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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
GM23125
 
Resource Report
Resource Website
Coriell Cat# GM23125, RRID:CVCL_5S75 Homo sapiens (Human) Autism spectrum disorder PMID:23495136
PMID:23665875
Transformed cell line Female 801-011 LCL Coriell GM23125 Coriell:GM23125,
Wikidata:Q54852899
CVCL_5S75 Cellosaurus 2026-09-26 06:53:17 0
GM23270
 
Resource Report
Resource Website
RRID:CVCL_5S86 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell:GM23270,
Wikidata:Q54852957
CVCL_5S86 Cellosaurus 2026-09-26 06:53:18 0
GM23264
 
Resource Report
Resource Website
Coriell Cat# GM23264, RRID:CVCL_5S85 Homo sapiens (Human) Chromosome 15q11-q13 duplication syndrome PMID:23495136
PMID:23665875
Transformed cell line Female 801-015 LCL Coriell GM23264 Coriell:GM23264,
Wikidata:Q54852947
CVCL_5S85 Cellosaurus 2026-09-26 06:53:18 0
GM23226
 
Resource Report
Resource Website
Coriell Cat# GM23226, RRID:CVCL_F170 Homo sapiens (Human) Type 1 diabetes mellitus Population: Native North American; Alaskan. PMID:23665875 Induced pluripotent stem cell Female GM23226*A Coriell GM23226 Coriell:GM23226,
SKIP:SKIP000182,
SKIP:SKIP004346,
Wikidata:Q54852921
cvcl_8518 CVCL_F170 Cellosaurus 2026-09-26 06:53:17 0
GM23354
 
Resource Report
Resource Website
RRID:CVCL_HK74 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Male Coriell:GM23354,
Wikidata:Q54853016
CVCL_HK74 Cellosaurus 2026-09-26 06:53:19 0
GM23302
 
Resource Report
Resource Website
Coriell Cat# GM23302, RRID:CVCL_5S87 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM23302 Coriell:GM23302,
Wikidata:Q54852981
CVCL_5S87 Cellosaurus 2026-09-26 06:53:18 0
GM23336
 
Resource Report
Resource Website
Coriell Cat# GM23336, RRID:CVCL_U546 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Female Coriell GM23336 Coriell:GM23336,
Wikidata:Q54853009
CVCL_U546 Cellosaurus 2026-09-26 06:53:19 0
GM23337
 
Resource Report
Resource Website
RRID:CVCL_BV43 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Male Coriell:GM23337,
Wikidata:Q54853010
CVCL_BV43 Cellosaurus 2026-09-26 06:53:19 0
GM23433
 
Resource Report
Resource Website
RRID:CVCL_5S89 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell:GM23433,
Wikidata:Q54853076
CVCL_5S89 Cellosaurus 2026-09-26 06:53:20 0
GM23425
 
Resource Report
Resource Website
Coriell Cat# GM23425, RRID:CVCL_U548 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Male Coriell GM23425 Coriell:GM23425,
Wikidata:Q54853068
CVCL_U548 Cellosaurus 2026-09-26 06:53:20 0
GM23432
 
Resource Report
Resource Website
RRID:CVCL_5S88 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM23432,
Wikidata:Q54853075
CVCL_5S88 Cellosaurus 2026-09-26 06:53:20 0
GM23488
 
Resource Report
Resource Website
Coriell Cat# GM23488, RRID:CVCL_5S90 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM23488 Coriell:GM23488,
Wikidata:Q54853108
CVCL_5S90 Cellosaurus 2026-09-26 06:53:21 0
GM23425
 
Resource Report
Resource Website
RRID:CVCL_U548 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Male Coriell:GM23425,
Wikidata:Q54853068
CVCL_U548 Cellosaurus 2026-09-26 06:53:20 0
GM23488
 
Resource Report
Resource Website
RRID:CVCL_5S90 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell:GM23488,
Wikidata:Q54853108
CVCL_5S90 Cellosaurus 2026-09-26 06:53:21 0
GM23432
 
Resource Report
Resource Website
Coriell Cat# GM23432, RRID:CVCL_5S88 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM23432 Coriell:GM23432,
Wikidata:Q54853075
CVCL_5S88 Cellosaurus 2026-09-26 06:53:20 0
GM23433
 
Resource Report
Resource Website
Coriell Cat# GM23433, RRID:CVCL_5S89 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM23433 Coriell:GM23433,
Wikidata:Q54853076
CVCL_5S89 Cellosaurus 2026-09-26 06:53:20 0
GM23493
 
Resource Report
Resource Website
Coriell Cat# GM23493, RRID:CVCL_5S93 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM23493 Coriell:GM23493,
Wikidata:Q54853113
CVCL_5S93 Cellosaurus 2026-09-26 06:53:21 0
GM23492
 
Resource Report
Resource Website
RRID:CVCL_5S92 Homo sapiens (Human) Autism spectrum disorder PMID:23495136
PMID:23665875
Transformed cell line Male 801-018 LCL Coriell:GM23492,
Wikidata:Q54853112
CVCL_5S92 Cellosaurus 2026-09-26 06:53:21 0
GM23504
 
Resource Report
Resource Website
RRID:CVCL_5S95 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell:GM23504,
Wikidata:Q54853125
CVCL_5S95 Cellosaurus 2026-09-26 06:53:21 0
GM23492
 
Resource Report
Resource Website
Coriell Cat# GM23492, RRID:CVCL_5S92 Homo sapiens (Human) Autism spectrum disorder PMID:23495136
PMID:23665875
Transformed cell line Male 801-018 LCL Coriell GM23492 Coriell:GM23492,
Wikidata:Q54853112
CVCL_5S92 Cellosaurus 2026-09-26 06:53:21 0

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