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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
GM00731
 
Resource Report
Resource Website
Coriell Cat# GM00731, RRID:CVCL_7301 Homo sapiens (Human) Population: Caucasian. PMID:3860870
PMID:15450399
Finite cell line Male GM0731, GM 0731, GM-731, GM 731, GM00731A, GM0731A, GM 0731A Coriell GM00731 CLO:CLO_0028816,
Coriell:GM00731,
Wikidata:Q54836423
CVCL_7301 2026-08-15 04:28:52 0
GM00773
 
Resource Report
Resource Website
Coriell Cat# GM00773, RRID:CVCL_V781 Homo sapiens (Human) Karyotypic information: 46,XX,t(4;7)(4qter->4p16::7q34->7qter;7pter->7q34::4p16->4pter) (Coriell=GM00773). PMID:891261 Finite cell line Female GM-773 Coriell GM00773 CLO:CLO_0028839,
Coriell:GM00773,
Wikidata:Q54836450
CVCL_V781 2026-08-15 04:28:52 0
GM00727
 
Resource Report
Resource Website
RRID:CVCL_1Y22 Homo sapiens (Human) Galactosemia Population: Caucasian. Finite cell line Female GM-727, GM00727A CLO:CLO_0028783,
Coriell:GM00727,
Wikidata:Q54836420
CVCL_1Y22 2026-08-15 04:28:52 0
GM00681
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00681, RRID:CVCL_X132 Homo sapiens (Human) PMID:694721 Finite cell line Male GM681 Coriell GM00681 Coriell:GM00681,
Wikidata:Q54836387
CVCL_X132 2026-08-15 04:28:51 0
GM00782
 
Resource Report
Resource Website
Coriell Cat# GM00782, RRID:CVCL_4E27 Homo sapiens (Human) PMID:23665875 Finite cell line Male GM-782 Coriell GM00782 CLO:CLO_0028841,
Coriell:GM00782,
Wikidata:Q54836455
CVCL_4E27 2026-08-15 04:28:52 0
GM00770
 
Resource Report
Resource Website
RRID:CVCL_V205 Homo sapiens (Human) Cystic fibrosis Population: Caucasian. Finite cell line Male GM-770, GM00770A CLO:CLO_0028840,
Coriell:GM00770,
Wikidata:Q54836449
CVCL_V205 2026-08-15 04:28:52 0
GM00722
 
Resource Report
Resource Website
Discontinued
Possibly Discontinued
Coriell Cat# GM00548, RRID:CVCL_L954 Homo sapiens (Human) Homocystinuria Finite cell line Male GM0722, GM-722, GM00548, GM0548 Coriell GM00548 CLO:CLO_0028794,
Coriell:GM00548,
Coriell:GM00722,
Wikidata:Q54836416
CVCL_L954 2026-08-15 04:28:52 0
GM00741
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00741, RRID:CVCL_CX36 Homo sapiens (Human) Neuronal ceroid lipofuscinosis type 4B Finite cell line Male GM-741 Coriell GM00741 Coriell:GM00741,
Wikidata:Q54836435
CVCL_CX36 2026-08-15 04:28:52 0
GM00683
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_CX20 Homo sapiens (Human) Glycogen storage disease type III Finite cell line Male GM-683 Coriell:GM00683,
Wikidata:Q54836389
CVCL_CX20 2026-08-15 04:28:51 0
GM00747
 
Resource Report
Resource Website
RRID:CVCL_CX01 Homo sapiens (Human) Glycine encephalopathy Population: Caucasian. Finite cell line Female GM0747, GM-747 CLO:CLO_0028824,
Coriell:GM00747,
Wikidata:Q54836438
CVCL_CX01 2026-08-15 04:28:52 0
GM00781
 
Resource Report
Resource Website
Coriell Cat# GM00781, RRID:CVCL_J108 Homo sapiens (Human) Ataxia telangiectasia syndrome PMID:761484
PMID:16166284
Transformed cell line Female GM-781 Coriell GM00781 CLO:CLO_0028842,
Coriell:GM00781,
Wikidata:Q54836452
CVCL_J108 2026-08-15 04:28:52 0
GM00701
 
Resource Report
Resource Website
RRID:CVCL_4N06 Homo sapiens (Human) Hyperlipoproteinemia, type IIa Population: Caucasian. PMID:6986448
PMID:29308438
Finite cell line Female GM-701, GM 701 GM00701B, GM00701C CLO:CLO_0028896,
Coriell:GM00701,
Wikidata:Q54836398
CVCL_4N06 2026-08-15 04:28:51 0
GM00738
 
Resource Report
Resource Website
RRID:CVCL_4J12 Homo sapiens (Human) Population: Caucasian. PMID:7803800 Finite cell line Male GM-738 CLO:CLO_0028813,
Coriell:GM00738,
Wikidata:Q54836432
CVCL_4J12 2026-08-15 04:28:52 0
GM00741
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_CX36 Homo sapiens (Human) Neuronal ceroid lipofuscinosis type 4B Finite cell line Male GM-741 Coriell:GM00741,
Wikidata:Q54836435
CVCL_CX36 2026-08-15 04:28:52 0
GM00754
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_CX51 Homo sapiens (Human) Finite cell line Female GM-754 Coriell:GM00754,
Wikidata:Q54836442
CVCL_CX51 2026-08-15 04:28:52 0
GM00773
 
Resource Report
Resource Website
RRID:CVCL_V781 Homo sapiens (Human) Karyotypic information: 46,XX,t(4;7)(4qter->4p16::7q34->7qter;7pter->7q34::4p16->4pter) (Coriell=GM00773). PMID:891261 Finite cell line Female GM-773 CLO:CLO_0028839,
Coriell:GM00773,
Wikidata:Q54836450
CVCL_V781 2026-08-15 04:28:52 0
GM00878
 
Resource Report
Resource Website
RRID:CVCL_0R28 Homo sapiens (Human) Population: Caucasian. Finite cell line Female GM-878 CLO:CLO_0029602,
Coriell:GM00878,
Wikidata:Q54836497
CVCL_0R28 2026-08-15 04:28:53 0
GM00861
 
Resource Report
Resource Website
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 CLO:CLO_0029634,
Coriell:GM00861,
Wikidata:Q54836482
CVCL_4D79 2026-08-15 04:28:53 0
GM00887
 
Resource Report
Resource Website
Coriell Cat# GM00887, RRID:CVCL_V530 Homo sapiens (Human) Hurler syndrome Population: Caucasian. PMID:8328452 Finite cell line Female GM-887, GM 00887 Coriell GM00887 CLO:CLO_0029583,
Coriell:GM00887,
Wikidata:Q54836510
CVCL_V530 2026-08-15 04:28:53 0
GM00851
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JB84 Homo sapiens (Human) Cystic fibrosis Finite cell line Male GM-851 Coriell:GM00851,
Wikidata:Q54836474
CVCL_JB84 2026-08-15 04:28:53 0

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