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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
GM22654
 
Resource Report
Resource Website
RRID:CVCL_5R96 Homo sapiens (Human) Primary open angle glaucoma Population: Caucasian. Transformed cell line Female Coriell:GM22654,
Wikidata:Q54852696
CVCL_5R96 2026-09-05 10:59:27 0
GM22704
 
Resource Report
Resource Website
Coriell Cat# GM22704, RRID:CVCL_BU85 Homo sapiens (Human) Transformed cell line Female Coriell GM22704 Coriell:GM22704,
Wikidata:Q54852741
CVCL_BU85 2026-09-05 10:59:28 0
GM22684
 
Resource Report
Resource Website
Coriell Cat# GM22684, RRID:CVCL_5S07 Homo sapiens (Human) Primary open angle glaucoma Population: African American. Transformed cell line Female Coriell GM22684 Coriell:GM22684,
Wikidata:Q54852732
CVCL_5S07 2026-09-05 10:59:28 0
GM22677
 
Resource Report
Resource Website
Coriell Cat# GM22677, RRID:CVCL_1P81 Homo sapiens (Human) Karyotypic information: 46,XX.arr(1-22,X)x2 (Coriell=GM22677)., Population: Caucasian., Part of: NIGMS collection of multiple cell lines from the same individual; EBV-transformed lymphoblasts. PMID:22374857
PMID:30075799
Transformed cell line Female Coriell GM22677 Coriell:GM22677,
Wikidata:Q54852725
CVCL_1P81 2026-09-05 10:59:28 0
GM22674
 
Resource Report
Resource Website
RRID:CVCL_1P79 Homo sapiens (Human) Population: Caucasian., Part of: NIGMS collection of multiple cell lines from the same individual; EBV-transformed lymphoblasts. PMID:22374857
PMID:30075799
Transformed cell line Female Coriell:GM22674,
Wikidata:Q54852723
CVCL_1P79 2026-09-05 10:59:28 0
GM22873
 
Resource Report
Resource Website
Coriell Cat# GM22873, RRID:CVCL_8A99 Homo sapiens (Human) Transformed cell line Female Coriell GM22873 Coriell:GM22873,
Wikidata:Q54852815
CVCL_8A99 2026-09-05 10:59:30 0
GM22871
 
Resource Report
Resource Website
RRID:CVCL_DB18 Homo sapiens (Human) Niemann-Pick disease, type C1 Donor information: Established from monozygotic twin of GM22227 (Cellosaurus=CVCL_DB13) and GM22871 (Cellosaurus=CVCL_DB17)., Population: Caucasian. Finite cell line Female Coriell:GM22871,
Wikidata:Q54852814
CVCL_DB18 2026-09-05 10:59:30 0
GM22873
 
Resource Report
Resource Website
RRID:CVCL_8A99 Homo sapiens (Human) Transformed cell line Female Coriell:GM22873,
Wikidata:Q54852815
CVCL_8A99 2026-09-05 10:59:30 0
GM22782
 
Resource Report
Resource Website
RRID:CVCL_5S17 Homo sapiens (Human) Primary open angle glaucoma Population: African American. Transformed cell line Female Coriell:GM22782,
Wikidata:Q54852802
CVCL_5S17 2026-09-05 10:59:29 0
GM22739
 
Resource Report
Resource Website
RRID:CVCL_1P93 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:GM22739,
Wikidata:Q54852769
CVCL_1P93 2026-09-05 10:59:29 0
GM22786
 
Resource Report
Resource Website
RRID:CVCL_DN53 Homo sapiens (Human) Marshall syndrome Population: African American. Finite cell line Female Coriell:GM22786,
Wikidata:Q54852809
CVCL_DN53 2026-09-05 10:59:30 0
GM22739
 
Resource Report
Resource Website
Coriell Cat# GM22739, RRID:CVCL_1P93 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 GM22739 Coriell:GM22739,
Wikidata:Q54852769
CVCL_1P93 2026-09-05 10:59:29 0
GM22777
 
Resource Report
Resource Website
Coriell Cat# GM22777, RRID:CVCL_5S16 Homo sapiens (Human) Primary open angle glaucoma Transformed cell line Female Coriell GM22777 Coriell:GM22777,
Wikidata:Q54852797
CVCL_5S16 2026-09-05 10:59:29 0
GM22779
 
Resource Report
Resource Website
RRID:CVCL_BV02 Homo sapiens (Human) Ehlers-Danlos syndrome, type IV Finite cell line Female Coriell:GM22779,
Wikidata:Q54852799
CVCL_BV02 2026-09-05 10:59:29 0
GM22767
 
Resource Report
Resource Website
RRID:CVCL_5K25 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell:GM22767,
Wikidata:Q54852786
CVCL_5K25 2026-09-05 10:59:29 0
GM22899
 
Resource Report
Resource Website
Coriell Cat# GM22899, RRID:CVCL_5S19 Homo sapiens (Human) 1p36 deletion syndrome Transformed cell line Female Coriell GM22899 Coriell:GM22899,
Wikidata:Q54852817
CVCL_5S19 2026-09-05 10:59:30 0
GM22714
 
Resource Report
Resource Website
RRID:CVCL_BU88 Homo sapiens (Human) Transformed cell line Female Coriell:GM22714,
Wikidata:Q54852750
CVCL_BU88 2026-09-05 10:59:29 0
GM22784
 
Resource Report
Resource Website
RRID:CVCL_BV06 Homo sapiens (Human) Transformed cell line Female Coriell:GM22784,
Wikidata:Q54852804
CVCL_BV06 2026-09-05 10:59:30 0
GM22753
 
Resource Report
Resource Website
RRID:CVCL_BU95 Homo sapiens (Human) Ehlers-Danlos syndrome, type IV Finite cell line Female Coriell:GM22753,
Wikidata:Q54852778
CVCL_BU95 2026-09-05 10:59:29 0
GM22899
 
Resource Report
Resource Website
RRID:CVCL_5S19 Homo sapiens (Human) 1p36 deletion syndrome Transformed cell line Female Coriell:GM22899,
Wikidata:Q54852817
CVCL_5S19 2026-09-05 10:59:30 0

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