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256,031 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
GM00909
 
Resource Report
Resource Website
RRID:CVCL_Y987 Homo sapiens (Human) Population: Caucasian. PMID:28649545 Finite cell line Female GM0909, GM-909 CLO:CLO_0029591,
Coriell:GM00909,
Wikidata:Q54836527
CVCL_Y987 2026-08-15 04:28:54 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 2026-08-15 04:28:54 0
GM00813
 
Resource Report
Resource Website
RRID:CVCL_2H04 Homo sapiens (Human) Population: Caucasian. Finite cell line Male GM0813, GM-813 CLO:CLO_0029647,
Coriell:GM00813,
Wikidata:Q54836467
CVCL_2H04 2026-08-15 04:28:53 0
GM00883
 
Resource Report
Resource Website
RRID:CVCL_2H08 Homo sapiens (Human) Population: Caucasian. Finite cell line Female GM0883, GM-883 CLO:CLO_0029610,
Coriell:GM00883,
Wikidata:Q54836507
CVCL_2H08 2026-08-15 04:28:53 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 2026-08-15 04:28:53 0
GM00883
 
Resource Report
Resource Website
Coriell Cat# GM00883, RRID:CVCL_2H08 Homo sapiens (Human) Population: Caucasian. Finite cell line Female GM0883, GM-883 Coriell GM00883 CLO:CLO_0029610,
Coriell:GM00883,
Wikidata:Q54836507
CVCL_2H08 2026-08-15 04:28:53 0
GM00803
 
Resource Report
Resource Website
Coriell Cat# GM00803, RRID:CVCL_X077 Homo sapiens (Human) Population: Caucasian. PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Male GM-803, GM 803 Coriell GM00803 CLO:CLO_0029645,
Coriell:GM00803,
Wikidata:Q54836462
CVCL_X077 2026-08-15 04:28:52 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 2026-08-15 04:28:54 0
GM00892
 
Resource Report
Resource Website
Coriell Cat# GM00892, RRID:CVCL_H136 Homo sapiens (Human) PMID:6661932 Transformed cell line Female GM-892, GM-0892, GM 892, GM0892, GM892, GM00892A, GM892A, GM00892B Coriell GM00892 CLO:CLO_0029582,
ChEMBL-Cells:CHEMBL3308595,
ChEMBL-Targets:CHEMBL614505,
Coriell:GM00892,
PubChem_Cell_line:CVCL_H136,
Wikidata:Q54836514
CVCL_H136 2026-08-15 04:28:53 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 2026-08-15 04:28:53 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 2026-08-15 04:28:54 0
GM00906
 
Resource Report
Resource Website
RRID:CVCL_CW98 Homo sapiens (Human) Population: Caucasian. PMID:28649545 Finite cell line Male GM0906, GM-906 CLO:CLO_0029599,
Coriell:GM00906,
Wikidata:Q54836524
CVCL_CW98 2026-08-15 04:28:54 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 2026-08-15 04:28:53 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 2026-08-15 04:28:53 0
GM00846
 
Resource Report
Resource Website
Coriell Cat# GM00846, RRID:CVCL_V783 Homo sapiens (Human) Karyotypic information: 46,XX,t(2;8)(2pter->2q37::8q13->8qter;8pter->8q13::2q37->2qter) (Coriell=GM00846)., Population: Caucasian. PMID:565692 Finite cell line Female GM-846 Coriell GM00846 CLO:CLO_0029653,
Coriell:GM00846,
Wikidata:Q54836471
CVCL_V783 2026-08-15 04:28:53 0
GM00847
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM00847, RRID:CVCL_7908 Homo sapiens (Human) Lesch-Nyhan syndrome Characteristics: Cell line positive for alternative lengthening of telomeres (ALT+) (CelloPub=CLPUB00712; PubMed=19935656)., Population: African American. PMID:174085
PMID:191830
PMID:1260760
PMID:3413074
PMID:9175740
PMID:11359895
PMID:12361951
PMID:19935656
PMID:26001292
Transformed cell line Male LN-SV, LNSV, GM-847, GM 847, GM847 Coriell GM00847 CLO:CLO_0029655,
EFO:EFO_0022519,
Coriell:GM00847,
Wikidata:Q54836472
cvcl_f127 CVCL_7908 2026-08-15 04:28:53 5
GM00861
 
Resource Report
Resource Website
Coriell Cat# GM00861, RRID:CVCL_4D79 Homo sapiens (Human) Karyotypic information: 46,XY,ins(5;1)(5pter->5q15::1q25->1q32::5q15->5qter;1pter->1q25::1q32->1qter) (Coriell=GM00861)., Population: Caucasian. Finite cell line Male GM-861 Coriell GM00861 CLO:CLO_0029634,
Coriell:GM00861,
Wikidata:Q54836482
CVCL_4D79 2026-08-15 04:28:53 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 2026-08-15 04:28:53 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 2026-08-15 04:28:54 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 2026-08-15 04:28:53 0

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