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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 Authority Record Last Update Mentions Count
GM13410
 
Resource Report
Resource Website
RRID:CVCL_2U27 Homo sapiens (Human) PMID:23665875 Transformed cell line Sex ambiguous CLO:CLO_0012856,
BioSample:SAMN00802346,
Coriell:GM13410,
Wikidata:Q54846508
CVCL_2U27 Cellosaurus 2026-10-17 06:16:49 0
GM13415
 
Resource Report
Resource Website
RRID:CVCL_1N83 Homo sapiens (Human) Beckwith-Wiedemann syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0012653,
BioSample:SAMN00802350,
Coriell:GM13415,
Wikidata:Q54846512
CVCL_1N83 Cellosaurus 2026-10-17 06:16:49 0
GM13321
 
Resource Report
Resource Website
RRID:CVCL_N207 Homo sapiens (Human) Population: African American., Part of: Human variation panel. PMID:16260726
PMID:23665875
Transformed cell line Male GM17174 CLO:CLO_0013224,
CLO:CLO_0014034,
BioSample:SAMN00802297,
Coriell:GM13321,
Coriell:GM17174,
GEO:GSM569746,
GEO:GSM596238,
GEO:GSM597033,
GEO:GSM924684,
Wikidata:Q54846458
CVCL_N207 Cellosaurus 2026-10-17 06:16:48 0
GM13323
 
Resource Report
Resource Website
RRID:CVCL_2N04 Homo sapiens (Human) Turner syndrome Donor information: Established from monozygotic twin of GM13324 (Cellosaurus=CVCL_2N05). PMID:23665875 Transformed cell line Female CLO:CLO_0013275,
Coriell:GM13323,
Wikidata:Q54846460
CVCL_2N04 Cellosaurus 2026-10-17 06:16:48 0
GM13434
 
Resource Report
Resource Website
RRID:CVCL_5P75 Homo sapiens (Human) Pelizaeus-Merzbacher disease PMID:7539213
PMID:23665875
Transformed cell line Male CLO:CLO_0012675,
Coriell:GM13434,
Wikidata:Q54846524
CVCL_5P75 Cellosaurus 2026-10-17 06:16:49 0
GM13325
 
Resource Report
Resource Website
Coriell Cat# GM13325, RRID:CVCL_2Y99 Homo sapiens (Human) 22q11.2 deletion syndrome Population: Caucasian. PMID:23665875 Finite cell line Female Coriell GM13325 CLO:CLO_0013273,
BioSample:SAMN00802301,
Coriell:GM13325,
Wikidata:Q54846462
CVCL_2Y99 Cellosaurus 2026-10-17 06:16:48 0
GM13321
 
Resource Report
Resource Website
Coriell Cat# GM17174, RRID:CVCL_N207 Homo sapiens (Human) Population: African American., Part of: Human variation panel. PMID:16260726
PMID:23665875
Transformed cell line Male GM17174 Coriell GM17174 CLO:CLO_0013224,
CLO:CLO_0014034,
BioSample:SAMN00802297,
Coriell:GM13321,
Coriell:GM17174,
GEO:GSM569746,
GEO:GSM596238,
GEO:GSM597033,
GEO:GSM924684,
Wikidata:Q54846458
CVCL_N207 Cellosaurus 2026-10-17 06:16:48 0
GM13325
 
Resource Report
Resource Website
RRID:CVCL_2Y99 Homo sapiens (Human) 22q11.2 deletion syndrome Population: Caucasian. PMID:23665875 Finite cell line Female CLO:CLO_0013273,
BioSample:SAMN00802301,
Coriell:GM13325,
Wikidata:Q54846462
CVCL_2Y99 Cellosaurus 2026-10-17 06:16:48 0
GM13461
 
Resource Report
Resource Website
Coriell Cat# GM13461, RRID:CVCL_5P82 Homo sapiens (Human) Williams syndrome Population: Caucasian. PMID:23665875 Transformed cell line Male Coriell GM13461 CLO:CLO_0012170,
BioSample:SAMN00802386,
Coriell:GM13461,
Wikidata:Q54846540
CVCL_5P82 Cellosaurus 2026-10-17 06:16:50 0
GM13478
 
Resource Report
Resource Website
RRID:CVCL_5P96 Homo sapiens (Human) Williams syndrome Population: Caucasian. PMID:23665875 Transformed cell line Female CLO:CLO_0012250,
BioSample:SAMN00802416,
Coriell:GM13478,
Wikidata:Q54846565
CVCL_5P96 Cellosaurus 2026-10-17 06:16:50 0
GM13485
 
Resource Report
Resource Website
Coriell Cat# GM13485, RRID:CVCL_5Q03 Homo sapiens (Human) Williams syndrome Population: Caucasian. PMID:23665875 Transformed cell line Male Coriell GM13485 CLO:CLO_0012265,
BioSample:SAMN00802430,
Coriell:GM13485,
Wikidata:Q54846574
CVCL_5Q03 Cellosaurus 2026-10-17 06:16:50 0
GM13470
 
Resource Report
Resource Website
RRID:CVCL_5P89 Homo sapiens (Human) Williams syndrome Population: Caucasian. PMID:23665875 Transformed cell line Female CLO:CLO_0012219,
BioSample:SAMN00802400,
Coriell:GM13470,
Wikidata:Q54846550
CVCL_5P89 Cellosaurus 2026-10-17 06:16:49 0
GM13463
 
Resource Report
Resource Website
Coriell Cat# GM13463, RRID:CVCL_5P83 Homo sapiens (Human) Williams syndrome Population: Caucasian. PMID:23665875 Transformed cell line Female Coriell GM13463 CLO:CLO_0012190,
BioSample:SAMN00802388,
Coriell:GM13463,
Wikidata:Q54846541
CVCL_5P83 Cellosaurus 2026-10-17 06:16:49 0
GM13476
 
Resource Report
Resource Website
Coriell Cat# GM13476, RRID:CVCL_5K11 Homo sapiens (Human) Smith-Magenis syndrome Population: Caucasian. PMID:23665875 Transformed cell line Female Coriell GM13476 CLO:CLO_0012235,
BioSample:SAMN00802412,
Coriell:GM13476,
Wikidata:Q54846563
CVCL_5K11 Cellosaurus 2026-10-17 06:16:50 0
GM13464
 
Resource Report
Resource Website
Coriell Cat# GM13464, RRID:CVCL_5P84 Homo sapiens (Human) Williams syndrome Population: Caucasian. PMID:23665875 Transformed cell line Male Coriell GM13464 CLO:CLO_0012187,
BioSample:SAMN00802390,
Coriell:GM13464,
Wikidata:Q54846542
CVCL_5P84 Cellosaurus 2026-10-17 06:16:50 0
GM13480
 
Resource Report
Resource Website
Coriell Cat# GM13480, RRID:CVCL_5P98 Homo sapiens (Human) Williams syndrome Population: Caucasian. PMID:23665875 Transformed cell line Female Coriell GM13480 CLO:CLO_0012253,
BioSample:SAMN00802420,
Coriell:GM13480,
Wikidata:Q54846567
CVCL_5P98 Cellosaurus 2026-10-17 06:16:50 0
GM13475
 
Resource Report
Resource Website
RRID:CVCL_5P94 Homo sapiens (Human) Williams syndrome Population: Caucasian. PMID:23665875 Transformed cell line Male CLO:CLO_0012237,
BioSample:SAMN00802410,
Coriell:GM13475,
Wikidata:Q54846562
CVCL_5P94 Cellosaurus 2026-10-17 06:16:50 0
GM13463
 
Resource Report
Resource Website
RRID:CVCL_5P83 Homo sapiens (Human) Williams syndrome Population: Caucasian. PMID:23665875 Transformed cell line Female CLO:CLO_0012190,
BioSample:SAMN00802388,
Coriell:GM13463,
Wikidata:Q54846541
CVCL_5P83 Cellosaurus 2026-10-17 06:16:49 0
GM13475
 
Resource Report
Resource Website
Coriell Cat# GM13475, RRID:CVCL_5P94 Homo sapiens (Human) Williams syndrome Population: Caucasian. PMID:23665875 Transformed cell line Male Coriell GM13475 CLO:CLO_0012237,
BioSample:SAMN00802410,
Coriell:GM13475,
Wikidata:Q54846562
CVCL_5P94 Cellosaurus 2026-10-17 06:16:50 0
GM13556
 
Resource Report
Resource Website
RRID:CVCL_U539 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0012477,
BioSample:SAMN00802476,
Coriell:GM13556,
Wikidata:Q54846634
CVCL_U539 Cellosaurus 2026-10-17 06:16:51 0

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