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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
GM02434
 
Resource Report
Resource Website
RRID:CVCL_GS55 Homo sapiens (Human) Adenosine deaminase deficiency Population: Caucasian. PMID:7380831 Finite cell line Male GM-2434, GM 2434, GM02434A CLO:CLO_0033277,
BioSample:SAMN00807771,
Coriell:GM02434,
Wikidata:Q54837486
CVCL_GS55 2026-07-25 04:32:33 0
GM02355
 
Resource Report
Resource Website
Coriell Cat# GM02355, RRID:CVCL_L945 Homo sapiens (Human) Familial adenomatous polyposis Population: Caucasian. Finite cell line Female GM2355 Coriell GM02355 CLO:CLO_0033110,
BioSample:SAMN00807733,
Coriell:GM02355,
Wikidata:Q54837455
CVCL_L945 2026-07-25 04:32:32 0
GM02442
 
Resource Report
Resource Website
Coriell Cat# GM02442, RRID:CVCL_GR98 Homo sapiens (Human) Type 1 diabetes mellitus Population: Native Central American; Pima. Finite cell line Female Coriell GM02442 CLO:CLO_0033317,
BioSample:SAMN00807779,
Coriell:GM02442,
Wikidata:Q54837496
CVCL_GR98 2026-07-25 04:32:33 0
GM02363
 
Resource Report
Resource Website
Coriell Cat# GM02363, RRID:CVCL_AK24 Homo sapiens (Human) Fanconi anemia, complementation group A Finite cell line Male GM-2363 Coriell GM02363 CLO:CLO_0033100,
Coriell:GM02363,
Wikidata:Q54837460
CVCL_AK24 2026-07-25 04:32:32 0
GM02362
 
Resource Report
Resource Website
RRID:CVCL_AK23 Homo sapiens (Human) Fanconi anemia, complementation group A Finite cell line Male GM-2362, GM02362A CLO:CLO_0033099,
Coriell:GM02362,
Wikidata:Q54837459
CVCL_AK23 2026-07-25 04:32:32 0
GM02439 GM1-iPSC clone 3
 
Resource Report
Resource Website
RRID:CVCL_VE86 Homo sapiens (Human) GM1 gangliosidosis Population: Turkish. PMID:25925601 Induced pluripotent stem cell Male GM1-iPSC-clone 3 SKIP:SKIP001350,
Wikidata:Q54837493
cvcl_w149 CVCL_VE86 2026-07-25 04:32:35 0
GM02439
 
Resource Report
Resource Website
RRID:CVCL_W149 Homo sapiens (Human) GM1 gangliosidosis Population: Turkish., From: Montreal Children's Hospital cell repository; Montreal; Canada. PMID:25925601 Finite cell line Male WG0406, WG406 CLO:CLO_0033291,
Coriell:GM02439,
Wikidata:Q54837491
CVCL_W149 2026-07-25 04:32:33 0
GM02431
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_L975 Homo sapiens (Human) Chediak-Higashi syndrome Transformed cell line Male GM02431A, GM02378 CLO:CLO_0033275,
BioSample:SAMN00807765,
Coriell:GM02378,
Coriell:GM02431,
Wikidata:Q54837482
CVCL_L975 2026-07-25 04:32:35 0
GM02380
 
Resource Report
Resource Website
Coriell Cat# GM02380, RRID:CVCL_H181 Homo sapiens (Human) PMID:6617268 Finite cell line Female GM 2380 Coriell GM02380 CLO:CLO_0033104,
Coriell:GM02380,
Wikidata:Q54837466
CVCL_H181 2026-07-25 04:32:33 0
GM02365
 
Resource Report
Resource Website
Coriell Cat# GM02365, RRID:CVCL_1R62 Homo sapiens (Human) Coffin-Lowry syndrome Population: Caucasian. PMID:23665875 Finite cell line Male GM02365A Coriell GM02365 CLO:CLO_0033101,
BioSample:SAMN00807737,
Coriell:GM02365,
Wikidata:Q54837463
CVCL_1R62 2026-07-25 04:32:32 0
GM02425
 
Resource Report
Resource Website
RRID:CVCL_9R69 Homo sapiens (Human) Mucolipidosis type IIIA Population: Caucasian. PMID:16465621 Finite cell line Male GM-2425 CLO:CLO_0033090,
BioSample:SAMN00807757,
Coriell:GM02425,
Wikidata:Q54837477
CVCL_9R69 2026-07-25 04:32:35 0
GM02419
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_UY61 Homo sapiens (Human) Finite cell line Female Coriell:GM02419,
Wikidata:Q93577635
CVCL_UY61 2026-07-25 04:32:34 0
GM02422
 
Resource Report
Resource Website
RRID:CVCL_H183 Homo sapiens (Human) Trisomy 18 PMID:6661932 Finite cell line Female GM 2422 CLO:CLO_0033089,
BioSample:SAMN00807755,
Coriell:GM02422,
Wikidata:Q54837476
CVCL_H183 2026-07-25 04:32:33 0
GM02346
 
Resource Report
Resource Website
RRID:CVCL_X091 Homo sapiens (Human) Karyotypic information: 46,XY,t(4;16)(4pter->4q35::16q22.1->16qter;16pter->16q22.1::4q35->4qter) (Coriell=GM02346)., Population: Caucasian. PMID:2095701
PMID:6617268
PMID:6661932
Finite cell line Male GM-2346, GM 2346, GM2346 CLO:CLO_0033112,
BioSample:SAMN00807729,
Coriell:GM02346,
Wikidata:Q54837453
CVCL_X091 2026-07-25 04:32:32 0
GM02432
 
Resource Report
Resource Website
Coriell Cat# GM17252, RRID:CVCL_M997 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:20889555 Transformed cell line Female GM17252 Coriell GM17252 CLO:CLO_0014392,
CLO:CLO_0033283,
BioSample:SAMN00807767,
Coriell:GM02432,
Coriell:GM17252,
GEO:GSM569642,
GEO:GSM596316,
GEO:GSM596675,
GEO:GSM924854,
Wikidata:Q54837483
CVCL_M997 2026-07-25 04:32:33 0
GM02364
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JD75 Homo sapiens (Human) Fanconi anemia Finite cell line Male GM-2364 Coriell:GM02364,
Wikidata:Q54837461
CVCL_JD75 2026-07-25 04:32:32 0
GM02340 iPSC clone 6
 
Resource Report
Resource Website
RRID:CVCL_B5QU Homo sapiens (Human) Sickle cell disease PMID:22905176 Induced pluripotent stem cell Female iPSC clone 6.1 GEO:GSM861005,
GEO:GSM1589943,
GEO:GSM1589955,
Wikidata:Q111733236
cvcl_l749 CVCL_B5QU 2026-07-25 04:32:34 0
GM02436
 
Resource Report
Resource Website
RRID:CVCL_GS56 Homo sapiens (Human) Adenosine deaminase deficiency Population: Caucasian; Swiss. PMID:1346349
PMID:1680289
PMID:2567118
PMID:7380831
Finite cell line Female GM-2436, GM 2436 CLO:CLO_0033293,
BioSample:SAMN00807775,
Coriell:GM02436,
Wikidata:Q54837488
CVCL_GS56 2026-07-25 04:32:33 0
GM02430
 
Resource Report
Resource Website
RRID:CVCL_M996 Homo sapiens (Human) Transformed cell line Female GM17321 CLO:CLO_0013646,
CLO:CLO_0033274,
BioSample:SAMN00807763,
Coriell:GM02430,
Coriell:GM17321,
Wikidata:Q54837481
CVCL_M996 2026-07-25 04:32:35 0
GM02437
 
Resource Report
Resource Website
Coriell Cat# GM02437, RRID:CVCL_5M73 Homo sapiens (Human) Dyggve-Melchior-Clausen syndrome Finite cell line Female Coriell GM02437 CLO:CLO_0033298,
Coriell:GM02437,
Wikidata:Q54837489
CVCL_5M73 2026-07-25 04:32:33 0

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