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10,882 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
GM00942
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_9W78 Homo sapiens (Human) Population: Caucasian. Finite cell line Female GM-942 CLO:CLO_0029552,
Coriell:GM00942,
Wikidata:Q54836551
CVCL_9W78 2026-09-05 10:54:13 1
GM01389
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_F028 Homo sapiens (Human) Xeroderma pigmentosum, complementation group E PMID:9584159
PMID:10655550
PMID:10777490
PMID:12812979
PMID:26184184
Finite cell line Female GM-1389, GM01389A, GM01389D, XP408BE CLO:CLO_0030821,
BioSample:SAMN00803846,
Coriell:GM01389,
Wikidata:Q54836798
CVCL_F028 2026-09-05 10:54:20 1
GM01582
 
Resource Report
Resource Website
1+ mentions
Discontinued
Possibly Discontinued
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 CLO:CLO_0031462,
BioSample:SAMN00806939,
Coriell:GM00240,
Coriell:GM01582,
GEO:GSM3124639,
Wikidata:Q54836927
CVCL_7323 2026-09-05 10:54:23 1
GM01651
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM01651, RRID:CVCL_7329 Homo sapiens (Human) Population: Caucasian. PMID:8643543
PMID:26984941
Finite cell line Female GM1651, GM-1651, GM 01651, GM01651A, GM1651A, GM 1651A, GM01651B Coriell GM01651 CLO:CLO_0031528,
BioSample:SAMN00807025,
Coriell:GM01651,
GEO:GSM1316973,
GEO:GSM1317010,
Wikidata:Q54836982
CVCL_7329 2026-09-05 10:54:24 1
GM01651
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_7329 Homo sapiens (Human) Population: Caucasian. PMID:8643543
PMID:26984941
Finite cell line Female GM1651, GM-1651, GM 01651, GM01651A, GM1651A, GM 1651A, GM01651B CLO:CLO_0031528,
BioSample:SAMN00807025,
Coriell:GM01651,
GEO:GSM1316973,
GEO:GSM1317010,
Wikidata:Q54836982
CVCL_7329 2026-09-05 10:54:24 1
GM01835
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM01835, RRID:CVCL_D873 Homo sapiens (Human) Schizophrenia Population: Jewish and Caucasian; Scandinavian. PMID:7847674
PMID:21490598
Finite cell line Female GM-1835 Coriell GM01835 CLO:CLO_0031421,
BioSample:SAMN00807213,
Coriell:GM01835,
Wikidata:Q54837112
CVCL_D873 2026-09-05 10:54:27 1
GM01972
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_F261 Homo sapiens (Human) Progeria Population: Caucasian. PMID:7253718
PMID:7471105
PMID:12714972
Finite cell line Female GM-1972, GM01972A, AG01972, AG-1972, AG 1972, AG1972, AG01972A, AG01972B CLO:CLO_0032341,
CLO:CLO_0036882,
BioSample:SAMN00807344,
Coriell:AG01972,
Coriell:GM01972,
GEO:GSM603044,
GEO:GSM603045,
Wikidata:Q54837209
CVCL_F261 2026-09-05 10:54:30 1
GM01983
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_F591 Homo sapiens (Human) Population: Caucasian. PMID:7438975 Finite cell line Female GM-1983 CLO:CLO_0032358,
BioSample:SAMN00807350,
Coriell:GM01983,
Wikidata:Q54837214
CVCL_F591 2026-09-05 10:54:30 1
GM02037
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM02037, RRID:CVCL_7349 Homo sapiens (Human) Karyotypic information: 46,XY [45]; 46,XY,t(4;16)(4qter->4p14::16q24->16qter;16pter->16q24::4p14->4pter) [5] (Coriell=GM02037)., Population: Caucasian. PMID:6223188
PMID:8643543
PMID:30567591
Finite cell line Male GM2037, GM-2037, GM 2037, GM02037A, GM2037A, GM 2037A, GM02037B, GM 2037B, GM02037C Coriell GM02037 BTO:BTO_0003842,
CLO:CLO_0032574,
BioSample:SAMN00807416,
Coriell:GM02037,
GEO:GSM3124641,
Wikidata:Q54837256
CVCL_7349 2026-09-05 10:54:31 1
GM02079
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM02079, RRID:CVCL_1H41 Homo sapiens (Human) Huntington's disease Population: Caucasian. PMID:6220707 Finite cell line Female GM-2079, GM 2079, GM02079A Coriell GM02079 CLO:CLO_0032509,
BioSample:SAMN00807468,
Coriell:GM02079,
Wikidata:Q54837291
CVCL_1H41 2026-09-05 10:54:31 1
GM02052
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_7350 Homo sapiens (Human) Ataxia telangiectasia syndrome Population: Jewish; Moroccan. PMID:761484
PMID:11313956
PMID:12446774
PMID:19896956
Finite cell line Female GM-2052, GM 2052, GM2052, GM02052A, AT19IJE-F CLO:CLO_0032553,
BioSample:SAMN00807434,
Coriell:GM02052,
Wikidata:Q54837268
CVCL_7350 2026-09-05 10:54:31 1
GM02048
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_M927 Homo sapiens (Human) Mucolipidosis type IV Population: Jewish; Ashkenazi. Finite cell line Female GM-2048 CLO:CLO_0032549,
BioSample:SAMN00807426,
Coriell:GM02048,
Wikidata:Q54837263
CVCL_M927 2026-09-05 10:54:31 2
GM02037
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_7349 Homo sapiens (Human) Karyotypic information: 46,XY [45]; 46,XY,t(4;16)(4qter->4p14::16q24->16qter;16pter->16q24::4p14->4pter) [5] (Coriell=GM02037)., Population: Caucasian. PMID:6223188
PMID:8643543
PMID:30567591
Finite cell line Male GM2037, GM-2037, GM 2037, GM02037A, GM2037A, GM 2037A, GM02037B, GM 2037B, GM02037C BTO:BTO_0003842,
CLO:CLO_0032574,
BioSample:SAMN00807416,
Coriell:GM02037,
GEO:GSM3124641,
Wikidata:Q54837256
CVCL_7349 2026-09-05 10:54:31 1
GM02183
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_W557 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease., Population: Caucasian. PMID:6220707
PMID:22748968
PMID:34746695
Finite cell line Female GM-2183, GM 2183, GM2183 CLO:CLO_0031788,
CLO:CLO_0037414,
BioSample:SAMN00807584,
Coriell:GM02183,
LINCS_LDP:LPC-1015,
Wikidata:Q54837357
CVCL_W557 2026-09-05 10:54:33 1
GM02171
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_1H55 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease., Population: Caucasian. PMID:6220707
PMID:25326100
Finite cell line Female GM-2171, GM 2171 CLO:CLO_0031767,
BioSample:SAMN00807564,
Coriell:GM02171,
GEO:GSM1266971,
Wikidata:Q54837347
CVCL_1H55 2026-09-05 10:54:33 3
GM02171
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM02171, RRID:CVCL_1H55 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease., Population: Caucasian. PMID:6220707
PMID:25326100
Finite cell line Female GM-2171, GM 2171 Coriell GM02171 CLO:CLO_0031767,
BioSample:SAMN00807564,
Coriell:GM02171,
GEO:GSM1266971,
Wikidata:Q54837347
CVCL_1H55 2026-09-05 10:54:33 3
GM02154
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM02154, RRID:CVCL_1H44 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease., Population: Caucasian. Transformed cell line Female GM-2154, GM02154B Coriell GM02154 CLO:CLO_0031857,
BioSample:SAMN00807530,
Coriell:GM02154,
Wikidata:Q54837328
CVCL_1H44 2026-09-05 10:54:32 1
GM02304
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_1U21 Homo sapiens (Human) Autosomal dominant torsion dystonia 1 Population: Caucasian. Finite cell line Female GM-2304 CLO:CLO_0032209,
BioSample:SAMN00807677,
Coriell:GM02304,
Wikidata:Q54837418
CVCL_1U21 2026-09-05 10:54:35 1
GM03652
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_7397 Homo sapiens (Human) Population: Caucasian. PMID:2897722
PMID:3863481
PMID:7847674
PMID:8247227
PMID:26184184
PMID:29125828
PMID:30567591
PMID:32291635
PMID:35850241
Finite cell line Male GM3652, GM3652A, GM03652C, C3652 CLO:CLO_0015442,
BioSample:SAMN00808487,
Coriell:GM03652,
GEO:GSM2794409,
GEO:GSM3124681,
Wikidata:Q54838179
CVCL_7397 2026-09-05 10:54:54 4
GM03672
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_8A60 Homo sapiens (Human) Leigh disease Population: Caucasian. PMID:2376596
PMID:30471880
PMID:34091428
Finite cell line Female GM3672 CLO:CLO_0015477,
BioSample:SAMN00808494,
Coriell:GM03672,
Wikidata:Q54838187
CVCL_8A60 2026-09-05 10:54:54 1

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