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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 Authority Record Last Update Mentions Count
GM23857
 
Resource Report
Resource Website
RRID:CVCL_U552 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Male Coriell:GM23857,
Wikidata:Q54853380
CVCL_U552 Cellosaurus 2026-10-17 06:19:33 0
GM23854
 
Resource Report
Resource Website
RRID:CVCL_5T23 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM23854,
Wikidata:Q54853378
CVCL_5T23 Cellosaurus 2026-10-17 06:19:33 0
GM23832
 
Resource Report
Resource Website
Coriell Cat# GM23832, RRID:CVCL_U550 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Female Coriell GM23832 Coriell:GM23832,
Wikidata:Q54853361
CVCL_U550 Cellosaurus 2026-10-17 06:19:33 0
GM23873
 
Resource Report
Resource Website
Coriell Cat# GM23873, RRID:CVCL_5T25 Homo sapiens (Human) PMID:23665875
PMID:26621101
PMID:29474986
Transformed cell line Female Coriell GM23873 Coriell:GM23873,
Wikidata:Q54853409
CVCL_5T25 Cellosaurus 2026-10-17 06:19:33 0
GM23862
 
Resource Report
Resource Website
RRID:CVCL_U553 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Female Coriell:GM23862,
Wikidata:Q54853384
CVCL_U553 Cellosaurus 2026-10-17 06:19:33 0
GM23922
 
Resource Report
Resource Website
RRID:CVCL_5T38 Homo sapiens (Human) Hyperglycerolemia PMID:23665875 Transformed cell line Male Coriell:GM23922,
Wikidata:Q54853442
CVCL_5T38 Cellosaurus 2026-10-17 06:19:34 0
GM23905
 
Resource Report
Resource Website
Coriell Cat# GM23905, RRID:CVCL_5T32 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM23905 Coriell:GM23905,
Wikidata:Q54853431
CVCL_5T32 Cellosaurus 2026-10-17 06:19:34 0
GM23906
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_5T33 Homo sapiens (Human) Hyperglycerolemia PMID:23665875 Transformed cell line Male Coriell:GM23906,
Wikidata:Q54853432
CVCL_5T33 Cellosaurus 2026-10-17 06:19:34 0
GM23900
 
Resource Report
Resource Website
Coriell Cat# GM23900, RRID:CVCL_5T30 Homo sapiens (Human) Turner syndrome PMID:23665875 Transformed cell line Female Coriell GM23900 Coriell:GM23900,
Wikidata:Q54853429
CVCL_5T30 Cellosaurus 2026-10-17 06:19:34 0
GM23905
 
Resource Report
Resource Website
RRID:CVCL_5T32 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell:GM23905,
Wikidata:Q54853431
CVCL_5T32 Cellosaurus 2026-10-17 06:19:34 0
GM23908
 
Resource Report
Resource Website
RRID:CVCL_5T35 Homo sapiens (Human) Congenital adrenal gland hypoplasia PMID:23665875 Transformed cell line Male Coriell:GM23908,
Wikidata:Q54853434
CVCL_5T35 Cellosaurus 2026-10-17 06:19:34 0
GM23904
 
Resource Report
Resource Website
RRID:CVCL_5T31 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM23904,
Wikidata:Q54853430
CVCL_5T31 Cellosaurus 2026-10-17 06:19:34 0
GM23922
 
Resource Report
Resource Website
Coriell Cat# GM23922, RRID:CVCL_5T38 Homo sapiens (Human) Hyperglycerolemia PMID:23665875 Transformed cell line Male Coriell GM23922 Coriell:GM23922,
Wikidata:Q54853442
CVCL_5T38 Cellosaurus 2026-10-17 06:19:34 0
GM23904
 
Resource Report
Resource Website
Coriell Cat# GM23904, RRID:CVCL_5T31 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM23904 Coriell:GM23904,
Wikidata:Q54853430
CVCL_5T31 Cellosaurus 2026-10-17 06:19:34 0
GM06979
 
Resource Report
Resource Website
Coriell Cat# GM06979, 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 Coriell GM06979 CLO:CLO_0036450,
Coriell:GM06979,
Wikidata:Q54842419
CVCL_5N54 Cellosaurus 2026-10-17 06:14:54 0
GM06960
 
Resource Report
Resource Website
Coriell Cat# GM06960, 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 Coriell GM06960 CLO:CLO_0036461,
Coriell:GM06960,
Wikidata:Q54842405
CVCL_5N53 Cellosaurus 2026-10-17 06:14:53 0
GM07151
 
Resource Report
Resource Website
RRID:CVCL_X048 Homo sapiens (Human) Tetralogy of Fallot Karyotypic information: 46,X,t(X;17)(p11.2;p11.2).arr(1-22,X)x2 (Coriell=GM07151)., Population: Caucasian. PMID:2498246
PMID:23665875
Finite cell line Female GM7151 CLO:CLO_0036891,
Coriell:GM07151,
Wikidata:Q54842547
CVCL_X048 Cellosaurus 2026-10-17 06:14:58 0
GM07212
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_5N58 Homo sapiens (Human) PMID:23665875 Finite cell line Female Coriell:GM07212,
Wikidata:Q54842579
CVCL_5N58 Cellosaurus 2026-10-17 06:14:58 0
GM07212
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM07212, RRID:CVCL_5N58 Homo sapiens (Human) PMID:23665875 Finite cell line Female Coriell GM07212 Coriell:GM07212,
Wikidata:Q54842579
CVCL_5N58 Cellosaurus 2026-10-17 06:14:58 0
GM07106
 
Resource Report
Resource Website
RRID:CVCL_5N55 Homo sapiens (Human) PMID:23665875 Finite cell line Male CLO:CLO_0036812,
Coriell:GM07106,
Wikidata:Q54842537
CVCL_5N55 Cellosaurus 2026-10-17 06:14:57 0

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