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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
GM14128
 
Resource Report
Resource Website
RRID:CVCL_W004 Homo sapiens (Human) Cri du chat syndrome PMID:8004090
PMID:23665875
Transformed cell line Female JL138 CLO:CLO_0034397,
Coriell:GM14128,
Wikidata:Q54847072
CVCL_W004 2026-09-12 05:35:01 0
GM14111
 
Resource Report
Resource Website
RRID:CVCL_0G27 Cricetulus griseus (Chinese hamster) Group: Human/rodent somatic cell hybrid. PMID:8004090 Hybrid cell line JH148 CLO:CLO_0034412,
Coriell:GM14111,
Wikidata:Q54847049
CVCL_0G27 2026-09-12 05:35:01 0
GM14142
 
Resource Report
Resource Website
RRID:CVCL_1M56 Homo sapiens (Human) Ataxia telangiectasia syndrome Transformed cell line Female CLO:CLO_0034387,
Coriell:GM14142,
Wikidata:Q54847080
CVCL_1M56 2026-09-12 05:35:02 0
GM14100
 
Resource Report
Resource Website
RRID:CVCL_1M52 Homo sapiens (Human) Ataxia telangiectasia syndrome Transformed cell line Male CLO:CLO_0034053,
Coriell:GM14100,
Wikidata:Q54847044
CVCL_1M52 2026-09-12 05:35:01 0
GM14076
 
Resource Report
Resource Website
RRID:CVCL_EH19 Homo sapiens (Human) Transformed cell line Male CLO:CLO_0033758,
Coriell:GM14076,
Wikidata:Q54847026
CVCL_EH19 2026-09-12 05:35:00 0
GM14116
 
Resource Report
Resource Website
RRID:CVCL_V992 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Male JL27 CLO:CLO_0034419,
Coriell:GM14116,
Wikidata:Q54847059
CVCL_V992 2026-09-12 05:35:01 0
GM14088
 
Resource Report
Resource Website
Coriell Cat# GM14088, RRID:CVCL_0Q28 Homo sapiens (Human) Thanatophoric dysplasia Population: Caucasian; Russian. Finite cell line Female Coriell GM14088 CLO:CLO_0034045,
Coriell:GM14088,
Wikidata:Q54847034
CVCL_0Q28 2026-09-12 05:35:00 0
GM14106
 
Resource Report
Resource Website
Coriell Cat# GM14106, RRID:CVCL_5Q35 Homo sapiens (Human) Hypogonadotropic hypogonadism with anosmia PMID:23665875 Transformed cell line Male Coriell GM14106 CLO:CLO_0034055,
Coriell:GM14106,
Wikidata:Q54847046
CVCL_5Q35 2026-09-12 05:35:01 0
GM14120
 
Resource Report
Resource Website
RRID:CVCL_V996 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Female JL54 CLO:CLO_0034427,
Coriell:GM14120,
Wikidata:Q54847063
CVCL_V996 2026-09-12 05:35:01 0
GM14152
 
Resource Report
Resource Website
Coriell Cat# GM14152, RRID:CVCL_1M57 Homo sapiens (Human) Ataxia telangiectasia syndrome Transformed cell line Female Coriell GM14152 CLO:CLO_0034389,
Coriell:GM14152,
Wikidata:Q54847081
CVCL_1M57 2026-09-12 05:35:02 0
GM14096
 
Resource Report
Resource Website
RRID:CVCL_W416 Homo sapiens (Human) BRCA1 syndrome Transformed cell line Female CLO:CLO_0034051,
Coriell:GM14096,
Wikidata:Q54847042
CVCL_W416 2026-09-12 05:35:01 0
GM14142
 
Resource Report
Resource Website
Coriell Cat# GM14142, RRID:CVCL_1M56 Homo sapiens (Human) Ataxia telangiectasia syndrome Transformed cell line Female Coriell GM14142 CLO:CLO_0034387,
Coriell:GM14142,
Wikidata:Q54847080
CVCL_1M56 2026-09-12 05:35:02 0
GM14081
 
Resource Report
Resource Website
RRID:CVCL_1K19 Homo sapiens (Human) Dentatorubral-pallidoluysian atrophy Transformed cell line Female CLO:CLO_0033760,
Coriell:GM14081,
Wikidata:Q54847028
CVCL_1K19 2026-09-12 05:35:00 0
GM14093
 
Resource Report
Resource Website
RRID:CVCL_5A78 Homo sapiens (Human) BRCA1 syndrome Transformed cell line Female CLO:CLO_0034047,
Coriell:GM14093,
Wikidata:Q54847039
CVCL_5A78 2026-09-12 05:35:01 0
GM14157
 
Resource Report
Resource Website
Coriell Cat# GM14157, 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 Coriell GM14157 CLO:CLO_0034379,
Coriell:GM14157,
Wikidata:Q54847084
CVCL_4E10 2026-09-12 05:35:02 0
GM14083
 
Resource Report
Resource Website
RRID:CVCL_1M49 Homo sapiens (Human) Ataxia telangiectasia syndrome Transformed cell line Female CLO:CLO_0034041,
Coriell:GM14083,
Wikidata:Q54847030
CVCL_1M49 2026-09-12 05:35:00 0
GM14108
 
Resource Report
Resource Website
RRID:CVCL_1K94 Homo sapiens (Human) Glycogen storage disease type II Transformed cell line Female Coriell:GM14108,
Wikidata:Q54847047
CVCL_1K94 2026-09-12 05:35:01 0
GM14082
 
Resource Report
Resource Website
Coriell Cat# GM14082, RRID:CVCL_9R53 Homo sapiens (Human) Spina bifida Transformed cell line Male Coriell GM14082 CLO:CLO_0034042,
Coriell:GM14082,
Wikidata:Q54847029
CVCL_9R53 2026-09-12 05:35:00 0
GM14164
 
Resource Report
Resource Website
RRID:CVCL_5M47 Homo sapiens (Human) Tetralogy of Fallot PMID:23665875 Transformed cell line Female CLO:CLO_0034357,
Coriell:GM14164,
Wikidata:Q54847088
CVCL_5M47 2026-09-12 05:35:02 0
GM14131
 
Resource Report
Resource Website
RRID:CVCL_W007 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Female JL142 CLO:CLO_0034401,
Coriell:GM14131,
Wikidata:Q54847075
CVCL_W007 2026-09-12 05:35:01 0

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