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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
GM16524
 
Resource Report
Resource Website
RRID:CVCL_9R39 Homo sapiens (Human) Neonatal adrenoleukodystrophy Finite cell line Male CLO:CLO_0017586,
Coriell:GM16524,
Wikidata:Q54848622
CVCL_9R39 2026-09-05 10:58:02 0
GM16482
 
Resource Report
Resource Website
RRID:CVCL_0E68 Homo sapiens (Human) Population: Caucasian. Transformed cell line Female CLO:CLO_0017515,
Coriell:GM16482,
Wikidata:Q54848589
CVCL_0E68 2026-09-05 10:58:02 0
GM16435
 
Resource Report
Resource Website
RRID:CVCL_0G30 Cricetulus griseus (Chinese hamster) Group: Human/rodent somatic cell hybrid. PMID:8004090 Hybrid cell line JH374 CLO:CLO_0017780,
Coriell:GM16435,
Wikidata:Q54848557
cvcl_0f83 CVCL_0G30 2026-09-05 10:58:01 0
GM16449
 
Resource Report
Resource Website
RRID:CVCL_0H48 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male JL314 CLO:CLO_0017800,
Coriell:GM16449,
Wikidata:Q54848569
CVCL_0H48 2026-09-05 10:58:02 0
GM16491
 
Resource Report
Resource Website
RRID:CVCL_9Z48 Homo sapiens (Human) Refsum disease Finite cell line Female CLO:CLO_0017519,
Coriell:GM16491,
Wikidata:Q54848605
CVCL_9Z48 2026-09-05 10:58:02 0
GM16444
 
Resource Report
Resource Website
RRID:CVCL_0H29 Cricetulus griseus (Chinese hamster) Group: Human/rodent somatic cell hybrid. Hybrid cell line JH478 CLO:CLO_0017787,
Coriell:GM16444,
Wikidata:Q54848565
CVCL_0H29 2026-09-05 10:58:01 0
GM16479
 
Resource Report
Resource Website
RRID:CVCL_9T94 Homo sapiens (Human) Population: Caucasian; Sicilian. Finite cell line Male CLO:CLO_0017531,
Coriell:GM16479,
Wikidata:Q54848586
CVCL_9T94 2026-09-05 10:58:02 0
GM16494
 
Resource Report
Resource Website
Coriell Cat# GM16494, RRID:CVCL_9Z51 Homo sapiens (Human) Infantile Refsum disease Transformed cell line Female Coriell GM16494 CLO:CLO_0017493,
Coriell:GM16494,
Wikidata:Q54848609
CVCL_9Z51 2026-09-05 10:58:02 0
GM16436
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM16436, RRID:CVCL_0H58 Homo sapiens (Human) Tourette syndrome Transformed cell line Male JL281 Coriell GM16436 Coriell:GM16436,
Wikidata:Q54848558
CVCL_0H58 2026-09-05 10:58:01 0
GM16485
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_DA46 Homo sapiens (Human) Neuronal ceroid lipofuscinosis type 2 Population: Latino or Hispanic. PMID:29631617 Finite cell line Female CABM011 CLO:CLO_0017518,
Coriell:GM16485,
Wikidata:Q54848591
CVCL_DA46 2026-09-05 10:58:02 1
GM16499
 
Resource Report
Resource Website
RRID:CVCL_JE96 Homo sapiens (Human) Donor information: Established from a donor with cleft hand and absent tibia., Population: Caucasian. Finite cell line Male CLO:CLO_0017487,
Coriell:GM16499,
Wikidata:Q54848612
CVCL_JE96 2026-09-05 10:58:02 0
GM16430
 
Resource Report
Resource Website
RRID:CVCL_LN90 Homo sapiens (Human) Facioscapulohumeral muscular dystrophy 1 Donor information: At sampling donor was not affected with facioscapulohumeral muscular dystrophy but at risk for disease. PMID:28161093 Transformed cell line Male Coriell:GM16430,
Wikidata:Q54848554
CVCL_LN90 2026-09-05 10:58:01 0
GM16453
 
Resource Report
Resource Website
Coriell Cat# GM16453, RRID:CVCL_0H50 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male JL360 Coriell GM16453 CLO:CLO_0017804,
Coriell:GM16453,
Wikidata:Q54848573
CVCL_0H50 2026-09-05 10:58:02 0
GM16512
 
Resource Report
Resource Website
RRID:CVCL_9R36 Homo sapiens (Human) Neonatal adrenoleukodystrophy Finite cell line Female CLO:CLO_0017482,
Coriell:GM16512,
Wikidata:Q54848615
CVCL_9R36 2026-09-05 10:58:02 0
GM16442
 
Resource Report
Resource Website
Coriell Cat# GM16442, RRID:CVCL_2U48 Homo sapiens (Human) Transformed cell line Male JL482 Coriell GM16442 CLO:CLO_0017788,
Coriell:GM16442,
Wikidata:Q54848563
CVCL_2U48 2026-09-05 10:58:01 0
GM16440
 
Resource Report
Resource Website
Coriell Cat# GM16440, RRID:CVCL_0H53 Homo sapiens (Human) Bipolar disorder PMID:23665875 Transformed cell line Female JL481 Coriell GM16440 CLO:CLO_0017791,
Coriell:GM16440,
Wikidata:Q54848562
CVCL_0H53 2026-09-05 10:58:01 0
GM16445
 
Resource Report
Resource Website
Coriell Cat# GM16445, RRID:CVCL_5L22 Homo sapiens (Human) Deletion 18p syndrome PMID:23665875 Transformed cell line Male JL439 Coriell GM16445 CLO:CLO_0017802,
Coriell:GM16445,
Wikidata:Q54848566
CVCL_5L22 2026-09-05 10:58:01 0
GM16492
 
Resource Report
Resource Website
RRID:CVCL_9Z49 Homo sapiens (Human) Refsum disease Finite cell line Female CLO:CLO_0017522,
Coriell:GM16492,
Wikidata:Q54848606
CVCL_9Z49 2026-09-05 10:58:02 0
GM16426
 
Resource Report
Resource Website
RRID:CVCL_UT80 Homo sapiens (Human) PMID:28161093 Transformed cell line Male Coriell:GM16426,
Wikidata:Q93845590
CVCL_UT80 2026-09-05 10:58:01 0
GM16427
 
Resource Report
Resource Website
RRID:CVCL_LN87 Homo sapiens (Human) Facioscapulohumeral muscular dystrophy 1 PMID:28161093 Transformed cell line Male Coriell:GM16427,
Wikidata:Q54848551
CVCL_LN87 2026-09-05 10:58:01 0

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