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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
46 | DISCUSSION | 0 | null | null | 20,198,134 | null | Good growth at 37 °C, though slower at 30 °C. | null | 45 | 42,119 | 0 | false | null | null | Good growth at 37 °C, though slower at 30 °C. | true | true | true | true | true | 7,290 |
46 | DISCUSSION | 0 | null | null | 20,198,134 | null | Good growth on MEA with 0.5 % acetic acid and CYA with 1 000 ppm propionic acid (pH 3.8). | null | 89 | 42,120 | 0 | false | null | null | Good growth on MEA with 0.5 % acetic acid and CYA with 1 000 ppm propionic acid (pH 3.8). | true | true | true | true | true | 7,290 |
46 | DISCUSSION | 0 | null | null | 20,198,134 | null | No growth observed on CYA with 5 % NaCl. | null | 40 | 42,121 | 0 | false | null | null | No growth observed on CYA with 5 % NaCl. | true | true | true | true | true | 7,290 |
46 | DISCUSSION | 0 | null | null | 20,198,134 | null | Poor growth and no acid production on CREA. | null | 43 | 42,122 | 0 | false | null | null | Poor growth and no acid production on CREA. | true | true | true | true | true | 7,290 |
47 | DISCUSSION | 0 | null | null | 20,198,134 | null | Morphological examination of various strains showed that this species forms fairly regularly branched, penicillium-like conidiophores, with ellipsoidal and/or cylindrical conidia without a distinct truncation. | null | 209 | 42,123 | 0 | false | null | null | Morphological examination of various strains showed that this species forms fairly regularly branched, penicillium-like conidiophores, with ellipsoidal and/or cylindrical conidia without a distinct truncation. | true | true | true | true | true | 7,291 |
47 | DISCUSSION | 0 | null | null | 20,198,134 | null | Chlamydospores present, hyaline and smooth walled. | null | 50 | 42,124 | 0 | false | null | null | Chlamydospores present, hyaline and smooth walled. | true | true | true | true | true | 7,291 |
47 | DISCUSSION | 0 | null | null | 20,198,134 | null | No teleomorph observed. | null | 23 | 42,125 | 0 | false | null | null | No teleomorph observed. | true | true | true | true | true | 7,291 |
48 | DISCUSSION | 0 | null | null | 20,198,134 | null | The production of extrolites depends very much on the growth medium; patulin or brefeldin A can be produced. | null | 108 | 42,126 | 0 | false | null | null | The production of extrolites depends very much on the growth medium; patulin or brefeldin A can be produced. | true | true | true | true | true | 7,292 |
49 | DISCUSSION | 1 | Sakaguchi et al. (1939) | [
"R41",
"R39",
"R31"
] | 20,198,134 | NA|NA|NA |
Paecilomyces saturatus is an easily recognisable species with its ellipsoidal and/or cylindrical conidia and its fairy regularly branched, penicillium-like conidiophores. | [
"Sakaguchi et al. (1939)",
"Raper & Thom (1949)",
"Luangsa-ard et al. 2004"
] | 176 | 42,127 | 0 | false | Paecilomyces saturatus is an easily recognisable species with its ellipsoidal and/or cylindrical conidia and its fairy regularly branched, penicillium-like conidiophores. | [] | Paecilomyces saturatus is an easily recognisable species with its ellipsoidal and/or cylindrical conidia and its fairy regularly branched, penicillium-like conidiophores. | true | true | true | true | true | 7,293 |
49 | DISCUSSION | 1 | Sakaguchi et al. (1939) | [
"R41",
"R39",
"R31"
] | 20,198,134 | NA|NA|NA | Sakaguchi et al. | [
"Sakaguchi et al. (1939)",
"Raper & Thom (1949)",
"Luangsa-ard et al. 2004"
] | 16 | 42,128 | 0 | false | Sakaguchi et al. | [] | Sakaguchi et al. | true | true | true | true | true | 7,293 |
49 | DISCUSSION | 1 | Sakaguchi et al. (1939) | [
"R41",
"R39",
"R31"
] | 20,198,134 | NA|NA|NA | (1939) described Penicillium viniferum and this species was subsequently placed in Paecilomyces by Raper & Thom (1949). | [
"Sakaguchi et al. (1939)",
"Raper & Thom (1949)",
"Luangsa-ard et al. 2004"
] | 119 | 42,129 | 0 | false | (1939) described Penicillium viniferum and this species was subsequently placed in Paecilomyces by Raper & Thom (1949). | [] | described Penicillium viniferum and this species was subsequently placed in Paecilomyces by Raper & Thom. | false | true | true | true | false | 7,293 |
49 | DISCUSSION | 1 | Sakaguchi et al. (1939) | [
"R41",
"R39",
"R31"
] | 20,198,134 | NA|NA|NA | In retrospect, the placement in Paecilomyces was correct, although this species could be interpreted, with its penicillium-like conidiophores and the presence of chlamydospores, as an intermediate form between Penicillium and Paecilomyces. | [
"Sakaguchi et al. (1939)",
"Raper & Thom (1949)",
"Luangsa-ard et al. 2004"
] | 239 | 42,130 | 0 | false | In retrospect, the placement in Paecilomyces was correct, although this species could be interpreted, with its penicillium-like conidiophores and the presence of chlamydospores, as an intermediate form between Penicillium and Paecilomyces. | [] | In retrospect, the placement in Paecilomyces was correct, although this species could be interpreted, with its penicillium-like conidiophores and the presence of chlamydospores, as an intermediate form between Penicillium and Paecilomyces. | true | true | true | true | true | 7,293 |
49 | DISCUSSION | 1 | Sakaguchi et al. (1939) | [
"R41",
"R39",
"R31"
] | 20,198,134 | NA|NA|NA | Molecular studies now show that this species belongs to the Byssochlamys clade and is different from other olive-brown coloured species such as Hamigera avellanea (Luangsa-ard et al. | [
"Sakaguchi et al. (1939)",
"Raper & Thom (1949)",
"Luangsa-ard et al. 2004"
] | 182 | 42,131 | 0 | false | Molecular studies now show that this species belongs to the Byssochlamys clade and is different from other olive-brown coloured species such as Hamigera avellanea (Luangsa-ard et al. | [] | Molecular studies now show that this species belongs to the Byssochlamys clade and is different from other olive-brown coloured species such as Hamigera avellanea (Luangsa-ard et al. | true | true | true | true | true | 7,293 |
49 | DISCUSSION | 1 | Sakaguchi et al. (1939) | [
"R41",
"R39",
"R31"
] | 20,198,134 | NA|NA|NA | 2004), Penicillium digitatum and P. cylindrosporum (unpubl. | [
"Sakaguchi et al. (1939)",
"Raper & Thom (1949)",
"Luangsa-ard et al. 2004"
] | 59 | 42,132 | 0 | false | 2004), Penicillium digitatum and P. cylindrosporum (unpubl. | [] | 2004), Penicillium digitatum and P. cylindrosporum (unpubl. | false | false | true | true | false | 7,293 |
50 | DISCUSSION | 0 | null | null | 20,198,134 | null | This species has been isolated from a variety of substrates, e.g. | null | 65 | 42,133 | 0 | false | null | null | This species has been isolated from a variety of substrates, e.g. | true | true | true | true | true | 7,294 |
50 | DISCUSSION | 0 | null | null | 20,198,134 | null | acetic acid, leather, medicine containing quinine, a dispersion of fenylacetate and dibutylmaleinate and Lepidium sativum. | null | 122 | 42,134 | 0 | false | null | null | acetic acid, leather, medicine containing quinine, a dispersion of fenylacetate and dibutylmaleinate and Lepidium sativum. | false | true | true | true | false | 7,294 |
51 | DISCUSSION | 1 | Scurti et al. 1973 | [
"R46",
"R11",
"R12",
"R2",
"R14",
"R11",
"R12",
"R54",
"R24",
"R27",
"R25",
"R46",
"R40",
"R10",
"R11",
"R12",
"R35",
"R40",
"R26",
"R40",
"R32"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA |
Byssochlamys and Paecilomyces species are often found in acidic habitats such as silage (Scurti et al. | [
"Scurti et al. 1973",
"Escoula 1975a",
"b",
"Anderson et al. 1979",
"Frisvad & Samson 2004",
"Escoula 1975a",
"b",
"Taniwaki 1995",
"Karow & Forster 1944",
"Kuehn 1958",
"Kis et al. (1969)",
"Scurti et al. (1973)",
"Rice et al. (1977)",
"Draughon & Ayres (1980)",
"Escoula 1975a",
"b",
... | 108 | 42,135 | 0 | false | Byssochlamys and Paecilomyces species are often found in acidic habitats such as silage (Scurti et al. | [] | Byssochlamys and Paecilomyces species are often found in acidic habitats such as silage (Scurti et al. | true | true | true | true | true | 7,295 |
51 | DISCUSSION | 1 | Scurti et al. 1973 | [
"R46",
"R11",
"R12",
"R2",
"R14",
"R11",
"R12",
"R54",
"R24",
"R27",
"R25",
"R46",
"R40",
"R10",
"R11",
"R12",
"R35",
"R40",
"R26",
"R40",
"R32"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | 1973, Escoula 1975a, b, Anderson et al. | [
"Scurti et al. 1973",
"Escoula 1975a",
"b",
"Anderson et al. 1979",
"Frisvad & Samson 2004",
"Escoula 1975a",
"b",
"Taniwaki 1995",
"Karow & Forster 1944",
"Kuehn 1958",
"Kis et al. (1969)",
"Scurti et al. (1973)",
"Rice et al. (1977)",
"Draughon & Ayres (1980)",
"Escoula 1975a",
"b",
... | 39 | 42,136 | 0 | false | 1973, Escoula 1975a, b, Anderson et al. | [] | 1973, Escoula 1975a, b, Anderson et al. | false | false | true | true | false | 7,295 |
51 | DISCUSSION | 1 | Frisvad & Samson 2004 | [
"R46",
"R11",
"R12",
"R2",
"R14",
"R11",
"R12",
"R54",
"R24",
"R27",
"R25",
"R46",
"R40",
"R10",
"R11",
"R12",
"R35",
"R40",
"R26",
"R40",
"R32"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | 1979), and in common with Penicillium series Roqueforti species (Frisvad & Samson 2004) can also tolerate microaerophilic conditions (Escoula 1975a, b, Taniwaki 1995). | [
"Scurti et al. 1973",
"Escoula 1975a",
"b",
"Anderson et al. 1979",
"Frisvad & Samson 2004",
"Escoula 1975a",
"b",
"Taniwaki 1995",
"Karow & Forster 1944",
"Kuehn 1958",
"Kis et al. (1969)",
"Scurti et al. (1973)",
"Rice et al. (1977)",
"Draughon & Ayres (1980)",
"Escoula 1975a",
"b",
... | 167 | 42,137 | 1 | false | 1979), and in common with Penicillium series Roqueforti species can also tolerate microaerophilic conditions. | [
"Frisvad & Samson 2004",
"Escoula 1975a, b, Taniwaki 1995"
] | 1979), and in common with Penicillium series Roqueforti species can also tolerate microaerophilic conditions. | false | false | true | true | false | 7,295 |
51 | DISCUSSION | 1 | Scurti et al. 1973 | [
"R46",
"R11",
"R12",
"R2",
"R14",
"R11",
"R12",
"R54",
"R24",
"R27",
"R25",
"R46",
"R40",
"R10",
"R11",
"R12",
"R35",
"R40",
"R26",
"R40",
"R32"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | Byssochlamys nivea was initially reported to produce patulin under the name Gymnoascus sp. | [
"Scurti et al. 1973",
"Escoula 1975a",
"b",
"Anderson et al. 1979",
"Frisvad & Samson 2004",
"Escoula 1975a",
"b",
"Taniwaki 1995",
"Karow & Forster 1944",
"Kuehn 1958",
"Kis et al. (1969)",
"Scurti et al. (1973)",
"Rice et al. (1977)",
"Draughon & Ayres (1980)",
"Escoula 1975a",
"b",
... | 90 | 42,138 | 0 | false | Byssochlamys nivea was initially reported to produce patulin under the name Gymnoascus sp. | [] | Byssochlamys nivea was initially reported to produce patulin under the name Gymnoascus sp. | true | true | true | true | true | 7,295 |
51 | DISCUSSION | 1 | Scurti et al. 1973 | [
"R46",
"R11",
"R12",
"R2",
"R14",
"R11",
"R12",
"R54",
"R24",
"R27",
"R25",
"R46",
"R40",
"R10",
"R11",
"R12",
"R35",
"R40",
"R26",
"R40",
"R32"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | (Karow & Forster 1944, Kuehn 1958), later confirmed by Kis et al. | [
"Scurti et al. 1973",
"Escoula 1975a",
"b",
"Anderson et al. 1979",
"Frisvad & Samson 2004",
"Escoula 1975a",
"b",
"Taniwaki 1995",
"Karow & Forster 1944",
"Kuehn 1958",
"Kis et al. (1969)",
"Scurti et al. (1973)",
"Rice et al. (1977)",
"Draughon & Ayres (1980)",
"Escoula 1975a",
"b",
... | 65 | 42,139 | 0 | false | , later confirmed by Kis et al. | [
"Karow & Forster 1944, Kuehn 1958"
] | , later confirmed by Kis et al. | false | false | true | true | false | 7,295 |
51 | DISCUSSION | 1 | Scurti et al. 1973 | [
"R46",
"R11",
"R12",
"R2",
"R14",
"R11",
"R12",
"R54",
"R24",
"R27",
"R25",
"R46",
"R40",
"R10",
"R11",
"R12",
"R35",
"R40",
"R26",
"R40",
"R32"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | (1969), Scurti et al. | [
"Scurti et al. 1973",
"Escoula 1975a",
"b",
"Anderson et al. 1979",
"Frisvad & Samson 2004",
"Escoula 1975a",
"b",
"Taniwaki 1995",
"Karow & Forster 1944",
"Kuehn 1958",
"Kis et al. (1969)",
"Scurti et al. (1973)",
"Rice et al. (1977)",
"Draughon & Ayres (1980)",
"Escoula 1975a",
"b",
... | 21 | 42,140 | 0 | false | (1969), Scurti et al. | [] | , Scurti et al. | false | false | true | true | false | 7,295 |
51 | DISCUSSION | 1 | Scurti et al. 1973 | [
"R46",
"R11",
"R12",
"R2",
"R14",
"R11",
"R12",
"R54",
"R24",
"R27",
"R25",
"R46",
"R40",
"R10",
"R11",
"R12",
"R35",
"R40",
"R26",
"R40",
"R32"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | Rice et al. | [
"Scurti et al. 1973",
"Escoula 1975a",
"b",
"Anderson et al. 1979",
"Frisvad & Samson 2004",
"Escoula 1975a",
"b",
"Taniwaki 1995",
"Karow & Forster 1944",
"Kuehn 1958",
"Kis et al. (1969)",
"Scurti et al. (1973)",
"Rice et al. (1977)",
"Draughon & Ayres (1980)",
"Escoula 1975a",
"b",
... | 11 | 42,141 | 0 | false | Rice et al. | [] | Rice et al. | true | true | true | true | true | 7,295 |
51 | DISCUSSION | 1 | Scurti et al. 1973 | [
"R46",
"R11",
"R12",
"R2",
"R14",
"R11",
"R12",
"R54",
"R24",
"R27",
"R25",
"R46",
"R40",
"R10",
"R11",
"R12",
"R35",
"R40",
"R26",
"R40",
"R32"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | (1977) and Draughon & Ayres (1980). | [
"Scurti et al. 1973",
"Escoula 1975a",
"b",
"Anderson et al. 1979",
"Frisvad & Samson 2004",
"Escoula 1975a",
"b",
"Taniwaki 1995",
"Karow & Forster 1944",
"Kuehn 1958",
"Kis et al. (1969)",
"Scurti et al. (1973)",
"Rice et al. (1977)",
"Draughon & Ayres (1980)",
"Escoula 1975a",
"b",
... | 35 | 42,142 | 0 | false | (1977) and Draughon & Ayres (1980). | [] | and Draughon & Ayres. | false | true | true | true | false | 7,295 |
51 | DISCUSSION | 1 | Scurti et al. 1973 | [
"R46",
"R11",
"R12",
"R2",
"R14",
"R11",
"R12",
"R54",
"R24",
"R27",
"R25",
"R46",
"R40",
"R10",
"R11",
"R12",
"R35",
"R40",
"R26",
"R40",
"R32"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | Byssochlamys fulva was also reported to produce patulin, albeit by few strains (Escoula 1975a, b, Percebois et al. | [
"Scurti et al. 1973",
"Escoula 1975a",
"b",
"Anderson et al. 1979",
"Frisvad & Samson 2004",
"Escoula 1975a",
"b",
"Taniwaki 1995",
"Karow & Forster 1944",
"Kuehn 1958",
"Kis et al. (1969)",
"Scurti et al. (1973)",
"Rice et al. (1977)",
"Draughon & Ayres (1980)",
"Escoula 1975a",
"b",
... | 114 | 42,143 | 0 | false | Byssochlamys fulva was also reported to produce patulin, albeit by few strains (Escoula 1975a, b, Percebois et al. | [] | Byssochlamys fulva was also reported to produce patulin, albeit by few strains (Escoula 1975a, b, Percebois et al. | true | true | true | true | true | 7,295 |
51 | DISCUSSION | 1 | Scurti et al. 1973 | [
"R46",
"R11",
"R12",
"R2",
"R14",
"R11",
"R12",
"R54",
"R24",
"R27",
"R25",
"R46",
"R40",
"R10",
"R11",
"R12",
"R35",
"R40",
"R26",
"R40",
"R32"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | 1975, Rice et al. | [
"Scurti et al. 1973",
"Escoula 1975a",
"b",
"Anderson et al. 1979",
"Frisvad & Samson 2004",
"Escoula 1975a",
"b",
"Taniwaki 1995",
"Karow & Forster 1944",
"Kuehn 1958",
"Kis et al. (1969)",
"Scurti et al. (1973)",
"Rice et al. (1977)",
"Draughon & Ayres (1980)",
"Escoula 1975a",
"b",
... | 17 | 42,144 | 0 | false | 1975, Rice et al. | [] | 1975, Rice et al. | false | false | true | true | false | 7,295 |
51 | DISCUSSION | 1 | Scurti et al. 1973 | [
"R46",
"R11",
"R12",
"R2",
"R14",
"R11",
"R12",
"R54",
"R24",
"R27",
"R25",
"R46",
"R40",
"R10",
"R11",
"R12",
"R35",
"R40",
"R26",
"R40",
"R32"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | Besides their presence in pasteurised fruit, B. fulva and B. nivea also form toxic extrolites, such as byssotoxin A and byssochlamic acid (Kramer et al. | [
"Scurti et al. 1973",
"Escoula 1975a",
"b",
"Anderson et al. 1979",
"Frisvad & Samson 2004",
"Escoula 1975a",
"b",
"Taniwaki 1995",
"Karow & Forster 1944",
"Kuehn 1958",
"Kis et al. (1969)",
"Scurti et al. (1973)",
"Rice et al. (1977)",
"Draughon & Ayres (1980)",
"Escoula 1975a",
"b",
... | 152 | 42,145 | 0 | false | Besides their presence in pasteurised fruit, B. fulva and B. nivea also form toxic extrolites, such as byssotoxin A and byssochlamic acid (Kramer et al. | [] | Besides their presence in pasteurised fruit, B. fulva and B. nivea also form toxic extrolites, such as byssotoxin A and byssochlamic acid (Kramer et al. | true | true | true | true | true | 7,295 |
51 | DISCUSSION | 1 | Scurti et al. 1973 | [
"R46",
"R11",
"R12",
"R2",
"R14",
"R11",
"R12",
"R54",
"R24",
"R27",
"R25",
"R46",
"R40",
"R10",
"R11",
"R12",
"R35",
"R40",
"R26",
"R40",
"R32"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | 1976, Rice et al. | [
"Scurti et al. 1973",
"Escoula 1975a",
"b",
"Anderson et al. 1979",
"Frisvad & Samson 2004",
"Escoula 1975a",
"b",
"Taniwaki 1995",
"Karow & Forster 1944",
"Kuehn 1958",
"Kis et al. (1969)",
"Scurti et al. (1973)",
"Rice et al. (1977)",
"Draughon & Ayres (1980)",
"Escoula 1975a",
"b",
... | 17 | 42,146 | 0 | false | 1976, Rice et al. | [] | 1976, Rice et al. | false | false | true | true | false | 7,295 |
51 | DISCUSSION | 1 | Scurti et al. 1973 | [
"R46",
"R11",
"R12",
"R2",
"R14",
"R11",
"R12",
"R54",
"R24",
"R27",
"R25",
"R46",
"R40",
"R10",
"R11",
"R12",
"R35",
"R40",
"R26",
"R40",
"R32"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | Besides mycotoxins, also an antitumor metabolite, byssochlamysol, a steroid against IGF-1 dependent cancer cells, is produced by B. nivea (Mori et al. | [
"Scurti et al. 1973",
"Escoula 1975a",
"b",
"Anderson et al. 1979",
"Frisvad & Samson 2004",
"Escoula 1975a",
"b",
"Taniwaki 1995",
"Karow & Forster 1944",
"Kuehn 1958",
"Kis et al. (1969)",
"Scurti et al. (1973)",
"Rice et al. (1977)",
"Draughon & Ayres (1980)",
"Escoula 1975a",
"b",
... | 150 | 42,147 | 0 | false | Besides mycotoxins, also an antitumor metabolite, byssochlamysol, a steroid against IGF-1 dependent cancer cells, is produced by B. nivea (Mori et al. | [] | Besides mycotoxins, also an antitumor metabolite, byssochlamysol, a steroid against IGF-1 dependent cancer cells, is produced by B. nivea (Mori et al. | true | true | true | true | true | 7,295 |
52 | DISCUSSION | 1 | Scott 1965 | [
"R45",
"R11",
"R12",
"R17",
"R23",
"R60",
"R53",
"R52",
"R50",
"R34",
"R33",
"R13",
"R18",
"R7",
"R8",
"R9",
"R4",
"R59",
"R29",
"R41",
"R1"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA |
Paecilomyces variotii s.l. | [
"Scott 1965",
"Escoula 1975a",
"b",
"Frommer et al. 1992",
"Jiu & Mizuba 1974",
"Wang et al. 2003",
"Takeuchi et al. 1959",
"1964",
"Suzuki et al. 1990",
"Omolo et al. 2000",
"Nakajima et al. 1991",
"Fields et al. 1996",
"Hegde et al. 2003",
"Burton 1949",
"Diekmann 1967",
"Domsch et a... | 32 | 42,148 | 0 | false | Paecilomyces variotii s.l. | [] | Paecilomyces variotii s.l. | true | true | true | true | true | 7,296 |
52 | DISCUSSION | 1 | Scott 1965 | [
"R45",
"R11",
"R12",
"R17",
"R23",
"R60",
"R53",
"R52",
"R50",
"R34",
"R33",
"R13",
"R18",
"R7",
"R8",
"R9",
"R4",
"R59",
"R29",
"R41",
"R1"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | also produces mycotoxins (Scott 1965), such as patulin (Escoula 1975a, b), sphingofungin E and F (Frommer et al. | [
"Scott 1965",
"Escoula 1975a",
"b",
"Frommer et al. 1992",
"Jiu & Mizuba 1974",
"Wang et al. 2003",
"Takeuchi et al. 1959",
"1964",
"Suzuki et al. 1990",
"Omolo et al. 2000",
"Nakajima et al. 1991",
"Fields et al. 1996",
"Hegde et al. 2003",
"Burton 1949",
"Diekmann 1967",
"Domsch et a... | 112 | 42,149 | 1 | false | also produces mycotoxins, such as patulin, sphingofungin E and F (Frommer et al. | [
"Scott 1965",
"Escoula 1975a, b"
] | also produces mycotoxins, such as patulin, sphingofungin E and F (Frommer et al. | false | true | true | true | false | 7,296 |
52 | DISCUSSION | 1 | Jiu & Mizuba 1974 | [
"R45",
"R11",
"R12",
"R17",
"R23",
"R60",
"R53",
"R52",
"R50",
"R34",
"R33",
"R13",
"R18",
"R7",
"R8",
"R9",
"R4",
"R59",
"R29",
"R41",
"R1"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | 1992) and viriditoxin, reported originally from an isolate named Spicaria divaricata (Jiu & Mizuba 1974). | [
"Scott 1965",
"Escoula 1975a",
"b",
"Frommer et al. 1992",
"Jiu & Mizuba 1974",
"Wang et al. 2003",
"Takeuchi et al. 1959",
"1964",
"Suzuki et al. 1990",
"Omolo et al. 2000",
"Nakajima et al. 1991",
"Fields et al. 1996",
"Hegde et al. 2003",
"Burton 1949",
"Diekmann 1967",
"Domsch et a... | 105 | 42,150 | 1 | false | 1992) and viriditoxin, reported originally from an isolate named Spicaria divaricata. | [
"Jiu & Mizuba 1974"
] | 1992) and viriditoxin, reported originally from an isolate named Spicaria divaricata. | false | false | true | true | false | 7,296 |
52 | DISCUSSION | 1 | Scott 1965 | [
"R45",
"R11",
"R12",
"R17",
"R23",
"R60",
"R53",
"R52",
"R50",
"R34",
"R33",
"R13",
"R18",
"R7",
"R8",
"R9",
"R4",
"R59",
"R29",
"R41",
"R1"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | Apart from being reported as being a potential mycotoxin, viriditoxin has also been reported to be a candidate for treatment of antibiotic resistant bacteria (Wang et al. | [
"Scott 1965",
"Escoula 1975a",
"b",
"Frommer et al. 1992",
"Jiu & Mizuba 1974",
"Wang et al. 2003",
"Takeuchi et al. 1959",
"1964",
"Suzuki et al. 1990",
"Omolo et al. 2000",
"Nakajima et al. 1991",
"Fields et al. 1996",
"Hegde et al. 2003",
"Burton 1949",
"Diekmann 1967",
"Domsch et a... | 170 | 42,151 | 0 | false | Apart from being reported as being a potential mycotoxin, viriditoxin has also been reported to be a candidate for treatment of antibiotic resistant bacteria (Wang et al. | [] | Apart from being reported as being a potential mycotoxin, viriditoxin has also been reported to be a candidate for treatment of antibiotic resistant bacteria (Wang et al. | true | true | true | true | true | 7,296 |
52 | DISCUSSION | 1 | Scott 1965 | [
"R45",
"R11",
"R12",
"R17",
"R23",
"R60",
"R53",
"R52",
"R50",
"R34",
"R33",
"R13",
"R18",
"R7",
"R8",
"R9",
"R4",
"R59",
"R29",
"R41",
"R1"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | Among the known extrolites are the antifungal drug variotin (Takeuchi et al. | [
"Scott 1965",
"Escoula 1975a",
"b",
"Frommer et al. 1992",
"Jiu & Mizuba 1974",
"Wang et al. 2003",
"Takeuchi et al. 1959",
"1964",
"Suzuki et al. 1990",
"Omolo et al. 2000",
"Nakajima et al. 1991",
"Fields et al. 1996",
"Hegde et al. 2003",
"Burton 1949",
"Diekmann 1967",
"Domsch et a... | 76 | 42,152 | 0 | false | Among the known extrolites are the antifungal drug variotin (Takeuchi et al. | [] | Among the known extrolites are the antifungal drug variotin (Takeuchi et al. | true | true | true | true | true | 7,296 |
52 | DISCUSSION | 1 | Scott 1965 | [
"R45",
"R11",
"R12",
"R17",
"R23",
"R60",
"R53",
"R52",
"R50",
"R34",
"R33",
"R13",
"R18",
"R7",
"R8",
"R9",
"R4",
"R59",
"R29",
"R41",
"R1"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | 1959, 1964, Suzuki et al. | [
"Scott 1965",
"Escoula 1975a",
"b",
"Frommer et al. 1992",
"Jiu & Mizuba 1974",
"Wang et al. 2003",
"Takeuchi et al. 1959",
"1964",
"Suzuki et al. 1990",
"Omolo et al. 2000",
"Nakajima et al. 1991",
"Fields et al. 1996",
"Hegde et al. 2003",
"Burton 1949",
"Diekmann 1967",
"Domsch et a... | 25 | 42,153 | 0 | false | 1959, 1964, Suzuki et al. | [] | 1959, 1964, Suzuki et al. | false | false | true | true | false | 7,296 |
52 | DISCUSSION | 1 | Scott 1965 | [
"R45",
"R11",
"R12",
"R17",
"R23",
"R60",
"R53",
"R52",
"R50",
"R34",
"R33",
"R13",
"R18",
"R7",
"R8",
"R9",
"R4",
"R59",
"R29",
"R41",
"R1"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | 1990, Omolo et al. | [
"Scott 1965",
"Escoula 1975a",
"b",
"Frommer et al. 1992",
"Jiu & Mizuba 1974",
"Wang et al. 2003",
"Takeuchi et al. 1959",
"1964",
"Suzuki et al. 1990",
"Omolo et al. 2000",
"Nakajima et al. 1991",
"Fields et al. 1996",
"Hegde et al. 2003",
"Burton 1949",
"Diekmann 1967",
"Domsch et a... | 18 | 42,154 | 0 | false | 1990, Omolo et al. | [] | 1990, Omolo et al. | false | false | true | true | false | 7,296 |
52 | DISCUSSION | 1 | Scott 1965 | [
"R45",
"R11",
"R12",
"R17",
"R23",
"R60",
"R53",
"R52",
"R50",
"R34",
"R33",
"R13",
"R18",
"R7",
"R8",
"R9",
"R4",
"R59",
"R29",
"R41",
"R1"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | 2000), and other drug candidates such as cornexistins (Nakajima et al. | [
"Scott 1965",
"Escoula 1975a",
"b",
"Frommer et al. 1992",
"Jiu & Mizuba 1974",
"Wang et al. 2003",
"Takeuchi et al. 1959",
"1964",
"Suzuki et al. 1990",
"Omolo et al. 2000",
"Nakajima et al. 1991",
"Fields et al. 1996",
"Hegde et al. 2003",
"Burton 1949",
"Diekmann 1967",
"Domsch et a... | 70 | 42,155 | 0 | false | 2000), and other drug candidates such as cornexistins (Nakajima et al. | [] | 2000), and other drug candidates such as cornexistins (Nakajima et al. | false | false | true | true | false | 7,296 |
52 | DISCUSSION | 1 | Scott 1965 | [
"R45",
"R11",
"R12",
"R17",
"R23",
"R60",
"R53",
"R52",
"R50",
"R34",
"R33",
"R13",
"R18",
"R7",
"R8",
"R9",
"R4",
"R59",
"R29",
"R41",
"R1"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | 1991, Fields et al. | [
"Scott 1965",
"Escoula 1975a",
"b",
"Frommer et al. 1992",
"Jiu & Mizuba 1974",
"Wang et al. 2003",
"Takeuchi et al. 1959",
"1964",
"Suzuki et al. 1990",
"Omolo et al. 2000",
"Nakajima et al. 1991",
"Fields et al. 1996",
"Hegde et al. 2003",
"Burton 1949",
"Diekmann 1967",
"Domsch et a... | 19 | 42,156 | 0 | false | 1991, Fields et al. | [] | 1991, Fields et al. | false | false | true | true | false | 7,296 |
52 | DISCUSSION | 1 | Scott 1965 | [
"R45",
"R11",
"R12",
"R17",
"R23",
"R60",
"R53",
"R52",
"R50",
"R34",
"R33",
"R13",
"R18",
"R7",
"R8",
"R9",
"R4",
"R59",
"R29",
"R41",
"R1"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | 1996), SCH 643432 (Hegde et al. | [
"Scott 1965",
"Escoula 1975a",
"b",
"Frommer et al. 1992",
"Jiu & Mizuba 1974",
"Wang et al. 2003",
"Takeuchi et al. 1959",
"1964",
"Suzuki et al. 1990",
"Omolo et al. 2000",
"Nakajima et al. 1991",
"Fields et al. 1996",
"Hegde et al. 2003",
"Burton 1949",
"Diekmann 1967",
"Domsch et a... | 31 | 42,157 | 0 | false | 1996), SCH 643432 (Hegde et al. | [] | 1996), SCH 643432 (Hegde et al. | false | false | true | true | false | 7,296 |
52 | DISCUSSION | 1 | Burton 1949 | [
"R45",
"R11",
"R12",
"R17",
"R23",
"R60",
"R53",
"R52",
"R50",
"R34",
"R33",
"R13",
"R18",
"R7",
"R8",
"R9",
"R4",
"R59",
"R29",
"R41",
"R1"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | 2003) and a penicillin-like compound (Burton 1949). | [
"Scott 1965",
"Escoula 1975a",
"b",
"Frommer et al. 1992",
"Jiu & Mizuba 1974",
"Wang et al. 2003",
"Takeuchi et al. 1959",
"1964",
"Suzuki et al. 1990",
"Omolo et al. 2000",
"Nakajima et al. 1991",
"Fields et al. 1996",
"Hegde et al. 2003",
"Burton 1949",
"Diekmann 1967",
"Domsch et a... | 51 | 42,158 | 1 | false | 2003) and a penicillin-like compound. | [
"Burton 1949"
] | 2003) and a penicillin-like compound. | false | false | true | true | false | 7,296 |
52 | DISCUSSION | 1 | Scott 1965 | [
"R45",
"R11",
"R12",
"R17",
"R23",
"R60",
"R53",
"R52",
"R50",
"R34",
"R33",
"R13",
"R18",
"R7",
"R8",
"R9",
"R4",
"R59",
"R29",
"R41",
"R1"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | The sideramins ferrirubrin and fusigen (Diekmann 1967, Domsch et al. | [
"Scott 1965",
"Escoula 1975a",
"b",
"Frommer et al. 1992",
"Jiu & Mizuba 1974",
"Wang et al. 2003",
"Takeuchi et al. 1959",
"1964",
"Suzuki et al. 1990",
"Omolo et al. 2000",
"Nakajima et al. 1991",
"Fields et al. 1996",
"Hegde et al. 2003",
"Burton 1949",
"Diekmann 1967",
"Domsch et a... | 68 | 42,159 | 0 | false | The sideramins ferrirubrin and fusigen (Diekmann 1967, Domsch et al. | [] | The sideramins ferrirubrin and fusigen (Diekmann 1967, Domsch et al. | true | true | true | true | true | 7,296 |
52 | DISCUSSION | 1 | Scott 1965 | [
"R45",
"R11",
"R12",
"R17",
"R23",
"R60",
"R53",
"R52",
"R50",
"R34",
"R33",
"R13",
"R18",
"R7",
"R8",
"R9",
"R4",
"R59",
"R29",
"R41",
"R1"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | 1980) and the organic acids 3-indole-acetic acid (Bakalinerov 1968, Voinova-Raikova et al. | [
"Scott 1965",
"Escoula 1975a",
"b",
"Frommer et al. 1992",
"Jiu & Mizuba 1974",
"Wang et al. 2003",
"Takeuchi et al. 1959",
"1964",
"Suzuki et al. 1990",
"Omolo et al. 2000",
"Nakajima et al. 1991",
"Fields et al. 1996",
"Hegde et al. 2003",
"Burton 1949",
"Diekmann 1967",
"Domsch et a... | 90 | 42,160 | 0 | false | 1980) and the organic acids 3-indole-acetic acid (Bakalinerov 1968, Voinova-Raikova et al. | [] | 1980) and the organic acids 3-indole-acetic acid (Bakalinerov 1968, Voinova-Raikova et al. | false | false | true | true | false | 7,296 |
52 | DISCUSSION | 1 | Loesecke 1945 | [
"R45",
"R11",
"R12",
"R17",
"R23",
"R60",
"R53",
"R52",
"R50",
"R34",
"R33",
"R13",
"R18",
"R7",
"R8",
"R9",
"R4",
"R59",
"R29",
"R41",
"R1"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | 1969), citric acid (Loesecke 1945), ethyleneoxide-α, β-dicarboxylic acid (Sakaguchi et al. | [
"Scott 1965",
"Escoula 1975a",
"b",
"Frommer et al. 1992",
"Jiu & Mizuba 1974",
"Wang et al. 2003",
"Takeuchi et al. 1959",
"1964",
"Suzuki et al. 1990",
"Omolo et al. 2000",
"Nakajima et al. 1991",
"Fields et al. 1996",
"Hegde et al. 2003",
"Burton 1949",
"Diekmann 1967",
"Domsch et a... | 90 | 42,161 | 1 | false | 1969), citric acid, ethyleneoxide-α, β-dicarboxylic acid (Sakaguchi et al. | [
"Loesecke 1945"
] | 1969), citric acid, ethyleneoxide-α, β-dicarboxylic acid (Sakaguchi et al. | false | false | true | true | false | 7,296 |
52 | DISCUSSION | 1 | Scott 1965 | [
"R45",
"R11",
"R12",
"R17",
"R23",
"R60",
"R53",
"R52",
"R50",
"R34",
"R33",
"R13",
"R18",
"R7",
"R8",
"R9",
"R4",
"R59",
"R29",
"R41",
"R1"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | 1939), (3Z,5E)-octa-3,5-diene -1,3,4-tricarboxylic acid 3,4-anhydride (Aldridge et al. | [
"Scott 1965",
"Escoula 1975a",
"b",
"Frommer et al. 1992",
"Jiu & Mizuba 1974",
"Wang et al. 2003",
"Takeuchi et al. 1959",
"1964",
"Suzuki et al. 1990",
"Omolo et al. 2000",
"Nakajima et al. 1991",
"Fields et al. 1996",
"Hegde et al. 2003",
"Burton 1949",
"Diekmann 1967",
"Domsch et a... | 86 | 42,162 | 0 | false | 1939), (3Z,5E)-octa-3,5-diene -1,3,4-tricarboxylic acid 3,4-anhydride (Aldridge et al. | [] | 1939), -octa-3,5-diene -1,3,4-tricarboxylic acid 3,4-anhydride (Aldridge et al. | false | false | true | true | false | 7,296 |
52 | DISCUSSION | 1 | Scott 1965 | [
"R45",
"R11",
"R12",
"R17",
"R23",
"R60",
"R53",
"R52",
"R50",
"R34",
"R33",
"R13",
"R18",
"R7",
"R8",
"R9",
"R4",
"R59",
"R29",
"R41",
"R1"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | 1980) have also been reported. | [
"Scott 1965",
"Escoula 1975a",
"b",
"Frommer et al. 1992",
"Jiu & Mizuba 1974",
"Wang et al. 2003",
"Takeuchi et al. 1959",
"1964",
"Suzuki et al. 1990",
"Omolo et al. 2000",
"Nakajima et al. 1991",
"Fields et al. 1996",
"Hegde et al. 2003",
"Burton 1949",
"Diekmann 1967",
"Domsch et a... | 30 | 42,163 | 0 | false | 1980) have also been reported. | [] | 1980) have also been reported. | false | false | true | true | false | 7,296 |
52 | DISCUSSION | 1 | Scott 1965 | [
"R45",
"R11",
"R12",
"R17",
"R23",
"R60",
"R53",
"R52",
"R50",
"R34",
"R33",
"R13",
"R18",
"R7",
"R8",
"R9",
"R4",
"R59",
"R29",
"R41",
"R1"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | The possible mycotoxins and/or potential drugs byssotoxin | [
"Scott 1965",
"Escoula 1975a",
"b",
"Frommer et al. 1992",
"Jiu & Mizuba 1974",
"Wang et al. 2003",
"Takeuchi et al. 1959",
"1964",
"Suzuki et al. 1990",
"Omolo et al. 2000",
"Nakajima et al. 1991",
"Fields et al. 1996",
"Hegde et al. 2003",
"Burton 1949",
"Diekmann 1967",
"Domsch et a... | 57 | 42,164 | 0 | false | The possible mycotoxins and/or potential drugs byssotoxin | [] | The possible mycotoxins and/or potential drugs byssotoxin | true | true | false | true | false | 7,296 |
52 | DISCUSSION | 1 | Scott 1965 | [
"R45",
"R11",
"R12",
"R17",
"R23",
"R60",
"R53",
"R52",
"R50",
"R34",
"R33",
"R13",
"R18",
"R7",
"R8",
"R9",
"R4",
"R59",
"R29",
"R41",
"R1"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | A, sphingofungin E and F, SCH 643432 and byssochlamysol were not available to us as standards. | [
"Scott 1965",
"Escoula 1975a",
"b",
"Frommer et al. 1992",
"Jiu & Mizuba 1974",
"Wang et al. 2003",
"Takeuchi et al. 1959",
"1964",
"Suzuki et al. 1990",
"Omolo et al. 2000",
"Nakajima et al. 1991",
"Fields et al. 1996",
"Hegde et al. 2003",
"Burton 1949",
"Diekmann 1967",
"Domsch et a... | 94 | 42,165 | 0 | false | A, sphingofungin E and F, SCH 643432 and byssochlamysol were not available to us as standards. | [] | A, sphingofungin E and F, SCH 643432 and byssochlamysol were not available to us as standards. | true | true | true | true | true | 7,296 |
52 | DISCUSSION | 1 | Scott 1965 | [
"R45",
"R11",
"R12",
"R17",
"R23",
"R60",
"R53",
"R52",
"R50",
"R34",
"R33",
"R13",
"R18",
"R7",
"R8",
"R9",
"R4",
"R59",
"R29",
"R41",
"R1"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | Given the taxonomic revision presented here, it remains to be seen which species produce these extrolites. | [
"Scott 1965",
"Escoula 1975a",
"b",
"Frommer et al. 1992",
"Jiu & Mizuba 1974",
"Wang et al. 2003",
"Takeuchi et al. 1959",
"1964",
"Suzuki et al. 1990",
"Omolo et al. 2000",
"Nakajima et al. 1991",
"Fields et al. 1996",
"Hegde et al. 2003",
"Burton 1949",
"Diekmann 1967",
"Domsch et a... | 106 | 42,166 | 0 | false | Given the taxonomic revision presented here, it remains to be seen which species produce these extrolites. | [] | Given the taxonomic revision presented here, it remains to be seen which species produce these extrolites. | true | true | true | true | true | 7,296 |
52 | DISCUSSION | 1 | Scott 1965 | [
"R45",
"R11",
"R12",
"R17",
"R23",
"R60",
"R53",
"R52",
"R50",
"R34",
"R33",
"R13",
"R18",
"R7",
"R8",
"R9",
"R4",
"R59",
"R29",
"R41",
"R1"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | Some connections between species and bioactive extrolites were confirmed or established here and several species had a high consistent extrolite profile. | [
"Scott 1965",
"Escoula 1975a",
"b",
"Frommer et al. 1992",
"Jiu & Mizuba 1974",
"Wang et al. 2003",
"Takeuchi et al. 1959",
"1964",
"Suzuki et al. 1990",
"Omolo et al. 2000",
"Nakajima et al. 1991",
"Fields et al. 1996",
"Hegde et al. 2003",
"Burton 1949",
"Diekmann 1967",
"Domsch et a... | 153 | 42,167 | 0 | false | Some connections between species and bioactive extrolites were confirmed or established here and several species had a high consistent extrolite profile. | [] | Some connections between species and bioactive extrolites were confirmed or established here and several species had a high consistent extrolite profile. | true | true | true | true | true | 7,296 |
52 | DISCUSSION | 1 | Scott 1965 | [
"R45",
"R11",
"R12",
"R17",
"R23",
"R60",
"R53",
"R52",
"R50",
"R34",
"R33",
"R13",
"R18",
"R7",
"R8",
"R9",
"R4",
"R59",
"R29",
"R41",
"R1"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | However, the chemotaxonomy of P. saturatus is unresolved, because there appear to be two chemotypes, which may or may not indicate that there are two species rather than one. | [
"Scott 1965",
"Escoula 1975a",
"b",
"Frommer et al. 1992",
"Jiu & Mizuba 1974",
"Wang et al. 2003",
"Takeuchi et al. 1959",
"1964",
"Suzuki et al. 1990",
"Omolo et al. 2000",
"Nakajima et al. 1991",
"Fields et al. 1996",
"Hegde et al. 2003",
"Burton 1949",
"Diekmann 1967",
"Domsch et a... | 174 | 42,168 | 0 | false | However, the chemotaxonomy of P. saturatus is unresolved, because there appear to be two chemotypes, which may or may not indicate that there are two species rather than one. | [] | However, the chemotaxonomy of P. saturatus is unresolved, because there appear to be two chemotypes, which may or may not indicate that there are two species rather than one. | true | true | true | true | true | 7,296 |
52 | DISCUSSION | 1 | Scott 1965 | [
"R45",
"R11",
"R12",
"R17",
"R23",
"R60",
"R53",
"R52",
"R50",
"R34",
"R33",
"R13",
"R18",
"R7",
"R8",
"R9",
"R4",
"R59",
"R29",
"R41",
"R1"
] | 20,198,134 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | Likewise, B. fulva appears to have two chemotypes, with only byssochlamic acid as a common extrolite in all isolates examined. | [
"Scott 1965",
"Escoula 1975a",
"b",
"Frommer et al. 1992",
"Jiu & Mizuba 1974",
"Wang et al. 2003",
"Takeuchi et al. 1959",
"1964",
"Suzuki et al. 1990",
"Omolo et al. 2000",
"Nakajima et al. 1991",
"Fields et al. 1996",
"Hegde et al. 2003",
"Burton 1949",
"Diekmann 1967",
"Domsch et a... | 126 | 42,169 | 0 | false | Likewise, B. fulva appears to have two chemotypes, with only byssochlamic acid as a common extrolite in all isolates examined. | [] | Likewise, B. fulva appears to have two chemotypes, with only byssochlamic acid as a common extrolite in all isolates examined. | true | true | true | true | true | 7,296 |
53 | DISCUSSION | 0 | null | null | 20,198,134 | null | Conidia with conspicuously truncate ends or a flattened base……………2 | null | 66 | 42,170 | 0 | false | null | null | Conidia with conspicuously truncate ends or a flattened base……………2 | true | true | false | true | false | 7,297 |
54 | DISCUSSION | 0 | null | null | 20,198,134 | null | Conidia ellipsoidal or cylindrical with inconspicuously truncate ends……………P. | null | 76 | 42,171 | 0 | false | null | null | Conidia ellipsoidal or cylindrical with inconspicuously truncate ends……………P. | true | true | true | true | true | 7,298 |
55 | DISCUSSION | 0 | null | null | 20,198,134 | null | Conidia predominantly ellipsoidal and/or cylindrical chlamydospores absent or present; Byssochlamys teleomorph absent or present……………3 | null | 134 | 42,172 | 0 | false | null | null | Conidia predominantly ellipsoidal and/or cylindrical chlamydospores absent or present; Byssochlamys teleomorph absent or present……………3 | true | true | false | true | false | 7,299 |
56 | DISCUSSION | 0 | null | null | 20,198,134 | null | Conidia predominantly globose to subglobose, chlamydospores present; | null | 68 | 42,173 | 0 | false | null | null | Conidia predominantly globose to subglobose, chlamydospores present; | true | true | false | true | false | 7,300 |
56 | DISCUSSION | 0 | null | null | 20,198,134 | null | Byssochlamys teleomorph present……………8 | null | 37 | 42,174 | 0 | false | null | null | Byssochlamys teleomorph present……………8 | true | true | false | true | false | 7,300 |
57 | DISCUSSION | 0 | null | null | 20,198,134 | null | Conidia cylindrical and/or ellipsoidal; measuring 3.4–4.2 × 1.7–2.1 μm, colonies on MEA restricted, attaining a diameter of less than 45 mm in 7 d at 30 °C ……………4 | null | 162 | 42,175 | 0 | false | null | null | Conidia cylindrical and/or ellipsoidal; measuring 3.4–4.2 × 1.7–2.1 μm, colonies on MEA restricted, attaining a diameter of less than 45 mm in 7 d at 30 °C ……………4 | true | true | false | true | false | 7,301 |
58 | DISCUSSION | 0 | null | null | 20,198,134 | null | Conidia larger 2.3–8(–13) | null | 25 | 42,176 | 0 | false | null | null | Conidia larger 2.3–8(–13) | true | true | false | true | false | 7,302 |
58 | DISCUSSION | 0 | null | null | 20,198,134 | null | × 1.5–4.5 μm, cylindrical or ellipsoidal, colonies on MEA larger than 45 mm after 7 d at 30 °C ……………5 | null | 101 | 42,177 | 0 | false | null | null | × 1.5–4.5 μm, cylindrical or ellipsoidal, colonies on MEA larger than 45 mm after 7 d at 30 °C ……………5 | false | false | false | true | false | 7,302 |
59 | DISCUSSION | 0 | null | null | 20,198,134 | null | Chlamydospores present, ratio between diameters on MEA at 37:30 °C between 0.25 and 0.45, colonies with well-defined margins ……………P. | null | 132 | 42,178 | 0 | false | null | null | Chlamydospores present, ratio between diameters on MEA at 37:30 °C between 0.25 and 0.45, colonies with well-defined margins ……………P. | true | true | true | true | true | 7,303 |
60 | DISCUSSION | 0 | null | null | 20,198,134 | null | Chlamydospores absent, ratio between diameters on MEA at 37:30 °C between 0.60 and 0.75, colonies with more or less feathery margins ……………P. | null | 140 | 42,179 | 0 | false | null | null | Chlamydospores absent, ratio between diameters on MEA at 37:30 °C between 0.60 and 0.75, colonies with more or less feathery margins ……………P. | true | true | true | true | true | 7,304 |
60 | DISCUSSION | 0 | null | null | 20,198,134 | null | divaricatus
** | null | 15 | 42,180 | 0 | false | null | null | divaricatus
** | false | true | false | true | false | 7,304 |
61 | DISCUSSION | 0 | null | null | 20,198,134 | null | Conidia predominantly ellipsoidal with truncate ends, chlamydospores present ……………6 | null | 83 | 42,181 | 0 | false | null | null | Conidia predominantly ellipsoidal with truncate ends, chlamydospores present ……………6 | true | true | false | true | false | 7,305 |
62 | DISCUSSION | 0 | null | null | 20,198,134 | null | Conidia predominantly cylindrical, chlamydospores absent…………… 7 | null | 63 | 42,182 | 0 | false | null | null | Conidia predominantly cylindrical, chlamydospores absent…………… 7 | true | true | false | true | false | 7,306 |
63 | DISCUSSION | 0 | null | null | 20,198,134 | null | Conidia measuring 3.7–5.6 × | null | 27 | 42,183 | 0 | false | null | null | Conidia measuring 3.7–5.6 × | true | true | false | true | false | 7,307 |
63 | DISCUSSION | 0 | null | null | 20,198,134 | null | 2.4–3.6 μm, no acid production on CREA; | null | 39 | 42,184 | 0 | false | null | null | 2.4–3.6 μm, no acid production on CREA; | false | false | false | true | false | 7,307 |
63 | DISCUSSION | 0 | null | null | 20,198,134 | null | Byssochlamys teleomorph produced in a heterothallic manner ……………B. | null | 66 | 42,185 | 0 | false | null | null | Byssochlamys teleomorph produced in a heterothallic manner ……………B. | true | true | true | true | true | 7,307 |
63 | DISCUSSION | 0 | null | null | 20,198,134 | null | spectabilis | null | 11 | 42,186 | 0 | false | null | null | spectabilis | false | true | false | true | false | 7,307 |
64 | DISCUSSION | 0 | null | null | 20,198,134 | null | Conidia measuring 3.2–5.7(–10) × 2–2.9(–3.4) μm, acid production under colony on CREA; | null | 86 | 42,187 | 0 | false | null | null | Conidia measuring 3.2–5.7(–10) × 2–2.9(–3.4) μm, acid production under colony on CREA; | true | true | false | true | false | 7,308 |
64 | DISCUSSION | 0 | null | null | 20,198,134 | null | Byssochlamys teleomorph absent ……………P. | null | 38 | 42,188 | 0 | false | null | null | Byssochlamys teleomorph absent ……………P. | true | true | true | true | true | 7,308 |
65 | DISCUSSION | 0 | null | null | 20,198,134 | null | Conidia measuring 4.5–6 × 1.7–2.2 μm; ascospores, smooth-walled, 5.5–6.5 × 3.5–4.1 μm, acid production under colony on CREA ……………B. | null | 131 | 42,189 | 0 | false | null | null | Conidia measuring 4.5–6 × 1.7–2.2 μm; ascospores, smooth-walled, 5.5–6.5 × 3.5–4.1 μm, acid production under colony on CREA ……………B. | true | true | true | true | true | 7,309 |
65 | DISCUSSION | 0 | null | null | 20,198,134 | null | fulva (Fig. | null | 11 | 42,190 | 0 | false | null | null | fulva (Fig. | false | true | true | true | false | 7,309 |
66 | DISCUSSION | 0 | null | null | 20,198,134 | null | Conidia measuring 9–11.8 × 2.5–4 μm; ascospores, verrucose and large, 7.1–8.1 × 5–5.7 μm, no acid production on CREA ……………B. | null | 124 | 42,191 | 0 | false | null | null | Conidia measuring 9–11.8 × 2.5–4 μm; ascospores, verrucose and large, 7.1–8.1 × 5–5.7 μm, no acid production on CREA ……………B. | true | true | true | true | true | 7,310 |
66 | DISCUSSION | 0 | null | null | 20,198,134 | null | verrucosa (Fig. | null | 15 | 42,192 | 0 | false | null | null | verrucosa (Fig. | false | true | true | true | false | 7,310 |
67 | DISCUSSION | 0 | null | null | 20,198,134 | null | Chlamydospores distinctly rough-walled ……………B. | null | 46 | 42,193 | 0 | false | null | null | Chlamydospores distinctly rough-walled ……………B. | true | true | true | true | true | 7,311 |
67 | DISCUSSION | 0 | null | null | 20,198,134 | null | zollerniae (Fig. | null | 16 | 42,194 | 0 | false | null | null | zollerniae (Fig. | false | true | true | true | false | 7,311 |
68 | DISCUSSION | 0 | null | null | 20,198,134 | null | Chlamydospores smooth walled or finely roughened ……………9 | null | 55 | 42,195 | 0 | false | null | null | Chlamydospores smooth walled or finely roughened ……………9 | true | true | false | true | false | 7,312 |
69 | DISCUSSION | 0 | null | null | 20,198,134 | null | Conidia measuring 3.1–3.8 × 2.5–3.2 μm, good growth on CYA ……………B. | null | 66 | 42,196 | 0 | false | null | null | Conidia measuring 3.1–3.8 × 2.5–3.2 μm, good growth on CYA ……………B. | true | true | true | true | true | 7,313 |
69 | DISCUSSION | 0 | null | null | 20,198,134 | null | lagunculariae | null | 13 | 42,197 | 0 | false | null | null | lagunculariae | false | true | false | true | false | 7,313 |
70 | DISCUSSION | 0 | null | null | 20,198,134 | null | Conidia measuring 3.1–4.3 × 2.6–3.4 μm, moderate growth on CYA ……………B. | null | 70 | 42,198 | 0 | false | null | null | Conidia measuring 3.1–4.3 × 2.6–3.4 μm, moderate growth on CYA ……………B. | true | true | true | true | true | 7,314 |
70 | DISCUSSION | 0 | null | null | 20,198,134 | null | nivea (Fig. | null | 11 | 42,199 | 0 | false | null | null | nivea (Fig. | false | true | true | true | false | 7,314 |
0 | DISCUSSION | 1 | 10 | [
"B10",
"B11"
] | 19,252,134 | pmid-16101480|pmid-17942768 | In this report, we describe the results of a genome-wide association scan in the GoKinD collection to identify loci associated with risk of diabetic nephropathy in type 1 diabetes. | [
"10",
"11"
] | 180 | 42,200 | 0 | false | In this report, we describe the results of a genome-wide association scan in the GoKinD collection to identify loci associated with risk of diabetic nephropathy in type 1 diabetes. | [] | In this report, we describe the results of a genome-wide association scan in the GoKinD collection to identify loci associated with risk of diabetic nephropathy in type 1 diabetes. | true | true | true | true | true | 7,315 |
0 | DISCUSSION | 1 | 10 | [
"B10",
"B11"
] | 19,252,134 | pmid-16101480|pmid-17942768 | The most significant associations were identified with variants located within four distinct chromosomal regions. | [
"10",
"11"
] | 113 | 42,201 | 0 | false | The most significant associations were identified with variants located within four distinct chromosomal regions. | [] | The most significant associations were identified with variants located within four distinct chromosomal regions. | true | true | true | true | true | 7,315 |
0 | DISCUSSION | 1 | 10 | [
"B10",
"B11"
] | 19,252,134 | pmid-16101480|pmid-17942768 | Although the biology underlying these associations remains to be elucidated, they implicate CHN2/CPVL, FRMD3, CARS, and an intergenic region on chromosome 13q as novel genes/genetic regions involved in the pathogenesis of diabetic nephropathy. | [
"10",
"11"
] | 243 | 42,202 | 0 | false | Although the biology underlying these associations remains to be elucidated, they implicate CHN2/CPVL, FRMD3, CARS, and an intergenic region on chromosome 13q as novel genes/genetic regions involved in the pathogenesis of diabetic nephropathy. | [] | Although the biology underlying these associations remains to be elucidated, they implicate CHN2/CPVL, FRMD3, CARS, and an intergenic region on chromosome 13q as novel genes/genetic regions involved in the pathogenesis of diabetic nephropathy. | true | true | true | true | true | 7,315 |
0 | DISCUSSION | 1 | 10 | [
"B10",
"B11"
] | 19,252,134 | pmid-16101480|pmid-17942768 | None of these loci overlap with previously reported associations between candidate genes and the development of any stage of diabetic nephropathy (10,11). | [
"10",
"11"
] | 154 | 42,203 | 0 | false | None of these loci overlap with previously reported associations between candidate genes and the development of any stage of diabetic nephropathy. | [
"10,11"
] | None of these loci overlap with previously reported associations between candidate genes and the development of any stage of diabetic nephropathy. | true | true | true | true | true | 7,315 |
0 | DISCUSSION | 1 | 10 | [
"B10",
"B11"
] | 19,252,134 | pmid-16101480|pmid-17942768 | Importantly, replication in a Cox proportional hazard analysis of the associations at the FRMD3 and CARS loci with time to the onset of severe nephropathy in the DCCT/EDIC study bolsters the significance of these two findings; that two studies having such different designs (one a case-control study and the other a pros... | [
"10",
"11"
] | 404 | 42,204 | 0 | false | Importantly, replication in a Cox proportional hazard analysis of the associations at the FRMD3 and CARS loci with time to the onset of severe nephropathy in the DCCT/EDIC study bolsters the significance of these two findings; that two studies having such different designs (one a case-control study and the other a pros... | [] | Importantly, replication in a Cox proportional hazard analysis of the associations at the FRMD3 and CARS loci with time to the onset of severe nephropathy in the DCCT/EDIC study bolsters the significance of these two findings; that two studies having such different designs (one a case-control study and the other a pros... | true | true | true | true | true | 7,315 |
1 | DISCUSSION | 1 | 26 | [
"B26",
"B27",
"B28",
"B29",
"B30",
"B26"
] | 19,252,134 | pmid-12601556|pmid-10712924|pmid-12631349|pmid-9757824|pmid-16626485|pmid-12601556 | FRMD3 encodes the 4.1O protein, a structural protein with unknown function and a member of the 4.1 family of proteins (26). | [
"26",
"27",
"28",
"29",
"30",
"26"
] | 123 | 42,205 | 1 | false | FRMD3 encodes the 4.1O protein, a structural protein with unknown function and a member of the 4.1 family of proteins. | [
"26"
] | FRMD3 encodes the 4.1O protein, a structural protein with unknown function and a member of the 4.1 family of proteins. | true | true | true | true | true | 7,316 |
1 | DISCUSSION | 1 | 26 | [
"B26",
"B27",
"B28",
"B29",
"B30",
"B26"
] | 19,252,134 | pmid-12601556|pmid-10712924|pmid-12631349|pmid-9757824|pmid-16626485|pmid-12601556 | Members of the 4.1 protein family have well-characterized roles as cytoskeletal proteins, maintaining both cellular shape and form, in a variety of cell types, including mouse nephron (27,28). | [
"26",
"27",
"28",
"29",
"30",
"26"
] | 192 | 42,206 | 0 | false | Members of the 4.1 protein family have well-characterized roles as cytoskeletal proteins, maintaining both cellular shape and form, in a variety of cell types, including mouse nephron. | [
"27,28"
] | Members of the 4.1 protein family have well-characterized roles as cytoskeletal proteins, maintaining both cellular shape and form, in a variety of cell types, including mouse nephron. | true | true | true | true | true | 7,316 |
1 | DISCUSSION | 1 | 26 | [
"B26",
"B27",
"B28",
"B29",
"B30",
"B26"
] | 19,252,134 | pmid-12601556|pmid-10712924|pmid-12631349|pmid-9757824|pmid-16626485|pmid-12601556 | Although membership of the 4.1O protein in this family has recently been questioned, it does contain a FERM domain, which is a module that is integral in maintaining cell integrity through its interactions with transmembrane proteins and actin filaments (29,30). | [
"26",
"27",
"28",
"29",
"30",
"26"
] | 262 | 42,207 | 0 | false | Although membership of the 4.1O protein in this family has recently been questioned, it does contain a FERM domain, which is a module that is integral in maintaining cell integrity through its interactions with transmembrane proteins and actin filaments. | [
"29,30"
] | Although membership of the 4.1O protein in this family has recently been questioned, it does contain a FERM domain, which is a module that is integral in maintaining cell integrity through its interactions with transmembrane proteins and actin filaments. | true | true | true | true | true | 7,316 |
1 | DISCUSSION | 1 | 26 | [
"B26",
"B27",
"B28",
"B29",
"B30",
"B26"
] | 19,252,134 | pmid-12601556|pmid-10712924|pmid-12631349|pmid-9757824|pmid-16626485|pmid-12601556 | FRMD3 is detectable in adult ovaries as well as in fetal skeletal muscle, brain, and thymus (26). | [
"26",
"27",
"28",
"29",
"30",
"26"
] | 97 | 42,208 | 1 | false | FRMD3 is detectable in adult ovaries as well as in fetal skeletal muscle, brain, and thymus. | [
"26"
] | FRMD3 is detectable in adult ovaries as well as in fetal skeletal muscle, brain, and thymus. | true | true | true | true | true | 7,316 |
1 | DISCUSSION | 1 | 26 | [
"B26",
"B27",
"B28",
"B29",
"B30",
"B26"
] | 19,252,134 | pmid-12601556|pmid-10712924|pmid-12631349|pmid-9757824|pmid-16626485|pmid-12601556 | Our data extend the expression profile of FRMD3 to specifically include mesangial and proximal tubular cells. | [
"26",
"27",
"28",
"29",
"30",
"26"
] | 109 | 42,209 | 0 | false | Our data extend the expression profile of FRMD3 to specifically include mesangial and proximal tubular cells. | [] | Our data extend the expression profile of FRMD3 to specifically include mesangial and proximal tubular cells. | true | true | true | true | true | 7,316 |
1 | DISCUSSION | 1 | 26 | [
"B26",
"B27",
"B28",
"B29",
"B30",
"B26"
] | 19,252,134 | pmid-12601556|pmid-10712924|pmid-12631349|pmid-9757824|pmid-16626485|pmid-12601556 | Interestingly, among 18 genes that contain FERM domains, including several members of the 4.1 protein family, we identified nominally significant associations with diabetic nephropathy for SNPs located in eight of these genes (supplementary Table 5), including FARP2 (FERM, RhoGEF and pleckstrin domain protein 2; P = 3.... | [
"26",
"27",
"28",
"29",
"30",
"26"
] | 405 | 42,210 | 0 | false | Interestingly, among 18 genes that contain FERM domains, including several members of the 4.1 protein family, we identified nominally significant associations with diabetic nephropathy for SNPs located in eight of these genes (supplementary Table 5), including FARP2 (FERM, RhoGEF and pleckstrin domain protein 2; P = 3.... | [] | Interestingly, among 18 genes that contain FERM domains, including several members of the 4.1 protein family, we identified nominally significant associations with diabetic nephropathy for SNPs located in eight of these genes (supplementary Table 5), including FARP2 and EPB41L2. | true | true | true | true | true | 7,316 |
1 | DISCUSSION | 1 | 26 | [
"B26",
"B27",
"B28",
"B29",
"B30",
"B26"
] | 19,252,134 | pmid-12601556|pmid-10712924|pmid-12631349|pmid-9757824|pmid-16626485|pmid-12601556 | Although these findings require further study, including replication in additional collections, it is interesting to speculate that these data may point to the involvement of new, previously unsuspected pathways in the pathogenesis of diabetic nephropathy. | [
"26",
"27",
"28",
"29",
"30",
"26"
] | 256 | 42,211 | 0 | false | Although these findings require further study, including replication in additional collections, it is interesting to speculate that these data may point to the involvement of new, previously unsuspected pathways in the pathogenesis of diabetic nephropathy. | [] | Although these findings require further study, including replication in additional collections, it is interesting to speculate that these data may point to the involvement of new, previously unsuspected pathways in the pathogenesis of diabetic nephropathy. | true | true | true | true | true | 7,316 |
2 | DISCUSSION | 1 | 31 | [
"B31",
"B32",
"B32"
] | 19,252,134 | pmid-18252769|pmid-18767960|pmid-18767960 | The CARS gene encodes cysteinyl-tRNA synthetase, one of several aminoacyl-tRNA synthetases (ARSs) that have been identified in humans (31,32). | [
"31",
"32",
"32"
] | 142 | 42,212 | 0 | false | The CARS gene encodes cysteinyl-tRNA synthetase, one of several aminoacyl-tRNA synthetases (ARSs) that have been identified in humans. | [
"31,32"
] | The CARS gene encodes cysteinyl-tRNA synthetase, one of several aminoacyl-tRNA synthetases (ARSs) that have been identified in humans. | true | true | true | true | true | 7,317 |
2 | DISCUSSION | 1 | 31 | [
"B31",
"B32",
"B32"
] | 19,252,134 | pmid-18252769|pmid-18767960|pmid-18767960 | ARSs are important regulators of intracellular amino acid concentrations and protein biosynthesis in both the cytoplasm and mitochondria (a process facilitated by specialized mitochondria-specific and bifunctional ARSs). | [
"31",
"32",
"32"
] | 220 | 42,213 | 0 | false | ARSs are important regulators of intracellular amino acid concentrations and protein biosynthesis in both the cytoplasm and mitochondria (a process facilitated by specialized mitochondria-specific and bifunctional ARSs). | [] | ARSs are important regulators of intracellular amino acid concentrations and protein biosynthesis in both the cytoplasm and mitochondria (a process facilitated by specialized mitochondria-specific and bifunctional ARSs). | true | true | true | true | true | 7,317 |
2 | DISCUSSION | 1 | 31 | [
"B31",
"B32",
"B32"
] | 19,252,134 | pmid-18252769|pmid-18767960|pmid-18767960 | In the initial steps of protein translation, the function of these enzymes is to attach amino acids to their cognate tRNA molecules. | [
"31",
"32",
"32"
] | 132 | 42,214 | 0 | false | In the initial steps of protein translation, the function of these enzymes is to attach amino acids to their cognate tRNA molecules. | [] | In the initial steps of protein translation, the function of these enzymes is to attach amino acids to their cognate tRNA molecules. | true | true | true | true | true | 7,317 |
2 | DISCUSSION | 1 | 32 | [
"B31",
"B32",
"B32"
] | 19,252,134 | pmid-18252769|pmid-18767960|pmid-18767960 | To date, both autosomal dominant and recessive mutations in ARS-encoding genes have been identified only in neurodegenerative disease, including missense changes in glycyl-tRNA synthetase (GARS) and both missense mutations and in-frame deletions in tyrosyl-tRNA synthetase (YARS) in Charcot-Marie-Tooth disease (32). | [
"31",
"32",
"32"
] | 316 | 42,215 | 1 | false | To date, both autosomal dominant and recessive mutations in ARS-encoding genes have been identified only in neurodegenerative disease, including missense changes in glycyl-tRNA synthetase (GARS) and both missense mutations and in-frame deletions in tyrosyl-tRNA synthetase (YARS) in Charcot-Marie-Tooth disease. | [
"32"
] | To date, both autosomal dominant and recessive mutations in ARS-encoding genes have been identified only in neurodegenerative disease, including missense changes in glycyl-tRNA synthetase (GARS) and both missense mutations and in-frame deletions in tyrosyl-tRNA synthetase (YARS) in Charcot-Marie-Tooth disease. | true | true | true | true | true | 7,317 |
3 | DISCUSSION | 1 | 33 | [
"B33",
"B34",
"B35"
] | 19,252,134 | pmid-4834888|pmid-12110740|pmid-9537412 | CARS has been implicated in cystinosis, an autosomal recessive renal tubule disorder caused by the accumulation of free cystine in cellular lysosomes (33,34). | [
"33",
"34",
"35"
] | 158 | 42,216 | 0 | false | CARS has been implicated in cystinosis, an autosomal recessive renal tubule disorder caused by the accumulation of free cystine in cellular lysosomes. | [
"33,34"
] | CARS has been implicated in cystinosis, an autosomal recessive renal tubule disorder caused by the accumulation of free cystine in cellular lysosomes. | true | true | true | true | true | 7,318 |
3 | DISCUSSION | 1 | 35 | [
"B33",
"B34",
"B35"
] | 19,252,134 | pmid-4834888|pmid-12110740|pmid-9537412 | A recent study identified defects in lysosomal cystine transport as the primary cause of the disease (35). | [
"33",
"34",
"35"
] | 106 | 42,217 | 1 | false | A recent study identified defects in lysosomal cystine transport as the primary cause of the disease. | [
"35"
] | A recent study identified defects in lysosomal cystine transport as the primary cause of the disease. | true | true | true | true | true | 7,318 |
3 | DISCUSSION | 1 | 33 | [
"B33",
"B34",
"B35"
] | 19,252,134 | pmid-4834888|pmid-12110740|pmid-9537412 | However, ESRD is prominent in this disorder, and such an outcome may be due to vulnerability of specific renal cells to damage by excess cystine. | [
"33",
"34",
"35"
] | 145 | 42,218 | 0 | false | However, ESRD is prominent in this disorder, and such an outcome may be due to vulnerability of specific renal cells to damage by excess cystine. | [] | However, ESRD is prominent in this disorder, and such an outcome may be due to vulnerability of specific renal cells to damage by excess cystine. | true | true | true | true | true | 7,318 |
Subsets and Splits
No community queries yet
The top public SQL queries from the community will appear here once available.