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256,031 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 Authority 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 Cellosaurus 2026-09-26 06:49:10 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 Cellosaurus 2026-09-26 06:49:10 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 Cellosaurus 2026-09-26 06:49:10 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 Cellosaurus 2026-09-26 06:49:09 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 Cellosaurus 2026-09-26 06:49:10 0
GM03780
 
Resource Report
Resource Website
RRID:CVCL_M942 Homo sapiens (Human) Duchenne muscular dystrophy Population: Caucasian; Iberian., Part of: Human variation panel. PMID:6726265
PMID:23665875
Transformed cell line Male GM 3780, GM3780, GM17091 CLO:CLO_0014526,
CLO:CLO_0015498,
BioSample:SAMN00808528,
Coriell:GM03780,
Coriell:GM17091,
Wikidata:Q54838230
CVCL_M942 Cellosaurus 2026-09-26 06:49:10 0
GM03825
 
Resource Report
Resource Website
Coriell Cat# GM03825, RRID:CVCL_AK80 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian; German. Transformed cell line Male Coriell GM03825 CLO:CLO_0015681,
BioSample:SAMN00808551,
Coriell:GM03825,
Wikidata:Q54838255
CVCL_AK80 Cellosaurus 2026-09-26 06:49:10 0
GM03784
 
Resource Report
Resource Website
Coriell Cat# GM03784, RRID:CVCL_DF22 Homo sapiens (Human) Macular dystrophy, retinal, 1 Transformed cell line Male Coriell GM03784 CLO:CLO_0015604,
BioSample:SAMN00808532,
Coriell:GM03784,
Wikidata:Q54838234
CVCL_DF22 Cellosaurus 2026-09-26 06:49:10 0
GM03773
 
Resource Report
Resource Website
RRID:CVCL_U398 Homo sapiens (Human) Tay-Sachs disease Donor information: Established from twin of GM03772 (Cellosaurus=CVCL_U397). Transformed cell line Male CLO:CLO_0015505,
BioSample:SAMN00808526,
Coriell:GM03773,
Wikidata:Q54838228
CVCL_U398 Cellosaurus 2026-09-26 06:49:10 0
GM03767
 
Resource Report
Resource Website
Coriell Cat# GM03767, RRID:CVCL_X111 Homo sapiens (Human) Deletion 18p syndrome Karyotypic information: 46,XY,del(18)(qter->p11) (Coriell=GM03767)., Population: Caucasian. PMID:6617268
PMID:6661932
Finite cell line Male GM 3767 Coriell GM03767 CLO:CLO_0015491,
BioSample:SAMN00808521,
Coriell:GM03767,
Wikidata:Q54838222
CVCL_X111 Cellosaurus 2026-09-26 06:49:10 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 Cellosaurus 2026-09-26 06:49:10 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 Cellosaurus 2026-09-26 06:49:10 0
GM03823
 
Resource Report
Resource Website
Coriell Cat# GM03823, RRID:CVCL_AK78 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian; German. PMID:6726265 Transformed cell line Male GM 3823, GM03823A Coriell GM03823 CLO:CLO_0015540,
BioSample:SAMN00808549,
Coriell:GM03823,
Wikidata:Q54838253
CVCL_AK78 Cellosaurus 2026-09-26 06:49:10 0
GM03747
 
Resource Report
Resource Website
RRID:CVCL_1H62 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 Male CLO:CLO_0015521,
BioSample:SAMN00808517,
Coriell:GM03747,
Wikidata:Q54838216
CVCL_1H62 Cellosaurus 2026-09-26 06:49:10 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 Cellosaurus 2026-09-26 06:49:10 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 Cellosaurus 2026-09-26 06:49:11 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 Cellosaurus 2026-09-26 06:49:10 0
GM03813
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_F172 Homo sapiens (Human) Spinal muscular atrophy type 2 Population: Caucasian., Problematic cell line: Misclassified. Originally thought to be a SMA type 1 (SMA1) cell line but shown to be from a SMA type 2 (SMA2) (PubMed=28284873).. PMID:3941662
PMID:26190808
PMID:26247043
PMID:28284873
Finite cell line Male GM 3813, SMA1FABE CLO:CLO_0015532,
BioSample:SAMN00808545,
Coriell:GM03813,
Wikidata:Q54838249
CVCL_F172 Cellosaurus 2026-09-26 06:49:10 2
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 Cellosaurus 2026-09-26 06:49:10 0
GM03733
 
Resource Report
Resource Website
RRID:CVCL_X110 Homo sapiens (Human) Karyotypic information: 46,XY,del(7)(pter->q34) (Coriell=GM03733)., Population: Caucasian. PMID:6617268
PMID:6661932
Finite cell line Male GM-3733, GM 3733 CLO:CLO_0015525,
BioSample:SAMN00808514,
Coriell:GM03733,
Wikidata:Q54838213
CVCL_X110 Cellosaurus 2026-09-26 06:49:09 0

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