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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
GM22738
 
Resource Report
Resource Website
Coriell Cat# GM22738, RRID:CVCL_1P92 Homo sapiens (Human) Population: African American., Part of: NIGMS collection of multiple cell lines from the same individual; EBV-transformed lymphoblasts. PMID:22374857
PMID:30075799
Transformed cell line Female Coriell GM22738 Coriell:GM22738,
Wikidata:Q54852768
CVCL_1P92 2026-09-05 10:59:29 0
GM22713
 
Resource Report
Resource Website
RRID:CVCL_BU87 Homo sapiens (Human) Rett syndrome Transformed cell line Female Coriell:GM22713,
Wikidata:Q54852749
CVCL_BU87 2026-09-05 10:59:29 0
GM22782
 
Resource Report
Resource Website
Coriell Cat# GM22782, RRID:CVCL_5S17 Homo sapiens (Human) Primary open angle glaucoma Population: African American. Transformed cell line Female Coriell GM22782 Coriell:GM22782,
Wikidata:Q54852802
CVCL_5S17 2026-09-05 10:59:29 0
GM22708
 
Resource Report
Resource Website
Coriell Cat# GM22708, RRID:CVCL_8A96 Homo sapiens (Human) Transformed cell line Female Coriell GM22708 Coriell:GM22708,
Wikidata:Q54852743
CVCL_8A96 2026-09-05 10:59:28 0
GM22783
 
Resource Report
Resource Website
RRID:CVCL_BV05 Homo sapiens (Human) Rett syndrome Transformed cell line Female Coriell:GM22783,
Wikidata:Q54852803
CVCL_BV05 2026-09-05 10:59:30 0
GM22752
 
Resource Report
Resource Website
RRID:CVCL_BU94 Homo sapiens (Human) Ehlers-Danlos syndrome, type IV Transformed cell line Female Coriell:GM22752,
Wikidata:Q54852777
CVCL_BU94 2026-09-05 10:59:29 0
GM22741
 
Resource Report
Resource Website
Coriell Cat# GM22741, RRID:CVCL_1P94 Homo sapiens (Human) Population: African American., Part of: NIGMS collection of multiple cell lines from the same individual; EBV-transformed lymphoblasts. PMID:22374857
PMID:30075799
Transformed cell line Female Coriell GM22741 Coriell:GM22741,
Wikidata:Q54852770
CVCL_1P94 2026-09-05 10:59:29 0
GM22741
 
Resource Report
Resource Website
RRID:CVCL_1P94 Homo sapiens (Human) Population: African American., Part of: NIGMS collection of multiple cell lines from the same individual; EBV-transformed lymphoblasts. PMID:22374857
PMID:30075799
Transformed cell line Female Coriell:GM22741,
Wikidata:Q54852770
CVCL_1P94 2026-09-05 10:59:29 0
GM22714
 
Resource Report
Resource Website
Coriell Cat# GM22714, RRID:CVCL_BU88 Homo sapiens (Human) Transformed cell line Female Coriell GM22714 Coriell:GM22714,
Wikidata:Q54852750
CVCL_BU88 2026-09-05 10:59:29 0
GM22737
 
Resource Report
Resource Website
Coriell Cat# GM22737, RRID:CVCL_1P91 Homo sapiens (Human) Population: African American., Part of: NIGMS collection of multiple cell lines from the same individual; EBV-transformed lymphoblasts. PMID:22374857
PMID:30075799
Transformed cell line Female Coriell GM22737 Coriell:GM22737,
Wikidata:Q54852767
CVCL_1P91 2026-09-05 10:59:29 0
GM22763
 
Resource Report
Resource Website
RRID:CVCL_BU97 Homo sapiens (Human) Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1 Transformed cell line Female Coriell:GM22763,
Wikidata:Q54852782
CVCL_BU97 2026-09-05 10:59:29 0
GM23001
 
Resource Report
Resource Website
RRID:CVCL_5S55 Homo sapiens (Human) 1p36 deletion syndrome Transformed cell line Female Coriell:GM23001,
Wikidata:Q54852863
CVCL_5S55 2026-09-05 10:59:31 0
GM22994
 
Resource Report
Resource Website
RRID:CVCL_5S51 Homo sapiens (Human) Transformed cell line Female Coriell:GM22994,
Wikidata:Q54852859
CVCL_5S51 2026-09-05 10:59:31 0
GM22916
 
Resource Report
Resource Website
Coriell Cat# GM22916, RRID:CVCL_5S27 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Female Coriell GM22916 Coriell:GM22916,
Wikidata:Q54852825
CVCL_5S27 2026-09-05 10:59:30 0
GM22926
 
Resource Report
Resource Website
Coriell Cat# GM22926, RRID:CVCL_5S30 Homo sapiens (Human) 1p36 deletion syndrome Transformed cell line Female Coriell GM22926 Coriell:GM22926,
Wikidata:Q54852831
CVCL_5S30 2026-09-05 10:59:30 0
GM22923
 
Resource Report
Resource Website
RRID:CVCL_5S28 Homo sapiens (Human) 1p36 deletion syndrome Transformed cell line Female Coriell:GM22923,
Wikidata:Q54852829
CVCL_5S28 2026-09-05 10:59:30 0
GM22904
 
Resource Report
Resource Website
Coriell Cat# GM22904, RRID:CVCL_5S22 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Female Coriell GM22904 Coriell:GM22904,
Wikidata:Q54852820
CVCL_5S22 2026-09-05 10:59:30 0
GM22963
 
Resource Report
Resource Website
RRID:CVCL_5S43 Homo sapiens (Human) 1p36 deletion syndrome Transformed cell line Female Coriell:GM22963,
Wikidata:Q54852845
CVCL_5S43 2026-09-05 10:59:31 0
GM23008
 
Resource Report
Resource Website
RRID:CVCL_5S62 Homo sapiens (Human) 1p36 deletion syndrome Transformed cell line Female Coriell:GM23008,
Wikidata:Q54852870
CVCL_5S62 2026-09-05 10:59:31 0
GM23004
 
Resource Report
Resource Website
RRID:CVCL_5S58 Homo sapiens (Human) 1p36 deletion syndrome Transformed cell line Female Coriell:GM23004,
Wikidata:Q54852866
CVCL_5S58 2026-09-05 10:59:31 0

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