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256,031 Results - per page

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Name Proper Citation Organism Disease Comments Defining Citation Category Sex Synonyms Vendor Catalog Number Cross References Hierarchy Originate from Same Individual ID Record Last Update Mentions Count
GM14100
 
Resource Report
Resource Website
Coriell Cat# GM14100, RRID:CVCL_1M52 Homo sapiens (Human) Ataxia telangiectasia syndrome Transformed cell line Male Coriell GM14100 CLO:CLO_0034053,
Coriell:GM14100,
Wikidata:Q54847044
CVCL_1M52 2026-08-15 04:32:06 0
GM14117
 
Resource Report
Resource Website
Coriell Cat# GM14117, RRID:CVCL_V993 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Male JL30 Coriell GM14117 CLO:CLO_0034422,
Coriell:GM14117,
Wikidata:Q54847060
CVCL_V993 2026-08-15 04:32:06 0
GM14122
 
Resource Report
Resource Website
Coriell Cat# GM14122, RRID:CVCL_V998 Homo sapiens (Human) Cri du chat syndrome PMID:8004090
PMID:23665875
Transformed cell line Female JL65 Coriell GM14122 CLO:CLO_0034431,
Coriell:GM14122,
Wikidata:Q54847065
CVCL_V998 2026-08-15 04:32:06 0
GM14081
 
Resource Report
Resource Website
Coriell Cat# GM14081, RRID:CVCL_1K19 Homo sapiens (Human) Dentatorubral-pallidoluysian atrophy Transformed cell line Female Coriell GM14081 CLO:CLO_0033760,
Coriell:GM14081,
Wikidata:Q54847028
CVCL_1K19 2026-08-15 04:32:06 0
GM14124
 
Resource Report
Resource Website
RRID:CVCL_W000 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Male JL72 CLO:CLO_0034409,
Coriell:GM14124,
Wikidata:Q54847067
CVCL_W000 2026-08-15 04:32:06 0
GM14157
 
Resource Report
Resource Website
RRID:CVCL_4E10 Homo sapiens (Human) Supernumerary circular chromosome Karyotypic information: 47,XX,+r(16).ish r(16)(D16Z1+) [27]; 48,XX,+r(1).ish r(1)(D1Z5+),+r(16).ish r(16)(D16Z1+) [15]; 47,XX,+r(1).ish r(1)(D1Z5+) [2]; 46,XX [6] (Coriell=GM14157)., Population: Hispanic. Finite cell line Female CLO:CLO_0034379,
Coriell:GM14157,
Wikidata:Q54847084
CVCL_4E10 2026-08-15 04:32:12 0
GM14089
 
Resource Report
Resource Website
RRID:CVCL_0Q29 Homo sapiens (Human) Thanatophoric dysplasia Population: Caucasian; Russian. Finite cell line Female CLO:CLO_0034044,
Coriell:GM14089,
Wikidata:Q54847035
CVCL_0Q29 2026-08-15 04:32:06 0
GM14162
 
Resource Report
Resource Website
RRID:CVCL_5Q37 Homo sapiens (Human) Williams syndrome PMID:23665875 Transformed cell line Male CLO:CLO_0034370,
Coriell:GM14162,
Wikidata:Q54847086
CVCL_5Q37 2026-08-15 04:32:12 0
GM14130
 
Resource Report
Resource Website
Coriell Cat# GM14130, RRID:CVCL_W006 Homo sapiens (Human) Cri du chat syndrome PMID:8004090
PMID:23665875
Transformed cell line Female JL140 Coriell GM14130 CLO:CLO_0034392,
Coriell:GM14130,
Wikidata:Q54847074
CVCL_W006 2026-08-15 04:32:12 0
GM14127
 
Resource Report
Resource Website
Coriell Cat# GM14127, RRID:CVCL_W003 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Female JL136 Coriell GM14127 CLO:CLO_0034395,
Coriell:GM14127,
Wikidata:Q54847071
CVCL_W003 2026-08-15 04:32:11 0
GM14113
 
Resource Report
Resource Website
RRID:CVCL_0G28 Cricetulus griseus (Chinese hamster) Group: Human/rodent somatic cell hybrid. PMID:8004090 Hybrid cell line JH199 CLO:CLO_0034435,
Coriell:GM14113,
Wikidata:Q54847056
CVCL_0G28 2026-08-15 04:32:06 0
GM14121
 
Resource Report
Resource Website
RRID:CVCL_V997 Homo sapiens (Human) Cri du chat syndrome PMID:8004090
PMID:23665875
Transformed cell line Female JL63 CLO:CLO_0034429,
Coriell:GM14121,
Wikidata:Q54847064
CVCL_V997 2026-08-15 04:32:06 0
GM14155
 
Resource Report
Resource Website
Coriell Cat# GM14155, RRID:CVCL_2Z79 Homo sapiens (Human) Nevoid basal cell carcinoma syndrome Transformed cell line Female Coriell GM14155 CLO:CLO_0034377,
Coriell:GM14155,
Wikidata:Q54847083
CVCL_2Z79 2026-08-15 04:32:07 0
GM14101
 
Resource Report
Resource Website
RRID:CVCL_1M53 Homo sapiens (Human) Ataxia telangiectasia syndrome Transformed cell line Female CLO:CLO_0034052,
Coriell:GM14101,
Wikidata:Q54847045
CVCL_1M53 2026-08-15 04:32:06 0
GM14124
 
Resource Report
Resource Website
Coriell Cat# GM14124, RRID:CVCL_W000 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Male JL72 Coriell GM14124 CLO:CLO_0034409,
Coriell:GM14124,
Wikidata:Q54847067
CVCL_W000 2026-08-15 04:32:11 0
GM14297
 
Resource Report
Resource Website
RRID:CVCL_5Q55 Homo sapiens (Human) Williams syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0031146,
Coriell:GM14297,
Wikidata:Q54847149
CVCL_5Q55 2026-08-15 04:32:08 0
GM14260
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM14260, RRID:CVCL_UI19 Homo sapiens (Human) Ataxia telangiectasia syndrome PMID:16166284 Transformed cell line Coriell GM14260 Coriell:GM14260,
Wikidata:Q93834971
CVCL_UI19 2026-08-15 04:32:12 0
GM14280
 
Resource Report
Resource Website
RRID:CVCL_DS43 Homo sapiens (Human) Morbid obesity Transformed cell line Female CLO:CLO_0031094,
Coriell:GM14280,
Wikidata:Q54847128
CVCL_DS43 2026-08-15 04:32:08 0
GM14286
 
Resource Report
Resource Website
RRID:CVCL_DS47 Homo sapiens (Human) Morbid obesity Transformed cell line Male CLO:CLO_0031089,
Coriell:GM14286,
Wikidata:Q54847132
CVCL_DS47 2026-08-15 04:32:08 0
GM14165
 
Resource Report
Resource Website
Coriell Cat# GM14165, RRID:CVCL_JF02 Homo sapiens (Human) Cleft palate Transformed cell line Male Coriell GM14165 CLO:CLO_0034355,
Coriell:GM14165,
Wikidata:Q54847089
CVCL_JF02 2026-08-15 04:32:07 0

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