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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
GM13556
 
Resource Report
Resource Website
Coriell Cat# GM13556, RRID:CVCL_U539 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Female Coriell GM13556 CLO:CLO_0012477,
BioSample:SAMN00802476,
Coriell:GM13556,
Wikidata:Q54846634
CVCL_U539 2026-09-19 05:30:09 0
GM13555
 
Resource Report
Resource Website
RRID:CVCL_U538 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Male CLO:CLO_0012476,
BioSample:SAMN00802474,
Coriell:GM13555,
Wikidata:Q54846633
CVCL_U538 2026-09-19 05:30:09 0
GM13685
 
Resource Report
Resource Website
RRID:CVCL_2U29 Homo sapiens (Human) PMID:23665875 Transformed cell line Female CLO:CLO_0032757,
BioSample:SAMN00802528,
Coriell:GM13685,
Wikidata:Q54846713
CVCL_2U29 2026-09-19 05:30:11 0
GM13688
 
Resource Report
Resource Website
RRID:CVCL_2U32 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0032752,
BioSample:SAMN00802534,
Coriell:GM13688,
Wikidata:Q54846717
CVCL_2U32 2026-09-19 05:30:11 0
GM13685
 
Resource Report
Resource Website
Coriell Cat# GM13685, RRID:CVCL_2U29 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM13685 CLO:CLO_0032757,
BioSample:SAMN00802528,
Coriell:GM13685,
Wikidata:Q54846713
CVCL_2U29 2026-09-19 05:30:11 0
GM13687
 
Resource Report
Resource Website
Coriell Cat# GM13687, RRID:CVCL_2U31 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM13687 CLO:CLO_0032755,
BioSample:SAMN00802532,
Coriell:GM13687,
Wikidata:Q54846715
CVCL_2U31 2026-09-19 05:30:11 0
GM13687
 
Resource Report
Resource Website
RRID:CVCL_2U31 Homo sapiens (Human) PMID:23665875 Transformed cell line Female CLO:CLO_0032755,
BioSample:SAMN00802532,
Coriell:GM13687,
Wikidata:Q54846715
CVCL_2U31 2026-09-19 05:30:11 0
GM13721
 
Resource Report
Resource Website
RRID:CVCL_5Q10 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0032797,
BioSample:SAMN00802574,
Coriell:GM13721,
Wikidata:Q54846751
CVCL_5Q10 2026-09-19 05:30:12 0
GM13734
 
Resource Report
Resource Website
RRID:CVCL_2U36 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0032764,
BioSample:SAMN00802582,
Coriell:GM13734,
Wikidata:Q54846767
CVCL_2U36 2026-09-19 05:30:12 0
GM13733
 
Resource Report
Resource Website
Coriell Cat# GM13733, RRID:CVCL_2U35 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM13733 CLO:CLO_0032762,
BioSample:SAMN00802580,
Coriell:GM13733,
Wikidata:Q54846754
CVCL_2U35 2026-09-19 05:30:12 0
GM13733
 
Resource Report
Resource Website
RRID:CVCL_2U35 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0032762,
BioSample:SAMN00802580,
Coriell:GM13733,
Wikidata:Q54846754
CVCL_2U35 2026-09-19 05:30:12 0
GM13744
 
Resource Report
Resource Website
Coriell Cat# GM13744, RRID:CVCL_2U38 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM13744 CLO:CLO_0032776,
BioSample:SAMN00802590,
Coriell:GM13744,
Wikidata:Q54846771
CVCL_2U38 2026-09-19 05:30:12 0
GM11957
 
Resource Report
Resource Website
Coriell Cat# GM11957, RRID:CVCL_5L13 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female Coriell GM11957 CLO:CLO_0020109,
Coriell:GM11957,
Wikidata:Q54845389
CVCL_5L13 2026-09-19 05:29:35 0
GM11949
 
Resource Report
Resource Website
RRID:CVCL_5P61 Homo sapiens (Human) PMID:23665875 Transformed cell line Female CLO:CLO_0020203,
Coriell:GM11949,
Wikidata:Q54845381
CVCL_5P61 2026-09-19 05:29:35 0
GM11962
 
Resource Report
Resource Website
RRID:CVCL_2U17 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0020110,
Coriell:GM11962,
Wikidata:Q54845394
CVCL_2U17 2026-09-19 05:29:35 0
GM11957
 
Resource Report
Resource Website
RRID:CVCL_5L13 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0020109,
Coriell:GM11957,
Wikidata:Q54845389
CVCL_5L13 2026-09-19 05:29:35 0
GM11964
 
Resource Report
Resource Website
RRID:CVCL_5L17 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male CLO:CLO_0020539,
Coriell:GM11964,
Wikidata:Q54845397
CVCL_5L17 2026-09-19 05:29:35 0
GM11954
 
Resource Report
Resource Website
RRID:CVCL_5L11 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0020123,
Coriell:GM11954,
Wikidata:Q54845387
CVCL_5L11 2026-09-19 05:29:35 0
GM11965
 
Resource Report
Resource Website
Coriell Cat# GM11965, RRID:CVCL_5L18 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male Coriell GM11965 CLO:CLO_0020544,
Coriell:GM11965,
Wikidata:Q54845398
CVCL_5L18 2026-09-19 05:29:35 0
GM11951
 
Resource Report
Resource Website
RRID:CVCL_5L08 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0020208,
Coriell:GM11951,
Wikidata:Q54845383
CVCL_5L08 2026-09-19 05:29:35 0

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