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  • References:pmid:23665875 (facet)

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1,669 Results - per page

Show More Columns | Download Top 1000 Results

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
GM03035
 
Resource Report
Resource Website
RRID:CVCL_X429 Homo sapiens (Human) X-linked ichthyosis Population: Caucasian; Sardinian. PMID:23665875 Finite cell line Male CLO:CLO_0012617,
BioSample:SAMN00808218,
Coriell:GM03035,
Wikidata:Q54837828
CVCL_X429 2026-09-12 05:32:22 0
GM03089
 
Resource Report
Resource Website
RRID:CVCL_X279 Homo sapiens (Human) Population: Puerto Rican. PMID:6661932
PMID:23665875
Finite cell line Female GM 3089 CLO:CLO_0013495,
BioSample:SAMN00808245,
Coriell:GM03089,
Wikidata:Q54837863
CVCL_X279 2026-09-12 05:32:22 0
GM03047
 
Resource Report
Resource Website
RRID:CVCL_X101 Homo sapiens (Human) Population: Caucasian. PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Male GM 3047 CLO:CLO_0013502,
BioSample:SAMN00808225,
Coriell:GM03047,
Wikidata:Q54837837
CVCL_X101 2026-09-12 05:32:22 0
GM03047
 
Resource Report
Resource Website
Coriell Cat# GM03047, RRID:CVCL_X101 Homo sapiens (Human) Population: Caucasian. PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Male GM 3047 Coriell GM03047 CLO:CLO_0013502,
BioSample:SAMN00808225,
Coriell:GM03047,
Wikidata:Q54837837
CVCL_X101 2026-09-12 05:32:22 0
GM03090
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_H187 Homo sapiens (Human) PMID:23665875 Finite cell line Female CLO:CLO_0013496,
BioSample:SAMN00808246,
Coriell:GM03090,
Wikidata:Q54837864
CVCL_H187 2026-09-12 05:32:22 0
GM06960
 
Resource Report
Resource Website
RRID:CVCL_5N53 Homo sapiens (Human) Karyotypic information: 46,X,i(X)(q22) (PubMed=10377420)., Population: African American. PMID:10377420
PMID:23665875
Finite cell line Female GM6960 CLO:CLO_0036461,
Coriell:GM06960,
Wikidata:Q54842405
CVCL_5N53 2026-09-12 05:33:12 0
GM06979
 
Resource Report
Resource Website
RRID:CVCL_5N54 Homo sapiens (Human) Karyotypic information: 92,XXYY.arr(1-22)x2,(XY)x1 (Coriell=GM06979)., Population: Caucasian. PMID:23665875 Finite cell line Male CLO:CLO_0036450,
Coriell:GM06979,
Wikidata:Q54842419
CVCL_5N54 2026-09-12 05:33:12 0
GM07158
 
Resource Report
Resource Website
Coriell Cat# GM07158, RRID:CVCL_0L58 Homo sapiens (Human) Intellectual developmental disorder PMID:23665875 Transformed cell line Male Coriell GM07158 CLO:CLO_0036896,
Coriell:GM07158,
Wikidata:Q54842560
CVCL_0L58 2026-09-12 05:33:16 0
GM07148
 
Resource Report
Resource Website
Coriell Cat# GM07148, RRID:CVCL_5N56 Homo sapiens (Human) Population: Native North American. PMID:23665875 Finite cell line Female Coriell GM07148 CLO:CLO_0036817,
Coriell:GM07148,
Wikidata:Q54842544
CVCL_5N56 2026-09-12 05:33:15 0
GM07213
 
Resource Report
Resource Website
RRID:CVCL_F610 Homo sapiens (Human) Karyotypic information: 46,X,i(X)(q28) (PubMed=10377420)., Population: African American. PMID:10377420
PMID:23665875
Finite cell line Female GM7213 CLO:CLO_0036924,
Coriell:GM07213,
Wikidata:Q54842580
CVCL_F610 2026-09-12 05:33:16 0
GM07150
 
Resource Report
Resource Website
Coriell Cat# GM07150, RRID:CVCL_2T29 Homo sapiens (Human) PMID:23665875 Finite cell line Female Coriell GM07150 CLO:CLO_0036885,
Coriell:GM07150,
Wikidata:Q54842546
CVCL_2T29 2026-09-12 05:33:15 0
GM07158
 
Resource Report
Resource Website
RRID:CVCL_0L58 Homo sapiens (Human) Intellectual developmental disorder PMID:23665875 Transformed cell line Male CLO:CLO_0036896,
Coriell:GM07158,
Wikidata:Q54842560
CVCL_0L58 2026-09-12 05:33:16 0
GM07213
 
Resource Report
Resource Website
Coriell Cat# GM07213, RRID:CVCL_F610 Homo sapiens (Human) Karyotypic information: 46,X,i(X)(q28) (PubMed=10377420)., Population: African American. PMID:10377420
PMID:23665875
Finite cell line Female GM7213 Coriell GM07213 CLO:CLO_0036924,
Coriell:GM07213,
Wikidata:Q54842580
CVCL_F610 2026-09-12 05:33:16 0
GM07148
 
Resource Report
Resource Website
RRID:CVCL_5N56 Homo sapiens (Human) Population: Native North American. PMID:23665875 Finite cell line Female CLO:CLO_0036817,
Coriell:GM07148,
Wikidata:Q54842544
CVCL_5N56 2026-09-12 05:33:15 0
GM07106
 
Resource Report
Resource Website
Coriell Cat# GM07106, RRID:CVCL_5N55 Homo sapiens (Human) PMID:23665875 Finite cell line Male Coriell GM07106 CLO:CLO_0036812,
Coriell:GM07106,
Wikidata:Q54842537
CVCL_5N55 2026-09-12 05:33:15 0
GM07215
 
Resource Report
Resource Website
Coriell Cat# GM07215, RRID:CVCL_2Y98 Homo sapiens (Human) 22q11.2 deletion syndrome Population: Caucasian. PMID:23665875 Finite cell line Female Coriell GM07215 CLO:CLO_0036922,
Coriell:GM07215,
Wikidata:Q54842582
CVCL_2Y98 2026-09-12 05:33:16 0
GM07216
 
Resource Report
Resource Website
Coriell Cat# GM07216, RRID:CVCL_5N59 Homo sapiens (Human) Holoprosencephaly Population: Caucasian. PMID:23665875 Finite cell line Female Coriell GM07216 CLO:CLO_0036923,
Coriell:GM07216,
Wikidata:Q54842583
CVCL_5N59 2026-09-12 05:33:16 0
GM07364
 
Resource Report
Resource Website
Coriell Cat# GM07364, RRID:CVCL_4D92 Homo sapiens (Human) Ring chromosome 14 syndrome Population: Caucasian. PMID:23665875 Finite cell line Male Coriell GM07364 CLO:CLO_0016948,
Coriell:GM07364,
Wikidata:Q54842689
CVCL_4D92 2026-09-12 05:33:19 0
GM07312
 
Resource Report
Resource Website
Coriell Cat# GM07312, RRID:CVCL_X141 Homo sapiens (Human) Sporadic retinoblastoma PMID:23665875 Transformed cell line Female GM7312, GM07312A Coriell GM07312 CLO:CLO_0035947,
Coriell:GM07312,
Wikidata:Q54842645
CVCL_X141 2026-09-12 05:33:18 0
GM07323
 
Resource Report
Resource Website
RRID:CVCL_5N60 Homo sapiens (Human) PMID:23665875 Transformed cell line Female CLO:CLO_0035939,
Coriell:GM07323,
Wikidata:Q54842656
CVCL_5N60 2026-09-12 05:33:18 0

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