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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
GM08135
 
Resource Report
Resource Website
RRID:CVCL_2T51 Homo sapiens (Human) Karyotypic information: 46,X,t(X;21)(q22.3;q11) (PubMed=10377420)., Population: Caucasian. PMID:10377420 Finite cell line Female GM8135 CLO:CLO_0010110,
Coriell:GM08135,
Wikidata:Q54843090
CVCL_2T51 2026-07-25 04:33:50 0
GM08197
 
Resource Report
Resource Website
Coriell Cat# GM08197, RRID:CVCL_GR14 Homo sapiens (Human) Cirrhosis Population: Caucasian. Finite cell line Female Coriell GM08197 CLO:CLO_0010114,
Coriell:GM08197,
Wikidata:Q54843098
CVCL_GR14 2026-07-25 04:33:50 0
GM08107
 
Resource Report
Resource Website
RRID:CVCL_AI56 Homo sapiens (Human) Hepatocyte nuclear factor 4-alpha associated monogenic diabetes Population: Caucasian., Part of: R-W pedigree MODY cell line collection. PMID:8945471 Transformed cell line Female GM08107B CLO:CLO_0010095,
Coriell:GM08107,
Wikidata:Q54843084
CVCL_AI56 2026-07-25 04:33:51 0
GM08148
 
Resource Report
Resource Website
Coriell Cat# GM08148, RRID:CVCL_6G93 Homo sapiens (Human) Population: Caucasian. Finite cell line Female Coriell GM08148 CLO:CLO_0010122,
Coriell:GM08148,
Wikidata:Q54843094
CVCL_6G93 2026-07-25 04:33:50 0
GM08070
 
Resource Report
Resource Website
RRID:CVCL_2T47 Homo sapiens (Human) Transformed cell line Male CLO:CLO_0010024,
Coriell:GM08070,
Wikidata:Q54843058
CVCL_2T47 2026-07-25 04:33:50 0
GM08100
 
Resource Report
Resource Website
Coriell Cat# GM08100, RRID:CVCL_N075 Homo sapiens (Human) HMG-CoA lyase deficiency Population: Egyptian. Finite cell line Male GM8100, GM17383 Coriell GM08100 CLO:CLO_0010010,
CLO:CLO_0012174,
Coriell:GM08100,
Coriell:GM17383,
Wikidata:Q54843075
CVCL_N075 2026-07-25 04:33:51 0
GM08146
 
Resource Report
Resource Website
Coriell Cat# GM08146, RRID:CVCL_5N82 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM08146 CLO:CLO_0010106,
Coriell:GM08146,
Wikidata:Q54843092
CVCL_5N82 2026-07-25 04:33:50 0
GM08085
 
Resource Report
Resource Website
Coriell Cat# GM08085, RRID:CVCL_AI48 Homo sapiens (Human) Population: Caucasian., Part of: R-W pedigree MODY cell line collection. PMID:8945471 Transformed cell line Female GM08085A Coriell GM08085 CLO:CLO_0010015,
Coriell:GM08085,
Wikidata:Q54843065
CVCL_AI48 2026-07-25 04:33:49 0
GM08084
 
Resource Report
Resource Website
RRID:CVCL_AI47 Homo sapiens (Human) Population: Caucasian., Part of: R-W pedigree MODY cell line collection. PMID:8945471 Transformed cell line Female CLO:CLO_0010019,
Coriell:GM08084,
Wikidata:Q54843064
CVCL_AI47 2026-07-25 04:33:49 0
GM08206
 
Resource Report
Resource Website
RRID:CVCL_1N82 Homo sapiens (Human) Beckwith-Wiedemann syndrome Karyotypic information: 46,XY.arr(1-22)x2,(XY)x1 (Coriell=GM08206)., Population: Caucasian. PMID:23665875 Finite cell line Male CLO:CLO_0010129,
Coriell:GM08206,
Wikidata:Q54843100
CVCL_1N82 2026-07-25 04:33:50 0
GM08211
 
Resource Report
Resource Website
Coriell Cat# GM08211, RRID:CVCL_0M99 Homo sapiens (Human) Cystic fibrosis Transformed cell line Female Coriell GM08211 CLO:CLO_0010055,
Coriell:GM08211,
Wikidata:Q54843103
CVCL_0M99 2026-07-25 04:33:52 0
GM08147
 
Resource Report
Resource Website
Coriell Cat# GM08147, RRID:CVCL_AT08 Homo sapiens (Human) Karyotypic information: 46,XY,9qh- (Coriell=GM08147)., Population: Caucasian. Finite cell line Male Coriell GM08147 CLO:CLO_0010124,
Coriell:GM08147,
Wikidata:Q54843093
CVCL_AT08 2026-07-25 04:33:51 0
GM08106
 
Resource Report
Resource Website
RRID:CVCL_AI55 Homo sapiens (Human) Hepatocyte nuclear factor 4-alpha associated monogenic diabetes Population: Caucasian., Part of: R-W pedigree MODY cell line collection. PMID:8945471 Transformed cell line Male CLO:CLO_0010103,
Coriell:GM08106,
Wikidata:Q54843076
CVCL_AI55 2026-07-25 04:33:50 0
GM08210
 
Resource Report
Resource Website
Coriell Cat# GM08210, RRID:CVCL_1Q56 Homo sapiens (Human) Population: Caucasian. PMID:23665875 Finite cell line Female Coriell GM08210 CLO:CLO_0010127,
Coriell:GM08210,
Wikidata:Q54843102
CVCL_1Q56 2026-07-25 04:33:50 0
GM08256
 
Resource Report
Resource Website
Coriell Cat# GM08256, RRID:CVCL_8A55 Homo sapiens (Human) Hereditary factor X deficiency Transformed cell line Male Coriell GM08256 CLO:CLO_0010067,
Coriell:GM08256,
Wikidata:Q54843108
CVCL_8A55 2026-07-25 04:33:52 0
GM08247
 
Resource Report
Resource Website
RRID:CVCL_EJ54 Homo sapiens (Human) Population: Caucasian. Finite cell line Female CLO:CLO_0010063,
Coriell:GM08247,
Wikidata:Q54843106
CVCL_EJ54 2026-07-25 04:33:50 0
GM08341
 
Resource Report
Resource Website
RRID:CVCL_0N06 Homo sapiens (Human) Population: Caucasian. Transformed cell line Male CLO:CLO_0010584,
BioSample:SAMN00798014,
Coriell:GM08341,
Wikidata:Q54843157
CVCL_0N06 2026-07-25 04:33:52 0
GM08281
 
Resource Report
Resource Website
RRID:CVCL_AI65 Homo sapiens (Human) Population: Caucasian., Part of: R-W pedigree MODY cell line collection. PMID:8945471 Transformed cell line Female CLO:CLO_0010082,
Coriell:GM08281,
Wikidata:Q54843120
CVCL_AI65 2026-07-25 04:33:52 0
GM08336
 
Resource Report
Resource Website
Coriell Cat# GM08336, RRID:CVCL_0N02 Homo sapiens (Human) Population: Caucasian. Transformed cell line Male Coriell GM08336 CLO:CLO_0010589,
BioSample:SAMN00798004,
Coriell:GM08336,
Wikidata:Q54843152
CVCL_0N02 2026-07-25 04:33:53 0
GM08288
 
Resource Report
Resource Website
Coriell Cat# GM18031, RRID:CVCL_N077 Homo sapiens (Human) Population: Caucasian., Part of: R-W pedigree MODY cell line collection., Part of: Human variation panel. PMID:8945471 Transformed cell line Female GM18031 Coriell GM18031 CLO:CLO_0010160,
CLO:CLO_0015581,
Coriell:GM08288,
Coriell:GM18031,
Wikidata:Q54843134
CVCL_N077 2026-07-25 04:33:51 0

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