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  • References:pmid:23665875 (facet)

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1,669 Results - per page

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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
GM08946
 
Resource Report
Resource Website
RRID:CVCL_5N93 Homo sapiens (Human) Population: Caucasian. PMID:23665875 Finite cell line Female CLO:CLO_0011042,
BioSample:SAMN00798296,
Coriell:GM08946,
Wikidata:Q54843421
CVCL_5N93 2026-02-14 08:16:36 0
GM08946
 
Resource Report
Resource Website
Coriell Cat# GM08946, RRID:CVCL_5N93 Homo sapiens (Human) Population: Caucasian. PMID:23665875 Finite cell line Female Coriell GM08946 CLO:CLO_0011042,
BioSample:SAMN00798296,
Coriell:GM08946,
Wikidata:Q54843421
CVCL_5N93 2026-02-14 08:16:36 0
GM09025
 
Resource Report
Resource Website
RRID:CVCL_4D94 Homo sapiens (Human) Supernumerary circular chromosome PMID:23665875 Transformed cell line Male CLO:CLO_0010836,
BioSample:SAMN00798441,
Coriell:GM09025,
Wikidata:Q54843508
CVCL_4D94 2026-02-14 08:16:37 0
GM09026
 
Resource Report
Resource Website
Coriell Cat# GM09026, RRID:CVCL_0L61 Homo sapiens (Human) Population: African American. PMID:23665875 Finite cell line Male Coriell GM09026 CLO:CLO_0010837,
BioSample:SAMN00798443,
Coriell:GM09026,
Wikidata:Q54843509
cvcl_0l60 CVCL_0L61 2026-02-14 08:16:38 0
GM09024
 
Resource Report
Resource Website
Coriell Cat# GM09024, RRID:CVCL_0L59 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Male Coriell GM09024 CLO:CLO_0010734,
BioSample:SAMN00798439,
Coriell:GM09024,
Wikidata:Q54843507
CVCL_0L59 2026-02-14 08:16:38 0
GM09101
 
Resource Report
Resource Website
Coriell Cat# GM09101, RRID:CVCL_5N94 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM09101 CLO:CLO_0010655,
BioSample:SAMN00798547,
Coriell:GM09101,
Wikidata:Q54843585
CVCL_5N94 2026-02-14 08:16:39 0
GM09189
 
Resource Report
Resource Website
Coriell Cat# GM09189, RRID:CVCL_5N97 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Female Coriell GM09189 CLO:CLO_0010631,
BioSample:SAMN00798575,
Coriell:GM09189,
Wikidata:Q54843603
CVCL_5N97 2026-02-14 08:16:40 0
GM09216
 
Resource Report
Resource Website
Coriell Cat# GM09216, RRID:CVCL_V823 Homo sapiens (Human) Population: African American. PMID:23665875 Transformed cell line Male Coriell GM09216 CLO:CLO_0010685,
BioSample:SAMN00798587,
Coriell:GM09216,
Wikidata:Q54843618
CVCL_V823 2026-02-14 08:16:40 0
GM09189
 
Resource Report
Resource Website
RRID:CVCL_5N97 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0010631,
BioSample:SAMN00798575,
Coriell:GM09189,
Wikidata:Q54843603
CVCL_5N97 2026-02-14 08:16:40 0
GM09101
 
Resource Report
Resource Website
RRID:CVCL_5N94 Homo sapiens (Human) PMID:23665875 Transformed cell line Female CLO:CLO_0010655,
BioSample:SAMN00798547,
Coriell:GM09101,
Wikidata:Q54843585
CVCL_5N94 2026-02-14 08:16:39 0
GM12959
 
Resource Report
Resource Website
Coriell Cat# GM12959, RRID:CVCL_5P71 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM12959 CLO:CLO_0022918,
Coriell:GM12959,
Wikidata:Q54846240
CVCL_5P71 2026-02-14 08:17:48 0
GM13031
 
Resource Report
Resource Website
RRID:CVCL_5P72 Homo sapiens (Human) PMID:11687795
PMID:23665875
Transformed cell line Male CLO:CLO_0014030,
Coriell:GM13031,
GEO:GSM808,
Wikidata:Q54846273
CVCL_5P72 2026-02-14 08:17:49 0
GM13031
 
Resource Report
Resource Website
Coriell Cat# GM13031, RRID:CVCL_5P72 Homo sapiens (Human) PMID:11687795
PMID:23665875
Transformed cell line Male Coriell GM13031 CLO:CLO_0014030,
Coriell:GM13031,
GEO:GSM808,
Wikidata:Q54846273
CVCL_5P72 2026-02-14 08:17:49 0
GM13019
 
Resource Report
Resource Website
RRID:CVCL_2N02 Homo sapiens (Human) Turner syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0013986,
Coriell:GM13019,
Wikidata:Q54846265
CVCL_2N02 2026-02-14 08:17:49 0
GM13019
 
Resource Report
Resource Website
Coriell Cat# GM13019, RRID:CVCL_2N02 Homo sapiens (Human) Turner syndrome PMID:23665875 Transformed cell line Female Coriell GM13019 CLO:CLO_0013986,
Coriell:GM13019,
Wikidata:Q54846265
CVCL_2N02 2026-02-14 08:17:49 0
GM13166
 
Resource Report
Resource Website
RRID:CVCL_2Q71 Homo sapiens (Human) Turner syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0013643,
Coriell:GM13166,
Wikidata:Q54846355
CVCL_2Q71 2026-02-14 08:17:51 0
GM13284
 
Resource Report
Resource Website
RRID:CVCL_2U25 Homo sapiens (Human) Population: Caucasian. PMID:23665875 Finite cell line Male CLO:CLO_0013286,
BioSample:SAMN00802254,
Coriell:GM13284,
Wikidata:Q54846420
CVCL_2U25 2026-02-14 08:17:53 0
GM13277
 
Resource Report
Resource Website
Coriell Cat# GM13277, RRID:CVCL_5P73 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM13277 CLO:CLO_0013290,
BioSample:SAMN00802246,
Coriell:GM13277,
Wikidata:Q54846416
CVCL_5P73 2026-02-14 08:17:52 0
GM13419
 
Resource Report
Resource Website
RRID:CVCL_1N85 Homo sapiens (Human) Beckwith-Wiedemann syndrome PMID:23665875 Transformed cell line Male CLO:CLO_0012646,
BioSample:SAMN00802356,
Coriell:GM13419,
Wikidata:Q54846515
CVCL_1N85 2026-02-14 08:17:54 0
GM13324
 
Resource Report
Resource Website
Coriell Cat# GM13324, RRID:CVCL_2N05 Homo sapiens (Human) Turner syndrome Donor information: Established from monozygotic twin of GM13323 (Cellosaurus=CVCL_2N04). PMID:23665875 Transformed cell line Female Coriell GM13324 CLO:CLO_0013274,
Coriell:GM13324,
Wikidata:Q54846461
CVCL_2N05 2026-02-14 08:17:54 0

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