain amphipathic CPPs can be exploited to bind anionic cargo molecules like nucleic acids non-covalently via ionic interactions (24–26). | [
"23",
"24",
"26"
] | 178 | 3,453 | 0 | false | Alternatively, the positive charges of certain amphipathic CPPs can be exploited to bind anionic cargo molecules like nucleic acids non-covalently via ionic interactions. | [
"24–26"
] | Alternatively, the positive charges of certain amphipathic CPPs can be exploited to bind anionic cargo molecules like nucleic acids non-covalently via ionic interactions. | true | true | true | true | true | 588 |
1 | INTRODUCTION | 1 | 23 | [
"b23",
"b24",
"b26"
] | 17,135,188 | pmid-16305500|pmid-9207018|pmid-11024364|pmid-12888501|pmid-12054897|NA|pmid-15386618|pmid-15576677 | Additional hydrophobic peptide/peptide interactions then drive the maturation of nanoparticles in a sandwich-like assembly reaction. | [
"23",
"24",
"26"
] | 132 | 3,454 | 0 | false | Additional hydrophobic peptide/peptide interactions then drive the maturation of nanoparticles in a sandwich-like assembly reaction. | [] | Additional hydrophobic peptide/peptide interactions then drive the maturation of nanoparticles in a sandwich-like assembly reaction. | true | true | true | true | true | 588 |
1 | INTRODUCTION | 1 | 23 | [
"b23",
"b24",
"b26"
] | 17,135,188 | pmid-16305500|pmid-9207018|pmid-11024364|pmid-12888501|pmid-12054897|NA|pmid-15386618|pmid-15576677 | As a result, such a CPP can in principle be combined with any given oligonucleotide. | [
"23",
"24",
"26"
] | 84 | 3,455 | 0 | false | As a result, such a CPP can in principle be combined with any given oligonucleotide. | [] | As a result, such a CPP can in principle be combined with any given oligonucleotide. | true | true | true | true | true | 588 |
2 | INTRODUCTION | 1 | 27 | [
"b27",
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"b50",
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] | 17,135,188 | pmid-9111037|pmid-15907190|pmid-12134943|pmid-16377019|pmid-12771197|pmid-16321967|pmid-15907190|pmid-9438412|pmid-16516138|pmid-12621426|pmid-15687999|pmid-15640444|pmid-15203910|pmid-15935328|pmid-15035618|pmid-15859953|pmid-11856307|pmid-15687490|pmid-12411431|pmid-15653149|pmid-3035599|pmid-11711547|pmid-15628847|p... | For many CPPs, the initial interaction with cells is supposed to be mediated by negatively charged glycosaminoglycan (GAG) receptors of the extracellular matrix, e.g. | [
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2 | INTRODUCTION | 1 | 27 | [
"b27",
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] | 39 | 3,457 | 0 | false | heparan sulphate proteoglycans. | [
"27–33"
] | heparan sulphate proteoglycans. | false | true | true | true | false | 589 |
2 | INTRODUCTION | 1 | 27 | [
"b27",
"b33",
"b34",
"b38",
"b39",
"b45",
"b33",
"b46",
"b49",
"b50",
"b51",
"b37",
"b52",
"b54",
"b41",
"b53",
"b55",
"b56"
] | 17,135,188 | pmid-9111037|pmid-15907190|pmid-12134943|pmid-16377019|pmid-12771197|pmid-16321967|pmid-15907190|pmid-9438412|pmid-16516138|pmid-12621426|pmid-15687999|pmid-15640444|pmid-15203910|pmid-15935328|pmid-15035618|pmid-15859953|pmid-11856307|pmid-15687490|pmid-12411431|pmid-15653149|pmid-3035599|pmid-11711547|pmid-15628847|p... | However, the mechanisms underlying the cellular translocation of CPPs are poorly understood and subject to controversial discussions. | [
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"49",
"50",
"51",
"37",
"52",
"54",
"41",
"53",
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] | 133 | 3,458 | 0 | false | However, the mechanisms underlying the cellular translocation of CPPs are poorly understood and subject to controversial discussions. | [] | However, the mechanisms underlying the cellular translocation of CPPs are poorly understood and subject to controversial discussions. | true | true | true | true | true | 589 |
2 | INTRODUCTION | 1 | 27 | [
"b27",
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"b50",
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"b52",
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] | 119 | 3,459 | 0 | false | Nonetheless, there is considerable evidence that for many CPPs endocytosis is a major route of internalisation. | [
"34–38"
] | Nonetheless, there is considerable evidence that for many CPPs endocytosis is a major route of internalisation. | true | true | true | true | true | 589 |
2 | INTRODUCTION | 1 | 27 | [
"b27",
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"b34",
"b38",
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"b50",
"b51",
"b37",
"b52",
"b54",
"b41",
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] | 17,135,188 | pmid-9111037|pmid-15907190|pmid-12134943|pmid-16377019|pmid-12771197|pmid-16321967|pmid-15907190|pmid-9438412|pmid-16516138|pmid-12621426|pmid-15687999|pmid-15640444|pmid-15203910|pmid-15935328|pmid-15035618|pmid-15859953|pmid-11856307|pmid-15687490|pmid-12411431|pmid-15653149|pmid-3035599|pmid-11711547|pmid-15628847|p... | On the other hand, there are examples in the literature proposing a direct penetration of the cell membrane independent of any endocytotic pathway (39–45), while others suggest both entry routes are used in parallel or under certain conditions (33,46–49). | [
"27",
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"37",
"52",
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] | 255 | 3,460 | 0 | false | On the other hand, there are examples in the literature proposing a direct penetration of the cell membrane independent of any endocytotic pathway, while others suggest both entry routes are used in parallel or under certain conditions. | [
"39–45",
"33,46–49"
] | On the other hand, there are examples in the literature proposing a direct penetration of the cell membrane independent of any endocytotic pathway, while others suggest both entry routes are used in parallel or under certain conditions. | true | true | true | true | true | 589 |
2 | INTRODUCTION | 1 | 27 | [
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"b38",
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"b49",
"b50",
"b51",
"b37",
"b52",
"b54",
"b41",
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] | 17,135,188 | pmid-9111037|pmid-15907190|pmid-12134943|pmid-16377019|pmid-12771197|pmid-16321967|pmid-15907190|pmid-9438412|pmid-16516138|pmid-12621426|pmid-15687999|pmid-15640444|pmid-15203910|pmid-15935328|pmid-15035618|pmid-15859953|pmid-11856307|pmid-15687490|pmid-12411431|pmid-15653149|pmid-3035599|pmid-11711547|pmid-15628847|p... | Furthermore, as at least four basic routes of endocytosis can be distinguished to date (50,51), it seems reasonable to speculate about multiple pathways involved in cellular entry of CPPs. | [
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] | 188 | 3,461 | 0 | false | Furthermore, as at least four basic routes of endocytosis can be distinguished to date, it seems reasonable to speculate about multiple pathways involved in cellular entry of CPPs. | [
"50,51"
] | Furthermore, as at least four basic routes of endocytosis can be distinguished to date, it seems reasonable to speculate about multiple pathways involved in cellular entry of CPPs. | true | true | true | true | true | 589 |
2 | INTRODUCTION | 1 | 27 | [
"b27",
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] | 194 | 3,462 | 0 | false | Then again, currently available data are based on studies using a variety of different cell lines and techniques, which renders a direct comparison of different approaches impossible. | [
"37,52–54"
] | Then again, currently available data are based on studies using a variety of different cell lines and techniques, which renders a direct comparison of different approaches impossible. | true | true | true | true | true | 589 |
2 | INTRODUCTION | 1 | 27 | [
"b27",
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] | 17,135,188 | pmid-9111037|pmid-15907190|pmid-12134943|pmid-16377019|pmid-12771197|pmid-16321967|pmid-15907190|pmid-9438412|pmid-16516138|pmid-12621426|pmid-15687999|pmid-15640444|pmid-15203910|pmid-15935328|pmid-15035618|pmid-15859953|pmid-11856307|pmid-15687490|pmid-12411431|pmid-15653149|pmid-3035599|pmid-11711547|pmid-15628847|p... | It has been shown that even minor changes of the physical state of a CPP (e.g. | [
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] | 78 | 3,463 | 0 | false | It has been shown that even minor changes of the physical state of a CPP (e.g. | [] | It has been shown that even minor changes of the physical state of a CPP (e.g. | true | true | true | true | true | 589 |
2 | INTRODUCTION | 1 | 27 | [
"b27",
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] | 90 | 3,464 | 0 | false | exchange of certain amino acids) can alter translocation properties significantly. | [
"41,53"
] | exchange of certain amino acids) can alter translocation properties significantly. | false | true | true | true | false | 589 |
2 | INTRODUCTION | 1 | 27 | [
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"b55",
"b56"
] | 17,135,188 | pmid-9111037|pmid-15907190|pmid-12134943|pmid-16377019|pmid-12771197|pmid-16321967|pmid-15907190|pmid-9438412|pmid-16516138|pmid-12621426|pmid-15687999|pmid-15640444|pmid-15203910|pmid-15935328|pmid-15035618|pmid-15859953|pmid-11856307|pmid-15687490|pmid-12411431|pmid-15653149|pmid-3035599|pmid-11711547|pmid-15628847|p... | This particularly holds true for the attachment of large cargo molecules (55,56). | [
"27",
"33",
"34",
"38",
"39",
"45",
"33",
"46",
"49",
"50",
"51",
"37",
"52",
"54",
"41",
"53",
"55",
"56"
] | 81 | 3,465 | 0 | false | This particularly holds true for the attachment of large cargo molecules. | [
"55,56"
] | This particularly holds true for the attachment of large cargo molecules. | true | true | true | true | true | 589 |
2 | INTRODUCTION | 1 | 27 | [
"b27",
"b33",
"b34",
"b38",
"b39",
"b45",
"b33",
"b46",
"b49",
"b50",
"b51",
"b37",
"b52",
"b54",
"b41",
"b53",
"b55",
"b56"
] | 17,135,188 | pmid-9111037|pmid-15907190|pmid-12134943|pmid-16377019|pmid-12771197|pmid-16321967|pmid-15907190|pmid-9438412|pmid-16516138|pmid-12621426|pmid-15687999|pmid-15640444|pmid-15203910|pmid-15935328|pmid-15035618|pmid-15859953|pmid-11856307|pmid-15687490|pmid-12411431|pmid-15653149|pmid-3035599|pmid-11711547|pmid-15628847|p... | Thus, it might not be possible to generalise results obtained with a given CPP, and it might be necessary to characterise each carrier/cargo complex individually. | [
"27",
"33",
"34",
"38",
"39",
"45",
"33",
"46",
"49",
"50",
"51",
"37",
"52",
"54",
"41",
"53",
"55",
"56"
] | 162 | 3,466 | 0 | false | Thus, it might not be possible to generalise results obtained with a given CPP, and it might be necessary to characterise each carrier/cargo complex individually. | [] | Thus, it might not be possible to generalise results obtained with a given CPP, and it might be necessary to characterise each carrier/cargo complex individually. | true | true | true | true | true | 589 |
2 | INTRODUCTION | 1 | 27 | [
"b27",
"b33",
"b34",
"b38",
"b39",
"b45",
"b33",
"b46",
"b49",
"b50",
"b51",
"b37",
"b52",
"b54",
"b41",
"b53",
"b55",
"b56"
] | 17,135,188 | pmid-9111037|pmid-15907190|pmid-12134943|pmid-16377019|pmid-12771197|pmid-16321967|pmid-15907190|pmid-9438412|pmid-16516138|pmid-12621426|pmid-15687999|pmid-15640444|pmid-15203910|pmid-15935328|pmid-15035618|pmid-15859953|pmid-11856307|pmid-15687490|pmid-12411431|pmid-15653149|pmid-3035599|pmid-11711547|pmid-15628847|p... | If CPPs are intended to be used for therapeutic purposes in the future, it is essential to focus on the attachment of functional cargos and analyse their biological effects inside the cell. | [
"27",
"33",
"34",
"38",
"39",
"45",
"33",
"46",
"49",
"50",
"51",
"37",
"52",
"54",
"41",
"53",
"55",
"56"
] | 189 | 3,467 | 0 | false | If CPPs are intended to be used for therapeutic purposes in the future, it is essential to focus on the attachment of functional cargos and analyse their biological effects inside the cell. | [] | If CPPs are intended to be used for therapeutic purposes in the future, it is essential to focus on the attachment of functional cargos and analyse their biological effects inside the cell. | true | true | true | true | true | 589 |
2 | INTRODUCTION | 1 | 27 | [
"b27",
"b33",
"b34",
"b38",
"b39",
"b45",
"b33",
"b46",
"b49",
"b50",
"b51",
"b37",
"b52",
"b54",
"b41",
"b53",
"b55",
"b56"
] | 17,135,188 | pmid-9111037|pmid-15907190|pmid-12134943|pmid-16377019|pmid-12771197|pmid-16321967|pmid-15907190|pmid-9438412|pmid-16516138|pmid-12621426|pmid-15687999|pmid-15640444|pmid-15203910|pmid-15935328|pmid-15035618|pmid-15859953|pmid-11856307|pmid-15687490|pmid-12411431|pmid-15653149|pmid-3035599|pmid-11711547|pmid-15628847|p... | Therefore, a quantitative comparison of the total amount of cargo taken up with functionally active cargo is an essential requirement in order to improve delivery. | [
"27",
"33",
"34",
"38",
"39",
"45",
"33",
"46",
"49",
"50",
"51",
"37",
"52",
"54",
"41",
"53",
"55",
"56"
] | 163 | 3,468 | 0 | false | Therefore, a quantitative comparison of the total amount of cargo taken up with functionally active cargo is an essential requirement in order to improve delivery. | [] | Therefore, a quantitative comparison of the total amount of cargo taken up with functionally active cargo is an essential requirement in order to improve delivery. | true | true | true | true | true | 589 |
2 | INTRODUCTION | 1 | 27 | [
"b27",
"b33",
"b34",
"b38",
"b39",
"b45",
"b33",
"b46",
"b49",
"b50",
"b51",
"b37",
"b52",
"b54",
"b41",
"b53",
"b55",
"b56"
] | 17,135,188 | pmid-9111037|pmid-15907190|pmid-12134943|pmid-16377019|pmid-12771197|pmid-16321967|pmid-15907190|pmid-9438412|pmid-16516138|pmid-12621426|pmid-15687999|pmid-15640444|pmid-15203910|pmid-15935328|pmid-15035618|pmid-15859953|pmid-11856307|pmid-15687490|pmid-12411431|pmid-15653149|pmid-3035599|pmid-11711547|pmid-15628847|p... | As a prerequisite, there is need for a sensitive method to quantify intracellular amounts of cargo in combination with sensitive and easy to handle reporter systems. | [
"27",
"33",
"34",
"38",
"39",
"45",
"33",
"46",
"49",
"50",
"51",
"37",
"52",
"54",
"41",
"53",
"55",
"56"
] | 165 | 3,469 | 0 | false | As a prerequisite, there is need for a sensitive method to quantify intracellular amounts of cargo in combination with sensitive and easy to handle reporter systems. | [] | As a prerequisite, there is need for a sensitive method to quantify intracellular amounts of cargo in combination with sensitive and easy to handle reporter systems. | true | true | true | true | true | 589 |
3 | INTRODUCTION | 1 | 24 | [
"b24",
"b57"
] | 17,135,188 | pmid-9207018|pmid-15196012|pmid-10751399|pmid-12746500|pmid-16682561 | In the present study we used the 27 amino acid peptide MPGα, a derivative of the original MPG peptide (24), as carrier for siRNA delivery. | [
"24",
"57"
] | 138 | 3,470 | 1 | false | In the present study we used the 27 amino acid peptide MPGα, a derivative of the original MPG peptide, as carrier for siRNA delivery. | [
"24"
] | In the present study we used the 27 amino acid peptide MPGα, a derivative of the original MPG peptide, as carrier for siRNA delivery. | true | true | true | true | true | 590 |
3 | INTRODUCTION | 1 | 57 | [
"b24",
"b57"
] | 17,135,188 | pmid-9207018|pmid-15196012|pmid-10751399|pmid-12746500|pmid-16682561 | The primary amphipathic peptide is composed of a hydrophobic domain, derived from the N-terminal fusion sequence of the HIV-1 glycoprotein 41, and a hydrophilic domain equivalent to the nuclear localisation sequence (NLS) of the SV40 large T antigen linked by the three amino acid spacer WSQ (57). | [
"24",
"57"
] | 297 | 3,471 | 1 | false | The primary amphipathic peptide is composed of a hydrophobic domain, derived from the N-terminal fusion sequence of the HIV-1 glycoprotein 41, and a hydrophilic domain equivalent to the nuclear localisation sequence (NLS) of the SV40 large T antigen linked by the three amino acid spacer WSQ. | [
"57"
] | The primary amphipathic peptide is composed of a hydrophobic domain, derived from the N-terminal fusion sequence of the HIV-1 glycoprotein 41, and a hydrophilic domain equivalent to the nuclear localisation sequence (NLS) of the SV40 large T antigen linked by the three amino acid spacer WSQ. | true | true | true | true | true | 590 |
3 | INTRODUCTION | 1 | 24 | [
"b24",
"b57"
] | 17,135,188 | pmid-9207018|pmid-15196012|pmid-10751399|pmid-12746500|pmid-16682561 | MPGα differs from the parent peptide by six amino acids in the hydrophobic part and is predicted to adopt a partially helical conformation. | [
"24",
"57"
] | 139 | 3,472 | 0 | false | MPGα differs from the parent peptide by six amino acids in the hydrophobic part and is predicted to adopt a partially helical conformation. | [] | MPGα differs from the parent peptide by six amino acids in the hydrophobic part and is predicted to adopt a partially helical conformation. | true | true | true | true | true | 590 |
3 | INTRODUCTION | 1 | 24 | [
"b24",
"b57"
] | 17,135,188 | pmid-9207018|pmid-15196012|pmid-10751399|pmid-12746500|pmid-16682561 | The peptide forms stable non-covalent complexes with nucleic acids in solution, which eventually assemble into nanoparticles of different sizes (S.V. | [
"24",
"57"
] | 149 | 3,473 | 0 | false | The peptide forms stable non-covalent complexes with nucleic acids in solution, which eventually assemble into nanoparticles of different sizes (S.V. | [] | The peptide forms stable non-covalent complexes with nucleic acids in solution, which eventually assemble into nanoparticles of different sizes (S.V. | true | true | true | true | true | 590 |
3 | INTRODUCTION | 1 | 24 | [
"b24",
"b57"
] | 17,135,188 | pmid-9207018|pmid-15196012|pmid-10751399|pmid-12746500|pmid-16682561 | and A.T., unpublished data). | [
"24",
"57"
] | 28 | 3,474 | 0 | false | and A.T., unpublished data). | [] | and A.T., unpublished data). | false | true | true | true | false | 590 |
3 | INTRODUCTION | 1 | 24 | [
"b24",
"b57"
] | 17,135,188 | pmid-9207018|pmid-15196012|pmid-10751399|pmid-12746500|pmid-16682561 | Utilising this model system, we provide a combination of methods for detailed quantitative analyses of peptide-mediated siRNA internalisation along with its biological effects. | [
"24",
"57"
] | 176 | 3,475 | 0 | false | Utilising this model system, we provide a combination of methods for detailed quantitative analyses of peptide-mediated siRNA internalisation along with its biological effects. | [] | Utilising this model system, we provide a combination of methods for detailed quantitative analyses of peptide-mediated siRNA internalisation along with its biological effects. | true | true | true | true | true | 590 |
3 | INTRODUCTION | 1 | 24 | [
"b24",
"b57"
] | 17,135,188 | pmid-9207018|pmid-15196012|pmid-10751399|pmid-12746500|pmid-16682561 | To the best of our knowledge, we present for the first time a detailed analysis on the number of siRNA molecules per cell required to observe half maximal inhibition of the target for peptide- versus cationic lipid-mediated delivery. | [
"24",
"57"
] | 233 | 3,476 | 0 | false | To the best of our knowledge, we present for the first time a detailed analysis on the number of siRNA molecules per cell required to observe half maximal inhibition of the target for peptide- versus cationic lipid-mediated delivery. | [] | To the best of our knowledge, we present for the first time a detailed analysis on the number of siRNA molecules per cell required to observe half maximal inhibition of the target for peptide- versus cationic lipid-mediated delivery. | true | true | true | true | true | 590 |
3 | INTRODUCTION | 1 | 24 | [
"b24",
"b57"
] | 17,135,188 | pmid-9207018|pmid-15196012|pmid-10751399|pmid-12746500|pmid-16682561 | Beyond this, the techniques described here are generally applicable for a characterisation of delivery systems of oligonucleotides. | [
"24",
"57"
] | 131 | 3,477 | 0 | false | Beyond this, the techniques described here are generally applicable for a characterisation of delivery systems of oligonucleotides. | [] | Beyond this, the techniques described here are generally applicable for a characterisation of delivery systems of oligonucleotides. | true | true | true | true | true | 590 |
0 | DISCUSSION | 1 | 24 | [
"b24",
"b57",
"b57"
] | 17,135,188 | pmid-12120257|pmid-15952901|pmid-12359866|pmid-14564000|NA|pmid-12654261|pmid-15578064|pmid-15272050|pmid-16839274|pmid-15538359|pmid-16565705|pmid-2849509|pmid-2849510|pmid-1777485|pmid-8290579|pmid-10664605|pmid-15485768|pmid-16254940|pmid-9207018|pmid-15196012|pmid-15196012 | The cell membrane is one of the major barriers for an application of therapeutically interesting bio-macromolecules like nucleic acids. | [
"24",
"57",
"57"
] | 135 | 3,478 | 0 | false | The cell membrane is one of the major barriers for an application of therapeutically interesting bio-macromolecules like nucleic acids. | [] | The cell membrane is one of the major barriers for an application of therapeutically interesting bio-macromolecules like nucleic acids. | true | true | true | true | true | 591 |
0 | DISCUSSION | 1 | 24 | [
"b24",
"b57",
"b57"
] | 17,135,188 | pmid-12120257|pmid-15952901|pmid-12359866|pmid-14564000|NA|pmid-12654261|pmid-15578064|pmid-15272050|pmid-16839274|pmid-15538359|pmid-16565705|pmid-2849509|pmid-2849510|pmid-1777485|pmid-8290579|pmid-10664605|pmid-15485768|pmid-16254940|pmid-9207018|pmid-15196012|pmid-15196012 | In the present study we exploited a CPP-approach for the delivery of siRNA as a general example for an oligonucleotide cargo using the peptide MPGα, a derivative of the original MPG peptide described by Morris et al. | [
"24",
"57",
"57"
] | 216 | 3,479 | 0 | false | In the present study we exploited a CPP-approach for the delivery of siRNA as a general example for an oligonucleotide cargo using the peptide MPGα, a derivative of the original MPG peptide described by Morris et al. | [] | In the present study we exploited a CPP-approach for the delivery of siRNA as a general example for an oligonucleotide cargo using the peptide MPGα, a derivative of the original MPG peptide described by Morris et al. | true | true | true | true | true | 591 |
0 | DISCUSSION | 1 | 57 | [
"b24",
"b57",
"b57"
] | 17,135,188 | pmid-12120257|pmid-15952901|pmid-12359866|pmid-14564000|NA|pmid-12654261|pmid-15578064|pmid-15272050|pmid-16839274|pmid-15538359|pmid-16565705|pmid-2849509|pmid-2849510|pmid-1777485|pmid-8290579|pmid-10664605|pmid-15485768|pmid-16254940|pmid-9207018|pmid-15196012|pmid-15196012 | MPGα differs from MPG by six amino acids in the hydrophobic part (57). | [
"24",
"57",
"57"
] | 70 | 3,480 | 1 | false | MPGα differs from MPG by six amino acids in the hydrophobic part. | [
"57"
] | MPGα differs from MPG by six amino acids in the hydrophobic part. | true | true | true | true | true | 591 |
0 | DISCUSSION | 1 | 57 | [
"b24",
"b57",
"b57"
] | 17,135,188 | pmid-12120257|pmid-15952901|pmid-12359866|pmid-14564000|NA|pmid-12654261|pmid-15578064|pmid-15272050|pmid-16839274|pmid-15538359|pmid-16565705|pmid-2849509|pmid-2849510|pmid-1777485|pmid-8290579|pmid-10664605|pmid-15485768|pmid-16254940|pmid-9207018|pmid-15196012|pmid-15196012 | These changes result in an alteration of the overall structure of the peptide towards a higher tendency of adopting a helical conformation (57). | [
"24",
"57",
"57"
] | 144 | 3,481 | 1 | false | These changes result in an alteration of the overall structure of the peptide towards a higher tendency of adopting a helical conformation. | [
"57"
] | These changes result in an alteration of the overall structure of the peptide towards a higher tendency of adopting a helical conformation. | true | true | true | true | true | 591 |
0 | DISCUSSION | 1 | 24 | [
"b24",
"b57",
"b57"
] | 17,135,188 | pmid-12120257|pmid-15952901|pmid-12359866|pmid-14564000|NA|pmid-12654261|pmid-15578064|pmid-15272050|pmid-16839274|pmid-15538359|pmid-16565705|pmid-2849509|pmid-2849510|pmid-1777485|pmid-8290579|pmid-10664605|pmid-15485768|pmid-16254940|pmid-9207018|pmid-15196012|pmid-15196012 | The peptide forms stable non-covalent complexes with nucleic acids. | [
"24",
"57",
"57"
] | 67 | 3,482 | 0 | false | The peptide forms stable non-covalent complexes with nucleic acids. | [] | The peptide forms stable non-covalent complexes with nucleic acids. | true | true | true | true | true | 591 |
0 | DISCUSSION | 1 | 24 | [
"b24",
"b57",
"b57"
] | 17,135,188 | pmid-12120257|pmid-15952901|pmid-12359866|pmid-14564000|NA|pmid-12654261|pmid-15578064|pmid-15272050|pmid-16839274|pmid-15538359|pmid-16565705|pmid-2849509|pmid-2849510|pmid-1777485|pmid-8290579|pmid-10664605|pmid-15485768|pmid-16254940|pmid-9207018|pmid-15196012|pmid-15196012 | Besides the mechanism of cellular uptake of MPGα/siRNA complexes our main focus was a comparative parallel analysis of uptake versus functional effects of the nucleic acid cargo. | [
"24",
"57",
"57"
] | 178 | 3,483 | 0 | false | Besides the mechanism of cellular uptake of MPGα/siRNA complexes our main focus was a comparative parallel analysis of uptake versus functional effects of the nucleic acid cargo. | [] | Besides the mechanism of cellular uptake of MPGα/siRNA complexes our main focus was a comparative parallel analysis of uptake versus functional effects of the nucleic acid cargo. | true | true | true | true | true | 591 |
0 | DISCUSSION | 1 | 24 | [
"b24",
"b57",
"b57"
] | 17,135,188 | pmid-12120257|pmid-15952901|pmid-12359866|pmid-14564000|NA|pmid-12654261|pmid-15578064|pmid-15272050|pmid-16839274|pmid-15538359|pmid-16565705|pmid-2849509|pmid-2849510|pmid-1777485|pmid-8290579|pmid-10664605|pmid-15485768|pmid-16254940|pmid-9207018|pmid-15196012|pmid-15196012 | For this purpose, we used a liquid hybridisation protocol in combination with a simple luciferase reporter system. | [
"24",
"57",
"57"
] | 114 | 3,484 | 0 | false | For this purpose, we used a liquid hybridisation protocol in combination with a simple luciferase reporter system. | [] | For this purpose, we used a liquid hybridisation protocol in combination with a simple luciferase reporter system. | true | true | true | true | true | 591 |
0 | DISCUSSION | 1 | 24 | [
"b24",
"b57",
"b57"
] | 17,135,188 | pmid-12120257|pmid-15952901|pmid-12359866|pmid-14564000|NA|pmid-12654261|pmid-15578064|pmid-15272050|pmid-16839274|pmid-15538359|pmid-16565705|pmid-2849509|pmid-2849510|pmid-1777485|pmid-8290579|pmid-10664605|pmid-15485768|pmid-16254940|pmid-9207018|pmid-15196012|pmid-15196012 | For comparison, the commercially available cationic lipid LF2000 was included into the study. | [
"24",
"57",
"57"
] | 93 | 3,485 | 0 | false | For comparison, the commercially available cationic lipid LF2000 was included into the study. | [] | For comparison, the commercially available cationic lipid LF2000 was included into the study. | true | true | true | true | true | 591 |
1 | DISCUSSION | 1 | 58 | [
"b58",
"b61",
"b65",
"b68",
"b64"
] | 17,135,188 | pmid-16305500|pmid-9207018|pmid-11024364|pmid-12888501|pmid-12054897|NA|pmid-15386618|pmid-15576677 | As shown in Figure 1, MPGα is capable of translocating siRNA into mammalian cells leading to a down-regulation of the target protein luciferase. | [
"58",
"61",
"65",
"68",
"64"
] | 144 | 3,486 | 0 | false | As shown in Figure 1, MPGα is capable of translocating siRNA into mammalian cells leading to a down-regulation of the target protein luciferase. | [] | As shown in Figure 1, MPGα is capable of translocating siRNA into mammalian cells leading to a down-regulation of the target protein luciferase. | true | true | true | true | true | 592 |
1 | DISCUSSION | 1 | 58 | [
"b58",
"b61",
"b65",
"b68",
"b64"
] | 17,135,188 | pmid-16305500|pmid-9207018|pmid-11024364|pmid-12888501|pmid-12054897|NA|pmid-15386618|pmid-15576677 | The observed effect was highly specific for siR206 and maximal inhibition was achieved with a charge ratio of 15:1, i.e. | [
"58",
"61",
"65",
"68",
"64"
] | 120 | 3,487 | 0 | false | The observed effect was highly specific for siR206 and maximal inhibition was achieved with a charge ratio of 15:1, i.e. | [] | The observed effect was highly specific for siR206 and maximal inhibition was achieved with a charge ratio of 15:1, i.e. | true | true | true | true | true | 592 |
1 | DISCUSSION | 1 | 58 | [
"b58",
"b61",
"b65",
"b68",
"b64"
] | 17,135,188 | pmid-16305500|pmid-9207018|pmid-11024364|pmid-12888501|pmid-12054897|NA|pmid-15386618|pmid-15576677 | positive (peptide) over negative (siRNA) charges (Supplementary Figure 1). | [
"58",
"61",
"65",
"68",
"64"
] | 74 | 3,488 | 0 | false | positive (peptide) over negative (siRNA) charges (Supplementary Figure 1). | [] | positive (peptide) over negative (siRNA) charges (Supplementary Figure 1). | false | true | true | true | false | 592 |
1 | DISCUSSION | 1 | 58 | [
"b58",
"b61",
"b65",
"b68",
"b64"
] | 17,135,188 | pmid-16305500|pmid-9207018|pmid-11024364|pmid-12888501|pmid-12054897|NA|pmid-15386618|pmid-15576677 | Additionally, we tested MPGα-mediated delivery of siRNA directed to two other targets, namely ICAM-1 and lamin A/C applying published protocols (58,61). | [
"58",
"61",
"65",
"68",
"64"
] | 152 | 3,489 | 0 | false | Additionally, we tested MPGα-mediated delivery of siRNA directed to two other targets, namely ICAM-1 and lamin A/C applying published protocols. | [
"58,61"
] | Additionally, we tested MPGα-mediated delivery of siRNA directed to two other targets, namely ICAM-1 and lamin A/C applying published protocols. | true | true | true | true | true | 592 |
1 | DISCUSSION | 1 | 58 | [
"b58",
"b61",
"b65",
"b68",
"b64"
] | 17,135,188 | pmid-16305500|pmid-9207018|pmid-11024364|pmid-12888501|pmid-12054897|NA|pmid-15386618|pmid-15576677 | In both cases we observed a substantial RNAi effect of the active siRNA as compared to a control siRNA (data not shown). | [
"58",
"61",
"65",
"68",
"64"
] | 120 | 3,490 | 0 | false | In both cases we observed a substantial RNAi effect of the active siRNA as compared to a control siRNA (data not shown). | [] | In both cases we observed a substantial RNAi effect of the active siRNA as compared to a control siRNA (data not shown). | true | true | true | true | true | 592 |
1 | DISCUSSION | 1 | 58 | [
"b58",
"b61",
"b65",
"b68",
"b64"
] | 17,135,188 | pmid-16305500|pmid-9207018|pmid-11024364|pmid-12888501|pmid-12054897|NA|pmid-15386618|pmid-15576677 | These data clearly indicate a specific siRNA-mediated inhibition of target protein expression rather than an unspecific effect, which might be caused by the transfection procedure. | [
"58",
"61",
"65",
"68",
"64"
] | 180 | 3,491 | 0 | false | These data clearly indicate a specific siRNA-mediated inhibition of target protein expression rather than an unspecific effect, which might be caused by the transfection procedure. | [] | These data clearly indicate a specific siRNA-mediated inhibition of target protein expression rather than an unspecific effect, which might be caused by the transfection procedure. | true | true | true | true | true | 592 |
1 | DISCUSSION | 1 | 58 | [
"b58",
"b61",
"b65",
"b68",
"b64"
] | 17,135,188 | pmid-16305500|pmid-9207018|pmid-11024364|pmid-12888501|pmid-12054897|NA|pmid-15386618|pmid-15576677 | Comparing the peptide with LF2000, the maximal achievable levels of siRNA-mediated target protein down-regulation are roughly the same. | [
"58",
"61",
"65",
"68",
"64"
] | 135 | 3,492 | 0 | false | Comparing the peptide with LF2000, the maximal achievable levels of siRNA-mediated target protein down-regulation are roughly the same. | [] | Comparing the peptide with LF2000, the maximal achievable levels of siRNA-mediated target protein down-regulation are roughly the same. | true | true | true | true | true | 592 |
1 | DISCUSSION | 1 | 58 | [
"b58",
"b61",
"b65",
"b68",
"b64"
] | 17,135,188 | pmid-16305500|pmid-9207018|pmid-11024364|pmid-12888501|pmid-12054897|NA|pmid-15386618|pmid-15576677 | However, an exact determination of the IC50 values of both carrier/cargo complexes revealed an ∼30-fold lower efficiency of MPGα compared to LF2000. | [
"58",
"61",
"65",
"68",
"64"
] | 148 | 3,493 | 0 | false | However, an exact determination of the IC50 values of both carrier/cargo complexes revealed an ∼30-fold lower efficiency of MPGα compared to LF2000. | [] | However, an exact determination of the IC50 values of both carrier/cargo complexes revealed an ∼30-fold lower efficiency of MPGα compared to LF2000. | true | true | true | true | true | 592 |
1 | DISCUSSION | 1 | 58 | [
"b58",
"b61",
"b65",
"b68",
"b64"
] | 17,135,188 | pmid-16305500|pmid-9207018|pmid-11024364|pmid-12888501|pmid-12054897|NA|pmid-15386618|pmid-15576677 | To investigate if this phenomenon was caused by different levels of uptake or insufficient bio-availability of the siRNA molecules, we quantified the intracellular amount of cargo. | [
"58",
"61",
"65",
"68",
"64"
] | 180 | 3,494 | 0 | false | To investigate if this phenomenon was caused by different levels of uptake or insufficient bio-availability of the siRNA molecules, we quantified the intracellular amount of cargo. | [] | To investigate if this phenomenon was caused by different levels of uptake or insufficient bio-availability of the siRNA molecules, we quantified the intracellular amount of cargo. | true | true | true | true | true | 592 |
1 | DISCUSSION | 1 | 58 | [
"b58",
"b61",
"b65",
"b68",
"b64"
] | 17,135,188 | pmid-16305500|pmid-9207018|pmid-11024364|pmid-12888501|pmid-12054897|NA|pmid-15386618|pmid-15576677 | From a number of diverse procedures described in the literature (65–68) we adapted a liquid hybridisation protocol described by Overhoff et al. | [
"58",
"61",
"65",
"68",
"64"
] | 143 | 3,495 | 0 | false | From a number of diverse procedures described in the literature we adapted a liquid hybridisation protocol described by Overhoff et al. | [
"65–68"
] | From a number of diverse procedures described in the literature we adapted a liquid hybridisation protocol described by Overhoff et al. | true | true | true | true | true | 592 |
1 | DISCUSSION | 1 | 58 | [
"b58",
"b61",
"b65",
"b68",
"b64"
] | 17,135,188 | pmid-16305500|pmid-9207018|pmid-11024364|pmid-12888501|pmid-12054897|NA|pmid-15386618|pmid-15576677 | This assay does not need any modification of the siRNA and exclusively detects intact molecules. | [
"58",
"61",
"65",
"68",
"64"
] | 96 | 3,496 | 0 | false | This assay does not need any modification of the siRNA and exclusively detects intact molecules. | [] | This assay does not need any modification of the siRNA and exclusively detects intact molecules. | true | true | true | true | true | 592 |
1 | DISCUSSION | 1 | 58 | [
"b58",
"b61",
"b65",
"b68",
"b64"
] | 17,135,188 | pmid-16305500|pmid-9207018|pmid-11024364|pmid-12888501|pmid-12054897|NA|pmid-15386618|pmid-15576677 | Thus, artefacts due to detached fluorescence labels or degraded cargos for example are precluded. | [
"58",
"61",
"65",
"68",
"64"
] | 97 | 3,497 | 0 | false | Thus, artefacts due to detached fluorescence labels or degraded cargos for example are precluded. | [] | Thus, artefacts due to detached fluorescence labels or degraded cargos for example are precluded. | true | true | true | true | true | 592 |
1 | DISCUSSION | 1 | 58 | [
"b58",
"b61",
"b65",
"b68",
"b64"
] | 17,135,188 | pmid-16305500|pmid-9207018|pmid-11024364|pmid-12888501|pmid-12054897|NA|pmid-15386618|pmid-15576677 | Overall, the liquid hybridisation protocol is a fast, easy to handle and highly reproducible procedure that can be carried out in any laboratory without the need of expensive equipment. | [
"58",
"61",
"65",
"68",
"64"
] | 185 | 3,498 | 0 | false | Overall, the liquid hybridisation protocol is a fast, easy to handle and highly reproducible procedure that can be carried out in any laboratory without the need of expensive equipment. | [] | Overall, the liquid hybridisation protocol is a fast, easy to handle and highly reproducible procedure that can be carried out in any laboratory without the need of expensive equipment. | true | true | true | true | true | 592 |
2 | DISCUSSION | 1 | 35 | [
"b35",
"b69",
"b70",
"b30",
"b32",
"b56",
"b71"
] | 17,135,188 | pmid-9111037|pmid-15907190|pmid-12134943|pmid-16377019|pmid-12771197|pmid-16321967|pmid-15907190|pmid-9438412|pmid-16516138|pmid-12621426|pmid-15687999|pmid-15640444|pmid-15203910|pmid-15935328|pmid-15035618|pmid-15859953|pmid-11856307|pmid-15687490|pmid-12411431|pmid-15653149|pmid-3035599|pmid-11711547|pmid-15628847|p... | Though, before we could perform quantitative uptake experiments, we had to establish a washing procedure in order to remove complexes bound to the surface of the cells. | [
"35",
"69",
"70",
"30",
"32",
"56",
"71"
] | 168 | 3,499 | 0 | false | Though, before we could perform quantitative uptake experiments, we had to establish a washing procedure in order to remove complexes bound to the surface of the cells. | [] | Though, before we could perform quantitative uptake experiments, we had to establish a washing procedure in order to remove complexes bound to the surface of the cells. | true | true | true | true | true | 593 |
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