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19,458 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
GM00805
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00805, RRID:CVCL_JD85 Homo sapiens (Human) Finite cell line Male GM-805 Coriell GM00805 Coriell:GM00805,
Wikidata:Q54836464
CVCL_JD85 2026-09-12 05:31:48 0
GM00894
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JE18 Homo sapiens (Human) Transformed cell line Female GM-894 Coriell:GM00894,
Wikidata:Q54836516
CVCL_JE18 2026-09-12 05:31:49 0
GM00811
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_U702 Homo sapiens (Human) Bloom syndrome Donor information: From Bloom Syndrome Registry patient 3(HoCo) (BSR3)., Population: Jewish; Ashkenazi. PMID:436333
PMID:908169
PMID:2878433
Finite cell line Male GM-811, GM0811, GM811, GM 811, GM00811B CLO:CLO_0029646,
Coriell:GM00811,
GEO:GSM1317007,
Wikidata:Q54836466
CVCL_U702 2026-09-12 05:31:48 0
GM00903
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_CX34 Homo sapiens (Human) Mucopolysaccharidosis type IIIA Finite cell line Male GM-903 Coriell:GM00903,
Wikidata:Q54836521
CVCL_CX34 2026-09-12 05:31:49 0
GM00868
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JD86 Homo sapiens (Human) 46,XY gonadal dysgenesis Finite cell line Sex ambiguous GM-868 Coriell:GM00868,
Wikidata:Q54836491
CVCL_JD86 2026-09-12 05:31:49 0
GM00904
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_CX39 Homo sapiens (Human) Farber lipogranulomatosis Finite cell line Female GM-904 Coriell:GM00904,
Wikidata:Q54836522
CVCL_CX39 2026-09-12 05:31:49 0
GM00853
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00853, RRID:CVCL_CX47 Homo sapiens (Human) Krabbe disease Finite cell line Female GM-853 Coriell GM00853 Coriell:GM00853,
Wikidata:Q54836476
CVCL_CX47 2026-09-12 05:31:48 0
GM00891
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00891, RRID:CVCL_JE19 Homo sapiens (Human) Transformed cell line Sex unspecified GM-891 Coriell GM00891 Coriell:GM00891,
Wikidata:Q54836513
CVCL_JE19 2026-09-12 05:31:49 0
GM00806
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00806, RRID:CVCL_CX43 Homo sapiens (Human) Galactosialidosis PMID:8910459 Finite cell line Female GM-806, GM 806 Coriell GM00806 Coriell:GM00806,
Wikidata:Q54836465
CVCL_CX43 2026-09-12 05:31:48 0
GM00898
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_CX65 Homo sapiens (Human) Niemann-Pick disease, type A Finite cell line Sex unspecified GM-898 Coriell:GM00898,
Wikidata:Q54836518
CVCL_CX65 2026-09-12 05:31:49 0
GM00891
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JE19 Homo sapiens (Human) Transformed cell line Sex unspecified GM-891 Coriell:GM00891,
Wikidata:Q54836513
CVCL_JE19 2026-09-12 05:31:49 0
GM00901
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00901, RRID:CVCL_CX32 Homo sapiens (Human) Hunter syndrome Finite cell line Male GM-901 Coriell GM00901 Coriell:GM00901,
Wikidata:Q54836519
CVCL_CX32 2026-09-12 05:31:49 0
GM00898
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00898, RRID:CVCL_CX65 Homo sapiens (Human) Niemann-Pick disease, type A Finite cell line Sex unspecified GM-898 Coriell GM00898 Coriell:GM00898,
Wikidata:Q54836518
CVCL_CX65 2026-09-12 05:31:49 0
GM00805
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JD85 Homo sapiens (Human) Finite cell line Male GM-805 Coriell:GM00805,
Wikidata:Q54836464
CVCL_JD85 2026-09-12 05:31:48 0
GM00904
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00904, RRID:CVCL_CX39 Homo sapiens (Human) Farber lipogranulomatosis Finite cell line Female GM-904 Coriell GM00904 Coriell:GM00904,
Wikidata:Q54836522
CVCL_CX39 2026-09-12 05:31:49 0
GM00860
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00860, RRID:CVCL_X238 Homo sapiens (Human) PMID:6661932
PMID:23665875
Finite cell line Female GM-860, GM 860 Coriell GM00860 CLO:CLO_0029629,
Coriell:GM00860,
Wikidata:Q54836481
CVCL_X238 2026-09-12 05:31:49 0
GM00869
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00869, RRID:CVCL_JC76 Homo sapiens (Human) Renal agenesis Finite cell line Female GM-869 Coriell GM00869 Coriell:GM00869,
Wikidata:Q54836492
CVCL_JC76 2026-09-12 05:31:49 0
GM00854
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00854, RRID:CVCL_CX48 Homo sapiens (Human) Krabbe disease Finite cell line Female GM-854 Coriell GM00854 Coriell:GM00854,
Wikidata:Q54836477
CVCL_CX48 2026-09-12 05:31:48 0
GM00806
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_CX43 Homo sapiens (Human) Galactosialidosis PMID:8910459 Finite cell line Female GM-806, GM 806 Coriell:GM00806,
Wikidata:Q54836465
CVCL_CX43 2026-09-12 05:31:48 0
GM00868
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00868, RRID:CVCL_JD86 Homo sapiens (Human) 46,XY gonadal dysgenesis Finite cell line Sex ambiguous GM-868 Coriell GM00868 Coriell:GM00868,
Wikidata:Q54836491
CVCL_JD86 2026-09-12 05:31:49 0

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