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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
GM01742
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_CX27 Homo sapiens (Human) I-cell disease Finite cell line Female GM-1742 Coriell:GM01742,
Wikidata:Q54837054
CVCL_CX27 2026-08-01 05:03:48 0
GM01706
 
Resource Report
Resource Website
Discontinued
Coriell Cat# GM00237, RRID:CVCL_7334 Homo sapiens (Human) Population: Caucasian. PMID:30567591 Finite cell line Female GM1706, GM-1706, GM 1706, GM01706A, GM1706A, GM00237, GM0237 Coriell GM00237 CLO:CLO_0030976,
BioSample:SAMN00807091,
Coriell:GM00237,
Coriell:GM01706,
GEO:GSM3124688,
Wikidata:Q54837025
CVCL_7334 2026-08-01 05:03:47 0
GM01740
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JC92 Homo sapiens (Human) Ataxia telangiectasia syndrome Finite cell line Male GM-1740, GM01740A BioSample:SAMN00807129,
Coriell:GM01740,
Wikidata:Q54837051
CVCL_JC92 2026-08-01 05:03:48 0
GM01724
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM01724, RRID:CVCL_X254 Homo sapiens (Human) Population: Caucasian. Finite cell line Female GM-1724 Coriell GM01724 Coriell:GM01724,
Wikidata:Q54837038
CVCL_X254 2026-08-01 05:03:47 0
GM01669
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JB62 Homo sapiens (Human) Niemann-Pick disease, type B Finite cell line Female GM-1669 Coriell:GM01669,
Wikidata:Q54837000
CVCL_JB62 2026-08-01 05:03:46 0
GM01669
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM01669, RRID:CVCL_JB62 Homo sapiens (Human) Niemann-Pick disease, type B Finite cell line Female GM-1669 Coriell GM01669 Coriell:GM01669,
Wikidata:Q54837000
CVCL_JB62 2026-08-01 05:03:47 0
GM01740
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM01740, RRID:CVCL_JC92 Homo sapiens (Human) Ataxia telangiectasia syndrome Finite cell line Male GM-1740, GM01740A Coriell GM01740 BioSample:SAMN00807129,
Coriell:GM01740,
Wikidata:Q54837051
CVCL_JC92 2026-08-01 05:03:47 0
GM01724
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_X254 Homo sapiens (Human) Population: Caucasian. Finite cell line Female GM-1724 Coriell:GM01724,
Wikidata:Q54837038
CVCL_X254 2026-08-01 05:03:47 0
GM01824
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM01824, RRID:CVCL_JC84 Homo sapiens (Human) Finite cell line Male GM-1824 Coriell GM01824 Coriell:GM01824,
Wikidata:Q54837105
CVCL_JC84 2026-08-01 05:03:49 0
GM01814
 
Resource Report
Resource Website
Discontinued
Coriell Cat# GM17215, RRID:CVCL_7339 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:62390
PMID:16260726
PMID:20889555
PMID:29959025
Transformed cell line Female GM-1814, GM1814, GM01814A, GM01072, GM-1072, GM1072, GM17215 Coriell GM17215 CLO:CLO_0013885,
CLO:CLO_0031057,
BioSample:SAMN00807207,
Coriell:GM01072,
Coriell:GM01814,
Coriell:GM17215,
GEO:GSM569641,
GEO:GSM596279,
GEO:GSM596639,
GEO:GSM924817,
Wikidata:Q54837102
CVCL_7339 2026-08-01 05:03:49 0
GM01767
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_L963 Homo sapiens (Human) Hyperlipoproteinemia, type IIa Transformed cell line Female GM-1767, GM01452, GM-1452 CLO:CLO_0031000,
Coriell:GM01452,
Coriell:GM01767,
Wikidata:Q54837064
CVCL_L963 2026-08-01 05:03:48 0
GM01785
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM01785, RRID:CVCL_JE08 Homo sapiens (Human) Metachromatic leukodystrophy Transformed cell line Female GM-1785 Coriell GM01785 Coriell:GM01785,
Wikidata:Q54837075
CVCL_JE08 2026-08-01 05:03:48 0
GM01814
 
Resource Report
Resource Website
Discontinued
Coriell Cat# GM01814, RRID:CVCL_7339 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:62390
PMID:16260726
PMID:20889555
PMID:29959025
Transformed cell line Female GM-1814, GM1814, GM01814A, GM01072, GM-1072, GM1072, GM17215 Coriell GM01814 CLO:CLO_0013885,
CLO:CLO_0031057,
BioSample:SAMN00807207,
Coriell:GM01072,
Coriell:GM01814,
Coriell:GM17215,
GEO:GSM569641,
GEO:GSM596279,
GEO:GSM596639,
GEO:GSM924817,
Wikidata:Q54837102
CVCL_7339 2026-08-01 05:03:49 0
GM01806
 
Resource Report
Resource Website
Discontinued
Coriell Cat# GM01074, RRID:CVCL_7338 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:16260726
PMID:20889555
PMID:29959025
Transformed cell line Male GM-1806, GM01074, GM-1074, GM17214 Coriell GM01074 CLO:CLO_0013886,
CLO:CLO_0031047,
BioSample:SAMN00807197,
Coriell:GM01074,
Coriell:GM01806,
Coriell:GM17214,
GEO:GSM569518,
GEO:GSM596278,
GEO:GSM596741,
GEO:GSM924816,
Wikidata:Q54837096
CVCL_7338 2026-08-01 05:03:49 0
GM01814
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_7339 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:62390
PMID:16260726
PMID:20889555
PMID:29959025
Transformed cell line Female GM-1814, GM1814, GM01814A, GM01072, GM-1072, GM1072, GM17215 CLO:CLO_0013885,
CLO:CLO_0031057,
BioSample:SAMN00807207,
Coriell:GM01072,
Coriell:GM01814,
Coriell:GM17215,
GEO:GSM569641,
GEO:GSM596279,
GEO:GSM596639,
GEO:GSM924817,
Wikidata:Q54837102
CVCL_7339 2026-08-01 05:03:49 0
GM01815
 
Resource Report
Resource Website
Discontinued
Coriell Cat# GM18004, RRID:CVCL_7340 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. Transformed cell line Male GM-1815, GM1815, GM01075, GM-1075, GM1075, GM18004 Coriell GM18004 CLO:CLO_0015995,
CLO:CLO_0031055,
BioSample:SAMN00807209,
Coriell:GM01075,
Coriell:GM01815,
Coriell:GM18004,
Wikidata:Q54837103
CVCL_7340 2026-08-01 05:03:50 0
GM01783
 
Resource Report
Resource Website
Discontinued
Coriell Cat# GM01783, RRID:CVCL_JE07 Homo sapiens (Human) Hyperlipoproteinemia, type IIb Transformed cell line Female GM-1783 Coriell GM01783 Coriell:GM01783,
Wikidata:Q54837073
CVCL_JE07 2026-08-01 05:03:48 0
GM01825
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JC85 Homo sapiens (Human) Transformed cell line Male GM-1825 Coriell:GM01825,
Wikidata:Q54837106
CVCL_JC85 2026-08-01 05:03:49 0
GM01769
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_L964 Homo sapiens (Human) Gaucher disease Transformed cell line Male GM01769B, GM01021, GM-1021 CLO:CLO_0031001,
BioSample:SAMN00807149,
Coriell:GM01021,
Coriell:GM01769,
Wikidata:Q54837065
CVCL_L964 2026-08-01 05:03:48 0
GM01805
 
Resource Report
Resource Website
Discontinued
Coriell Cat# GM17213, RRID:CVCL_7337 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:62390
PMID:16260726
PMID:20889555
PMID:29959025
Transformed cell line Female GM-1805, GM01805A, GM01073, GM-1073, GM17213 Coriell GM17213 CLO:CLO_0013893,
CLO:CLO_0031046,
BioSample:SAMN00807195,
Coriell:GM01073,
Coriell:GM01805,
Coriell:GM17213,
GEO:GSM569542,
GEO:GSM596277,
GEO:GSM596638,
GEO:GSM924815,
Wikidata:Q54837091
CVCL_7337 2026-08-01 05:03:48 0

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