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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1 | INTRODUCTION | 1 | 1 | [
"B1",
"B2"
] | 19,503,677 | NA|NA | For example, adult independence refers to a person who does not require external care in daily life, whereas child independence includes care within the family and school life. | [
"1",
"2"
] | 176 | 38,016 | 0 | false | For example, adult independence refers to a person who does not require external care in daily life, whereas child independence includes care within the family and school life. | [] | For example, adult independence refers to a person who does not require external care in daily life, whereas child independence includes care within the family and school life. | true | true | true | true | true | 6,521 |
1 | INTRODUCTION | 1 | 1 | [
"B1",
"B2"
] | 19,503,677 | NA|NA | Such personal factors have been nurtured through development in the community and belong to the community's values and customs. | [
"1",
"2"
] | 127 | 38,017 | 0 | false | Such personal factors have been nurtured through development in the community and belong to the community's values and customs. | [] | Such personal factors have been nurtured through development in the community and belong to the community's values and customs. | true | true | true | true | true | 6,521 |
1 | INTRODUCTION | 1 | 1 | [
"B1",
"B2"
] | 19,503,677 | NA|NA | The universal factors, on the other hand, are measured against the common rule of humanbeings. | [
"1",
"2"
] | 94 | 38,018 | 0 | false | The universal factors, on the other hand, are measured against the common rule of humanbeings. | [] | The universal factors, on the other hand, are measured against the common rule of humanbeings. | true | true | true | true | true | 6,521 |
1 | INTRODUCTION | 1 | 1 | [
"B1",
"B2"
] | 19,503,677 | NA|NA | Furthermore, disability evaluation should also include assessment for the supporting system in the community-based rehabilitation (CBR) and other problems. | [
"1",
"2"
] | 155 | 38,019 | 0 | false | Furthermore, disability evaluation should also include assessment for the supporting system in the community-based rehabilitation (CBR) and other problems. | [] | Furthermore, disability evaluation should also include assessment for the supporting system in the community-based rehabilitation (CBR) and other problems. | true | true | true | true | true | 6,521 |
1 | INTRODUCTION | 1 | 1 | [
"B1",
"B2"
] | 19,503,677 | NA|NA | These other problems, which relate to objective signs, the timing of evaluation and multiple impairments, are still under fierce debate. | [
"1",
"2"
] | 136 | 38,020 | 0 | false | These other problems, which relate to objective signs, the timing of evaluation and multiple impairments, are still under fierce debate. | [] | These other problems, which relate to objective signs, the timing of evaluation and multiple impairments, are still under fierce debate. | true | true | true | true | true | 6,521 |
2 | INTRODUCTION | 0 | null | null | 19,503,677 | null | Generally, it is accepted that disabilities differ from impairment to impairment. | null | 81 | 38,021 | 0 | false | null | null | Generally, it is accepted that disabilities differ from impairment to impairment. | true | true | true | true | true | 6,522 |
2 | INTRODUCTION | 0 | null | null | 19,503,677 | null | In addition, the needs of patients vary by disability types. | null | 60 | 38,022 | 0 | false | null | null | In addition, the needs of patients vary by disability types. | true | true | true | true | true | 6,522 |
2 | INTRODUCTION | 0 | null | null | 19,503,677 | null | As such, Japan officially recognizes three forms of the identification booklet for the disabled, one for physical disability, one for mental disability, and another for psychological disability. | null | 194 | 38,023 | 0 | false | null | null | As such, Japan officially recognizes three forms of the identification booklet for the disabled, one for physical disability, one for mental disability, and another for psychological disability. | true | true | true | true | true | 6,522 |
0 | DISCUSSION | 0 | null | null | 19,503,677 | null | In Japan, disability is categorized under three identification booklets: 1) physical disability, which is classified by four subgroups, 2) mental disability, and 3) psychological disability. | null | 190 | 38,024 | 0 | false | null | null | In Japan, disability is categorized under three identification booklets: 1) physical disability, which is classified by four subgroups, 2) mental disability, and 3) psychological disability. | true | true | true | true | true | 6,523 |
1 | DISCUSSION | 0 | null | null | 19,503,677 | NA|NA | The classification of the physically disabled subgroups (Table 1-4) was very useful for determining the problems for government policy on welfare and public health. | null | 164 | 38,025 | 0 | false | null | null | The classification of the physically disabled subgroups (Table 1-4) was very useful for determining the problems for government policy on welfare and public health. | true | true | true | true | true | 6,524 |
1 | DISCUSSION | 0 | null | null | 19,503,677 | NA|NA | The increasing rate of internal disorders within the physically disabled has become a major theme for following global welfare services in the future. | null | 150 | 38,026 | 0 | false | null | null | The increasing rate of internal disorders within the physically disabled has become a major theme for following global welfare services in the future. | true | true | true | true | true | 6,524 |
1 | DISCUSSION | 0 | null | null | 19,503,677 | NA|NA | A multi-system for evaluating disabilities has resulted in many welfare services, depending on the various kinds of disabilities. | null | 129 | 38,027 | 0 | false | null | null | A multi-system for evaluating disabilities has resulted in many welfare services, depending on the various kinds of disabilities. | true | true | true | true | true | 6,524 |
1 | DISCUSSION | 0 | null | null | 19,503,677 | NA|NA | However, the achievements of the welfare system, based on different types of disabilities, have led to a complex or confused service system. | null | 140 | 38,028 | 0 | false | null | null | However, the achievements of the welfare system, based on different types of disabilities, have led to a complex or confused service system. | true | true | true | true | true | 6,524 |
1 | DISCUSSION | 0 | null | null | 19,503,677 | NA|NA | The system has also been affected yearly by the changing social community around persons with disabilities. | null | 107 | 38,029 | 0 | false | null | null | The system has also been affected yearly by the changing social community around persons with disabilities. | true | true | true | true | true | 6,524 |
1 | DISCUSSION | 0 | null | null | 19,503,677 | NA|NA | For example, the data showed a sharp rise in the elderly with disabilities. | null | 75 | 38,030 | 0 | false | null | null | For example, the data showed a sharp rise in the elderly with disabilities. | true | true | true | true | true | 6,524 |
1 | DISCUSSION | 0 | null | null | 19,503,677 | NA|NA | Accordingly, the increasing ratio of the elderly population has prompted the development of a new disability evaluation related to practical ADL. | null | 145 | 38,031 | 0 | false | null | null | Accordingly, the increasing ratio of the elderly population has prompted the development of a new disability evaluation related to practical ADL. | true | true | true | true | true | 6,524 |
1 | DISCUSSION | 0 | null | null | 19,503,677 | NA|NA | To cite another example, mental disability has been evaluated from infancy because of a lack of social response. | null | 112 | 38,032 | 0 | false | null | null | To cite another example, mental disability has been evaluated from infancy because of a lack of social response. | true | true | true | true | true | 6,524 |
1 | DISCUSSION | 0 | null | null | 19,503,677 | NA|NA | As such, most people with mental disability usually tend to receive the identification booklet up to the age of 18 yr. | null | 118 | 38,033 | 0 | false | null | null | As such, most people with mental disability usually tend to receive the identification booklet up to the age of 18 yr. | true | true | true | true | true | 6,524 |
1 | DISCUSSION | 0 | null | null | 19,503,677 | NA|NA | However, Table 5 shows that, in Japan, adults with mental disability tend to be less adaptive to the community than those with physical disability. | null | 147 | 38,034 | 0 | false | null | null | However, Table 5 shows that, in Japan, adults with mental disability tend to be less adaptive to the community than those with physical disability. | true | true | true | true | true | 6,524 |
1 | DISCUSSION | 0 | null | null | 19,503,677 | NA|NA | Therefore, the Ministry of Health, Labor and Welfare of Japanese Government has started to rearrange many welfare services to be more suitable to a small community around persons with disabilities. | null | 197 | 38,035 | 0 | false | null | null | Therefore, the Ministry of Health, Labor and Welfare of Japanese Government has started to rearrange many welfare services to be more suitable to a small community around persons with disabilities. | true | true | true | true | true | 6,524 |
2 | DISCUSSION | 0 | null | null | 19,503,677 | null | Moreover, the concept of preventing disabilities is emphasized not only in rehabilitation medicine, but also in CBR, indicating that disability evaluation needs another factor of support system based on their community. | null | 219 | 38,036 | 0 | false | null | null | Moreover, the concept of preventing disabilities is emphasized not only in rehabilitation medicine, but also in CBR, indicating that disability evaluation needs another factor of support system based on their community. | true | true | true | true | true | 6,525 |
2 | DISCUSSION | 0 | null | null | 19,503,677 | null | Thus, it is important to think about the disability evaluation according to the characteristics of age, impairment and assistive environment. | null | 141 | 38,037 | 0 | false | null | null | Thus, it is important to think about the disability evaluation according to the characteristics of age, impairment and assistive environment. | true | true | true | true | true | 6,525 |
2 | DISCUSSION | 0 | null | null | 19,503,677 | null | In the field of CBR, disability evaluation has recently become important for measuring the effects of rehabilitation treatment in medical insurance and decision of the grade of welfare service volume in Japan. | null | 209 | 38,038 | 0 | false | null | null | In the field of CBR, disability evaluation has recently become important for measuring the effects of rehabilitation treatment in medical insurance and decision of the grade of welfare service volume in Japan. | true | true | true | true | true | 6,525 |
3 | DISCUSSION | 0 | null | null | 19,503,677 | null | While the first and second groups have been historically well-established without any disagreement on the classifications of disability type, the third group concerning psychological disability has recently been questioned with respect to the visibly less apparent disabilities relating to cognition, memory, attention, ... | null | 377 | 38,039 | 0 | false | null | null | While the first and second groups have been historically well-established without any disagreement on the classifications of disability type, the third group concerning psychological disability has recently been questioned with respect to the visibly less apparent disabilities relating to cognition, memory, attention, ... | true | true | true | true | true | 6,526 |
3 | DISCUSSION | 0 | null | null | 19,503,677 | null | Although the new system to evaluate and support such a disability group is under development throughout the country, problems with classification continue to be debated. | null | 169 | 38,040 | 0 | false | null | null | Although the new system to evaluate and support such a disability group is under development throughout the country, problems with classification continue to be debated. | true | true | true | true | true | 6,526 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B6",
"B4",
"B7"
] | 18,003,655 | pmid-15277680|pmid-15479734|pmid-15003273|pmid-15803138|pmid-2839775|pmid-2839690|pmid-15803138|pmid-11050335|pmid-14960583 | Selective translation of messenger RNAs (mRNAs) has emerged as an important mechanism that regulates gene expression, particularly in response to various physiological and pathophysiological conditions that require rapid changes in gene expression profiles. | [
"1",
"2",
"3",
"4",
"5",
"6",
"4",
"7"
] | 257 | 38,041 | 0 | false | Selective translation of messenger RNAs (mRNAs) has emerged as an important mechanism that regulates gene expression, particularly in response to various physiological and pathophysiological conditions that require rapid changes in gene expression profiles. | [] | Selective translation of messenger RNAs (mRNAs) has emerged as an important mechanism that regulates gene expression, particularly in response to various physiological and pathophysiological conditions that require rapid changes in gene expression profiles. | true | true | true | true | true | 6,527 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B6",
"B4",
"B7"
] | 18,003,655 | pmid-15277680|pmid-15479734|pmid-15003273|pmid-15803138|pmid-2839775|pmid-2839690|pmid-15803138|pmid-11050335|pmid-14960583 | mRNAs that employ selective translation utilize various regulatory elements, most often located within their 5′ untranslated regions (UTRs) that allow preferential translation. | [
"1",
"2",
"3",
"4",
"5",
"6",
"4",
"7"
] | 176 | 38,042 | 0 | false | mRNAs that employ selective translation utilize various regulatory elements, most often located within their 5′ untranslated regions (UTRs) that allow preferential translation. | [] | mRNAs that employ selective translation utilize various regulatory elements, most often located within their 5′ untranslated regions (UTRs) that allow preferential translation. | false | true | true | true | false | 6,527 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B6",
"B4",
"B7"
] | 18,003,655 | pmid-15277680|pmid-15479734|pmid-15003273|pmid-15803138|pmid-2839775|pmid-2839690|pmid-15803138|pmid-11050335|pmid-14960583 | For example, the 5′ UTR of the transcription factor ATF4 contains two short upstream open reading frames that render translation of the ATF4 reading frame inefficient (1,2). | [
"1",
"2",
"3",
"4",
"5",
"6",
"4",
"7"
] | 173 | 38,043 | 0 | false | For example, the 5′ UTR of the transcription factor ATF4 contains two short upstream open reading frames that render translation of the ATF4 reading frame inefficient. | [
"1,2"
] | For example, the 5′ UTR of the transcription factor ATF4 contains two short upstream open reading frames that render translation of the ATF4 reading frame inefficient. | true | true | true | true | true | 6,527 |
0 | INTRODUCTION | 1 | 3 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B6",
"B4",
"B7"
] | 18,003,655 | pmid-15277680|pmid-15479734|pmid-15003273|pmid-15803138|pmid-2839775|pmid-2839690|pmid-15803138|pmid-11050335|pmid-14960583 | However, translation of ATF4 is specifically increased under conditions of increased eIF2α phosphorylation, such as during endoplasmic reticulum (ER) stress and the unfolded protein response, although the rate of global protein synthesis is reduced (3). | [
"1",
"2",
"3",
"4",
"5",
"6",
"4",
"7"
] | 253 | 38,044 | 1 | false | However, translation of ATF4 is specifically increased under conditions of increased eIF2α phosphorylation, such as during endoplasmic reticulum (ER) stress and the unfolded protein response, although the rate of global protein synthesis is reduced. | [
"3"
] | However, translation of ATF4 is specifically increased under conditions of increased eIF2α phosphorylation, such as during endoplasmic reticulum (ER) stress and the unfolded protein response, although the rate of global protein synthesis is reduced. | true | true | true | true | true | 6,527 |
0 | INTRODUCTION | 1 | 4 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B6",
"B4",
"B7"
] | 18,003,655 | pmid-15277680|pmid-15479734|pmid-15003273|pmid-15803138|pmid-2839775|pmid-2839690|pmid-15803138|pmid-11050335|pmid-14960583 | Another stress-induced mode of translation initiation takes advantage of internal ribosome entry site (IRES) elements located within 5′ UTRs that permit cap-independent translation (4). | [
"1",
"2",
"3",
"4",
"5",
"6",
"4",
"7"
] | 185 | 38,045 | 1 | false | Another stress-induced mode of translation initiation takes advantage of internal ribosome entry site (IRES) elements located within 5′ UTRs that permit cap-independent translation. | [
"4"
] | Another stress-induced mode of translation initiation takes advantage of internal ribosome entry site (IRES) elements located within 5′ UTRs that permit cap-independent translation. | true | true | true | true | true | 6,527 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B6",
"B4",
"B7"
] | 18,003,655 | pmid-15277680|pmid-15479734|pmid-15003273|pmid-15803138|pmid-2839775|pmid-2839690|pmid-15803138|pmid-11050335|pmid-14960583 | IRES were originally discovered in picornaviruses, where they initiate translation of naturally uncapped viral RNAs (5,6). | [
"1",
"2",
"3",
"4",
"5",
"6",
"4",
"7"
] | 122 | 38,046 | 0 | false | IRES were originally discovered in picornaviruses, where they initiate translation of naturally uncapped viral RNAs. | [
"5,6"
] | IRES were originally discovered in picornaviruses, where they initiate translation of naturally uncapped viral RNAs. | true | true | true | true | true | 6,527 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B6",
"B4",
"B7"
] | 18,003,655 | pmid-15277680|pmid-15479734|pmid-15003273|pmid-15803138|pmid-2839775|pmid-2839690|pmid-15803138|pmid-11050335|pmid-14960583 | Interestingly, cellular IRES are found largely in mRNAs that encode proteins with important roles in differentiation, cell growth and proliferation and the regulation of apoptosis, suggesting that the selective modulation of IRES-mediated translation is critical for the regulation of cell death and survival (4,7). | [
"1",
"2",
"3",
"4",
"5",
"6",
"4",
"7"
] | 315 | 38,047 | 0 | false | Interestingly, cellular IRES are found largely in mRNAs that encode proteins with important roles in differentiation, cell growth and proliferation and the regulation of apoptosis, suggesting that the selective modulation of IRES-mediated translation is critical for the regulation of cell death and survival. | [
"4,7"
] | Interestingly, cellular IRES are found largely in mRNAs that encode proteins with important roles in differentiation, cell growth and proliferation and the regulation of apoptosis, suggesting that the selective modulation of IRES-mediated translation is critical for the regulation of cell death and survival. | true | true | true | true | true | 6,527 |
1 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B4",
"B10 B11 B12 B13",
"B14",
"B15"
] | 18,003,655 | pmid-15094769|pmid-15818406|pmid-15803138|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-16174738|pmid-16932749|pmid-9049310|pmid-9030685|pmid-9032289|NA|pmid-9030685|pmid-9372926|pmid-9878069|pmid-9049310|pmid-9030685|pmid-11032820|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-15803138|pmi... | The precise molecular mechanism of cellular IRES-mediated translation is not fully understood. | [
"8",
"9",
"4",
"10–13",
"14",
"15"
] | 94 | 38,048 | 0 | false | The precise molecular mechanism of cellular IRES-mediated translation is not fully understood. | [] | The precise molecular mechanism of cellular IRES-mediated translation is not fully understood. | true | true | true | true | true | 6,528 |
1 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B4",
"B10 B11 B12 B13",
"B14",
"B15"
] | 18,003,655 | pmid-15094769|pmid-15818406|pmid-15803138|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-16174738|pmid-16932749|pmid-9049310|pmid-9030685|pmid-9032289|NA|pmid-9030685|pmid-9372926|pmid-9878069|pmid-9049310|pmid-9030685|pmid-11032820|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-15803138|pmi... | Several studies have shown that most, if not all, cellular IRES require various auxiliary proteins termed ITAFs (IRES trans-acting factors) for efficient IRES-mediated translation (8,9). | [
"8",
"9",
"4",
"10–13",
"14",
"15"
] | 186 | 38,049 | 0 | false | Several studies have shown that most, if not all, cellular IRES require various auxiliary proteins termed ITAFs (IRES trans-acting factors) for efficient IRES-mediated translation. | [
"8,9"
] | Several studies have shown that most, if not all, cellular IRES require various auxiliary proteins termed ITAFs (IRES trans-acting factors) for efficient IRES-mediated translation. | true | true | true | true | true | 6,528 |
1 | INTRODUCTION | 1 | 4 | [
"B8",
"B9",
"B4",
"B10 B11 B12 B13",
"B14",
"B15"
] | 18,003,655 | pmid-15094769|pmid-15818406|pmid-15803138|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-16174738|pmid-16932749|pmid-9049310|pmid-9030685|pmid-9032289|NA|pmid-9030685|pmid-9372926|pmid-9878069|pmid-9049310|pmid-9030685|pmid-11032820|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-15803138|pmi... | While the requirement for ITAFs is not the same for all cellular IRES, it is generally believed that these factors may function as RNA chaperones that aid in the remodeling of proper IRES conformation and therefore allow access of the ribosome (4). | [
"8",
"9",
"4",
"10–13",
"14",
"15"
] | 248 | 38,050 | 1 | false | While the requirement for ITAFs is not the same for all cellular IRES, it is generally believed that these factors may function as RNA chaperones that aid in the remodeling of proper IRES conformation and therefore allow access of the ribosome. | [
"4"
] | While the requirement for ITAFs is not the same for all cellular IRES, it is generally believed that these factors may function as RNA chaperones that aid in the remodeling of proper IRES conformation and therefore allow access of the ribosome. | true | true | true | true | true | 6,528 |
1 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B4",
"B10 B11 B12 B13",
"B14",
"B15"
] | 18,003,655 | pmid-15094769|pmid-15818406|pmid-15803138|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-16174738|pmid-16932749|pmid-9049310|pmid-9030685|pmid-9032289|NA|pmid-9030685|pmid-9372926|pmid-9878069|pmid-9049310|pmid-9030685|pmid-11032820|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-15803138|pmi... | Alternatively, ITAFs may also directly recruit the ribosome to an IRES through interaction with ribosomal subunits. | [
"8",
"9",
"4",
"10–13",
"14",
"15"
] | 115 | 38,051 | 0 | false | Alternatively, ITAFs may also directly recruit the ribosome to an IRES through interaction with ribosomal subunits. | [] | Alternatively, ITAFs may also directly recruit the ribosome to an IRES through interaction with ribosomal subunits. | true | true | true | true | true | 6,528 |
1 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B4",
"B10 B11 B12 B13",
"B14",
"B15"
] | 18,003,655 | pmid-15094769|pmid-15818406|pmid-15803138|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-16174738|pmid-16932749|pmid-9049310|pmid-9030685|pmid-9032289|NA|pmid-9030685|pmid-9372926|pmid-9878069|pmid-9049310|pmid-9030685|pmid-11032820|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-15803138|pmi... | The requirement for canonical initiation factors in IRES-mediated translation is even less understood. | [
"8",
"9",
"4",
"10–13",
"14",
"15"
] | 102 | 38,052 | 0 | false | The requirement for canonical initiation factors in IRES-mediated translation is even less understood. | [] | The requirement for canonical initiation factors in IRES-mediated translation is even less understood. | true | true | true | true | true | 6,528 |
1 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B4",
"B10 B11 B12 B13",
"B14",
"B15"
] | 18,003,655 | pmid-15094769|pmid-15818406|pmid-15803138|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-16174738|pmid-16932749|pmid-9049310|pmid-9030685|pmid-9032289|NA|pmid-9030685|pmid-9372926|pmid-9878069|pmid-9049310|pmid-9030685|pmid-11032820|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-15803138|pmi... | Several studies have suggested that members of the eIF4G family may be required for cellular IRES-mediated translation, in particular during conditions of cellular stress and compromised global protein synthesis. | [
"8",
"9",
"4",
"10–13",
"14",
"15"
] | 212 | 38,053 | 0 | false | Several studies have suggested that members of the eIF4G family may be required for cellular IRES-mediated translation, in particular during conditions of cellular stress and compromised global protein synthesis. | [] | Several studies have suggested that members of the eIF4G family may be required for cellular IRES-mediated translation, in particular during conditions of cellular stress and compromised global protein synthesis. | true | true | true | true | true | 6,528 |
1 | INTRODUCTION | 1 | 10–13 | [
"B8",
"B9",
"B4",
"B10 B11 B12 B13",
"B14",
"B15"
] | 18,003,655 | pmid-15094769|pmid-15818406|pmid-15803138|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-16174738|pmid-16932749|pmid-9049310|pmid-9030685|pmid-9032289|NA|pmid-9030685|pmid-9372926|pmid-9878069|pmid-9049310|pmid-9030685|pmid-11032820|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-15803138|pmi... | It was shown that caspase-cleaved fragments of two family members, eIF4GI and DAP5/p97, can specifically enhance translation mediated by several cellular IRES, including those of Apaf-1, c-myc, HIAP2, XIAP and DAP5/p97 mRNAs (10–13). | [
"8",
"9",
"4",
"10–13",
"14",
"15"
] | 233 | 38,054 | 1 | false | It was shown that caspase-cleaved fragments of two family members, eIF4GI and DAP5/p97, can specifically enhance translation mediated by several cellular IRES, including those of Apaf-1, c-myc, HIAP2, XIAP and DAP5/p97 mRNAs. | [
"10–13"
] | It was shown that caspase-cleaved fragments of two family members, eIF4GI and DAP5/p97, can specifically enhance translation mediated by several cellular IRES, including those of Apaf-1, c-myc, HIAP2, XIAP and DAP5/p97 mRNAs. | true | true | true | true | true | 6,528 |
1 | INTRODUCTION | 1 | 14 | [
"B8",
"B9",
"B4",
"B10 B11 B12 B13",
"B14",
"B15"
] | 18,003,655 | pmid-15094769|pmid-15818406|pmid-15803138|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-16174738|pmid-16932749|pmid-9049310|pmid-9030685|pmid-9032289|NA|pmid-9030685|pmid-9372926|pmid-9878069|pmid-9049310|pmid-9030685|pmid-11032820|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-15803138|pmi... | Furthermore, using a HeLa cell-free translation system, the full-length DAP5/p97 was shown to support translation mediated by the c-myc, HIAP2 and XIAP IRES elements in eIF4G-depleted extracts (14). | [
"8",
"9",
"4",
"10–13",
"14",
"15"
] | 198 | 38,055 | 1 | false | Furthermore, using a HeLa cell-free translation system, the full-length DAP5/p97 was shown to support translation mediated by the c-myc, HIAP2 and XIAP IRES elements in eIF4G-depleted extracts. | [
"14"
] | Furthermore, using a HeLa cell-free translation system, the full-length DAP5/p97 was shown to support translation mediated by the c-myc, HIAP2 and XIAP IRES elements in eIF4G-depleted extracts. | true | true | true | true | true | 6,528 |
1 | INTRODUCTION | 1 | 15 | [
"B8",
"B9",
"B4",
"B10 B11 B12 B13",
"B14",
"B15"
] | 18,003,655 | pmid-15094769|pmid-15818406|pmid-15803138|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-16174738|pmid-16932749|pmid-9049310|pmid-9030685|pmid-9032289|NA|pmid-9030685|pmid-9372926|pmid-9878069|pmid-9049310|pmid-9030685|pmid-11032820|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-15803138|pmi... | More recently, DAP5/p97 was suggested to control cell proliferation by regulating the translation of cell cycle proteins such as p27Kip1 (15). | [
"8",
"9",
"4",
"10–13",
"14",
"15"
] | 142 | 38,056 | 1 | false | More recently, DAP5/p97 was suggested to control cell proliferation by regulating the translation of cell cycle proteins such as p27Kip1. | [
"15"
] | More recently, DAP5/p97 was suggested to control cell proliferation by regulating the translation of cell cycle proteins such as p27Kip1. | true | true | true | true | true | 6,528 |
2 | INTRODUCTION | 0 | null | null | 18,003,655 | pmid-16174738|NA|NA|NA|pmid-11032820|NA|pmid-16932749|pmid-16932749|pmid-11032820 | In this study, we have investigated the role of DAP5/p97 in modulating selective translation of IRES-containing mRNAs during ER stress. | null | 135 | 38,057 | 0 | false | null | null | In this study, we have investigated the role of DAP5/p97 in modulating selective translation of IRES-containing mRNAs during ER stress. | true | true | true | true | true | 6,529 |
2 | INTRODUCTION | 0 | null | null | 18,003,655 | pmid-16174738|NA|NA|NA|pmid-11032820|NA|pmid-16932749|pmid-16932749|pmid-11032820 | We show that DAP5/p97 is necessary for specific activation of at least two cellular IRES elements during pharmacologically induced ER stress. | null | 141 | 38,058 | 0 | false | null | null | We show that DAP5/p97 is necessary for specific activation of at least two cellular IRES elements during pharmacologically induced ER stress. | true | true | true | true | true | 6,529 |
2 | INTRODUCTION | 0 | null | null | 18,003,655 | pmid-16174738|NA|NA|NA|pmid-11032820|NA|pmid-16932749|pmid-16932749|pmid-11032820 | We find that expression of DAP5/p97 and an inhibitor of apoptosis protein HIAP2 are enhanced during ER stress; their mRNAs are selectively recruited to the polysomes via IRES elements located in their respective 5′ UTRs. | null | 220 | 38,059 | 0 | false | null | null | We find that expression of DAP5/p97 and an inhibitor of apoptosis protein HIAP2 are enhanced during ER stress; their mRNAs are selectively recruited to the polysomes via IRES elements located in their respective 5′ UTRs. | true | true | true | true | true | 6,529 |
2 | INTRODUCTION | 0 | null | null | 18,003,655 | pmid-16174738|NA|NA|NA|pmid-11032820|NA|pmid-16932749|pmid-16932749|pmid-11032820 | We further find that this process is dependent on DAP5/p97, as reducing the levels of endogenous DAP5/p97 by RNA interference abrogated the IRES-mediated translation of both DAP5/p97 and HIAP2 during ER stress. | null | 210 | 38,060 | 0 | false | null | null | We further find that this process is dependent on DAP5/p97, as reducing the levels of endogenous DAP5/p97 by RNA interference abrogated the IRES-mediated translation of both DAP5/p97 and HIAP2 during ER stress. | true | true | true | true | true | 6,529 |
2 | INTRODUCTION | 0 | null | null | 18,003,655 | pmid-16174738|NA|NA|NA|pmid-11032820|NA|pmid-16932749|pmid-16932749|pmid-11032820 | Moreover, we find that proteolytic cleavage of DAP5/p97 to the DAP5/p86 isoform is not required for the translational induction of DAP5/p97 during ER stress. | null | 157 | 38,061 | 0 | false | null | null | Moreover, we find that proteolytic cleavage of DAP5/p97 to the DAP5/p86 isoform is not required for the translational induction of DAP5/p97 during ER stress. | true | true | true | true | true | 6,529 |
2 | INTRODUCTION | 0 | null | null | 18,003,655 | pmid-16174738|NA|NA|NA|pmid-11032820|NA|pmid-16932749|pmid-16932749|pmid-11032820 | Thus, a positive feedback loop exists in which ER stress results in elevated levels of DAP5/p97 that, in turn, activate translation of specific mRNAs such as HIAP2 and DAP5/p97 itself under conditions of reduced cap-dependent translation. | null | 238 | 38,062 | 0 | false | null | null | Thus, a positive feedback loop exists in which ER stress results in elevated levels of DAP5/p97 that, in turn, activate translation of specific mRNAs such as HIAP2 and DAP5/p97 itself under conditions of reduced cap-dependent translation. | true | true | true | true | true | 6,529 |
0 | DISCUSSION | 1 | 11 | [
"B11"
] | 18,003,655 | pmid-15277680|pmid-15479734|pmid-15003273|pmid-15803138|pmid-2839775|pmid-2839690|pmid-15803138|pmid-11050335|pmid-14960583 | In this work, we demonstrate that a member of the eIF4G translation initiation factor family, DAP5/p97, is necessary for the specific activation of at least two cellular IRES elements during pharmacologically induced ER stress. | [
"11"
] | 227 | 38,063 | 0 | false | In this work, we demonstrate that a member of the eIF4G translation initiation factor family, DAP5/p97, is necessary for the specific activation of at least two cellular IRES elements during pharmacologically induced ER stress. | [] | In this work, we demonstrate that a member of the eIF4G translation initiation factor family, DAP5/p97, is necessary for the specific activation of at least two cellular IRES elements during pharmacologically induced ER stress. | true | true | true | true | true | 6,530 |
0 | DISCUSSION | 1 | 11 | [
"B11"
] | 18,003,655 | pmid-15277680|pmid-15479734|pmid-15003273|pmid-15803138|pmid-2839775|pmid-2839690|pmid-15803138|pmid-11050335|pmid-14960583 | We find that DAP5/p97 and HIAP2 protein levels are enhanced during ER stress; their mRNAs are selectively recruited to the polysomes via IRES elements located within their respective 5′ UTRs. | [
"11"
] | 191 | 38,064 | 0 | false | We find that DAP5/p97 and HIAP2 protein levels are enhanced during ER stress; their mRNAs are selectively recruited to the polysomes via IRES elements located within their respective 5′ UTRs. | [] | We find that DAP5/p97 and HIAP2 protein levels are enhanced during ER stress; their mRNAs are selectively recruited to the polysomes via IRES elements located within their respective 5′ UTRs. | true | true | true | true | true | 6,530 |
0 | DISCUSSION | 1 | 11 | [
"B11"
] | 18,003,655 | pmid-15277680|pmid-15479734|pmid-15003273|pmid-15803138|pmid-2839775|pmid-2839690|pmid-15803138|pmid-11050335|pmid-14960583 | We further find that this process is dependent on DAP5/p97, as reducing the levels of endogenous DAP5/p97 by RNA interference abrogated both the translation and IRES activity of DAP5/p97 and HIAP2 during ER stress. | [
"11"
] | 214 | 38,065 | 0 | false | We further find that this process is dependent on DAP5/p97, as reducing the levels of endogenous DAP5/p97 by RNA interference abrogated both the translation and IRES activity of DAP5/p97 and HIAP2 during ER stress. | [] | We further find that this process is dependent on DAP5/p97, as reducing the levels of endogenous DAP5/p97 by RNA interference abrogated both the translation and IRES activity of DAP5/p97 and HIAP2 during ER stress. | true | true | true | true | true | 6,530 |
0 | DISCUSSION | 1 | 11 | [
"B11"
] | 18,003,655 | pmid-15277680|pmid-15479734|pmid-15003273|pmid-15803138|pmid-2839775|pmid-2839690|pmid-15803138|pmid-11050335|pmid-14960583 | Thus, in a positive feedback loop the triggering of ER stress results in elevated levels of DAP5/p97 that, in turn, activate translation of specific mRNAs such as HIAP2 and DAP5/p97 itself under conditions of reduced cap-dependent translation. | [
"11"
] | 243 | 38,066 | 0 | false | Thus, in a positive feedback loop the triggering of ER stress results in elevated levels of DAP5/p97 that, in turn, activate translation of specific mRNAs such as HIAP2 and DAP5/p97 itself under conditions of reduced cap-dependent translation. | [] | Thus, in a positive feedback loop the triggering of ER stress results in elevated levels of DAP5/p97 that, in turn, activate translation of specific mRNAs such as HIAP2 and DAP5/p97 itself under conditions of reduced cap-dependent translation. | true | true | true | true | true | 6,530 |
0 | DISCUSSION | 1 | 11 | [
"B11"
] | 18,003,655 | pmid-15277680|pmid-15479734|pmid-15003273|pmid-15803138|pmid-2839775|pmid-2839690|pmid-15803138|pmid-11050335|pmid-14960583 | Moreover, while cleavage of p97 to the DAP5/p86 isoform is required for the induction of HIAP2 IRES activity during ER stress (11), the translational induction of DAP5/p97 during ER stress is mediated by DAP5/p97 itself in a caspase-independent manner. | [
"11"
] | 252 | 38,067 | 1 | false | Moreover, while cleavage of p97 to the DAP5/p86 isoform is required for the induction of HIAP2 IRES activity during ER stress, the translational induction of DAP5/p97 during ER stress is mediated by DAP5/p97 itself in a caspase-independent manner. | [
"11"
] | Moreover, while cleavage of p97 to the DAP5/p86 isoform is required for the induction of HIAP2 IRES activity during ER stress, the translational induction of DAP5/p97 during ER stress is mediated by DAP5/p97 itself in a caspase-independent manner. | true | true | true | true | true | 6,530 |
0 | DISCUSSION | 1 | 11 | [
"B11"
] | 18,003,655 | pmid-15277680|pmid-15479734|pmid-15003273|pmid-15803138|pmid-2839775|pmid-2839690|pmid-15803138|pmid-11050335|pmid-14960583 | The pivotal role of DAP5/p97 is further strengthened by our observation that siRNA-mediated reduction of DAP5/p97 results in cell death. | [
"11"
] | 136 | 38,068 | 0 | false | The pivotal role of DAP5/p97 is further strengthened by our observation that siRNA-mediated reduction of DAP5/p97 results in cell death. | [] | The pivotal role of DAP5/p97 is further strengthened by our observation that siRNA-mediated reduction of DAP5/p97 results in cell death. | true | true | true | true | true | 6,530 |
1 | DISCUSSION | 1 | 28 | [
"B28",
"B29",
"B30",
"B31",
"B29",
"B32",
"B33",
"B28",
"B29",
"B34",
"B10 B11 B12 B13",
"B4",
"B7",
"B11",
"B31"
] | 18,003,655 | pmid-15094769|pmid-15818406|pmid-15803138|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-16174738|pmid-16932749|pmid-9049310|pmid-9030685|pmid-9032289|NA|pmid-9030685|pmid-9372926|pmid-9878069|pmid-9049310|pmid-9030685|pmid-11032820|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-15803138|pmi... | DAP5/p97 was identified by several groups by virtue of its homology to eIF4G (28), as a target of the APOBEC-1 editing enzyme that is heavily edited in the liver (29) and in a functional screening assay to identify modulators of interferon γ-induced apoptosis (30). | [
"28",
"29",
"30",
"31",
"29",
"32",
"33",
"28",
"29",
"34",
"10–13",
"4",
"7",
"11",
"31"
] | 265 | 38,069 | 1 | false | DAP5/p97 was identified by several groups by virtue of its homology to eIF4G, as a target of the APOBEC-1 editing enzyme that is heavily edited in the liver and in a functional screening assay to identify modulators of interferon γ-induced apoptosis. | [
"28",
"29",
"30"
] | DAP5/p97 was identified by several groups by virtue of its homology to eIF4G, as a target of the APOBEC-1 editing enzyme that is heavily edited in the liver and in a functional screening assay to identify modulators of interferon γ-induced apoptosis. | true | true | true | true | true | 6,531 |
1 | DISCUSSION | 1 | 31 | [
"B28",
"B29",
"B30",
"B31",
"B29",
"B32",
"B33",
"B28",
"B29",
"B34",
"B10 B11 B12 B13",
"B4",
"B7",
"B11",
"B31"
] | 18,003,655 | pmid-15094769|pmid-15818406|pmid-15803138|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-16174738|pmid-16932749|pmid-9049310|pmid-9030685|pmid-9032289|NA|pmid-9030685|pmid-9372926|pmid-9878069|pmid-9049310|pmid-9030685|pmid-11032820|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-15803138|pmi... | DAP5/p97 shares significant homology to eIF4G; however, this homology is restricted to the central and C-terminal portions of eIF4G (31). | [
"28",
"29",
"30",
"31",
"29",
"32",
"33",
"28",
"29",
"34",
"10–13",
"4",
"7",
"11",
"31"
] | 137 | 38,070 | 1 | false | DAP5/p97 shares significant homology to eIF4G; however, this homology is restricted to the central and C-terminal portions of eIF4G. | [
"31"
] | DAP5/p97 shares significant homology to eIF4G; however, this homology is restricted to the central and C-terminal portions of eIF4G. | true | true | true | true | true | 6,531 |
1 | DISCUSSION | 1 | 28 | [
"B28",
"B29",
"B30",
"B31",
"B29",
"B32",
"B33",
"B28",
"B29",
"B34",
"B10 B11 B12 B13",
"B4",
"B7",
"B11",
"B31"
] | 18,003,655 | pmid-15094769|pmid-15818406|pmid-15803138|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-16174738|pmid-16932749|pmid-9049310|pmid-9030685|pmid-9032289|NA|pmid-9030685|pmid-9372926|pmid-9878069|pmid-9049310|pmid-9030685|pmid-11032820|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-15803138|pmi... | Like eIF4G, DAP5/p97 can interact with eIF3, eIF4A and Mnk-1 (29,32,33). | [
"28",
"29",
"30",
"31",
"29",
"32",
"33",
"28",
"29",
"34",
"10–13",
"4",
"7",
"11",
"31"
] | 72 | 38,071 | 0 | false | Like eIF4G, DAP5/p97 can interact with eIF3, eIF4A and Mnk-1. | [
"29,32,33"
] | Like eIF4G, DAP5/p97 can interact with eIF3, eIF4A and Mnk-1. | true | true | true | true | true | 6,531 |
1 | DISCUSSION | 1 | 28 | [
"B28",
"B29",
"B30",
"B31",
"B29",
"B32",
"B33",
"B28",
"B29",
"B34",
"B10 B11 B12 B13",
"B4",
"B7",
"B11",
"B31"
] | 18,003,655 | pmid-15094769|pmid-15818406|pmid-15803138|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-16174738|pmid-16932749|pmid-9049310|pmid-9030685|pmid-9032289|NA|pmid-9030685|pmid-9372926|pmid-9878069|pmid-9049310|pmid-9030685|pmid-11032820|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-15803138|pmi... | Unlike eIF4G, however, DAP5/p97 lacks the amino-terminal portion that includes the eIF4E and PABP-binding domains. | [
"28",
"29",
"30",
"31",
"29",
"32",
"33",
"28",
"29",
"34",
"10–13",
"4",
"7",
"11",
"31"
] | 114 | 38,072 | 0 | false | Unlike eIF4G, however, DAP5/p97 lacks the amino-terminal portion that includes the eIF4E and PABP-binding domains. | [] | Unlike eIF4G, however, DAP5/p97 lacks the amino-terminal portion that includes the eIF4E and PABP-binding domains. | true | true | true | true | true | 6,531 |
1 | DISCUSSION | 1 | 28 | [
"B28",
"B29",
"B30",
"B31",
"B29",
"B32",
"B33",
"B28",
"B29",
"B34",
"B10 B11 B12 B13",
"B4",
"B7",
"B11",
"B31"
] | 18,003,655 | pmid-15094769|pmid-15818406|pmid-15803138|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-16174738|pmid-16932749|pmid-9049310|pmid-9030685|pmid-9032289|NA|pmid-9030685|pmid-9372926|pmid-9878069|pmid-9049310|pmid-9030685|pmid-11032820|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-15803138|pmi... | Therefore, it is believed that DAP5/p97 cannot support cap-dependent translation initiation. | [
"28",
"29",
"30",
"31",
"29",
"32",
"33",
"28",
"29",
"34",
"10–13",
"4",
"7",
"11",
"31"
] | 92 | 38,073 | 0 | false | Therefore, it is believed that DAP5/p97 cannot support cap-dependent translation initiation. | [] | Therefore, it is believed that DAP5/p97 cannot support cap-dependent translation initiation. | true | true | true | true | true | 6,531 |
1 | DISCUSSION | 1 | 28 | [
"B28",
"B29",
"B30",
"B31",
"B29",
"B32",
"B33",
"B28",
"B29",
"B34",
"B10 B11 B12 B13",
"B4",
"B7",
"B11",
"B31"
] | 18,003,655 | pmid-15094769|pmid-15818406|pmid-15803138|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-16174738|pmid-16932749|pmid-9049310|pmid-9030685|pmid-9032289|NA|pmid-9030685|pmid-9372926|pmid-9878069|pmid-9049310|pmid-9030685|pmid-11032820|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-15803138|pmi... | Consistent with this idea, overexpression of DAP5/p97 was found to repress both cap-dependent and EMCV IRES-dependent translation, presumably by sequestering eIF3 and eIF4A in inactive complexes (28,29). | [
"28",
"29",
"30",
"31",
"29",
"32",
"33",
"28",
"29",
"34",
"10–13",
"4",
"7",
"11",
"31"
] | 203 | 38,074 | 0 | false | Consistent with this idea, overexpression of DAP5/p97 was found to repress both cap-dependent and EMCV IRES-dependent translation, presumably by sequestering eIF3 and eIF4A in inactive complexes. | [
"28,29"
] | Consistent with this idea, overexpression of DAP5/p97 was found to repress both cap-dependent and EMCV IRES-dependent translation, presumably by sequestering eIF3 and eIF4A in inactive complexes. | true | true | true | true | true | 6,531 |
1 | DISCUSSION | 1 | 34 | [
"B28",
"B29",
"B30",
"B31",
"B29",
"B32",
"B33",
"B28",
"B29",
"B34",
"B10 B11 B12 B13",
"B4",
"B7",
"B11",
"B31"
] | 18,003,655 | pmid-15094769|pmid-15818406|pmid-15803138|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-16174738|pmid-16932749|pmid-9049310|pmid-9030685|pmid-9032289|NA|pmid-9030685|pmid-9372926|pmid-9878069|pmid-9049310|pmid-9030685|pmid-11032820|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-15803138|pmi... | In contrast, however, DAP5/p97-null ES cells have normal levels of global protein synthesis and show no differences in the activities of several IRES (34). | [
"28",
"29",
"30",
"31",
"29",
"32",
"33",
"28",
"29",
"34",
"10–13",
"4",
"7",
"11",
"31"
] | 155 | 38,075 | 1 | false | In contrast, however, DAP5/p97-null ES cells have normal levels of global protein synthesis and show no differences in the activities of several IRES. | [
"34"
] | In contrast, however, DAP5/p97-null ES cells have normal levels of global protein synthesis and show no differences in the activities of several IRES. | true | true | true | true | true | 6,531 |
1 | DISCUSSION | 1 | 10–13 | [
"B28",
"B29",
"B30",
"B31",
"B29",
"B32",
"B33",
"B28",
"B29",
"B34",
"B10 B11 B12 B13",
"B4",
"B7",
"B11",
"B31"
] | 18,003,655 | pmid-15094769|pmid-15818406|pmid-15803138|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-16174738|pmid-16932749|pmid-9049310|pmid-9030685|pmid-9032289|NA|pmid-9030685|pmid-9372926|pmid-9878069|pmid-9049310|pmid-9030685|pmid-11032820|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-15803138|pmi... | Furthermore, many studies have shown that the caspase-cleaved fragment of DAP5/p97 (termed DAP5/p86), but not the full-length DAP5/p97, is capable of specifically enhancing the translation mediated by the Apaf-1, c-myc, XIAP, and HIAP2 IRES elements (10–13). | [
"28",
"29",
"30",
"31",
"29",
"32",
"33",
"28",
"29",
"34",
"10–13",
"4",
"7",
"11",
"31"
] | 258 | 38,076 | 1 | false | Furthermore, many studies have shown that the caspase-cleaved fragment of DAP5/p97 (termed DAP5/p86), but not the full-length DAP5/p97, is capable of specifically enhancing the translation mediated by the Apaf-1, c-myc, XIAP, and HIAP2 IRES elements. | [
"10–13"
] | Furthermore, many studies have shown that the caspase-cleaved fragment of DAP5/p97 (termed DAP5/p86), but not the full-length DAP5/p97, is capable of specifically enhancing the translation mediated by the Apaf-1, c-myc, XIAP, and HIAP2 IRES elements. | true | true | true | true | true | 6,531 |
1 | DISCUSSION | 1 | 28 | [
"B28",
"B29",
"B30",
"B31",
"B29",
"B32",
"B33",
"B28",
"B29",
"B34",
"B10 B11 B12 B13",
"B4",
"B7",
"B11",
"B31"
] | 18,003,655 | pmid-15094769|pmid-15818406|pmid-15803138|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-16174738|pmid-16932749|pmid-9049310|pmid-9030685|pmid-9032289|NA|pmid-9030685|pmid-9372926|pmid-9878069|pmid-9049310|pmid-9030685|pmid-11032820|pmid-12458215|pmid-14960583|pmid-11943866|pmid-10611228|pmid-15803138|pmi... | Thus a model has emerged in which DAP5/p97 is activated by caspase cleavage and the resulting DAP5/p86 fragment functions as a specific translation initiation factor for cellular IRES, in particular during conditions of pathophysiological stress (4,7,11,31). | [
"28",
"29",
"30",
"31",
"29",
"32",
"33",
"28",
"29",
"34",
"10–13",
"4",
"7",
"11",
"31"
] | 258 | 38,077 | 0 | false | Thus a model has emerged in which DAP5/p97 is activated by caspase cleavage and the resulting DAP5/p86 fragment functions as a specific translation initiation factor for cellular IRES, in particular during conditions of pathophysiological stress. | [
"4,7,11,31"
] | Thus a model has emerged in which DAP5/p97 is activated by caspase cleavage and the resulting DAP5/p86 fragment functions as a specific translation initiation factor for cellular IRES, in particular during conditions of pathophysiological stress. | true | true | true | true | true | 6,531 |
2 | DISCUSSION | 1 | 14 | [
"B14",
"B27",
"B35",
"B27",
"B34",
"B35",
"B15",
"B15",
"B34"
] | 18,003,655 | pmid-16174738|NA|NA|NA|pmid-11032820|NA|pmid-16932749|pmid-16932749|pmid-11032820 | However, several recent publications have challenged this model. | [
"14",
"27",
"35",
"27",
"34",
"35",
"15",
"15",
"34"
] | 64 | 38,078 | 0 | false | However, several recent publications have challenged this model. | [] | However, several recent publications have challenged this model. | true | true | true | true | true | 6,532 |
2 | DISCUSSION | 1 | 14 | [
"B14",
"B27",
"B35",
"B27",
"B34",
"B35",
"B15",
"B15",
"B34"
] | 18,003,655 | pmid-16174738|NA|NA|NA|pmid-11032820|NA|pmid-16932749|pmid-16932749|pmid-11032820 | It was shown that the addition of exogenous DAP5/p97 can stimulate the activity of the XIAP, c-myc, DAP5/p97 and HIAP2 IRES elements in a HeLa-based cell-free translation system depleted of eIF4G (14). | [
"14",
"27",
"35",
"27",
"34",
"35",
"15",
"15",
"34"
] | 201 | 38,079 | 1 | false | It was shown that the addition of exogenous DAP5/p97 can stimulate the activity of the XIAP, c-myc, DAP5/p97 and HIAP2 IRES elements in a HeLa-based cell-free translation system depleted of eIF4G. | [
"14"
] | It was shown that the addition of exogenous DAP5/p97 can stimulate the activity of the XIAP, c-myc, DAP5/p97 and HIAP2 IRES elements in a HeLa-based cell-free translation system depleted of eIF4G. | true | true | true | true | true | 6,532 |
2 | DISCUSSION | 1 | 14 | [
"B14",
"B27",
"B35",
"B27",
"B34",
"B35",
"B15",
"B15",
"B34"
] | 18,003,655 | pmid-16174738|NA|NA|NA|pmid-11032820|NA|pmid-16932749|pmid-16932749|pmid-11032820 | More recently, it was shown that DAP5/p97 can function as an activator of translation in vivo and this function of DAP5/p97 does not necessarily requires proteolytic processing (27,35). | [
"14",
"27",
"35",
"27",
"34",
"35",
"15",
"15",
"34"
] | 185 | 38,080 | 0 | false | More recently, it was shown that DAP5/p97 can function as an activator of translation in vivo and this function of DAP5/p97 does not necessarily requires proteolytic processing. | [
"27,35"
] | More recently, it was shown that DAP5/p97 can function as an activator of translation in vivo and this function of DAP5/p97 does not necessarily requires proteolytic processing. | true | true | true | true | true | 6,532 |
2 | DISCUSSION | 1 | 14 | [
"B14",
"B27",
"B35",
"B27",
"B34",
"B35",
"B15",
"B15",
"B34"
] | 18,003,655 | pmid-16174738|NA|NA|NA|pmid-11032820|NA|pmid-16932749|pmid-16932749|pmid-11032820 | In these experiments, DAP5/p97 was found to be associated with polysomes, overexpression of DAP5/p97 resulted in the activation of cap-dependent reporter mRNA translation and global protein synthesis and siRNA-mediated knockdown of DAP5/p97 led to a reduction of global protein synthesis. | [
"14",
"27",
"35",
"27",
"34",
"35",
"15",
"15",
"34"
] | 288 | 38,081 | 0 | false | In these experiments, DAP5/p97 was found to be associated with polysomes, overexpression of DAP5/p97 resulted in the activation of cap-dependent reporter mRNA translation and global protein synthesis and siRNA-mediated knockdown of DAP5/p97 led to a reduction of global protein synthesis. | [] | In these experiments, DAP5/p97 was found to be associated with polysomes, overexpression of DAP5/p97 resulted in the activation of cap-dependent reporter mRNA translation and global protein synthesis and siRNA-mediated knockdown of DAP5/p97 led to a reduction of global protein synthesis. | true | true | true | true | true | 6,532 |
2 | DISCUSSION | 1 | 14 | [
"B14",
"B27",
"B35",
"B27",
"B34",
"B35",
"B15",
"B15",
"B34"
] | 18,003,655 | pmid-16174738|NA|NA|NA|pmid-11032820|NA|pmid-16932749|pmid-16932749|pmid-11032820 | These observations are all consistent with the role of DAP5/p97 as an activator of translation. | [
"14",
"27",
"35",
"27",
"34",
"35",
"15",
"15",
"34"
] | 95 | 38,082 | 0 | false | These observations are all consistent with the role of DAP5/p97 as an activator of translation. | [] | These observations are all consistent with the role of DAP5/p97 as an activator of translation. | true | true | true | true | true | 6,532 |
2 | DISCUSSION | 1 | 14 | [
"B14",
"B27",
"B35",
"B27",
"B34",
"B35",
"B15",
"B15",
"B34"
] | 18,003,655 | pmid-16174738|NA|NA|NA|pmid-11032820|NA|pmid-16932749|pmid-16932749|pmid-11032820 | In addition, reduced DAP5/p97 levels result in a reduction in cell viability and embryonic lethality in both zebrafish and mouse (27,34,35). | [
"14",
"27",
"35",
"27",
"34",
"35",
"15",
"15",
"34"
] | 140 | 38,083 | 0 | false | In addition, reduced DAP5/p97 levels result in a reduction in cell viability and embryonic lethality in both zebrafish and mouse. | [
"27,34,35"
] | In addition, reduced DAP5/p97 levels result in a reduction in cell viability and embryonic lethality in both zebrafish and mouse. | true | true | true | true | true | 6,532 |
2 | DISCUSSION | 1 | 14 | [
"B14",
"B27",
"B35",
"B27",
"B34",
"B35",
"B15",
"B15",
"B34"
] | 18,003,655 | pmid-16174738|NA|NA|NA|pmid-11032820|NA|pmid-16932749|pmid-16932749|pmid-11032820 | Our data confirm the observation that DAP5/p97 knockdown is not compatible with cell survival. | [
"14",
"27",
"35",
"27",
"34",
"35",
"15",
"15",
"34"
] | 94 | 38,084 | 0 | false | Our data confirm the observation that DAP5/p97 knockdown is not compatible with cell survival. | [] | Our data confirm the observation that DAP5/p97 knockdown is not compatible with cell survival. | true | true | true | true | true | 6,532 |
2 | DISCUSSION | 1 | 15 | [
"B14",
"B27",
"B35",
"B27",
"B34",
"B35",
"B15",
"B15",
"B34"
] | 18,003,655 | pmid-16174738|NA|NA|NA|pmid-11032820|NA|pmid-16932749|pmid-16932749|pmid-11032820 | However, in contrast to the data of Lee and McCormick (15), we find that a reduction in DAP5/p97 levels does not affect global protein synthesis (Figure 4A). | [
"14",
"27",
"35",
"27",
"34",
"35",
"15",
"15",
"34"
] | 157 | 38,085 | 1 | false | However, in contrast to the data of Lee and McCormick, we find that a reduction in DAP5/p97 levels does not affect global protein synthesis (Figure 4A). | [
"15"
] | However, in contrast to the data of Lee and McCormick, we find that a reduction in DAP5/p97 levels does not affect global protein synthesis (Figure 4A). | true | true | true | true | true | 6,532 |
2 | DISCUSSION | 1 | 14 | [
"B14",
"B27",
"B35",
"B27",
"B34",
"B35",
"B15",
"B15",
"B34"
] | 18,003,655 | pmid-16174738|NA|NA|NA|pmid-11032820|NA|pmid-16932749|pmid-16932749|pmid-11032820 | The likely explanation for this discrepancy is that, while Lee and McCormick assessed protein synthesis 48 h post- | [
"14",
"27",
"35",
"27",
"34",
"35",
"15",
"15",
"34"
] | 114 | 38,086 | 0 | false | The likely explanation for this discrepancy is that, while Lee and McCormick assessed protein synthesis 48 h post- | [] | The likely explanation for this discrepancy is that, while Lee and McCormick assessed protein synthesis 48 h post- | true | true | false | true | false | 6,532 |
2 | DISCUSSION | 1 | 14 | [
"B14",
"B27",
"B35",
"B27",
"B34",
"B35",
"B15",
"B15",
"B34"
] | 18,003,655 | pmid-16174738|NA|NA|NA|pmid-11032820|NA|pmid-16932749|pmid-16932749|pmid-11032820 | DAP5/p97 knockdown, in our experiments polysome profiling was performed 24 h after siRNA treatment because we observed a significant loss of cell viability after this timepoint. | [
"14",
"27",
"35",
"27",
"34",
"35",
"15",
"15",
"34"
] | 177 | 38,087 | 0 | false | DAP5/p97 knockdown, in our experiments polysome profiling was performed 24 h after siRNA treatment because we observed a significant loss of cell viability after this timepoint. | [] | DAP5/p97 knockdown, in our experiments polysome profiling was performed 24 h after siRNA treatment because we observed a significant loss of cell viability after this timepoint. | true | true | true | true | true | 6,532 |
2 | DISCUSSION | 1 | 14 | [
"B14",
"B27",
"B35",
"B27",
"B34",
"B35",
"B15",
"B15",
"B34"
] | 18,003,655 | pmid-16174738|NA|NA|NA|pmid-11032820|NA|pmid-16932749|pmid-16932749|pmid-11032820 | It should also be noted that DAP5/p97-null ES cells do not display a defect in global protein synthesis (15,34) suggesting that the role of DAP5/97 in the regulation of global translation may be cell-type specific. | [
"14",
"27",
"35",
"27",
"34",
"35",
"15",
"15",
"34"
] | 214 | 38,088 | 0 | false | It should also be noted that DAP5/p97-null ES cells do not display a defect in global protein synthesis suggesting that the role of DAP5/97 in the regulation of global translation may be cell-type specific. | [
"15,34"
] | It should also be noted that DAP5/p97-null ES cells do not display a defect in global protein synthesis suggesting that the role of DAP5/97 in the regulation of global translation may be cell-type specific. | true | true | true | true | true | 6,532 |
3 | DISCUSSION | 1 | 10–12 | [
"B10 B11 B12",
"B11",
"B36",
"B27"
] | 18,003,655 | pmid-12458215|pmid-14960583|pmid-11943866|pmid-14960583|pmid-15302935|NA | We and others have shown previously that overexpression of the p86 fragment of DAP5/p97 is sufficient to activate the DAP5/p97 and HIAP2 IRES elements (10–12). | [
"10–12",
"11",
"36",
"27"
] | 159 | 38,089 | 1 | false | We and others have shown previously that overexpression of the p86 fragment of DAP5/p97 is sufficient to activate the DAP5/p97 and HIAP2 IRES elements. | [
"10–12"
] | We and others have shown previously that overexpression of the p86 fragment of DAP5/p97 is sufficient to activate the DAP5/p97 and HIAP2 IRES elements. | true | true | true | true | true | 6,533 |
3 | DISCUSSION | 1 | 10–12 | [
"B10 B11 B12",
"B11",
"B36",
"B27"
] | 18,003,655 | pmid-12458215|pmid-14960583|pmid-11943866|pmid-14960583|pmid-15302935|NA | Here we have extended these observations by demonstrating that both DAP5/p97 and HIAP2 IRES-mediated translation are dependent on DAP5/p97, since the knockdown of p97 significantly reduces translation of DAP5/p97 itself and HIAP2 during ER stress by precluding activation of their respective IRES elements. | [
"10–12",
"11",
"36",
"27"
] | 306 | 38,090 | 0 | false | Here we have extended these observations by demonstrating that both DAP5/p97 and HIAP2 IRES-mediated translation are dependent on DAP5/p97, since the knockdown of p97 significantly reduces translation of DAP5/p97 itself and HIAP2 during ER stress by precluding activation of their respective IRES elements. | [] | Here we have extended these observations by demonstrating that both DAP5/p97 and HIAP2 IRES-mediated translation are dependent on DAP5/p97, since the knockdown of p97 significantly reduces translation of DAP5/p97 itself and HIAP2 during ER stress by precluding activation of their respective IRES elements. | true | true | true | true | true | 6,533 |
3 | DISCUSSION | 1 | 11 | [
"B10 B11 B12",
"B11",
"B36",
"B27"
] | 18,003,655 | pmid-12458215|pmid-14960583|pmid-11943866|pmid-14960583|pmid-15302935|NA | However, in contrast to the requirement of caspase-mediated cleavage of DAP5/p97 to the p86 isoform for induction of HIAP2 IRES activity (11), we find that the translational induction of DAP5/p97 following ER stress does not require caspase activity. | [
"10–12",
"11",
"36",
"27"
] | 250 | 38,091 | 1 | false | However, in contrast to the requirement of caspase-mediated cleavage of DAP5/p97 to the p86 isoform for induction of HIAP2 IRES activity, we find that the translational induction of DAP5/p97 following ER stress does not require caspase activity. | [
"11"
] | However, in contrast to the requirement of caspase-mediated cleavage of DAP5/p97 to the p86 isoform for induction of HIAP2 IRES activity, we find that the translational induction of DAP5/p97 following ER stress does not require caspase activity. | true | true | true | true | true | 6,533 |
3 | DISCUSSION | 1 | 10–12 | [
"B10 B11 B12",
"B11",
"B36",
"B27"
] | 18,003,655 | pmid-12458215|pmid-14960583|pmid-11943866|pmid-14960583|pmid-15302935|NA | Since DAP5/p97 is absolutely required for the translational induction of DAP5/p97 during ER stress, we conclude that DAP5/p97 enhances the activity of its IRES in a caspase-independent manner. | [
"10–12",
"11",
"36",
"27"
] | 192 | 38,092 | 0 | false | Since DAP5/p97 is absolutely required for the translational induction of DAP5/p97 during ER stress, we conclude that DAP5/p97 enhances the activity of its IRES in a caspase-independent manner. | [] | Since DAP5/p97 is absolutely required for the translational induction of DAP5/p97 during ER stress, we conclude that DAP5/p97 enhances the activity of its IRES in a caspase-independent manner. | true | true | true | true | true | 6,533 |
3 | DISCUSSION | 1 | 10–12 | [
"B10 B11 B12",
"B11",
"B36",
"B27"
] | 18,003,655 | pmid-12458215|pmid-14960583|pmid-11943866|pmid-14960583|pmid-15302935|NA | These data support the hypothesis that DAP5/p97 can function as a translational activator in the absence of proteolytic processing. | [
"10–12",
"11",
"36",
"27"
] | 131 | 38,093 | 0 | false | These data support the hypothesis that DAP5/p97 can function as a translational activator in the absence of proteolytic processing. | [] | These data support the hypothesis that DAP5/p97 can function as a translational activator in the absence of proteolytic processing. | true | true | true | true | true | 6,533 |
3 | DISCUSSION | 1 | 10–12 | [
"B10 B11 B12",
"B11",
"B36",
"B27"
] | 18,003,655 | pmid-12458215|pmid-14960583|pmid-11943866|pmid-14960583|pmid-15302935|NA | It is possible that other post-translational modifications of DAP5/p97 during ER stress control its ability to modulate IRES activity. | [
"10–12",
"11",
"36",
"27"
] | 134 | 38,094 | 0 | false | It is possible that other post-translational modifications of DAP5/p97 during ER stress control its ability to modulate IRES activity. | [] | It is possible that other post-translational modifications of DAP5/p97 during ER stress control its ability to modulate IRES activity. | true | true | true | true | true | 6,533 |
3 | DISCUSSION | 1 | 36 | [
"B10 B11 B12",
"B11",
"B36",
"B27"
] | 18,003,655 | pmid-12458215|pmid-14960583|pmid-11943866|pmid-14960583|pmid-15302935|NA | Indeed, phosphorylation of DAP5/p97 at threonine 508 was identified by a large-scale proteomics study (36) and it has been suggested that phosphorylation of DAP5/p97 controls its activity in response to growth factor signaling (27). | [
"10–12",
"11",
"36",
"27"
] | 232 | 38,095 | 1 | false | Indeed, phosphorylation of DAP5/p97 at threonine 508 was identified by a large-scale proteomics study and it has been suggested that phosphorylation of DAP5/p97 controls its activity in response to growth factor signaling. | [
"36",
"27"
] | Indeed, phosphorylation of DAP5/p97 at threonine 508 was identified by a large-scale proteomics study and it has been suggested that phosphorylation of DAP5/p97 controls its activity in response to growth factor signaling. | true | true | true | true | true | 6,533 |
3 | DISCUSSION | 1 | 10–12 | [
"B10 B11 B12",
"B11",
"B36",
"B27"
] | 18,003,655 | pmid-12458215|pmid-14960583|pmid-11943866|pmid-14960583|pmid-15302935|NA | Further investigations of the signaling pathways that modulate DAP5/p97 activity during cellular stress or following growth factor stimulation should prove to be enlightening. | [
"10–12",
"11",
"36",
"27"
] | 175 | 38,096 | 0 | false | Further investigations of the signaling pathways that modulate DAP5/p97 activity during cellular stress or following growth factor stimulation should prove to be enlightening. | [] | Further investigations of the signaling pathways that modulate DAP5/p97 activity during cellular stress or following growth factor stimulation should prove to be enlightening. | true | true | true | true | true | 6,533 |
4 | DISCUSSION | 0 | null | null | 18,003,655 | null | We sought to mechanistically determine how full-length DAP5/p97 differentiates between distinct mRNA molecules such as DAP5/p97 and HIAP2. | null | 138 | 38,097 | 0 | false | null | null | We sought to mechanistically determine how full-length DAP5/p97 differentiates between distinct mRNA molecules such as DAP5/p97 and HIAP2. | true | true | true | true | true | 6,534 |
4 | DISCUSSION | 0 | null | null | 18,003,655 | null | Our data indicate that both full-length DAP5/p97 and the truncated p86 fragment are capable of binding DAP5/p97 and HIAP2 endogenous mRNAs equally well. | null | 152 | 38,098 | 0 | false | null | null | Our data indicate that both full-length DAP5/p97 and the truncated p86 fragment are capable of binding DAP5/p97 and HIAP2 endogenous mRNAs equally well. | true | true | true | true | true | 6,534 |
4 | DISCUSSION | 0 | null | null | 18,003,655 | null | Thus, the simple model whereby DAP5/p97 associates with a particular pool of cellular mRNAs while its DAP5/p86 truncated isoform associates with a different cohort of mRNAs is unlikely. | null | 185 | 38,099 | 0 | false | null | null | Thus, the simple model whereby DAP5/p97 associates with a particular pool of cellular mRNAs while its DAP5/p86 truncated isoform associates with a different cohort of mRNAs is unlikely. | true | true | true | true | true | 6,534 |
4 | DISCUSSION | 0 | null | null | 18,003,655 | null | Our observations raise the possibility that full-length DAP5/p97 preassembles with several mRNAs, but is only able to enhance IRES-dependent translation following a particular post-translational modification, which may be different depending on the target mRNA molecule. | null | 270 | 38,100 | 0 | false | null | null | Our observations raise the possibility that full-length DAP5/p97 preassembles with several mRNAs, but is only able to enhance IRES-dependent translation following a particular post-translational modification, which may be different depending on the target mRNA molecule. | true | true | true | true | true | 6,534 |
4 | DISCUSSION | 0 | null | null | 18,003,655 | null | For example, caspase cleavage of DAP5/p97 to generate the DAP5/p86 isoform enhances both DAP5/p97 and HIAP2 IRES activity, whereas other post-translational modifications (such as phosphorylation) may be sufficient to allow full-length DAP5/p97 to enhance the activity of its own IRES. | null | 284 | 38,101 | 0 | false | null | null | For example, caspase cleavage of DAP5/p97 to generate the DAP5/p86 isoform enhances both DAP5/p97 and HIAP2 IRES activity, whereas other post-translational modifications (such as phosphorylation) may be sufficient to allow full-length DAP5/p97 to enhance the activity of its own IRES. | true | true | true | true | true | 6,534 |
5 | DISCUSSION | 1 | 35 | [
"B35"
] | 18,003,655 | NA | In summary, our data provide direct evidence that DAP5/p97 can function as a translational activator of at least two IRES-containing cellular mRNAs during conditions of pathophysiological stress. | [
"35"
] | 195 | 38,102 | 0 | false | In summary, our data provide direct evidence that DAP5/p97 can function as a translational activator of at least two IRES-containing cellular mRNAs during conditions of pathophysiological stress. | [] | In summary, our data provide direct evidence that DAP5/p97 can function as a translational activator of at least two IRES-containing cellular mRNAs during conditions of pathophysiological stress. | true | true | true | true | true | 6,535 |
5 | DISCUSSION | 1 | 35 | [
"B35"
] | 18,003,655 | NA | Together with previously published observations (35), these findings support the hypothesis that DAP5/p97 controls translation of select, rather than all, mRNAs. | [
"35"
] | 161 | 38,103 | 1 | false | Together with previously published observations, these findings support the hypothesis that DAP5/p97 controls translation of select, rather than all, mRNAs. | [
"35"
] | Together with previously published observations, these findings support the hypothesis that DAP5/p97 controls translation of select, rather than all, mRNAs. | true | true | true | true | true | 6,535 |
5 | DISCUSSION | 1 | 35 | [
"B35"
] | 18,003,655 | NA | Importantly, the fact that the DAP5/p97 IRES itself is activated by DAP5/p97 during ER stress suggests the existence of a positive feedback loop that ensures elevated levels of DAP5/p97 to support IRES-dependent translation of select mRNAs during conditions of reduced global protein synthesis. | [
"35"
] | 294 | 38,104 | 0 | false | Importantly, the fact that the DAP5/p97 IRES itself is activated by DAP5/p97 during ER stress suggests the existence of a positive feedback loop that ensures elevated levels of DAP5/p97 to support IRES-dependent translation of select mRNAs during conditions of reduced global protein synthesis. | [] | Importantly, the fact that the DAP5/p97 IRES itself is activated by DAP5/p97 during ER stress suggests the existence of a positive feedback loop that ensures elevated levels of DAP5/p97 to support IRES-dependent translation of select mRNAs during conditions of reduced global protein synthesis. | true | true | true | true | true | 6,535 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B3",
"B4"
] | 17,066,524 | pmid-4020086|pmid-1778144|pmid-2919305|pmid-4020086|pmid-4020086|pmid-11693342|pmid-11693342|pmid-4020086 | Hamartomatous polyps of the colon are rare in adults, and nearly all cases are associated with hereditary or familial polyposis syndromes.1-3 Colonic hamartomas are non-neoplastic lesions1, and these mucosal protuberances contain mesenchymal elements of excess vascular and/or fibrous stroma and glandular proliferation ... | [
"1",
"3",
"4"
] | 343 | 38,105 | 0 | false | Hamartomatous polyps of the colon are rare in adults, and nearly all cases are associated with hereditary or familial polyposis syndromes.1-3 Colonic hamartomas are non-neoplastic lesions1, and these mucosal protuberances contain mesenchymal elements of excess vascular and/or fibrous stroma and glandular proliferation ... | [] | Hamartomatous polyps of the colon are rare in adults, and nearly all cases are associated with hereditary or familial polyposis syndromes.1-3 Colonic hamartomas are non-neoplastic lesions1, and these mucosal protuberances contain mesenchymal elements of excess vascular and/or fibrous stroma and glandular proliferation ... | true | true | true | true | true | 6,536 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B3",
"B4"
] | 17,066,524 | pmid-4020086|pmid-1778144|pmid-2919305|pmid-4020086|pmid-4020086|pmid-11693342|pmid-11693342|pmid-4020086 | Mesenchymal proliferation disorders are heterogeneous, and excessive growth may be a post-natal indication of an underlying developmental abnormality.4 | [
"1",
"3",
"4"
] | 151 | 38,106 | 0 | false | Mesenchymal proliferation disorders are heterogeneous, and excessive growth may be a post-natal indication of an underlying developmental abnormality.4 | [] | Mesenchymal proliferation disorders are heterogeneous, and excessive growth may be a post-natal indication of an underlying developmental abnormality.4 | true | true | false | true | false | 6,536 |
1 | INTRODUCTION | 0 | null | null | 17,066,524 | pmid-4317531 | Here, we report an unusual case of a giant colonic hamartoma in a 48-year-old man that is not associated with other hereditary or familial polyposis syndromes. | null | 159 | 38,107 | 0 | false | null | null | Here, we report an unusual case of a giant colonic hamartoma in a 48-year-old man that is not associated with other hereditary or familial polyposis syndromes. | true | true | true | true | true | 6,537 |
0 | DISCUSSION | 1 | 1 | [
"B1",
"B1",
"B2",
"B2",
"B1"
] | 17,066,524 | pmid-4020086|pmid-1778144|pmid-2919305|pmid-4020086|pmid-4020086|pmid-11693342|pmid-11693342|pmid-4020086 | Colonic hamartomas, or juvenile polyps, are acquired lesions most commonly found in individuals between 1 and 7 years of age. | [
"1",
"1",
"2",
"2",
"1"
] | 125 | 38,108 | 0 | false | Colonic hamartomas, or juvenile polyps, are acquired lesions most commonly found in individuals between 1 and 7 years of age. | [] | Colonic hamartomas, or juvenile polyps, are acquired lesions most commonly found in individuals between 1 and 7 years of age. | true | true | true | true | true | 6,538 |
0 | DISCUSSION | 1 | 1 | [
"B1",
"B1",
"B2",
"B2",
"B1"
] | 17,066,524 | pmid-4020086|pmid-1778144|pmid-2919305|pmid-4020086|pmid-4020086|pmid-11693342|pmid-11693342|pmid-4020086 | The lesions are usually associated with hereditary or familial polyposis syndromes. | [
"1",
"1",
"2",
"2",
"1"
] | 83 | 38,109 | 0 | false | The lesions are usually associated with hereditary or familial polyposis syndromes. | [] | The lesions are usually associated with hereditary or familial polyposis syndromes. | true | true | true | true | true | 6,538 |
0 | DISCUSSION | 1 | 1 | [
"B1",
"B1",
"B2",
"B2",
"B1"
] | 17,066,524 | pmid-4020086|pmid-1778144|pmid-2919305|pmid-4020086|pmid-4020086|pmid-11693342|pmid-11693342|pmid-4020086 | These colonic polyps are usually less than 4 cm in size, although larger polyps have been found.1 A MEDLINE search from 1966 to 2003 using hamartoma, colonic polyp, and giant hamartoma as search items was performed. | [
"1",
"1",
"2",
"2",
"1"
] | 215 | 38,110 | 0 | false | These colonic polyps are usually less than 4 cm in size, although larger polyps have been found.1 A MEDLINE search from 1966 to 2003 using hamartoma, colonic polyp, and giant hamartoma as search items was performed. | [] | These colonic polyps are usually less than 4 cm in size, although larger polyps have been found.1 A MEDLINE search from 1966 to 2003 using hamartoma, colonic polyp, and giant hamartoma as search items was performed. | true | true | true | true | true | 6,538 |
0 | DISCUSSION | 1 | 1 | [
"B1",
"B1",
"B2",
"B2",
"B1"
] | 17,066,524 | pmid-4020086|pmid-1778144|pmid-2919305|pmid-4020086|pmid-4020086|pmid-11693342|pmid-11693342|pmid-4020086 | After excluding hereditary and familial polyposis syndromes, only three relevant articles were found in English language journals. | [
"1",
"1",
"2",
"2",
"1"
] | 130 | 38,111 | 0 | false | After excluding hereditary and familial polyposis syndromes, only three relevant articles were found in English language journals. | [] | After excluding hereditary and familial polyposis syndromes, only three relevant articles were found in English language journals. | true | true | true | true | true | 6,538 |
0 | DISCUSSION | 1 | 1 | [
"B1",
"B1",
"B2",
"B2",
"B1"
] | 17,066,524 | pmid-4020086|pmid-1778144|pmid-2919305|pmid-4020086|pmid-4020086|pmid-11693342|pmid-11693342|pmid-4020086 | Colonic hamartoma, particularly of a large size and without mucocutaneous lesions, is rare and has been reported only twice.1,2 One report involved a 50-year-old man with ulcerative colitis. | [
"1",
"1",
"2",
"2",
"1"
] | 190 | 38,112 | 0 | false | Colonic hamartoma, particularly of a large size and without mucocutaneous lesions, is rare and has been reported only twice.1,2 One report involved a 50-year-old man with ulcerative colitis. | [] | Colonic hamartoma, particularly of a large size and without mucocutaneous lesions, is rare and has been reported only twice.1,2 One report involved a 50-year-old man with ulcerative colitis. | true | true | true | true | true | 6,538 |
0 | DISCUSSION | 1 | 1 | [
"B1",
"B1",
"B2",
"B2",
"B1"
] | 17,066,524 | pmid-4020086|pmid-1778144|pmid-2919305|pmid-4020086|pmid-4020086|pmid-11693342|pmid-11693342|pmid-4020086 | In this case, the lesion was located in the ascending colon and was approximately 5 cm in length. | [
"1",
"1",
"2",
"2",
"1"
] | 97 | 38,113 | 0 | false | In this case, the lesion was located in the ascending colon and was approximately 5 cm in length. | [] | In this case, the lesion was located in the ascending colon and was approximately 5 cm in length. | true | true | true | true | true | 6,538 |
0 | DISCUSSION | 1 | 1 | [
"B1",
"B1",
"B2",
"B2",
"B1"
] | 17,066,524 | pmid-4020086|pmid-1778144|pmid-2919305|pmid-4020086|pmid-4020086|pmid-11693342|pmid-11693342|pmid-4020086 | Resection was performed, because the large polypoid mass could not be distinguished from a possibly malignant mass.2 The other case involved a 26-year-old man with multiple large bowel polyps and a single immense colonic Peutz-Jeghers polyp.1 An endoscopic biopsy showed this to be an inflammatory polyp. | [
"1",
"1",
"2",
"2",
"1"
] | 304 | 38,114 | 0 | false | Resection was performed, because the large polypoid mass could not be distinguished from a possibly malignant mass.2 The other case involved a 26-year-old man with multiple large bowel polyps and a single immense colonic Peutz-Jeghers polyp.1 An endoscopic biopsy showed this to be an inflammatory polyp. | [] | Resection was performed, because the large polypoid mass could not be distinguished from a possibly malignant mass.2 The other case involved a 26-year-old man with multiple large bowel polyps and a single immense colonic Peutz-Jeghers polyp.1 An endoscopic biopsy showed this to be an inflammatory polyp. | true | true | true | true | true | 6,538 |
0 | DISCUSSION | 1 | 1 | [
"B1",
"B1",
"B2",
"B2",
"B1"
] | 17,066,524 | pmid-4020086|pmid-1778144|pmid-2919305|pmid-4020086|pmid-4020086|pmid-11693342|pmid-11693342|pmid-4020086 | The lesion was postoperatively diagnosed as a hamartoma. | [
"1",
"1",
"2",
"2",
"1"
] | 56 | 38,115 | 0 | false | The lesion was postoperatively diagnosed as a hamartoma. | [] | The lesion was postoperatively diagnosed as a hamartoma. | true | true | true | true | true | 6,538 |
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