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  • References:pmid:23665875 (facet)

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1,669 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
GM02003
 
Resource Report
Resource Website
RRID:CVCL_X085 Homo sapiens (Human) Population: Caucasian. PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Female GM-2003, GM 2003 CLO:CLO_0032295,
BioSample:SAMN00807372,
Coriell:GM02003,
Wikidata:Q54837229
CVCL_X085 Cellosaurus 2026-10-10 05:25:37 0
GM02003
 
Resource Report
Resource Website
Coriell Cat# GM02003, RRID:CVCL_X085 Homo sapiens (Human) Population: Caucasian. PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Female GM-2003, GM 2003 Coriell GM02003 CLO:CLO_0032295,
BioSample:SAMN00807372,
Coriell:GM02003,
Wikidata:Q54837229
CVCL_X085 Cellosaurus 2026-10-10 05:25:36 0
GM01921
 
Resource Report
Resource Website
Coriell Cat# GM01921, RRID:CVCL_V465 Homo sapiens (Human) Down syndrome Population: Caucasian. PMID:6617268
PMID:23665875
Transformed cell line Male GM-1921, GM 1921, GM01921A Coriell GM01921 CLO:CLO_0032392,
BioSample:SAMN00807314,
Coriell:GM01921,
Wikidata:Q54837187
CVCL_V465 Cellosaurus 2026-10-10 05:25:35 0
GM02008
 
Resource Report
Resource Website
RRID:CVCL_X086 Homo sapiens (Human) Population: African American. PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Female GM-2008, GM 2008 CLO:CLO_0032298,
BioSample:SAMN00807378,
Coriell:GM02008,
Wikidata:Q54837233
CVCL_X086 Cellosaurus 2026-10-10 05:25:37 0
GM01921
 
Resource Report
Resource Website
RRID:CVCL_V465 Homo sapiens (Human) Down syndrome Population: Caucasian. PMID:6617268
PMID:23665875
Transformed cell line Male GM-1921, GM 1921, GM01921A CLO:CLO_0032392,
BioSample:SAMN00807314,
Coriell:GM01921,
Wikidata:Q54837187
CVCL_V465 Cellosaurus 2026-10-10 05:25:35 0
GM01941
 
Resource Report
Resource Website
RRID:CVCL_X084 Homo sapiens (Human) Turner syndrome Population: Caucasian. PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Female GM-1941, GM 1941 CLO:CLO_0032323,
BioSample:SAMN00807328,
Coriell:GM01941,
Wikidata:Q54837198
CVCL_X084 Cellosaurus 2026-10-10 05:25:36 0
GM02030
 
Resource Report
Resource Website
Coriell Cat# GM02030, RRID:CVCL_X259 Homo sapiens (Human) Trisomy 8 Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Male GM-2030, GM 2030 Coriell GM02030 CLO:CLO_0032576,
BioSample:SAMN00807404,
Coriell:GM02030,
Wikidata:Q54837249
CVCL_X259 Cellosaurus 2026-10-10 05:25:37 0
GM02025
 
Resource Report
Resource Website
Coriell Cat# GM02025, RRID:CVCL_V825 Homo sapiens (Human) Population: Caucasian. PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Male GM-2025, GM 2025, GM2025 Coriell GM02025 CLO:CLO_0032577,
BioSample:SAMN00807400,
Coriell:GM02025,
Wikidata:Q54837244
CVCL_V825 Cellosaurus 2026-10-10 05:25:37 0
GM03884
 
Resource Report
Resource Website
RRID:CVCL_1N62 Homo sapiens (Human) Klippel-Feil syndrome Karyotypic information: 46,X,t(X;16)(q26;q24) (PubMed=10377420)., Population: Caucasian. PMID:2498246
PMID:3495225
PMID:10377420
PMID:23665875
Finite cell line Female GM 3884, GM3884 CLO:CLO_0016011,
BioSample:SAMN00808591,
Coriell:GM03884,
Wikidata:Q54838299
CVCL_1N62 Cellosaurus 2026-10-10 05:26:07 0
GM03887
 
Resource Report
Resource Website
Coriell Cat# GM03887, RRID:CVCL_X113 Homo sapiens (Human) PMID:6617268
PMID:6661932
PMID:23665875
Transformed cell line Female GM 3887 Coriell GM03887 CLO:CLO_0016009,
BioSample:SAMN00808593,
Coriell:GM03887,
Wikidata:Q54838301
CVCL_X113 Cellosaurus 2026-10-10 05:26:07 0
GM03883
 
Resource Report
Resource Website
Coriell Cat# GM03883, RRID:CVCL_X112 Homo sapiens (Human) Karyotypic information: 46,XX,inv(5)(q15;q33)pat.arr(1-22,X)x2 (Coriell=GM03883)., Population: Caucasian. PMID:6617268
PMID:23665875
Finite cell line Female GM 3883 Coriell GM03883 CLO:CLO_0016013,
BioSample:SAMN00808590,
Coriell:GM03883,
Wikidata:Q54838298
CVCL_X112 Cellosaurus 2026-10-10 05:26:07 0
GM03883
 
Resource Report
Resource Website
RRID:CVCL_X112 Homo sapiens (Human) Karyotypic information: 46,XX,inv(5)(q15;q33)pat.arr(1-22,X)x2 (Coriell=GM03883)., Population: Caucasian. PMID:6617268
PMID:23665875
Finite cell line Female GM 3883 CLO:CLO_0016013,
BioSample:SAMN00808590,
Coriell:GM03883,
Wikidata:Q54838298
CVCL_X112 Cellosaurus 2026-10-10 05:26:07 0
GM03884
 
Resource Report
Resource Website
Coriell Cat# GM03884, RRID:CVCL_1N62 Homo sapiens (Human) Klippel-Feil syndrome Karyotypic information: 46,X,t(X;16)(q26;q24) (PubMed=10377420)., Population: Caucasian. PMID:2498246
PMID:3495225
PMID:10377420
PMID:23665875
Finite cell line Female GM 3884, GM3884 Coriell GM03884 CLO:CLO_0016011,
BioSample:SAMN00808591,
Coriell:GM03884,
Wikidata:Q54838299
CVCL_1N62 Cellosaurus 2026-10-10 05:26:07 0
GM03912
 
Resource Report
Resource Website
RRID:CVCL_X114 Homo sapiens (Human) Cri du chat syndrome PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Male GM 3912 CLO:CLO_0016130,
Coriell:GM03912,
Wikidata:Q54838319
CVCL_X114 Cellosaurus 2026-10-10 05:26:08 0
GM03923
 
Resource Report
Resource Website
RRID:CVCL_X116 Homo sapiens (Human) Karyotypic information: 46,X,del(X)(q13;q22) (PubMed=10377420)., Population: Caucasian; English. PMID:6617268
PMID:6661932
PMID:10377420
PMID:23665875
Finite cell line Female GM 3923, GM3923 CLO:CLO_0016127,
Coriell:GM03923,
Wikidata:Q54838327
CVCL_X116 Cellosaurus 2026-10-10 05:26:08 0
GM04100
 
Resource Report
Resource Website
RRID:CVCL_5M90 Homo sapiens (Human) Duchenne muscular dystrophy Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:6726265
PMID:21354051
PMID:23665875
Transformed cell line Male RB 4100 CLO:CLO_0016212,
Coriell:GM04100,
Wikidata:Q54838387
CVCL_5M90 Cellosaurus 2026-10-10 05:26:09 0
GM03997
 
Resource Report
Resource Website
Coriell Cat# GM03997, RRID:CVCL_5M88 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM03997 CLO:CLO_0016075,
Coriell:GM03997,
Wikidata:Q54838363
CVCL_5M88 Cellosaurus 2026-10-10 05:26:09 0
GM03999
 
Resource Report
Resource Website
Coriell Cat# GM03999, RRID:CVCL_X117 Homo sapiens (Human) Population: African American. PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Female GM 3999 Coriell GM03999 CLO:CLO_0016070,
Coriell:GM03999,
Wikidata:Q54838365
CVCL_X117 Cellosaurus 2026-10-10 05:26:09 0
GM04127
 
Resource Report
Resource Website
RRID:CVCL_X303 Homo sapiens (Human) Population: African American. PMID:6661932
PMID:23665875
Finite cell line Female GM 4127 CLO:CLO_0016194,
Coriell:GM04127,
Wikidata:Q54838393
CVCL_X303 Cellosaurus 2026-10-10 05:26:10 0
GM04250
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# AG04250, RRID:CVCL_N015 Homo sapiens (Human) Sporadic retinoblastoma Population: Japanese., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:20889555
PMID:23665875
PMID:29959025
Finite cell line Female GM17052, AG04250, AG4250, RB9T Coriell AG04250 CLO:CLO_0014647,
CLO:CLO_0019479,
Coriell:AG04250,
Coriell:GM04250,
Coriell:GM17052,
JCRB:KURB2685,
Wikidata:Q54838453
CVCL_N015 Cellosaurus 2026-10-10 05:26:11 0

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