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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
GM16337
 
Resource Report
Resource Website
RRID:CVCL_UD09 Homo sapiens (Human) Facioscapulohumeral muscular dystrophy 1 PMID:28161093 Transformed cell line Female Coriell:GM16337,
Wikidata:Q93844475
CVCL_UD09 2026-08-15 04:32:38 0
GM16339
 
Resource Report
Resource Website
RRID:CVCL_UD11 Homo sapiens (Human) Facioscapulohumeral muscular dystrophy 1 Donor information: At sampling donor was not affected with facioscapulohumeral muscular dystrophy but at risk for disease. PMID:28161093 Transformed cell line Female Coriell:GM16339,
Wikidata:Q93844480
CVCL_UD11 2026-08-15 04:32:38 0
GM16333
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_A5WM Homo sapiens (Human) Facioscapulohumeral muscular dystrophy 1 PMID:28161093 Transformed cell line Female Coriell:GM16333,
Wikidata:Q107115161
CVCL_A5WM 2026-08-15 04:32:38 0
GM16350
 
Resource Report
Resource Website
RRID:CVCL_DB90 Homo sapiens (Human) PMID:28161093 Transformed cell line Female CLO:CLO_0019422,
Coriell:GM16350,
Wikidata:Q54848467
CVCL_DB90 2026-08-15 04:32:38 0
GM16334
 
Resource Report
Resource Website
RRID:CVCL_UD06 Homo sapiens (Human) Facioscapulohumeral muscular dystrophy 1 PMID:28161093 Transformed cell line Female Coriell:GM16334,
Wikidata:Q93844457
CVCL_UD06 2026-08-15 04:32:38 0
GM16338
 
Resource Report
Resource Website
RRID:CVCL_UD10 Homo sapiens (Human) Facioscapulohumeral muscular dystrophy 1 PMID:28161093 Transformed cell line Female Coriell:GM16338,
Wikidata:Q93844477
CVCL_UD10 2026-08-15 04:32:38 0
GM16401
 
Resource Report
Resource Website
Coriell Cat# GM16401, RRID:CVCL_DS04 Homo sapiens (Human) Atrioventricular septal defect Transformed cell line Female Coriell GM16401 CLO:CLO_0019508,
Coriell:GM16401,
Wikidata:Q54848510
CVCL_DS04 2026-08-15 04:32:39 0
GM16400
 
Resource Report
Resource Website
RRID:CVCL_N264 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. Transformed cell line Female GM18094 CLO:CLO_0015758,
CLO:CLO_0019509,
Coriell:GM16400,
Coriell:GM18094,
Wikidata:Q54848509
CVCL_N264 2026-08-15 04:32:39 0
GM16348
 
Resource Report
Resource Website
RRID:CVCL_HQ06 Homo sapiens (Human) Facioscapulohumeral muscular dystrophy 1 PMID:28161093 Transformed cell line Female CLO:CLO_0019426,
Coriell:GM16348,
Wikidata:Q54848465
CVCL_HQ06 2026-08-15 04:32:38 0
GM16400
 
Resource Report
Resource Website
Coriell Cat# GM18094, RRID:CVCL_N264 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. Transformed cell line Female GM18094 Coriell GM18094 CLO:CLO_0015758,
CLO:CLO_0019509,
Coriell:GM16400,
Coriell:GM18094,
Wikidata:Q54848509
CVCL_N264 2026-08-15 04:32:39 0
GM16349
 
Resource Report
Resource Website
RRID:CVCL_DB89 Homo sapiens (Human) PMID:28161093 Transformed cell line Female CLO:CLO_0019429,
Coriell:GM16349,
Wikidata:Q54848466
CVCL_DB89 2026-08-15 04:32:38 0
GM16391
 
Resource Report
Resource Website
RRID:CVCL_4Z81 Homo sapiens (Human) Trichothiodystrophy Population: Caucasian; Welsh. Finite cell line Female CLO:CLO_0019526,
Coriell:GM16391,
Wikidata:Q54848501
CVCL_4Z81 2026-08-15 04:32:38 0
GM16401
 
Resource Report
Resource Website
RRID:CVCL_DS04 Homo sapiens (Human) Atrioventricular septal defect Transformed cell line Female CLO:CLO_0019508,
Coriell:GM16401,
Wikidata:Q54848510
CVCL_DS04 2026-08-15 04:32:39 0
GM16332
 
Resource Report
Resource Website
RRID:CVCL_LN75 Homo sapiens (Human) PMID:28161093 Transformed cell line Female Coriell:GM16332,
Wikidata:Q54848463
CVCL_LN75 2026-08-15 04:32:38 0
GM16336
 
Resource Report
Resource Website
RRID:CVCL_UD08 Homo sapiens (Human) Facioscapulohumeral muscular dystrophy 1 PMID:28161093 Transformed cell line Female Coriell:GM16336,
Wikidata:Q93844464
CVCL_UD08 2026-08-15 04:32:38 0
GM16423
 
Resource Report
Resource Website
RRID:CVCL_UT77 Homo sapiens (Human) Facioscapulohumeral muscular dystrophy 1 PMID:28161093 Transformed cell line Female Coriell:GM16423,
Wikidata:Q93845575
CVCL_UT77 2026-08-15 04:32:39 0
GM16418
 
Resource Report
Resource Website
RRID:CVCL_LN83 Homo sapiens (Human) PMID:28161093 Transformed cell line Female Coriell:GM16418,
Wikidata:Q54848521
CVCL_LN83 2026-08-15 04:32:39 0
GM16393
 
Resource Report
Resource Website
RRID:CVCL_AT40 Homo sapiens (Human) Glutaric acidemia type 1 Finite cell line Female CLO:CLO_0019506,
Coriell:GM16393,
Wikidata:Q54848503
CVCL_AT40 2026-08-15 04:32:38 0
GM16349
 
Resource Report
Resource Website
Coriell Cat# GM16349, RRID:CVCL_DB89 Homo sapiens (Human) PMID:28161093 Transformed cell line Female Coriell GM16349 CLO:CLO_0019429,
Coriell:GM16349,
Wikidata:Q54848466
CVCL_DB89 2026-08-15 04:32:38 0
GM16500
 
Resource Report
Resource Website
RRID:CVCL_0E70 Homo sapiens (Human) Cystinuria Population: Caucasian. Transformed cell line Female CLO:CLO_0017485,
Coriell:GM16500,
Wikidata:Q54848613
CVCL_0E70 2026-08-15 04:32:40 0

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