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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
GM20201
 
Resource Report
Resource Website
RRID:CVCL_5R05 Homo sapiens (Human) Autism spectrum disorder PMID:23665875 Transformed cell line Female CLO:CLO_0027994,
Coriell:GM20201,
Wikidata:Q54850842
CVCL_5R05 Cellosaurus 2026-10-17 06:18:30 0
GM20027
 
Resource Report
Resource Website
Coriell Cat# GM20027, RRID:CVCL_2N06 Homo sapiens (Human) Turner syndrome PMID:23665875 Transformed cell line Female Coriell GM20027 CLO:CLO_0028353,
Coriell:GM20027,
Wikidata:Q54850785
CVCL_2N06 Cellosaurus 2026-10-17 06:18:29 0
GM20200
 
Resource Report
Resource Website
RRID:CVCL_5R04 Homo sapiens (Human) Isodicentric chromosome PMID:23665875 Transformed cell line Male CLO:CLO_0027992,
Coriell:GM20200,
Wikidata:Q54850841
CVCL_5R04 Cellosaurus 2026-10-17 06:18:30 0
GM20311
 
Resource Report
Resource Website
RRID:CVCL_2U60 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0027880,
Coriell:GM20311,
Wikidata:Q54850914
CVCL_2U60 Cellosaurus 2026-10-17 06:18:32 0
GM20305
 
Resource Report
Resource Website
RRID:CVCL_5R08 Homo sapiens (Human) PMID:23665875 Transformed cell line Female CLO:CLO_0027886,
Coriell:GM20305,
Wikidata:Q54850911
CVCL_5R08 Cellosaurus 2026-10-17 06:18:32 0
GM20409
 
Resource Report
Resource Website
RRID:CVCL_5R11 Homo sapiens (Human) Angelman syndrome PMID:23665875 Transformed cell line Male CLO:CLO_0029516,
Coriell:GM20409,
Wikidata:Q54851011
CVCL_5R11 Cellosaurus 2026-10-17 06:18:34 0
GM20375
 
Resource Report
Resource Website
RRID:CVCL_5R10 Homo sapiens (Human) Angelman syndrome PMID:23665875 Transformed cell line Male CLO:CLO_0029626,
Coriell:GM20375,
Wikidata:Q54850986
CVCL_5R10 Cellosaurus 2026-10-17 06:18:34 0
GM20375
 
Resource Report
Resource Website
Coriell Cat# GM20375, RRID:CVCL_5R10 Homo sapiens (Human) Angelman syndrome PMID:23665875 Transformed cell line Male Coriell GM20375 CLO:CLO_0029626,
Coriell:GM20375,
Wikidata:Q54850986
CVCL_5R10 Cellosaurus 2026-10-17 06:18:34 0
GM20366
 
Resource Report
Resource Website
RRID:CVCL_5R09 Homo sapiens (Human) Isodicentric chromosome PMID:23665875 Transformed cell line Male CLO:CLO_0029625,
Coriell:GM20366,
Wikidata:Q54850985
CVCL_5R09 Cellosaurus 2026-10-17 06:18:34 0
GM20408
 
Resource Report
Resource Website
RRID:CVCL_U541 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0029517,
Coriell:GM20408,
Wikidata:Q54851010
CVCL_U541 Cellosaurus 2026-10-17 06:18:34 0
GM21681
 
Resource Report
Resource Website
RRID:CVCL_5R35 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM21681,
Wikidata:Q54852080
CVCL_5R35 Cellosaurus 2026-10-17 06:19:03 0
GM21729
 
Resource Report
Resource Website
RRID:CVCL_5R38 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM21729,
Wikidata:Q54852104
CVCL_5R38 Cellosaurus 2026-10-17 06:19:04 0
GM21729
 
Resource Report
Resource Website
Coriell Cat# GM21729, RRID:CVCL_5R38 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM21729 Coriell:GM21729,
Wikidata:Q54852104
CVCL_5R38 Cellosaurus 2026-10-17 06:19:04 0
GM21698
 
Resource Report
Resource Website
Coriell Cat# GM21698, RRID:CVCL_4J60 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM21698 CLO:CLO_0014013,
Coriell:GM21698,
Wikidata:Q54852088
CVCL_4J60 Cellosaurus 2026-10-17 06:19:03 0
GM21715
 
Resource Report
Resource Website
Coriell Cat# GM21715, RRID:CVCL_5R37 Homo sapiens (Human) Autism spectrum disorder Population: African American. PMID:23495136
PMID:23665875
Transformed cell line Male 801-002 LCL Coriell GM21715 Coriell:GM21715,
Wikidata:Q54852090
CVCL_5R37 Cellosaurus 2026-10-17 06:19:03 0
GM21698
 
Resource Report
Resource Website
RRID:CVCL_4J60 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0014013,
Coriell:GM21698,
Wikidata:Q54852088
CVCL_4J60 Cellosaurus 2026-10-17 06:19:03 0
GM21699
 
Resource Report
Resource Website
RRID:CVCL_4J61 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0014010,
Coriell:GM21699,
Wikidata:Q54852089
CVCL_4J61 Cellosaurus 2026-10-17 06:19:03 0
GM21886
 
Resource Report
Resource Website
RRID:CVCL_5R45 Homo sapiens (Human) Supernumerary circular chromosome PMID:23665875 Transformed cell line Male Coriell:GM21886,
Wikidata:Q54852208
CVCL_5R45 Cellosaurus 2026-10-17 06:19:06 0
GM21890
 
Resource Report
Resource Website
RRID:CVCL_U543 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Finite cell line Male Coriell:GM21890,
Wikidata:Q54852211
CVCL_U543 Cellosaurus 2026-10-17 06:19:07 0
GM21889
 
Resource Report
Resource Website
Coriell Cat# GM21889, RRID:CVCL_U542 Homo sapiens (Human) Prader-Willi syndrome Population: African American. PMID:23665875
PMID:24816254
Finite cell line Male Coriell GM21889 Coriell:GM21889,
Wikidata:Q54852210
CVCL_U542 Cellosaurus 2026-10-17 06:19:07 0

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