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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 Authority Record Last Update Mentions Count
GM01441
 
Resource Report
Resource Website
RRID:CVCL_X248 Homo sapiens (Human) Population: Caucasian. PMID:6661932 Finite cell line Male GM-1441, GM 1441 CLO:CLO_0030890,
BioSample:SAMN00803888,
Coriell:GM01441,
Wikidata:Q54836829
CVCL_X248 Cellosaurus 2026-09-26 06:48:43 0
GM01411
 
Resource Report
Resource Website
Coriell Cat# GM01411, RRID:CVCL_0P92 Homo sapiens (Human) Karyotypic information: 46,X,t(X;21)(q11;p11) (PubMed=10377420)., Population: African American. PMID:10377420 Finite cell line Female GM-1411, GM1411 Coriell GM01411 CLO:CLO_0030790,
BioSample:SAMN00803866,
Coriell:GM01411,
Wikidata:Q54836811
CVCL_0P92 Cellosaurus 2026-09-26 06:48:42 0
GM01410
 
Resource Report
Resource Website
RRID:CVCL_J116 Homo sapiens (Human) Hepatocyte nuclear factor 4-alpha associated monogenic diabetes Population: Caucasian., Part of: R-W pedigree MODY cell line collection. PMID:7313555
PMID:8945471
Transformed cell line Female GM-1410, GM 1410 CLO:CLO_0030803,
Coriell:GM01410,
Wikidata:Q54836810
CVCL_J116 Cellosaurus 2026-09-26 06:48:42 0
GM01446
 
Resource Report
Resource Website
Coriell Cat# GM01446, RRID:CVCL_2H16 Homo sapiens (Human) Transformed cell line Female GM-1446 Coriell GM01446 CLO:CLO_0030898,
BioSample:SAMN00803896,
Coriell:GM01446,
Wikidata:Q54836834
CVCL_2H16 Cellosaurus 2026-09-26 06:48:43 0
GM01444
 
Resource Report
Resource Website
RRID:CVCL_0M11 Homo sapiens (Human) Transformed cell line Female GM-1444 CLO:CLO_0030894,
Coriell:GM01444,
Wikidata:Q54836832
CVCL_0M11 Cellosaurus 2026-09-26 06:48:43 0
GM01393
 
Resource Report
Resource Website
Coriell Cat# GM01393, RRID:CVCL_1V15 Homo sapiens (Human) Population: Caucasian. PMID:21418647
PMID:24555846
PMID:25326100
Finite cell line Male GM-1393 Coriell GM01393 CLO:CLO_0030812,
BioSample:SAMN00803854,
Coriell:GM01393,
GEO:GSM651114,
GEO:GSM651115,
GEO:GSM1257695,
GEO:GSM1266963,
GEO:GSM1267044,
GEO:GSM1288430,
Wikidata:Q54836803
CVCL_1V15 Cellosaurus 2026-09-26 06:48:42 0
GM01404
 
Resource Report
Resource Website
RRID:CVCL_JC90 Homo sapiens (Human) Androgen insensitivity syndrome Karyotypic information: 46,XY; but phenotypically female (Coriell=GM01404)., Population: African American. Finite cell line Sex ambiguous GM-1404 CLO:CLO_0030807,
BioSample:SAMN00803860,
Coriell:GM01404,
Wikidata:Q54836806
CVCL_JC90 Cellosaurus 2026-09-26 06:48:42 0
GM01355
 
Resource Report
Resource Website
RRID:CVCL_4N09 Homo sapiens (Human) Hyperlipoproteinemia, type IIa Population: Caucasian. Finite cell line Female GM-1355, GM01355A CLO:CLO_0030905,
BioSample:SAMN00803810,
Coriell:GM01355,
Wikidata:Q54836777
CVCL_4N09 Cellosaurus 2026-09-26 06:48:42 0
GM01381
 
Resource Report
Resource Website
Coriell Cat# GM01381, RRID:CVCL_7319 Homo sapiens (Human) PMID:7329430
PMID:7471105
Finite cell line Male GM1381, GM-1381, GM 1381, GM1381A, GM01381B Coriell GM01381 CLO:CLO_0030837,
Coriell:GM01381,
Wikidata:Q54836793
CVCL_7319 Cellosaurus 2026-09-26 06:48:42 0
GM01408
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_DF17 Homo sapiens (Human) Retinoblastoma PMID:7253718 Finite cell line Female GM-1408, AG01408, AG-1408, AG 1408, AG1408 CLO:CLO_0030799,
BioSample:SAMN00803864,
Coriell:AG01408,
Coriell:GM01408,
Wikidata:Q54836808
CVCL_DF17 Cellosaurus 2026-09-26 06:48:42 0
GM01408
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM01408, RRID:CVCL_DF17 Homo sapiens (Human) Retinoblastoma PMID:7253718 Finite cell line Female GM-1408, AG01408, AG-1408, AG 1408, AG1408 Coriell GM01408 CLO:CLO_0030799,
BioSample:SAMN00803864,
Coriell:AG01408,
Coriell:GM01408,
Wikidata:Q54836808
CVCL_DF17 Cellosaurus 2026-09-26 06:48:42 0
GM01376
 
Resource Report
Resource Website
RRID:CVCL_2H15 Homo sapiens (Human) Caution: Indicated by Coriell to originate from father of GM01374 but does not contain the same CBS mutation, therefore the pedigree relationship may be incorrect (PubMed=8528202)., Population: Caucasian. PMID:8528202
PMID:24555846
PMID:25326100
Finite cell line Male GM1376, GM-1376 CLO:CLO_0030831,
BioSample:SAMN00803832,
Coriell:GM01376,
GEO:GSM1257684,
GEO:GSM1266960,
GEO:GSM1267042,
GEO:GSM1288428,
Wikidata:Q54836789
CVCL_2H15 Cellosaurus 2026-09-26 06:48:42 0
GM01426
 
Resource Report
Resource Website
RRID:CVCL_0M01 Homo sapiens (Human) Mucopolysaccharidosis type IIIB Population: Caucasian. PMID:30933722
PMID:34411609
Finite cell line Female GM-1426 CLO:CLO_0030778,
BioSample:SAMN00803880,
Coriell:GM01426,
Wikidata:Q54836823
CVCL_0M01 Cellosaurus 2026-09-26 06:48:43 0
GM01387
 
Resource Report
Resource Website
Coriell Cat# GM01387, RRID:CVCL_J114 Homo sapiens (Human) Karyotypic information: 46,XX,+der(9)(9pter->9q21.2::13q12.1->13qter)mat,-13 (Coriell=GM01387)., Population: Caucasian. PMID:6661932 Finite cell line Female GM-1387, GM 1387 Coriell GM01387 CLO:CLO_0030825,
BioSample:SAMN00803842,
Coriell:GM01387,
Wikidata:Q54836796
CVCL_J114 Cellosaurus 2026-09-26 06:48:42 0
GM01420
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM01420, RRID:CVCL_JD99 Homo sapiens (Human) Finite cell line Female GM-1420 Coriell GM01420 Coriell:GM01420,
Wikidata:Q54836820
CVCL_JD99 Cellosaurus 2026-09-26 06:48:43 0
GM01430
 
Resource Report
Resource Website
RRID:CVCL_AI26 Homo sapiens (Human) Hepatocyte nuclear factor 4-alpha associated monogenic diabetes Population: Caucasian., Part of: R-W pedigree MODY cell line collection. PMID:8945471
PMID:29990710
Finite cell line Male GM-1430 CLO:CLO_0030772,
Coriell:GM01430,
Wikidata:Q54836826
CVCL_AI26 Cellosaurus 2026-09-26 06:48:43 0
GM01416
 
Resource Report
Resource Website
RRID:CVCL_F657 Homo sapiens (Human) Population: Caucasian. PMID:6661932
PMID:23665875
Transformed cell line Female GM-1416, GM 1416, GM1416, GM01416B CLO:CLO_0030788,
BioSample:SAMN00803874,
Coriell:GM01416,
Wikidata:Q54836816
CVCL_F657 Cellosaurus 2026-09-26 06:48:43 0
GM01368
 
Resource Report
Resource Website
RRID:CVCL_GY15 Homo sapiens (Human) Hereditary persistence of fetal hemoglobin Population: African American. Finite cell line Male GM-1368 CLO:CLO_0030847,
BioSample:SAMN00803826,
Coriell:GM01368,
Wikidata:Q54836786
CVCL_GY15 Cellosaurus 2026-09-26 06:48:42 0
GM01444
 
Resource Report
Resource Website
Coriell Cat# GM01444, RRID:CVCL_0M11 Homo sapiens (Human) Transformed cell line Female GM-1444 Coriell GM01444 CLO:CLO_0030894,
Coriell:GM01444,
Wikidata:Q54836832
CVCL_0M11 Cellosaurus 2026-09-26 06:48:43 0
GM01354
 
Resource Report
Resource Website
RRID:CVCL_4N08 Homo sapiens (Human) Hyperlipoproteinemia, type IIa Population: Caucasian. Finite cell line Female GM-1354 CLO:CLO_0030906,
BioSample:SAMN00803808,
Coriell:GM01354,
Wikidata:Q54836776
CVCL_4N08 Cellosaurus 2026-09-26 06:48:42 0

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