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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
GM10441
 
Resource Report
Resource Website
Coriell Cat# GM10441, RRID:CVCL_EG74 Homo sapiens (Human) Transformed cell line Female Coriell GM10441 CLO:CLO_0028519,
BioSample:SAMN00800027,
Coriell:GM10441,
Wikidata:Q54844471
CVCL_EG74 2026-09-12 05:34:01 0
GM10459
 
Resource Report
Resource Website
Coriell Cat# GM10459, RRID:CVCL_4I19 Homo sapiens (Human) Depression Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Transformed cell line Female Coriell GM10459 CLO:CLO_0028507,
Coriell:GM10459,
Wikidata:Q54844474
CVCL_4I19 2026-09-12 05:34:01 0
GM10417
 
Resource Report
Resource Website
RRID:CVCL_X449 Homo sapiens (Human) Aspartylglycosaminuria Population: Caucasian; Finnish. Transformed cell line Female GM10417A CLO:CLO_0028632,
BioSample:SAMN00800003,
Coriell:GM10417,
Wikidata:Q54844442
CVCL_X449 2026-09-12 05:34:01 0
GM10471
 
Resource Report
Resource Website
RRID:CVCL_N357 Homo sapiens (Human) Population: African; Biaka pygmies., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository. PMID:14583597 Transformed cell line Female JK742 CLO:CLO_0028495,
Coriell:GM10471,
Wikidata:Q54844483
CVCL_N357 2026-09-12 05:34:01 0
GM10420
 
Resource Report
Resource Website
Coriell Cat# GM10420, RRID:CVCL_DS22 Homo sapiens (Human) Sialic acid storage disease Transformed cell line Female Coriell GM10420 CLO:CLO_0028640,
BioSample:SAMN00800009,
Coriell:GM10420,
Wikidata:Q54844446
CVCL_DS22 2026-09-12 05:34:01 0
GM10502
 
Resource Report
Resource Website
RRID:CVCL_1R96 Homo sapiens (Human) Characteristics: Hybrid for chromosome 17 mapping (PubMed=9441767)., Group: Human/rodent somatic cell hybrid. PMID:3130306
PMID:9441767
Hybrid cell line MH-41 CLO:CLO_0024246,
Coriell:GM10502,
Wikidata:Q54844502
CVCL_1R96 2026-09-12 05:34:02 0
GM10482
 
Resource Report
Resource Website
Coriell Cat# GM10482, RRID:CVCL_1R92 Homo sapiens (Human) Characteristics: Hybrid for chromosome 11 mapping (PubMed=9441767)., Group: Human/rodent somatic cell hybrid. PMID:9441767 Hybrid cell line MCH110.1 C4, MCH110.1C4 Coriell GM10482 CLO:CLO_0028498,
Coriell:GM10482,
Wikidata:Q54844487
CVCL_1R92 2026-09-12 05:34:02 0
GM10482
 
Resource Report
Resource Website
RRID:CVCL_1R92 Homo sapiens (Human) Characteristics: Hybrid for chromosome 11 mapping (PubMed=9441767)., Group: Human/rodent somatic cell hybrid. PMID:9441767 Hybrid cell line MCH110.1 C4, MCH110.1C4 CLO:CLO_0028498,
Coriell:GM10482,
Wikidata:Q54844487
CVCL_1R92 2026-09-12 05:34:02 0
GM10494
 
Resource Report
Resource Website
Coriell Cat# GM10494, RRID:CVCL_N361 Homo sapiens (Human) Population: African; Mbuti Pygmy., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository. PMID:14583597 Transformed cell line Male JK1031 Coriell GM10494 CLO:CLO_0024251,
Coriell:GM10494,
Wikidata:Q54844493
CVCL_N361 2026-09-12 05:34:02 0
GM10432
 
Resource Report
Resource Website
RRID:CVCL_N143 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. Transformed cell line Female GM17294 CLO:CLO_0013138,
CLO:CLO_0028628,
BioSample:SAMN00800019,
Coriell:GM10432,
Coriell:GM17294,
GEO:GSM569762,
GEO:GSM596358,
GEO:GSM596775,
GEO:GSM924896,
Wikidata:Q54844452
CVCL_N143 2026-09-12 05:34:01 0
GM10497
 
Resource Report
Resource Website
RRID:CVCL_U717 Homo sapiens (Human) Osteogenesis imperfecta Finite cell line Female CLO:CLO_0024248,
Coriell:GM10497,
Wikidata:Q54844497
CVCL_U717 2026-09-12 05:34:02 0
GM10507
 
Resource Report
Resource Website
Coriell Cat# GM10507, RRID:CVCL_GT63 Homo sapiens (Human) Hypophosphatasia Population: Caucasian. Finite cell line Sex unspecified Coriell GM10507 CLO:CLO_0024242,
BioSample:SAMN00800049,
Coriell:GM10507,
Wikidata:Q54844506
CVCL_GT63 2026-09-12 05:34:02 0
GM10402
 
Resource Report
Resource Website
RRID:CVCL_1Y30 Homo sapiens (Human) Transformed cell line Male CLO:CLO_0028672,
BioSample:SAMN00799993,
Coriell:GM10402,
Wikidata:Q54844435
CVCL_1Y30 2026-09-12 05:34:01 0
GM10460
 
Resource Report
Resource Website
RRID:CVCL_4I20 Homo sapiens (Human) Depression Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Transformed cell line Male CLO:CLO_0028504,
Coriell:GM10460,
Wikidata:Q54844475
CVCL_4I20 2026-09-12 05:34:01 0
GM10501
 
Resource Report
Resource Website
RRID:CVCL_1R95 Cricetulus griseus (Chinese hamster) Characteristics: Hybrid for chromosomes 17 and X mapping (PubMed=9441767)., Group: Human/rodent somatic cell hybrid. PMID:3130306
PMID:9441767
Hybrid cell line 88H-5 CLO:CLO_0024243,
Coriell:GM10501,
Wikidata:Q54844501
CVCL_1R95 2026-09-12 05:34:02 0
GM10461
 
Resource Report
Resource Website
RRID:CVCL_V343 Homo sapiens (Human) Population: African American. Finite cell line Female CLO:CLO_0028530,
BioSample:SAMN00800033,
Coriell:GM10461,
Wikidata:Q54844476
CVCL_V343 2026-09-12 05:34:01 0
GM10406
 
Resource Report
Resource Website
Coriell Cat# GM10406, RRID:CVCL_AJ39 Homo sapiens (Human) Population: Caucasian., Part of: R-W pedigree MODY cell line collection. PMID:8945471 Transformed cell line Male Coriell GM10406 CLO:CLO_0028661,
Coriell:GM10406,
Wikidata:Q54844438
CVCL_AJ39 2026-09-12 05:34:01 0
GM10503
 
Resource Report
Resource Website
RRID:CVCL_DD83 Homo sapiens (Human) Osteogenesis imperfecta type II Population: Caucasian. PMID:2914942 Finite cell line Female JIMM-69 CLO:CLO_0024245,
Coriell:GM10503,
Wikidata:Q54844503
CVCL_DD83 2026-09-12 05:34:02 0
GM10450
 
Resource Report
Resource Website
Coriell Cat# GM10450, RRID:CVCL_N144 Homo sapiens (Human) Population: Caucasian., Part of: R-W pedigree MODY cell line collection., Part of: Human variation panel. PMID:8945471 Transformed cell line Male GM10450A, GM18050 Coriell GM10450 CLO:CLO_0015650,
CLO:CLO_0028514,
BioSample:SAMN00800029,
Coriell:GM10450,
Coriell:GM18050,
Wikidata:Q54844472
CVCL_N144 2026-09-12 05:34:01 0
GM10433
 
Resource Report
Resource Website
RRID:CVCL_V051 Homo sapiens (Human) Marfan syndrome Transformed cell line Female GM10433A CLO:CLO_0028629,
BioSample:SAMN00800021,
Coriell:GM10433,
Wikidata:Q54844467
CVCL_V051 2026-09-12 05:34:01 0

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