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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
GM01582
 
Resource Report
Resource Website
1+ mentions
Discontinued
Possibly Discontinued
Coriell Cat# GM00240, RRID:CVCL_7323 Homo sapiens (Human) Population: Caucasian. PMID:12665480
PMID:30567591
Finite cell line Female GM1582, GM-1582, GM01582A, GM1582A, GM00240, GM0240, GM-240 Coriell GM00240 CLO:CLO_0031462,
BioSample:SAMN00806939,
Coriell:GM00240,
Coriell:GM01582,
GEO:GSM3124639,
Wikidata:Q54836927
CVCL_7323 2026-08-29 04:27:40 1
GM01609
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JB87 Homo sapiens (Human) Wolfram syndrome Finite cell line Female GM-1609 Coriell:GM01609,
Wikidata:Q54836945
CVCL_JB87 2026-08-29 04:27:45 0
GM01582
 
Resource Report
Resource Website
1+ mentions
Possibly Discontinued
Discontinued
Coriell Cat# GM01582, RRID:CVCL_7323 Homo sapiens (Human) Population: Caucasian. PMID:12665480
PMID:30567591
Finite cell line Female GM1582, GM-1582, GM01582A, GM1582A, GM00240, GM0240, GM-240 Coriell GM01582 CLO:CLO_0031462,
BioSample:SAMN00806939,
Coriell:GM00240,
Coriell:GM01582,
GEO:GSM3124639,
Wikidata:Q54836927
CVCL_7323 2026-08-29 04:27:44 1
GM01581
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JD78 Homo sapiens (Human) Finite cell line Female GM-1581 Coriell:GM01581,
Wikidata:Q54836925
CVCL_JD78 2026-08-29 04:27:40 0
GM01612
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM01612, RRID:CVCL_JB63 Homo sapiens (Human) Niemann-Pick disease Finite cell line Male GM-1612 Coriell GM01612 Coriell:GM01612,
Wikidata:Q54836948
CVCL_JB63 2026-08-29 04:27:45 0
GM01609
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM01609, RRID:CVCL_JB87 Homo sapiens (Human) Wolfram syndrome Finite cell line Female GM-1609 Coriell GM01609 Coriell:GM01609,
Wikidata:Q54836945
CVCL_JB87 2026-08-29 04:27:41 0
GM01708
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_L959 Homo sapiens (Human) Population: Caucasian. Finite cell line Male GM-1708, GM-1010, GM01010 CLO:CLO_0030974,
BioSample:SAMN00807095,
Coriell:GM01010,
Coriell:GM01708,
Wikidata:Q54837027
CVCL_L959 2026-08-29 04:27:43 0
GM01706
 
Resource Report
Resource Website
Discontinued
Coriell Cat# GM01706, RRID:CVCL_7334 Homo sapiens (Human) Population: Caucasian. PMID:30567591 Finite cell line Female GM1706, GM-1706, GM 1706, GM01706A, GM1706A, GM00237, GM0237 Coriell GM01706 CLO:CLO_0030976,
BioSample:SAMN00807091,
Coriell:GM00237,
Coriell:GM01706,
GEO:GSM3124688,
Wikidata:Q54837025
CVCL_7334 2026-08-29 04:27:43 0
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 2026-08-29 04:27:48 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 2026-08-29 04:27:43 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 2026-08-29 04:27:48 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 2026-08-29 04:27:44 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 2026-08-29 04:27:42 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 2026-08-29 04:27:46 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 2026-08-29 04:27:44 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 2026-08-29 04:27:43 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 2026-08-29 04:27:45 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 2026-08-29 04:27:46 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 2026-08-29 04:27:44 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 2026-08-29 04:27:44 0

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