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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
GM05335
 
Resource Report
Resource Website
Coriell Cat# GM05335, RRID:CVCL_W027 Homo sapiens (Human) GM1 gangliosidosis Population: Caucasian. Finite cell line Female Coriell GM05335 CLO:CLO_0024914,
Coriell:GM05335,
Wikidata:Q54838969
CVCL_W027 2026-08-08 05:00:25 0
GM05321
 
Resource Report
Resource Website
RRID:CVCL_AL02 Homo sapiens (Human) Retinitis pigmentosa Finite cell line Female CLO:CLO_0024924,
Coriell:GM05321,
Wikidata:Q54838968
CVCL_AL02 2026-08-08 05:00:25 0
GM05228
 
Resource Report
Resource Website
RRID:CVCL_GQ52 Homo sapiens (Human) Anorexia nervosa Finite cell line Female CLO:CLO_0025223,
Coriell:GM05228,
Wikidata:Q54838935
CVCL_GQ52 2026-08-08 05:00:25 0
GM05267
 
Resource Report
Resource Website
Coriell Cat# GM05267, RRID:CVCL_F608 Mus musculus (Mouse) Karyotypic information: 84% of cells lack a Y chromosome (Coriell=GM05267). PMID:6947233 Transformed cell line Male 6TGR-SV-tfm Coriell GM05267 CLO:CLO_0024956,
Coriell:GM05267,
Wikidata:Q54838954
CVCL_F608 2026-08-08 05:00:26 0
GM05294
 
Resource Report
Resource Website
RRID:CVCL_9Y65 Homo sapiens (Human) Karyotypic information: 46,XY [44]; 46,XY,t(3;11)(p21;q23) [6] (Coriell=GM05294)., Population: African American. Finite cell line Male GM5294 CLO:CLO_0024944,
Coriell:GM05294,
Wikidata:Q54838959
CVCL_9Y65 2026-08-08 05:00:25 0
GM05255
 
Resource Report
Resource Website
RRID:CVCL_0P46 Homo sapiens (Human) Population: Caucasian. Finite cell line Female CLO:CLO_0025235,
Coriell:GM05255,
Wikidata:Q54838942
CVCL_0P46 2026-08-08 05:00:24 0
GM05335
 
Resource Report
Resource Website
RRID:CVCL_W027 Homo sapiens (Human) GM1 gangliosidosis Population: Caucasian. Finite cell line Female CLO:CLO_0024914,
Coriell:GM05335,
Wikidata:Q54838969
CVCL_W027 2026-08-08 05:00:25 0
GM05345
 
Resource Report
Resource Website
Coriell Cat# GM05345, RRID:CVCL_AL03 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian. Finite cell line Male Coriell GM05345 CLO:CLO_0024910,
Coriell:GM05345,
Wikidata:Q54838976
CVCL_AL03 2026-08-08 05:00:25 0
GM05345
 
Resource Report
Resource Website
RRID:CVCL_AL03 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian. Finite cell line Male CLO:CLO_0024910,
Coriell:GM05345,
Wikidata:Q54838976
CVCL_AL03 2026-08-08 05:00:27 0
GM05296
 
Resource Report
Resource Website
RRID:CVCL_X318 Homo sapiens (Human) Karyotypic information: 46,XX,der(11)(11pter->11p13::10q21->10q24::11p13->11qter)mat (Coriell=GM05296)., Population: Caucasian. PMID:6661932
PMID:11687795
Finite cell line Female GM 5296 CLO:CLO_0024929,
Coriell:GM05296,
GEO:GSM804,
Wikidata:Q54838960
CVCL_X318 2026-08-08 05:00:25 0
GM05259
 
Resource Report
Resource Website
RRID:CVCL_0P50 Homo sapiens (Human) Hepatolenticular degeneration Population: Caucasian. Finite cell line Female CLO:CLO_0025231,
Coriell:GM05259,
Wikidata:Q54838947
CVCL_0P50 2026-08-08 05:00:24 0
GM05227
 
Resource Report
Resource Website
Coriell Cat# GM05227, RRID:CVCL_GQ51 Homo sapiens (Human) Bipolar disorder Finite cell line Female GM05227A Coriell GM05227 CLO:CLO_0025224,
Coriell:GM05227,
Wikidata:Q54838934
CVCL_GQ51 2026-08-08 05:00:24 0
GM05237
 
Resource Report
Resource Website
Coriell Cat# GM05237, RRID:CVCL_DB62 Homo sapiens (Human) Transformed cell line Male GM05237B Coriell GM05237 CLO:CLO_0025230,
Coriell:GM05237,
Wikidata:Q54838938
CVCL_DB62 2026-08-08 05:00:24 0
GM05297
 
Resource Report
Resource Website
Coriell Cat# GM05297, RRID:CVCL_4D85 Homo sapiens (Human) Karyotypic information: 46,XX,ins(11;10)(11pter->11p13::10q21->10q24::11p13->11qter;10pter->10q21::10q24->10qter) (Coriell=GM05297)., Population: Caucasian. PMID:2570029 Finite cell line Female GM5297 Coriell GM05297 CLO:CLO_0024925,
Coriell:GM05297,
Wikidata:Q54838961
CVCL_4D85 2026-08-08 05:00:25 0
GM05236
 
Resource Report
Resource Website
RRID:CVCL_GQ53 Homo sapiens (Human) Bipolar disorder Transformed cell line Male CLO:CLO_0025229,
Coriell:GM05236,
Wikidata:Q54838937
CVCL_GQ53 2026-08-08 05:00:24 0
GM05339
 
Resource Report
Resource Website
Coriell Cat# GM05339, RRID:CVCL_0P52 Homo sapiens (Human) Hepatolenticular degeneration Population: Caucasian. Finite cell line Female Coriell GM05339 CLO:CLO_0024899,
Coriell:GM05339,
Wikidata:Q54838971
CVCL_0P52 2026-08-08 05:00:26 0
GM05225
 
Resource Report
Resource Website
RRID:CVCL_GQ49 Homo sapiens (Human) Bipolar disorder Population: Caucasian. Finite cell line Male CLO:CLO_0025222,
Coriell:GM05225,
Wikidata:Q54838932
CVCL_GQ49 2026-08-08 05:00:25 0
GM05220
 
Resource Report
Resource Website
RRID:CVCL_GQ45 Homo sapiens (Human) Bipolar disorder Finite cell line Male CLO:CLO_0025226,
Coriell:GM05220,
Wikidata:Q54838928
CVCL_GQ45 2026-08-08 05:00:24 0
GM05347
 
Resource Report
Resource Website
RRID:CVCL_X322 Homo sapiens (Human) Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Male GM 5347 CLO:CLO_0024906,
Coriell:GM05347,
Wikidata:Q54838978
CVCL_X322 2026-08-08 05:00:25 0
GM05342
 
Resource Report
Resource Website
Coriell Cat# GM05342, RRID:CVCL_0P55 Homo sapiens (Human) Hepatolenticular degeneration Population: Caucasian. Transformed cell line Female Coriell GM05342 CLO:CLO_0024902,
Coriell:GM05342,
Wikidata:Q54838974
CVCL_0P55 2026-08-08 05:00:26 0

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