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236,573 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
GM13880
 
Resource Report
Resource Website
Coriell Cat# GM13880, RRID:CVCL_5Q11 Homo sapiens (Human) Orofacial cleft 1 Transformed cell line Female Coriell GM13880 CLO:CLO_0033217,
BioSample:SAMN00802690,
Coriell:GM13880,
Wikidata:Q54846889
CVCL_5Q11 2026-08-01 05:07:17 0
GM13886
 
Resource Report
Resource Website
Coriell Cat# GM13886, RRID:CVCL_HL90 Homo sapiens (Human) Transformed cell line Male Coriell GM13886 BioSample:SAMN00802698,
Coriell:GM13886,
Wikidata:Q54846893
CVCL_HL90 2026-08-01 05:07:16 0
GM13909
 
Resource Report
Resource Website
RRID:CVCL_1M15 Homo sapiens (Human) Ataxia telangiectasia syndrome Transformed cell line Female CLO:CLO_0033917,
BioSample:SAMN00802722,
Coriell:GM13909,
Wikidata:Q54846911
CVCL_1M15 2026-08-01 05:07:16 0
GM13894
 
Resource Report
Resource Website
RRID:CVCL_EG48 Homo sapiens (Human) Cleft palate Transformed cell line Male CLO:CLO_0033959,
BioSample:SAMN00802704,
Coriell:GM13894,
Wikidata:Q54846898
CVCL_EG48 2026-08-01 05:07:16 0
GM13934
 
Resource Report
Resource Website
Coriell Cat# GM13934, RRID:CVCL_FV97 Homo sapiens (Human) Progressive familial intrahepatic cholestasis Transformed cell line Male Coriell GM13934 CLO:CLO_0034031,
BioSample:SAMN00802740,
Coriell:GM13934,
Wikidata:Q54846926
CVCL_FV97 2026-08-01 05:07:17 0
GM13944
 
Resource Report
Resource Website
Coriell Cat# GM13944, RRID:CVCL_5Q18 Homo sapiens (Human) Williams syndrome Transformed cell line Male Coriell GM13944 CLO:CLO_0033989,
BioSample:SAMN00802756,
Coriell:GM13944,
Wikidata:Q54846935
CVCL_5Q18 2026-08-01 05:07:17 0
GM13915
 
Resource Report
Resource Website
Coriell Cat# GM13915, RRID:CVCL_N458 Homo sapiens (Human) Population: Caucasian; Russian., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository. Transformed cell line Female JK3536 Coriell GM13915 CLO:CLO_0033932,
Coriell:GM13915,
Wikidata:Q54846918
CVCL_N458 2026-08-01 05:07:14 0
GM13922
 
Resource Report
Resource Website
RRID:CVCL_1M19 Homo sapiens (Human) Ataxia telangiectasia syndrome Transformed cell line Female CLO:CLO_0033940,
BioSample:SAMN00802732,
Coriell:GM13922,
Wikidata:Q54846922
CVCL_1M19 2026-08-01 05:07:17 0
GM13958
 
Resource Report
Resource Website
RRID:CVCL_0R43 Homo sapiens (Human) Hermansky-Pudlak syndrome 1 Transformed cell line Female CLO:CLO_0033844,
Coriell:GM13958,
Wikidata:Q54846949
CVCL_0R43 2026-08-01 05:07:18 0
GM14043
 
Resource Report
Resource Website
RRID:CVCL_5Q32 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM14043,
Wikidata:Q54846998
CVCL_5Q32 2026-08-01 05:07:20 0
GM14060
 
Resource Report
Resource Website
Coriell Cat# GM14060, RRID:CVCL_CZ45 Homo sapiens (Human) Population: Caucasian; Amish. Transformed cell line Male Coriell GM14060 CLO:CLO_0033772,
BioSample:SAMN00802872,
Coriell:GM14060,
Wikidata:Q54847019
CVCL_CZ45 2026-08-01 05:07:16 0
GM14000
 
Resource Report
Resource Website
Coriell Cat# GM14000, RRID:CVCL_1M36 Homo sapiens (Human) Ataxia telangiectasia syndrome Transformed cell line Female Coriell GM14000 CLO:CLO_0033904,
Coriell:GM14000,
Wikidata:Q54846976
CVCL_1M36 2026-08-01 05:07:15 0
GM14033
 
Resource Report
Resource Website
Coriell Cat# GM14033, RRID:CVCL_5Q31 Homo sapiens (Human) Williams syndrome PMID:23665875 Transformed cell line Female Coriell GM14033 CLO:CLO_0033867,
Coriell:GM14033,
Wikidata:Q54846995
CVCL_5Q31 2026-08-01 05:07:18 0
GM14038
 
Resource Report
Resource Website
RRID:CVCL_1M42 Homo sapiens (Human) Ataxia telangiectasia syndrome Transformed cell line Male CLO:CLO_0033788,
Coriell:GM14038,
Wikidata:Q54846996
CVCL_1M42 2026-08-01 05:07:20 0
GM13961
 
Resource Report
Resource Website
RRID:CVCL_1M27 Homo sapiens (Human) Ataxia telangiectasia syndrome Transformed cell line Male CLO:CLO_0033846,
BioSample:SAMN00802784,
Coriell:GM13961,
Wikidata:Q54846951
CVCL_1M27 2026-08-01 05:07:19 0
GM13977
 
Resource Report
Resource Website
RRID:CVCL_L267 Homo sapiens (Human) Cornelia de Lange syndrome Donor information: Established from monozygotic twin of GM13976 (Cellosaurus=CVCL_L266)., Part of: ENCODE project common cell types; tier 3. Transformed cell line Female CLO:CLO_0033829,
EFO:EFO_0005346,
BioSample:SAMN00802797,
Coriell:GM13977,
ENCODE:ENCBS221AAA,
GEO:GSM1008556,
Wikidata:Q54846967
CVCL_L267 2026-08-01 05:07:15 0
GM13988
 
Resource Report
Resource Website
RRID:CVCL_5Q28 Homo sapiens (Human) Orofacial cleft 1 Transformed cell line Male CLO:CLO_0033825,
BioSample:SAMN00802801,
Coriell:GM13988,
Wikidata:Q54846970
CVCL_5Q28 2026-08-01 05:07:17 0
GM13997
 
Resource Report
Resource Website
Coriell Cat# GM13997, RRID:CVCL_1M35 Homo sapiens (Human) Ataxia telangiectasia syndrome Transformed cell line Male Coriell GM13997 CLO:CLO_0033910,
BioSample:SAMN00802811,
Coriell:GM13997,
Wikidata:Q54846975
CVCL_1M35 2026-08-01 05:07:17 0
GM14006
 
Resource Report
Resource Website
RRID:CVCL_UY71 Homo sapiens (Human) Cleft palate Transformed cell line Male CLO:CLO_0033894,
Coriell:GM14006,
Wikidata:Q93833903
CVCL_UY71 2026-08-01 05:07:15 0
GM13972
 
Resource Report
Resource Website
Coriell Cat# GM13972, RRID:CVCL_1M30 Homo sapiens (Human) Ataxia telangiectasia syndrome Transformed cell line Female Coriell GM13972 CLO:CLO_0033832,
BioSample:SAMN00802793,
Coriell:GM13972,
Wikidata:Q54846964
CVCL_1M30 2026-08-01 05:07:19 0

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