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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
GM05744
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM05744, RRID:CVCL_US88 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Male GM05744Z Coriell GM05744 Coriell:GM05744,
Wikidata:Q93789658
CVCL_US88 2026-08-08 05:00:33 0
GM05758
 
Resource Report
Resource Website
Coriell Cat# GM05758, RRID:CVCL_7438 Homo sapiens (Human) Population: African American. PMID:2705456
PMID:17668376
Finite cell line Male GM5758 Coriell GM05758 CLO:CLO_0024668,
Coriell:GM05758,
Wikidata:Q54841933
CVCL_7438 2026-08-08 05:00:31 0
GM05879
 
Resource Report
Resource Website
RRID:CVCL_7444 Homo sapiens (Human) Population: Caucasian. PMID:29125828
PMID:32291635
Finite cell line Female GM05879B, GM5879A, C5879 CLO:CLO_0024225,
Coriell:GM05879,
GEO:GSM2794411,
Wikidata:Q54841978
CVCL_7444 2026-08-08 05:00:32 0
GM05747
 
Resource Report
Resource Website
RRID:CVCL_DD80 Homo sapiens (Human) Osteogenesis imperfecta Population: Colombian. Finite cell line Male GM05747A CLO:CLO_0024637,
Coriell:GM05747,
Wikidata:Q54841924
CVCL_DD80 2026-08-08 05:00:31 0
GM05888
 
Resource Report
Resource Website
Coriell Cat# GM05888, RRID:CVCL_4F95 Homo sapiens (Human) Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Transformed cell line Male GM05888A Coriell GM05888 CLO:CLO_0024220,
Coriell:GM05888,
Wikidata:Q54841982
CVCL_4F95 2026-08-08 05:00:32 0
GM05757
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM05757, RRID:CVCL_7437 Homo sapiens (Human) Population: African American. PMID:30567591 Finite cell line Male GM5757 Coriell GM05757 CLO:CLO_0024667,
Coriell:GM05757,
GEO:GSM3124631,
Wikidata:Q54841932
CVCL_7437 2026-08-08 05:00:33 2
GM05881
 
Resource Report
Resource Website
RRID:CVCL_5N37 Homo sapiens (Human) Population: Iraqi. PMID:23665875 Transformed cell line Female CLO:CLO_0024223,
Coriell:GM05881,
Wikidata:Q54841980
CVCL_5N37 2026-08-08 05:00:34 0
GM05867
 
Resource Report
Resource Website
RRID:CVCL_V254 Bos taurus (Bovine) Donor information: Cell line originating from a cow that was a carrier for bovine congenital erythropoietic porphyria. Finite cell line Female CLO:CLO_0024230,
Coriell:GM05867,
Wikidata:Q54841967
CVCL_V254 2026-08-08 05:00:32 0
GM05740
 
Resource Report
Resource Website
Coriell Cat# GM05740, RRID:CVCL_Y893 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Male GM05740A Coriell GM05740 CLO:CLO_0024640,
Coriell:GM05740,
Wikidata:Q54841923
CVCL_Y893 2026-08-08 05:00:31 0
GM05724
 
Resource Report
Resource Website
Coriell Cat# GM05724, RRID:CVCL_1J26 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Male GM05724A Coriell GM05724 CLO:CLO_0024646,
Coriell:GM05724,
Wikidata:Q54841919
CVCL_1J26 2026-08-08 05:00:31 0
GM05883
 
Resource Report
Resource Website
Coriell Cat# GM05883, RRID:CVCL_GQ57 Homo sapiens (Human) Bipolar disorder Transformed cell line Female Coriell GM05883 CLO:CLO_0024222,
Coriell:GM05883,
Wikidata:Q54841981
CVCL_GQ57 2026-08-08 05:00:32 0
GM05735
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_UR87 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Male GM05735Z Coriell:GM05735,
Wikidata:Q93789629
CVCL_UR87 2026-08-08 05:00:32 0
GM05761
 
Resource Report
Resource Website
RRID:CVCL_0P61 Homo sapiens (Human) Population: Caucasian. Transformed cell line Female GM05761A CLO:CLO_0024659,
Coriell:GM05761,
Wikidata:Q54841935
CVCL_0P61 2026-08-08 05:00:31 0
GM05852
 
Resource Report
Resource Website
RRID:CVCL_AL07 Homo sapiens (Human) Retinitis pigmentosa Transformed cell line Female CLO:CLO_0024706,
Coriell:GM05852,
Wikidata:Q54841960
CVCL_AL07 2026-08-08 05:00:33 0
GM05852
 
Resource Report
Resource Website
Coriell Cat# GM05852, RRID:CVCL_AL07 Homo sapiens (Human) Retinitis pigmentosa Transformed cell line Female Coriell GM05852 CLO:CLO_0024706,
Coriell:GM05852,
Wikidata:Q54841960
CVCL_AL07 2026-08-08 05:00:32 0
GM05795
 
Resource Report
Resource Website
RRID:CVCL_0Q56 Homo sapiens (Human) Population: Caucasian. Transformed cell line Female CLO:CLO_0024684,
Coriell:GM05795,
Wikidata:Q54841943
CVCL_0Q56 2026-08-08 05:00:33 0
GM05868
 
Resource Report
Resource Website
RRID:CVCL_V255 Bos taurus (Bovine) Donor information: Cell line originating from a cow that was a carrier for bovine protoporphyria. Finite cell line Female CLO:CLO_0024229,
Coriell:GM05868,
Wikidata:Q54841968
CVCL_V255 2026-08-08 05:00:34 0
GM05752
 
Resource Report
Resource Website
RRID:CVCL_7435 Homo sapiens (Human) Farber lipogranulomatosis Population: Caucasian. PMID:9458280 Finite cell line Female GM 05752 CLO:CLO_0003531,
CLO:CLO_0024641,
CLDB:cl1498,
Coriell:GM05752,
Wikidata:Q54841928
CVCL_7435 2026-08-08 05:00:33 0
GM05751
 
Resource Report
Resource Website
RRID:CVCL_DF26 Homo sapiens (Human) Transformed cell line Female CLO:CLO_0024644,
Coriell:GM05751,
Wikidata:Q54841927
CVCL_DF26 2026-08-08 05:00:31 0
GM05747
 
Resource Report
Resource Website
Coriell Cat# GM05747, RRID:CVCL_DD80 Homo sapiens (Human) Osteogenesis imperfecta Population: Colombian. Finite cell line Male GM05747A Coriell GM05747 CLO:CLO_0024637,
Coriell:GM05747,
Wikidata:Q54841924
CVCL_DD80 2026-08-08 05:00:31 0

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