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95,747 Results - per page

Show More Columns | Download Top 1000 Results

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
GM25267
 
Resource Report
Resource Website
RRID:CVCL_1N93 Homo sapiens (Human) Long QT syndrome 3 Population: Latino or Hispanic. PMID:24268663 Induced pluripotent stem cell Female GM25267*D, LQT3 iPS Coriell:GM25267,
SKIP:SKIP000737,
Wikidata:Q54853861
CVCL_1N93 2026-09-05 10:59:53 0
GM25379
 
Resource Report
Resource Website
Coriell Cat# GM25379, RRID:CVCL_5K93 Homo sapiens (Human) Smith-Magenis syndrome Transformed cell line Female Coriell GM25379 Coriell:GM25379,
Wikidata:Q54853911
CVCL_5K93 2026-09-05 10:59:54 0
GM25375
 
Resource Report
Resource Website
RRID:CVCL_5K90 Homo sapiens (Human) Smith-Magenis syndrome Transformed cell line Female Coriell:GM25375,
Wikidata:Q54853908
CVCL_5K90 2026-09-05 10:59:54 0
GM25380
 
Resource Report
Resource Website
RRID:CVCL_5K94 Homo sapiens (Human) Transformed cell line Female Coriell:GM25380,
Wikidata:Q54853912
CVCL_5K94 2026-09-05 10:59:54 0
GM25375
 
Resource Report
Resource Website
Coriell Cat# GM25375, RRID:CVCL_5K90 Homo sapiens (Human) Smith-Magenis syndrome Transformed cell line Female Coriell GM25375 Coriell:GM25375,
Wikidata:Q54853908
CVCL_5K90 2026-09-05 10:59:54 0
GM25364
 
Resource Report
Resource Website
Coriell Cat# GM25364, RRID:CVCL_5K82 Homo sapiens (Human) Transformed cell line Female Coriell GM25364 Coriell:GM25364,
Wikidata:Q54853895
CVCL_5K82 2026-09-05 10:59:54 0
GM25309
 
Resource Report
Resource Website
Coriell Cat# GM25309, RRID:CVCL_BW49 Homo sapiens (Human) Turner syndrome Transformed cell line Female Coriell GM25309 Coriell:GM25309,
Wikidata:Q54853870
CVCL_BW49 2026-09-05 10:59:53 0
GM25341
 
Resource Report
Resource Website
RRID:CVCL_BX25 Homo sapiens (Human) Population: Hispanic. Transformed cell line Female Coriell:GM25341,
Wikidata:Q54853879
CVCL_BX25 2026-09-05 10:59:54 0
GM25390
 
Resource Report
Resource Website
RRID:CVCL_BX32 Homo sapiens (Human) Transformed cell line Female Coriell:GM25390,
Wikidata:Q54853919
CVCL_BX32 2026-09-05 10:59:55 0
GM25380
 
Resource Report
Resource Website
Coriell Cat# GM25380, RRID:CVCL_5K94 Homo sapiens (Human) Transformed cell line Female Coriell GM25380 Coriell:GM25380,
Wikidata:Q54853912
CVCL_5K94 2026-09-05 10:59:54 0
GM25370
 
Resource Report
Resource Website
Coriell Cat# GM25370, RRID:CVCL_BA18 Homo sapiens (Human) Smith-Magenis syndrome Transformed cell line Female Coriell GM25370 Coriell:GM25370,
Wikidata:Q54853903
CVCL_BA18 2026-09-05 10:59:54 0
GM25364
 
Resource Report
Resource Website
RRID:CVCL_5K82 Homo sapiens (Human) Transformed cell line Female Coriell:GM25364,
Wikidata:Q54853895
CVCL_5K82 2026-09-05 10:59:54 0
GM25377
 
Resource Report
Resource Website
Coriell Cat# GM25377, RRID:CVCL_5K91 Homo sapiens (Human) Smith-Magenis syndrome Transformed cell line Female Coriell GM25377 Coriell:GM25377,
Wikidata:Q54853909
CVCL_5K91 2026-09-05 10:59:54 0
GM25336
 
Resource Report
Resource Website
RRID:CVCL_HQ18 Homo sapiens (Human) Nemaline myopathy 3 Finite cell line Female Coriell:GM25336,
Wikidata:Q54853877
CVCL_HQ18 2026-09-05 10:59:54 0
GM25371
 
Resource Report
Resource Website
RRID:CVCL_BA19 Homo sapiens (Human) Smith-Magenis syndrome Finite cell line Female Coriell:GM25371,
Wikidata:Q54853904
CVCL_BA19 2026-09-05 10:59:54 0
GM25409
 
Resource Report
Resource Website
RRID:CVCL_HL85 Homo sapiens (Human) Transformed cell line Female Coriell:GM25409,
Wikidata:Q54853936
CVCL_HL85 2026-09-05 10:59:55 0
GM25355
 
Resource Report
Resource Website
RRID:CVCL_5K77 Homo sapiens (Human) Transformed cell line Female Coriell:GM25355,
Wikidata:Q54853890
CVCL_5K77 2026-09-05 10:59:54 0
GM25374
 
Resource Report
Resource Website
Coriell Cat# GM25374, RRID:CVCL_5K89 Homo sapiens (Human) Smith-Magenis syndrome Finite cell line Female Coriell GM25374 Coriell:GM25374,
Wikidata:Q54853907
CVCL_5K89 2026-09-05 10:59:54 0
GM25378
 
Resource Report
Resource Website
Coriell Cat# GM25378, RRID:CVCL_5K92 Homo sapiens (Human) Smith-Magenis syndrome Finite cell line Female Coriell GM25378 Coriell:GM25378,
Wikidata:Q54853910
CVCL_5K92 2026-09-05 10:59:54 0
GM25367
 
Resource Report
Resource Website
Coriell Cat# GM25367, RRID:CVCL_5K84 Homo sapiens (Human) Smith-Magenis syndrome Finite cell line Female Coriell GM25367 Coriell:GM25367,
Wikidata:Q54853897
CVCL_5K84 2026-09-05 10:59:54 0

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