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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
GM16328
 
Resource Report
Resource Website
Coriell Cat# GM16328, RRID:CVCL_LN72 Homo sapiens (Human) PMID:28161093 Transformed cell line Male Coriell GM16328 Coriell:GM16328,
Wikidata:Q54848460
CVCL_LN72 2026-09-05 10:57:59 0
GM16353
 
Resource Report
Resource Website
Coriell Cat# GM16353, RRID:CVCL_UT72 Homo sapiens (Human) PMID:28161093 Transformed cell line Male Coriell GM16353 Coriell:GM16353,
Wikidata:Q93844603
CVCL_UT72 2026-09-05 10:58:00 0
GM16356
 
Resource Report
Resource Website
RRID:CVCL_UT75 Homo sapiens (Human) PMID:28161093 Transformed cell line Male Coriell:GM16356,
Wikidata:Q93844615
CVCL_UT75 2026-09-05 10:58:00 0
GM16334
 
Resource Report
Resource Website
RRID:CVCL_UD06 Homo sapiens (Human) Facioscapulohumeral muscular dystrophy 1 PMID:28161093 Transformed cell line Female Coriell:GM16334,
Wikidata:Q93844457
CVCL_UD06 2026-09-05 10:58:00 0
GM16390
 
Resource Report
Resource Website
RRID:CVCL_V269 Homo sapiens (Human) Xeroderma pigmentosum, complementation group D Population: Caucasian; Scottish. Finite cell line Male CLO:CLO_0019389,
Coriell:GM16390,
Wikidata:Q54848500
CVCL_V269 2026-09-05 10:58:00 0
GM16338
 
Resource Report
Resource Website
RRID:CVCL_UD10 Homo sapiens (Human) Facioscapulohumeral muscular dystrophy 1 PMID:28161093 Transformed cell line Female Coriell:GM16338,
Wikidata:Q93844477
CVCL_UD10 2026-09-05 10:58:00 0
GM16401
 
Resource Report
Resource Website
Coriell Cat# GM16401, RRID:CVCL_DS04 Homo sapiens (Human) Atrioventricular septal defect Transformed cell line Female Coriell GM16401 CLO:CLO_0019508,
Coriell:GM16401,
Wikidata:Q54848510
CVCL_DS04 2026-09-05 10:58:01 0
GM16395
 
Resource Report
Resource Website
RRID:CVCL_AT42 Homo sapiens (Human) Glutaric acidemia type 1 Finite cell line Male CLO:CLO_0019504,
Coriell:GM16395,
Wikidata:Q54848506
CVCL_AT42 2026-09-05 10:58:01 0
GM16400
 
Resource Report
Resource Website
RRID:CVCL_N264 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. Transformed cell line Female GM18094 CLO:CLO_0015758,
CLO:CLO_0019509,
Coriell:GM16400,
Coriell:GM18094,
Wikidata:Q54848509
CVCL_N264 2026-09-05 10:58:01 0
GM16378
 
Resource Report
Resource Website
Coriell Cat# GM16378, RRID:CVCL_9Y35 Homo sapiens (Human) Donohue syndrome Transformed cell line Male Coriell GM16378 CLO:CLO_0019414,
Coriell:GM16378,
Wikidata:Q54848486
CVCL_9Y35 2026-09-05 10:58:00 0
GM16378
 
Resource Report
Resource Website
RRID:CVCL_9Y35 Homo sapiens (Human) Donohue syndrome Transformed cell line Male CLO:CLO_0019414,
Coriell:GM16378,
Wikidata:Q54848486
CVCL_9Y35 2026-09-05 10:58:00 0
GM16348
 
Resource Report
Resource Website
RRID:CVCL_HQ06 Homo sapiens (Human) Facioscapulohumeral muscular dystrophy 1 PMID:28161093 Transformed cell line Female CLO:CLO_0019426,
Coriell:GM16348,
Wikidata:Q54848465
CVCL_HQ06 2026-09-05 10:58:00 0
GM16340
 
Resource Report
Resource Website
Coriell Cat# GM16340, RRID:CVCL_UD12 Homo sapiens (Human) PMID:28161093 Transformed cell line Male Coriell GM16340 Coriell:GM16340,
Wikidata:Q93844482
CVCL_UD12 2026-09-05 10:58:00 0
GM16400
 
Resource Report
Resource Website
Coriell Cat# GM18094, RRID:CVCL_N264 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. Transformed cell line Female GM18094 Coriell GM18094 CLO:CLO_0015758,
CLO:CLO_0019509,
Coriell:GM16400,
Coriell:GM18094,
Wikidata:Q54848509
CVCL_N264 2026-09-05 10:58:01 0
GM16335
 
Resource Report
Resource Website
RRID:CVCL_UD07 Homo sapiens (Human) PMID:28161093 Transformed cell line Male Coriell:GM16335,
Wikidata:Q93844460
CVCL_UD07 2026-09-05 10:58:00 0
GM16349
 
Resource Report
Resource Website
RRID:CVCL_DB89 Homo sapiens (Human) PMID:28161093 Transformed cell line Female CLO:CLO_0019429,
Coriell:GM16349,
Wikidata:Q54848466
CVCL_DB89 2026-09-05 10:58:00 0
GM16353
 
Resource Report
Resource Website
RRID:CVCL_UT72 Homo sapiens (Human) PMID:28161093 Transformed cell line Male Coriell:GM16353,
Wikidata:Q93844603
CVCL_UT72 2026-09-05 10:58:00 0
GM16375
 
Resource Report
Resource Website
RRID:CVCL_7651 Homo sapiens (Human) Bloom syndrome Donor information: From Bloom Syndrome Registry patient 81(MaGrou) (BSR81)., Population: Caucasian; French Canadian. PMID:436333
PMID:10521302
PMID:11325959
PMID:17407155
Transformed cell line Male HG1525 CLO:CLO_0019421,
Coriell:GM16375,
Wikidata:Q54848484
CVCL_7651 2026-09-05 10:58:00 0
GM16419
 
Resource Report
Resource Website
RRID:CVCL_LN84 Homo sapiens (Human) PMID:28161093 Transformed cell line Male Coriell:GM16419,
Wikidata:Q54848522
CVCL_LN84 2026-09-05 10:58:01 0
GM16396
 
Resource Report
Resource Website
RRID:CVCL_AT43 Homo sapiens (Human) Glutaric acidemia type 1 Finite cell line Male CLO:CLO_0019513,
Coriell:GM16396,
Wikidata:Q54848507
CVCL_AT43 2026-09-05 10:58:01 0

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