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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
GM13250
 
Resource Report
Resource Website
Coriell Cat# GM13250, RRID:CVCL_V139 Homo sapiens (Human) Von Hippel-Lindau syndrome Transformed cell line Female Coriell GM13250 CLO:CLO_0013078,
BioSample:SAMN00802210,
Coriell:GM13250,
Wikidata:Q54846396
CVCL_V139 2026-08-15 04:31:53 0
GM13273
 
Resource Report
Resource Website
Coriell Cat# GM13273, RRID:CVCL_4F70 Homo sapiens (Human) Zellweger syndrome Population: Caucasian. Finite cell line Female Coriell GM13273 CLO:CLO_0013287,
BioSample:SAMN00802240,
Coriell:GM13273,
Wikidata:Q54846413
CVCL_4F70 2026-08-15 04:31:54 0
GM13301
 
Resource Report
Resource Website
Coriell Cat# GM13301, RRID:CVCL_FV89 Homo sapiens (Human) Progressive familial intrahepatic cholestasis Population: Caucasian; Amish. Transformed cell line Female Coriell GM13301 CLO:CLO_0013318,
BioSample:SAMN00802273,
Coriell:GM13301,
Wikidata:Q54846431
CVCL_FV89 2026-08-15 04:31:54 0
GM13249
 
Resource Report
Resource Website
RRID:CVCL_V138 Homo sapiens (Human) Von Hippel-Lindau syndrome Transformed cell line Male CLO:CLO_0013079,
Coriell:GM13249,
Wikidata:Q54846395
CVCL_V138 2026-08-15 04:31:53 0
GM13281
 
Resource Report
Resource Website
Coriell Cat# GM13281, RRID:CVCL_N206 Homo sapiens (Human) Population: South American (Brazil, Guyana, Venezuela)., Part of: Human variation panel. Transformed cell line Female GM17320 Coriell GM13281 CLO:CLO_0013283,
CLO:CLO_0013642,
BioSample:SAMN00802252,
Coriell:GM13281,
Coriell:GM17320,
Wikidata:Q54846419
CVCL_N206 2026-08-15 04:31:54 0
GM13298
 
Resource Report
Resource Website
Coriell Cat# GM13298, RRID:CVCL_9R32 Homo sapiens (Human) Neonatal adrenoleukodystrophy Population: Caucasian. Finite cell line Male Coriell GM13298 CLO:CLO_0013327,
BioSample:SAMN00802271,
Coriell:GM13298,
Wikidata:Q54846430
CVCL_9R32 2026-08-15 04:31:54 0
GM13278
 
Resource Report
Resource Website
RRID:CVCL_GS83 Homo sapiens (Human) Pancreatic lipase deficiency PMID:11393534 Transformed cell line Female CLO:CLO_0013279,
BioSample:SAMN00802248,
Coriell:GM13278,
Wikidata:Q54846417
CVCL_GS83 2026-08-15 04:31:54 0
GM13268
 
Resource Report
Resource Website
RRID:CVCL_9R31 Homo sapiens (Human) Neonatal adrenoleukodystrophy Population: Caucasian. Finite cell line Male CLO:CLO_0013108,
BioSample:SAMN00802234,
Coriell:GM13268,
Wikidata:Q54846410
CVCL_9R31 2026-08-15 04:31:57 0
GM13311
 
Resource Report
Resource Website
Coriell Cat# GM13311, RRID:CVCL_4F07 Homo sapiens (Human) Ellis-Van Creveld syndrome Population: Caucasian; Amish. Transformed cell line Female Coriell GM13311 CLO:CLO_0013215,
BioSample:SAMN00802287,
Coriell:GM13311,
Wikidata:Q54846451
CVCL_4F07 2026-08-15 04:31:54 0
GM13305
 
Resource Report
Resource Website
RRID:CVCL_1K71 Homo sapiens (Human) Transformed cell line Female BioSample:SAMN00802277,
Coriell:GM13305,
Wikidata:Q54846445
CVCL_1K71 2026-08-15 04:31:54 0
GM13254
 
Resource Report
Resource Website
RRID:CVCL_V142 Homo sapiens (Human) Von Hippel-Lindau syndrome Transformed cell line Male CLO:CLO_0013093,
BioSample:SAMN00802214,
Coriell:GM13254,
Wikidata:Q54846399
CVCL_V142 2026-08-15 04:31:56 0
GM13289
 
Resource Report
Resource Website
RRID:CVCL_V396 Homo sapiens (Human) Glycogen storage disease type Ia Transformed cell line Female CLO:CLO_0013350,
BioSample:SAMN00802260,
Coriell:GM13289,
Wikidata:Q54846423
CVCL_V396 2026-08-15 04:31:54 0
GM13301
 
Resource Report
Resource Website
RRID:CVCL_FV89 Homo sapiens (Human) Progressive familial intrahepatic cholestasis Population: Caucasian; Amish. Transformed cell line Female CLO:CLO_0013318,
BioSample:SAMN00802273,
Coriell:GM13301,
Wikidata:Q54846431
CVCL_FV89 2026-08-15 04:31:57 0
GM13307
 
Resource Report
Resource Website
Coriell Cat# GM13307, RRID:CVCL_9R95 Homo sapiens (Human) Holt-Oram syndrome Population: Caucasian. Finite cell line Female Coriell GM13307 CLO:CLO_0013243,
BioSample:SAMN00802281,
Coriell:GM13307,
Wikidata:Q54846448
CVCL_9R95 2026-08-15 04:31:54 0
GM13293
 
Resource Report
Resource Website
RRID:CVCL_L931 Homo sapiens (Human) Population: African American., Part of: Human variation panel. Transformed cell line Female GM17173 CLO:CLO_0013331,
CLO:CLO_0014026,
BioSample:SAMN00802265,
Coriell:GM13293,
Coriell:GM17173,
GEO:GSM569745,
GEO:GSM596237,
GEO:GSM597032,
GEO:GSM924683,
IPD-IMGT/HLA:17383,
Wikidata:Q54846426
CVCL_L931 2026-08-15 04:31:57 0
GM13239
 
Resource Report
Resource Website
Coriell Cat# GM13239, RRID:CVCL_9Y33 Homo sapiens (Human) Sly syndrome Population: Mexican. Finite cell line Female Coriell GM13239 CLO:CLO_0013192,
BioSample:SAMN00802198,
Coriell:GM13239,
Wikidata:Q54846385
CVCL_9Y33 2026-08-15 04:31:53 0
GM13335
 
Resource Report
Resource Website
Coriell Cat# GM13335, RRID:CVCL_7531 Homo sapiens (Human) Population: Caucasian. PMID:30567591 Finite cell line Male GM00967B Coriell GM13335 CLO:CLO_0012883,
BioSample:SAMN00802313,
Coriell:GM13335,
GEO:GSM3124664,
Wikidata:Q54846468
CVCL_7531 2026-08-15 04:31:58 0
GM13448
 
Resource Report
Resource Website
RRID:CVCL_1S75 Homo sapiens (Human) Group: Human/rodent somatic cell hybrid. PMID:1559705 Hybrid cell line HAL26-12 CLO:CLO_0012167,
Coriell:GM13448,
Wikidata:Q54846534
cvcl_f739 CVCL_1S75 2026-08-15 04:31:56 0
GM13342
 
Resource Report
Resource Website
RRID:CVCL_1S71 Homo sapiens (Human) Characteristics: Hybrid for chromosome 3 mapping (PubMed=9441767)., Group: Human/rodent somatic cell hybrid. PMID:7713507
PMID:9441767
Hybrid cell line LG63-13, LG-63-13 CLO:CLO_0012885,
Coriell:GM13342,
Wikidata:Q54846473
cvcl_1r77 CVCL_1S71 2026-08-15 04:31:58 0
GM13316
 
Resource Report
Resource Website
Coriell Cat# GM13316, RRID:CVCL_4I84 Homo sapiens (Human) Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Transformed cell line Female Coriell GM13316 CLO:CLO_0013222,
Coriell:GM13316,
Wikidata:Q54846457
CVCL_4I84 2026-08-15 04:31:54 0

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