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19,458 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
GM00283
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_L936 Homo sapiens (Human) Hyperlipoproteinemia, type IIa Population: Caucasian. Finite cell line Female GM-283, GM0283, GM00102, GM0102 CLO:CLO_0025527,
Coriell:GM00102,
Coriell:GM00283,
Wikidata:Q54836127
CVCL_L936 2026-09-05 10:54:04 0
GM00217
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00217, RRID:CVCL_V758 Homo sapiens (Human) PMID:1132255
PMID:6661932
Finite cell line Male GM-217, GM-0217, GM 217 Coriell GM00217 Coriell:GM00217,
Wikidata:Q54836096
CVCL_V758 2026-09-05 10:54:03 0
GM00222
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00222, RRID:CVCL_JB94 Homo sapiens (Human) Ichthyosis Finite cell line Female GM-222 Coriell GM00222 Coriell:GM00222,
Wikidata:Q54836101
CVCL_JB94 2026-09-05 10:54:03 0
GM00282
 
Resource Report
Resource Website
Discontinued
Coriell Cat# GM00061, RRID:CVCL_L935 Homo sapiens (Human) Fructose-1,6-bisphosphatase deficiency Finite cell line Female GM-282, GM00061 Coriell GM00061 CLO:CLO_0025520,
Coriell:GM00061,
Coriell:GM00282,
Wikidata:Q54836125
CVCL_L935 2026-09-05 10:54:04 0
GM00158
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_V427 Homo sapiens (Human) Lesch-Nyhan syndrome PMID:180603 Finite cell line Male GM-158, GM 158 Coriell:GM00158,
Wikidata:Q54836070
CVCL_V427 2026-09-05 10:54:03 0
GM00260
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_L934 Homo sapiens (Human) Population: Caucasian. PMID:6661932 Finite cell line Male GM-260, GM-0260, GM 260, GM00069 CLO:CLO_0025494,
Coriell:GM00069,
Coriell:GM00260,
Wikidata:Q54836117
CVCL_L934 2026-09-05 10:54:04 0
GM00222
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JB94 Homo sapiens (Human) Ichthyosis Finite cell line Female GM-222 Coriell:GM00222,
Wikidata:Q54836101
CVCL_JB94 2026-09-05 10:54:03 0
GM00283
 
Resource Report
Resource Website
Discontinued
Coriell Cat# GM00283, RRID:CVCL_L936 Homo sapiens (Human) Hyperlipoproteinemia, type IIa Population: Caucasian. Finite cell line Female GM-283, GM0283, GM00102, GM0102 Coriell GM00283 CLO:CLO_0025527,
Coriell:GM00102,
Coriell:GM00283,
Wikidata:Q54836127
CVCL_L936 2026-09-05 10:54:04 0
GM00217
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_V758 Homo sapiens (Human) PMID:1132255
PMID:6661932
Finite cell line Male GM-217, GM-0217, GM 217 Coriell:GM00217,
Wikidata:Q54836096
CVCL_V758 2026-09-05 10:54:03 0
GM00164
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00164, RRID:CVCL_CX26 Homo sapiens (Human) I-cell disease Finite cell line Male GM-164 Coriell GM00164 Coriell:GM00164,
Wikidata:Q54836072
CVCL_CX26 2026-09-05 10:54:03 0
GM00264
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00264, RRID:CVCL_CX16 Homo sapiens (Human) Galactosemia Finite cell line Male GM-264 Coriell GM00264 Coriell:GM00264,
Wikidata:Q54836118
CVCL_CX16 2026-09-05 10:54:04 0
GM00185
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00185, RRID:CVCL_JD92 Homo sapiens (Human) Finite cell line Female GM-185 Coriell GM00185 Coriell:GM00185,
Wikidata:Q54836076
CVCL_JD92 2026-09-05 10:54:03 0
GM07854
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_0M89 Homo sapiens (Human) Transformed cell line Male GM07854B CLO:CLO_0010289,
Coriell:GM07854,
Wikidata:Q54842967
CVCL_0M89 2026-09-05 10:55:47 0
GM07993
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_5N77 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell:GM07993,
Wikidata:Q54843038
CVCL_5N77 2026-09-05 10:55:49 0
GM08582
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM08582, RRID:CVCL_VL36 Homo sapiens (Human) Bloom syndrome PMID:2805228 Transformed cell line GM8582 Coriell GM08582 Coriell:GM08582,
Wikidata:Q93799070
CVCL_VL36 2026-09-05 10:55:53 0
GM08762
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_5N87 Homo sapiens (Human) Finite cell line Male GM08762A Coriell:GM08762,
Wikidata:Q54843269
CVCL_5N87 2026-09-05 10:55:54 0
GM04614
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_V474 Homo sapiens (Human) Down syndrome PMID:6661932 Finite cell line Female GM 4614 CLO:CLO_0018905,
Coriell:GM04614,
Wikidata:Q54838600
CVCL_V474 2026-09-05 10:55:04 0
GM04614
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM04614, RRID:CVCL_V474 Homo sapiens (Human) Down syndrome PMID:6661932 Finite cell line Female GM 4614 Coriell GM04614 CLO:CLO_0018905,
Coriell:GM04614,
Wikidata:Q54838600
CVCL_V474 2026-09-05 10:55:04 0
GM05222
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_GQ47 Homo sapiens (Human) Bipolar disorder Finite cell line Male CLO:CLO_0025228,
Coriell:GM05222,
Wikidata:Q54838930
CVCL_GQ47 2026-09-05 10:55:12 0
GM05439
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM05439, RRID:CVCL_UR98 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Female GM05439Z Coriell GM05439 Coriell:GM05439,
Wikidata:Q93788985
CVCL_UR98 2026-09-05 10:55:14 0

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