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95,747 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
GM03810
 
Resource Report
Resource Website
Coriell Cat# GM03810, RRID:CVCL_X300 Homo sapiens (Human) PMID:6661932 Finite cell line Female GM 3810 Coriell GM03810 CLO:CLO_0015556,
BioSample:SAMN00808543,
Coriell:GM03810,
Wikidata:Q54838247
CVCL_X300 2026-08-08 05:00:08 0
GM03814
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_F173 Homo sapiens (Human) Population: Caucasian. PMID:3941662
PMID:26190808
PMID:26247043
PMID:26651604
PMID:28284873
PMID:33197628
Finite cell line Female GM 3814, SMAM1FABE CLO:CLO_0015534,
CLO:CLO_0037413,
BioSample:SAMN00808546,
Coriell:GM03814,
LINCS_LDP:LPC-1014,
Wikidata:Q54838250
CVCL_F173 2026-08-08 05:00:08 1
GM03790
 
Resource Report
Resource Website
Coriell Cat# GM03790, RRID:CVCL_1H64 Homo sapiens (Human) Huntington's disease Transformed cell line Female Coriell GM03790 CLO:CLO_0015569,
BioSample:SAMN00808535,
Coriell:GM03790,
Wikidata:Q54838239
CVCL_1H64 2026-08-08 05:00:08 0
GM03727
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_UT41 Homo sapiens (Human) Population: African American. Transformed cell line Female Coriell:GM03727,
Wikidata:Q93585468
CVCL_UT41 2026-08-08 05:00:07 0
GM03811
 
Resource Report
Resource Website
Coriell Cat# GM03811, RRID:CVCL_2S95 Homo sapiens (Human) Finite cell line Female Coriell GM03811 CLO:CLO_0015553,
BioSample:SAMN00808544,
Coriell:GM03811,
Wikidata:Q54838248
CVCL_2S95 2026-08-08 05:00:08 0
GM03786
 
Resource Report
Resource Website
Coriell Cat# GM03786, RRID:CVCL_N012 Homo sapiens (Human) Karyotypic information: 45,XX,dic(13;14)(13qter->13p11::14p11->14qter) (Coriell=GM03786)., Population: Caucasian; Greek., Part of: Human variation panel. Finite cell line Female GM17375 Coriell GM03786 CLO:CLO_0013696,
CLO:CLO_0015567,
BioSample:SAMN00808534,
Coriell:GM03786,
Coriell:GM17375,
Wikidata:Q54838238
CVCL_N012 2026-08-08 05:00:08 0
GM03827
 
Resource Report
Resource Website
RRID:CVCL_X057 Homo sapiens (Human) Karyotypic information: 46,X,del(X)(pter->q21) (Coriell=GM03827)., Population: African American. PMID:6617268
PMID:6661932
Finite cell line Female GM 3827 CLO:CLO_0015670,
BioSample:SAMN00808553,
Coriell:GM03827,
Wikidata:Q54838257
CVCL_X057 2026-08-08 05:00:08 0
GM03774
 
Resource Report
Resource Website
Coriell Cat# GM03774, RRID:CVCL_2M99 Homo sapiens (Human) Turner syndrome Population: Caucasian. PMID:23665875 Finite cell line Female Coriell GM03774 CLO:CLO_0015499,
BioSample:SAMN00808527,
Coriell:GM03774,
Wikidata:Q54838229
CVCL_2M99 2026-08-08 05:00:07 0
GM03835
 
Resource Report
Resource Website
Coriell Cat# GM03835, RRID:CVCL_AK86 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian. Finite cell line Female Coriell GM03835 CLO:CLO_0015668,
BioSample:SAMN00808559,
Coriell:GM03835,
Wikidata:Q54838263
CVCL_AK86 2026-08-08 05:00:08 0
GM03799
 
Resource Report
Resource Website
Coriell Cat# GM03799, RRID:CVCL_2S94 Homo sapiens (Human) Transformed cell line Female Coriell GM03799 CLO:CLO_0015547,
BioSample:SAMN00808540,
Coriell:GM03799,
Wikidata:Q54838244
CVCL_2S94 2026-08-08 05:00:08 0
GM03786
 
Resource Report
Resource Website
Coriell Cat# GM17375, RRID:CVCL_N012 Homo sapiens (Human) Karyotypic information: 45,XX,dic(13;14)(13qter->13p11::14p11->14qter) (Coriell=GM03786)., Population: Caucasian; Greek., Part of: Human variation panel. Finite cell line Female GM17375 Coriell GM17375 CLO:CLO_0013696,
CLO:CLO_0015567,
BioSample:SAMN00808534,
Coriell:GM03786,
Coriell:GM17375,
Wikidata:Q54838238
CVCL_N012 2026-08-08 05:00:07 0
GM03828
 
Resource Report
Resource Website
Coriell Cat# GM03828, RRID:CVCL_X058 Homo sapiens (Human) Karyotypic information: 46,X,del(X)(pter->q21) (Coriell=GM03828)., Population: African American. PMID:6617268
PMID:6661932
Finite cell line Female GM 3828 Coriell GM03828 CLO:CLO_0015676,
BioSample:SAMN00808554,
Coriell:GM03828,
Wikidata:Q54838258
CVCL_X058 2026-08-08 05:00:08 0
GM03828
 
Resource Report
Resource Website
RRID:CVCL_X058 Homo sapiens (Human) Karyotypic information: 46,X,del(X)(pter->q21) (Coriell=GM03828)., Population: African American. PMID:6617268
PMID:6661932
Finite cell line Female GM 3828 CLO:CLO_0015676,
BioSample:SAMN00808554,
Coriell:GM03828,
Wikidata:Q54838258
CVCL_X058 2026-08-08 05:00:08 0
GM03746
 
Resource Report
Resource Website
RRID:CVCL_1H61 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease. Transformed cell line Female CLO:CLO_0015522,
BioSample:SAMN00808516,
Coriell:GM03746,
Wikidata:Q54838215
CVCL_1H61 2026-08-08 05:00:07 0
GM03809
 
Resource Report
Resource Website
RRID:CVCL_JE58 Homo sapiens (Human) WAGR syndrome PMID:2570029 Finite cell line Female GM3809 CLO:CLO_0015559,
BioSample:SAMN00808542,
Coriell:GM03809,
Wikidata:Q54838246
CVCL_JE58 2026-08-08 05:00:08 0
GM03831
 
Resource Report
Resource Website
Coriell Cat# GM03831, RRID:CVCL_AK82 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian. Finite cell line Female Coriell GM03831 CLO:CLO_0015674,
BioSample:SAMN00808555,
Coriell:GM03831,
Wikidata:Q54838259
CVCL_AK82 2026-08-08 05:00:08 0
GM03911
 
Resource Report
Resource Website
RRID:CVCL_AK95 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian. PMID:6726265 Transformed cell line Female GM 3911, GM03911A CLO:CLO_0016123,
Coriell:GM03911,
Wikidata:Q54838318
CVCL_AK95 2026-08-08 05:00:09 0
GM03910
 
Resource Report
Resource Website
Coriell Cat# GM03910, RRID:CVCL_AK94 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian. Finite cell line Female Coriell GM03910 CLO:CLO_0015996,
Coriell:GM03910,
Wikidata:Q54838317
CVCL_AK94 2026-08-08 05:00:09 0
GM03870
 
Resource Report
Resource Website
RRID:CVCL_1H75 Homo sapiens (Human) Population: Caucasian. Finite cell line Female GM03870A CLO:CLO_0016028,
BioSample:SAMN00808582,
Coriell:GM03870,
Wikidata:Q54838289
CVCL_1H75 2026-08-08 05:00:09 0
GM03863
 
Resource Report
Resource Website
RRID:CVCL_1H68 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 CLO:CLO_0015734,
BioSample:SAMN00808575,
Coriell:GM03863,
Wikidata:Q54838282
CVCL_1H68 2026-08-08 05:00:09 0

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