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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
GM10403
 
Resource Report
Resource Website
Coriell Cat# GM10403, RRID:CVCL_GT61 Homo sapiens (Human) Hypophosphatasia Population: African American. Finite cell line Female Coriell GM10403 CLO:CLO_0028675,
BioSample:SAMN00799995,
Coriell:GM10403,
Wikidata:Q54844436
CVCL_GT61 2026-08-01 05:06:05 0
GM10463
 
Resource Report
Resource Website
RRID:CVCL_0Q11 Homo sapiens (Human) Transformed cell line Female CLO:CLO_0028501,
BioSample:SAMN00800037,
Coriell:GM10463,
Wikidata:Q54844478
CVCL_0Q11 2026-08-01 05:06:04 0
GM10463
 
Resource Report
Resource Website
Coriell Cat# GM10463, RRID:CVCL_0Q11 Homo sapiens (Human) Transformed cell line Female Coriell GM10463 CLO:CLO_0028501,
BioSample:SAMN00800037,
Coriell:GM10463,
Wikidata:Q54844478
CVCL_0Q11 2026-08-01 05:06:04 0
GM10472
 
Resource Report
Resource Website
Coriell Cat# GM10472, RRID:CVCL_N358 Homo sapiens (Human) Population: African; Biaka pygmies., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository. PMID:14583597 Transformed cell line Female GM10472A, JK745 Coriell GM10472 CLO:CLO_0028493,
Coriell:GM10472,
Wikidata:Q54844484
CVCL_N358 2026-08-01 05:06:04 0
GM10439
 
Resource Report
Resource Website
RRID:CVCL_EG72 Homo sapiens (Human) Generalized arterial calcification of infancy 1 Population: Caucasian. Finite cell line Female CLO:CLO_0028526,
BioSample:SAMN00800023,
Coriell:GM10439,
Wikidata:Q54844469
CVCL_EG72 2026-08-01 05:06:04 0
GM10490
 
Resource Report
Resource Website
Coriell Cat# GM17170, RRID:CVCL_N146 Homo sapiens (Human) Congenital adrenal gland hypoplasia Population: African American., Part of: Human variation panel. Transformed cell line Female GM10490A, GM17170 Coriell GM17170 CLO:CLO_0014022,
CLO:CLO_0024254,
BioSample:SAMN00800043,
Coriell:GM10490,
Coriell:GM17170,
GEO:GSM569696,
GEO:GSM596234,
GEO:GSM597029,
GEO:GSM924680,
IPD-IMGT/HLA:19225,
Wikidata:Q54844490
CVCL_N146 2026-08-01 05:06:04 0
GM10474
 
Resource Report
Resource Website
RRID:CVCL_GT62 Homo sapiens (Human) Hypophosphatasia Finite cell line Female GM10474A CLO:CLO_0028475,
Coriell:GM10474,
Wikidata:Q54844486
CVCL_GT62 2026-08-01 05:06:04 0
GM10506
 
Resource Report
Resource Website
RRID:CVCL_AU94 Homo sapiens (Human) Usher syndrome type 1 Population: Caucasian; Acadian. Transformed cell line Female CLO:CLO_0024239,
BioSample:SAMN00800047,
Coriell:GM10506,
Wikidata:Q54844505
CVCL_AU94 2026-08-01 05:06:05 0
GM10490
 
Resource Report
Resource Website
RRID:CVCL_N146 Homo sapiens (Human) Congenital adrenal gland hypoplasia Population: African American., Part of: Human variation panel. Transformed cell line Female GM10490A, GM17170 CLO:CLO_0014022,
CLO:CLO_0024254,
BioSample:SAMN00800043,
Coriell:GM10490,
Coriell:GM17170,
GEO:GSM569696,
GEO:GSM596234,
GEO:GSM597029,
GEO:GSM924680,
IPD-IMGT/HLA:19225,
Wikidata:Q54844490
CVCL_N146 2026-08-01 05:06:06 0
GM10431
 
Resource Report
Resource Website
RRID:CVCL_0I30 Homo sapiens (Human) Transformed cell line Female CLO:CLO_0028627,
BioSample:SAMN00800017,
Coriell:GM10431,
Wikidata:Q54844450
CVCL_0I30 2026-08-01 05:06:04 0
GM10474
 
Resource Report
Resource Website
Coriell Cat# GM10474, RRID:CVCL_GT62 Homo sapiens (Human) Hypophosphatasia Finite cell line Female GM10474A Coriell GM10474 CLO:CLO_0028475,
Coriell:GM10474,
Wikidata:Q54844486
CVCL_GT62 2026-08-01 05:06:04 0
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 2026-08-01 05:06:04 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 2026-08-01 05:06:06 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 2026-08-01 05:06:05 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 2026-08-01 05:06:04 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 2026-08-01 05:06:04 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 2026-08-01 05:06:05 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 2026-08-01 05:06:05 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 2026-08-01 05:06:06 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 2026-08-01 05:06:05 0

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