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95,747 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
GM04506
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM04506, RRID:CVCL_7413 Homo sapiens (Human) Donor information: Established from monozygotic twin of GM04505 (Cellosaurus=CVCL_7412)., Population: Caucasian. PMID:21490598 Finite cell line Female GM04506A, HF25 Coriell GM04506 CLO:CLO_0018815,
Coriell:GM04506,
Wikidata:Q54838546
CVCL_7413 2026-08-08 05:00:16 3
GM04586
 
Resource Report
Resource Website
RRID:CVCL_AA23 Homo sapiens (Human) Population: Caucasian. Finite cell line Female CLO:CLO_0018885,
Coriell:GM04586,
Wikidata:Q54838575
CVCL_AA23 2026-08-08 05:00:15 0
GM04430
 
Resource Report
Resource Website
RRID:CVCL_X306 Homo sapiens (Human) Isodicentric chromosome Population: Caucasian. PMID:6661932 Finite cell line Female GM 4430, GM04430A CLO:CLO_0019687,
Coriell:GM04430,
Wikidata:Q54838527
CVCL_X306 2026-08-08 05:00:14 0
GM04479
 
Resource Report
Resource Website
RRID:CVCL_V567 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female GM04479A CLO:CLO_0019662,
Coriell:GM04479,
Wikidata:Q54838533
CVCL_V567 2026-08-08 05:00:14 0
GM04543
 
Resource Report
Resource Website
RRID:CVCL_0M36 Homo sapiens (Human) Population: Caucasian. Finite cell line Female CLO:CLO_0018875,
Coriell:GM04543,
Wikidata:Q54838566
CVCL_0M36 2026-08-08 05:00:15 0
GM04488
 
Resource Report
Resource Website
RRID:CVCL_4F50 Homo sapiens (Human) Medium-chain acyl-CoA dehydrogenase deficiency Population: Caucasian. Finite cell line Female CLO:CLO_0019664,
Coriell:GM04488,
Wikidata:Q54838535
CVCL_4F50 2026-08-08 05:00:15 0
GM04515
 
Resource Report
Resource Website
RRID:CVCL_AW69 Homo sapiens (Human) Sideroblastic anemia Population: Caucasian. Transformed cell line Female CLO:CLO_0018851,
Coriell:GM04515,
Wikidata:Q54838553
CVCL_AW69 2026-08-08 05:00:16 0
GM04536
 
Resource Report
Resource Website
RRID:CVCL_X120 Homo sapiens (Human) PMID:6617268 Finite cell line Female GM 4536 CLO:CLO_0018862,
Coriell:GM04536,
Wikidata:Q54838562
CVCL_X120 2026-08-08 05:00:16 0
GM04515
 
Resource Report
Resource Website
Coriell Cat# GM04515, RRID:CVCL_AW69 Homo sapiens (Human) Sideroblastic anemia Population: Caucasian. Transformed cell line Female Coriell GM04515 CLO:CLO_0018851,
Coriell:GM04515,
Wikidata:Q54838553
CVCL_AW69 2026-08-08 05:00:15 0
GM04567
 
Resource Report
Resource Website
RRID:CVCL_AW53 Homo sapiens (Human) Dystrophia myotonica 1 Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:23680132 Transformed cell line Female CLO:CLO_0018879,
Coriell:GM04567,
Wikidata:Q54838570
CVCL_AW53 2026-08-08 05:00:15 0
GM04482
 
Resource Report
Resource Website
RRID:CVCL_1I19 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Female CLO:CLO_0019663,
Coriell:GM04482,
Wikidata:Q54838534
CVCL_1I19 2026-08-08 05:00:15 0
GM04479
 
Resource Report
Resource Website
Coriell Cat# GM04479, RRID:CVCL_V567 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female GM04479A Coriell GM04479 CLO:CLO_0019662,
Coriell:GM04479,
Wikidata:Q54838533
CVCL_V567 2026-08-08 05:00:14 0
GM04500
 
Resource Report
Resource Website
RRID:CVCL_2T05 Homo sapiens (Human) Karyotypic information: 46,XX,t(1;3)(1qter->1p36::3q13.3->3qter;3pter->3q13.3::1p36->1pter) (Coriell=GM04500)., Population: Caucasian. Finite cell line Female CLO:CLO_0018817,
Coriell:GM04500,
Wikidata:Q54838540
CVCL_2T05 2026-08-08 05:00:15 0
GM04520
 
Resource Report
Resource Website
RRID:CVCL_5L51 Homo sapiens (Human) Tuberous sclerosis 2 Population: Caucasian. Finite cell line Female CLO:CLO_0018844,
Coriell:GM04520,
Wikidata:Q54838558
CVCL_5L51 2026-08-08 05:00:15 0
GM04585
 
Resource Report
Resource Website
RRID:CVCL_AA22 Homo sapiens (Human) Population: Caucasian. Transformed cell line Female CLO:CLO_0018901,
Coriell:GM04585,
Wikidata:Q54838574
CVCL_AA22 2026-08-08 05:00:15 0
GM04539
 
Resource Report
Resource Website
RRID:CVCL_0M33 Homo sapiens (Human) Cystic fibrosis Population: Caucasian. Finite cell line Female CLO:CLO_0018881,
Coriell:GM04539,
Wikidata:Q54838563
CVCL_0M33 2026-08-08 05:00:15 0
GM04478
 
Resource Report
Resource Website
RRID:CVCL_V566 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Female CLO:CLO_0019661,
Coriell:GM04478,
Wikidata:Q54838532
CVCL_V566 2026-08-08 05:00:14 0
GM04465
 
Resource Report
Resource Website
Coriell Cat# GM04465, RRID:CVCL_CV41 Homo sapiens (Human) Schwartz-Jampel syndrome Population: Caucasian. Finite cell line Female Coriell GM04465 CLO:CLO_0019686,
Coriell:GM04465,
Wikidata:Q54838529
CVCL_CV41 2026-08-08 05:00:15 0
GM08878
 
Resource Report
Resource Website
RRID:CVCL_HJ76 Homo sapiens (Human) Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Transformed cell line Female Coriell:GM08878,
Wikidata:Q54843363
CVCL_HJ76 2026-08-08 05:01:12 0
GM08922
 
Resource Report
Resource Website
RRID:CVCL_9R02 Homo sapiens (Human) Multiple sclerosis Transformed cell line Female GM08922A CLO:CLO_0011220,
BioSample:SAMN00798270,
Coriell:GM08922,
Wikidata:Q54843405
CVCL_9R02 2026-08-08 05:01:16 0

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