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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
GM18331
 
Resource Report
Resource Website
RRID:CVCL_5Q87 Homo sapiens (Human) Azoospermia PMID:23665875 Transformed cell line Male CLO:CLO_0031063,
Coriell:GM18331,
Wikidata:Q54849499
CVCL_5Q87 Cellosaurus 2026-10-17 06:17:55 0
GM18324
 
Resource Report
Resource Website
RRID:CVCL_5K17 Homo sapiens (Human) Smith-Magenis syndrome PMID:23665875 Transformed cell line Male CLO:CLO_0031074,
Coriell:GM18324,
Wikidata:Q54849496
CVCL_5K17 Cellosaurus 2026-10-17 06:17:54 0
GM18326
 
Resource Report
Resource Website
Coriell Cat# GM18326, RRID:CVCL_5K19 Homo sapiens (Human) Smith-Magenis syndrome PMID:23665875 Transformed cell line Male Coriell GM18326 CLO:CLO_0031064,
Coriell:GM18326,
Wikidata:Q54849498
CVCL_5K19 Cellosaurus 2026-10-17 06:17:55 0
GM18311
 
Resource Report
Resource Website
RRID:CVCL_5Q86 Homo sapiens (Human) Holoprosencephaly PMID:23665875 Transformed cell line Female CLO:CLO_0031073,
Coriell:GM18311,
Wikidata:Q54849489
CVCL_5Q86 Cellosaurus 2026-10-17 06:17:54 0
GM18332
 
Resource Report
Resource Website
Coriell Cat# GM18332, RRID:CVCL_5Q88 Homo sapiens (Human) Azoospermia PMID:23665875 Transformed cell line Male Coriell GM18332 CLO:CLO_0031062,
Coriell:GM18332,
Wikidata:Q54849500
CVCL_5Q88 Cellosaurus 2026-10-17 06:17:55 0
GM18337
 
Resource Report
Resource Website
RRID:CVCL_5Q93 Homo sapiens (Human) Azoospermia PMID:23665875 Transformed cell line Male CLO:CLO_0031067,
Coriell:GM18337,
Wikidata:Q54849505
CVCL_5Q93 Cellosaurus 2026-10-17 06:17:55 0
GM18378
 
Resource Report
Resource Website
RRID:CVCL_5Q97 Homo sapiens (Human) Holoprosencephaly PMID:23665875 Transformed cell line Female Coriell:GM18378,
Wikidata:Q54849517
CVCL_5Q97 Cellosaurus 2026-10-17 06:17:55 0
GM18381
 
Resource Report
Resource Website
Coriell Cat# GM18381, RRID:CVCL_5Q99 Homo sapiens (Human) Pseudotrisomy 13 syndrome PMID:23665875 Transformed cell line Male Coriell GM18381 CLO:CLO_0031096,
Coriell:GM18381,
Wikidata:Q54849519
CVCL_5Q99 Cellosaurus 2026-10-17 06:17:55 0
GM18826
 
Resource Report
Resource Website
Coriell Cat# GM18826, RRID:CVCL_2U52 Homo sapiens (Human) Developmental delay Population: Caucasian. PMID:23665875 Transformed cell line Female Coriell GM18826 CLO:CLO_0026218,
Coriell:GM18826,
Wikidata:Q54849860
CVCL_2U52 Cellosaurus 2026-10-17 06:18:04 0
GM18828
 
Resource Report
Resource Website
RRID:CVCL_2U54 Homo sapiens (Human) Developmental delay Population: Caucasian. PMID:23665875 Transformed cell line Male CLO:CLO_0026216,
Coriell:GM18828,
Wikidata:Q54849862
CVCL_2U54 Cellosaurus 2026-10-17 06:18:04 0
GM18825
 
Resource Report
Resource Website
Coriell Cat# GM18825, RRID:CVCL_2U51 Homo sapiens (Human) Developmental delay Population: Caucasian. PMID:23665875 Transformed cell line Female Coriell GM18825 CLO:CLO_0026217,
Coriell:GM18825,
Wikidata:Q54849859
CVCL_2U51 Cellosaurus 2026-10-17 06:18:04 0
GM18827
 
Resource Report
Resource Website
RRID:CVCL_2U53 Homo sapiens (Human) Developmental delay Population: Caucasian. PMID:23665875 Transformed cell line Female CLO:CLO_0026215,
Coriell:GM18827,
Wikidata:Q54849861
CVCL_2U53 Cellosaurus 2026-10-17 06:18:04 0
GM18827
 
Resource Report
Resource Website
Coriell Cat# GM18827, RRID:CVCL_2U53 Homo sapiens (Human) Developmental delay Population: Caucasian. PMID:23665875 Transformed cell line Female Coriell GM18827 CLO:CLO_0026215,
Coriell:GM18827,
Wikidata:Q54849861
CVCL_2U53 Cellosaurus 2026-10-17 06:18:04 0
GM21715
 
Resource Report
Resource Website
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,
Wikidata:Q54852090
CVCL_5R37 Cellosaurus 2026-10-17 06:19:03 0
GM21699
 
Resource Report
Resource Website
Coriell Cat# GM21699, RRID:CVCL_4J61 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM21699 CLO:CLO_0014010,
Coriell:GM21699,
Wikidata:Q54852089
CVCL_4J61 Cellosaurus 2026-10-17 06:19:03 0
GM21889
 
Resource Report
Resource Website
RRID:CVCL_U542 Homo sapiens (Human) Prader-Willi syndrome Population: African American. PMID:23665875
PMID:24816254
Finite cell line Male Coriell:GM21889,
Wikidata:Q54852210
CVCL_U542 Cellosaurus 2026-10-17 06:19:07 0
GM21893
 
Resource Report
Resource Website
Coriell Cat# GM21893, RRID:CVCL_5R48 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM21893 Coriell:GM21893,
Wikidata:Q54852214
CVCL_5R48 Cellosaurus 2026-10-17 06:19:07 0
GM21878
 
Resource Report
Resource Website
RRID:CVCL_5R41 Homo sapiens (Human) PMID:23665875 Finite cell line Female Coriell:GM21878,
Wikidata:Q54852196
CVCL_5R41 Cellosaurus 2026-10-17 06:19:06 0
GM21890
 
Resource Report
Resource Website
Coriell Cat# GM21890, RRID:CVCL_U543 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Finite cell line Male Coriell GM21890 Coriell:GM21890,
Wikidata:Q54852211
CVCL_U543 Cellosaurus 2026-10-17 06:19:07 0
GM21877
 
Resource Report
Resource Website
RRID:CVCL_F109 Homo sapiens (Human) PMID:23665875 Finite cell line Female Coriell:GM21877,
Wikidata:Q54852195
CVCL_F109 Cellosaurus 2026-10-17 06:19:06 0

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