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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
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 2026-02-14 08:17:57 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 2026-02-14 08:18:00 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 2026-02-14 08:18:00 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 2026-02-14 08:18:00 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 2026-02-14 08:18:00 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 2026-02-14 08:18:00 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 2026-02-14 08:18:00 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 2026-02-14 08:18:00 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 2026-02-14 08:18:00 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 2026-02-14 08:18:00 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 2026-02-14 08:18:01 0
GM13940
 
Resource Report
Resource Website
Coriell Cat# GM13940, RRID:CVCL_5Q16 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM13940 CLO:CLO_0034026,
BioSample:SAMN00802748,
Coriell:GM13940,
Wikidata:Q54846931
CVCL_5Q16 2026-02-14 08:18:05 0
GM13940
 
Resource Report
Resource Website
RRID:CVCL_5Q16 Homo sapiens (Human) PMID:23665875 Transformed cell line Female CLO:CLO_0034026,
BioSample:SAMN00802748,
Coriell:GM13940,
Wikidata:Q54846931
CVCL_5Q16 2026-02-14 08:18:05 0
GM14043
 
Resource Report
Resource Website
RRID:CVCL_5Q32 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM14043,
Wikidata:Q54846998
CVCL_5Q32 2026-02-14 08:18:07 0
GM14033
 
Resource Report
Resource Website
Coriell Cat# GM14033, RRID:CVCL_5Q31 Homo sapiens (Human) Williams syndrome PMID:23665875 Transformed cell line Female Coriell GM14033 CLO:CLO_0033867,
Coriell:GM14033,
Wikidata:Q54846995
CVCL_5Q31 2026-02-14 08:18:07 0
GM14033
 
Resource Report
Resource Website
RRID:CVCL_5Q31 Homo sapiens (Human) Williams syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0033867,
Coriell:GM14033,
Wikidata:Q54846995
CVCL_5Q31 2026-02-14 08:18:07 0
GM14126
 
Resource Report
Resource Website
RRID:CVCL_W002 Homo sapiens (Human) Cri du chat syndrome PMID:8004090
PMID:23665875
Transformed cell line Female JL135 CLO:CLO_0034407,
Coriell:GM14126,
Wikidata:Q54847069
CVCL_W002 2026-02-14 08:18:09 0
GM14116
 
Resource Report
Resource Website
Coriell Cat# GM14116, RRID:CVCL_V992 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Male JL27 Coriell GM14116 CLO:CLO_0034419,
Coriell:GM14116,
Wikidata:Q54847059
CVCL_V992 2026-02-14 08:18:08 0
GM14126
 
Resource Report
Resource Website
Coriell Cat# GM14126, RRID:CVCL_W002 Homo sapiens (Human) Cri du chat syndrome PMID:8004090
PMID:23665875
Transformed cell line Female JL135 Coriell GM14126 CLO:CLO_0034407,
Coriell:GM14126,
Wikidata:Q54847069
CVCL_W002 2026-02-14 08:18:09 0
GM14129
 
Resource Report
Resource Website
Coriell Cat# GM14129, RRID:CVCL_W005 Homo sapiens (Human) Cri du chat syndrome PMID:8004090
PMID:23665875
Transformed cell line Male JL139 Coriell GM14129 CLO:CLO_0034390,
Coriell:GM14129,
Wikidata:Q54847073
CVCL_W005 2026-02-14 08:18:09 0

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