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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
GM16268
 
Resource Report
Resource Website
RRID:CVCL_5Q65 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell:GM16268,
Wikidata:Q54848411
CVCL_5Q65 Cellosaurus 2026-10-17 06:17:32 0
GM16268
 
Resource Report
Resource Website
Coriell Cat# GM16268, RRID:CVCL_5Q65 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM16268 Coriell:GM16268,
Wikidata:Q54848411
CVCL_5Q65 Cellosaurus 2026-10-17 06:17:32 0
GM16362
 
Resource Report
Resource Website
RRID:CVCL_5Q66 Homo sapiens (Human) Donor information: Established from monozygotic twin of GM16363 (Cellosaurus=CVCL_5Q67). PMID:23665875 Transformed cell line Male Coriell:GM16362,
Wikidata:Q54848471
CVCL_5Q66 Cellosaurus 2026-10-17 06:17:34 0
GM16457
 
Resource Report
Resource Website
RRID:CVCL_5L24 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female JL404 CLO:CLO_0017820,
Coriell:GM16457,
Wikidata:Q54848577
CVCL_5L24 Cellosaurus 2026-10-17 06:17:36 0
GM16440
 
Resource Report
Resource Website
RRID:CVCL_0H53 Homo sapiens (Human) Bipolar disorder PMID:23665875 Transformed cell line Female JL481 CLO:CLO_0017791,
Coriell:GM16440,
Wikidata:Q54848562
CVCL_0H53 Cellosaurus 2026-10-17 06:17:35 0
GM16449
 
Resource Report
Resource Website
Coriell Cat# GM16449, RRID:CVCL_0H48 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male JL314 Coriell GM16449 CLO:CLO_0017800,
Coriell:GM16449,
Wikidata:Q54848569
CVCL_0H48 Cellosaurus 2026-10-17 06:17:36 0
GM16438
 
Resource Report
Resource Website
RRID:CVCL_0H47 Homo sapiens (Human) PMID:23665875 Transformed cell line Male JL480 CLO:CLO_0017782,
Coriell:GM16438,
Wikidata:Q54848560
CVCL_0H47 Cellosaurus 2026-10-17 06:17:35 0
GM16447
 
Resource Report
Resource Website
Coriell Cat# GM16447, RRID:CVCL_5L23 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male JL288 Coriell GM16447 CLO:CLO_0017803,
Coriell:GM16447,
Wikidata:Q54848567
CVCL_5L23 Cellosaurus 2026-10-17 06:17:36 0
GM16455
 
Resource Report
Resource Website
RRID:CVCL_0H51 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female JL401 CLO:CLO_0017811,
Coriell:GM16455,
Wikidata:Q54848575
CVCL_0H51 Cellosaurus 2026-10-17 06:17:36 0
GM16445
 
Resource Report
Resource Website
RRID:CVCL_5L22 Homo sapiens (Human) Deletion 18p syndrome PMID:23665875 Transformed cell line Male JL439 CLO:CLO_0017802,
Coriell:GM16445,
Wikidata:Q54848566
CVCL_5L22 Cellosaurus 2026-10-17 06:17:35 0
GM16449
 
Resource Report
Resource Website
RRID:CVCL_0H48 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male JL314 CLO:CLO_0017800,
Coriell:GM16449,
Wikidata:Q54848569
CVCL_0H48 Cellosaurus 2026-10-17 06:17:36 0
GM16453
 
Resource Report
Resource Website
Coriell Cat# GM16453, RRID:CVCL_0H50 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male JL360 Coriell GM16453 CLO:CLO_0017804,
Coriell:GM16453,
Wikidata:Q54848573
CVCL_0H50 Cellosaurus 2026-10-17 06:17:36 0
GM16440
 
Resource Report
Resource Website
Coriell Cat# GM16440, RRID:CVCL_0H53 Homo sapiens (Human) Bipolar disorder PMID:23665875 Transformed cell line Female JL481 Coriell GM16440 CLO:CLO_0017791,
Coriell:GM16440,
Wikidata:Q54848562
CVCL_0H53 Cellosaurus 2026-10-17 06:17:35 0
GM16445
 
Resource Report
Resource Website
Coriell Cat# GM16445, RRID:CVCL_5L22 Homo sapiens (Human) Deletion 18p syndrome PMID:23665875 Transformed cell line Male JL439 Coriell GM16445 CLO:CLO_0017802,
Coriell:GM16445,
Wikidata:Q54848566
CVCL_5L22 Cellosaurus 2026-10-17 06:17:35 0
GM16451
 
Resource Report
Resource Website
RRID:CVCL_0H49 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male JL359 CLO:CLO_0017806,
Coriell:GM16451,
Wikidata:Q54848571
CVCL_0H49 Cellosaurus 2026-10-17 06:17:36 0
GM16598
 
Resource Report
Resource Website
RRID:CVCL_5Q74 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Male JL88 CLO:CLO_0017405,
Coriell:GM16598,
Wikidata:Q54848671
CVCL_5Q74 Cellosaurus 2026-10-17 06:17:37 0
GM16586
 
Resource Report
Resource Website
Coriell Cat# GM16586, RRID:CVCL_0G75 Homo sapiens (Human) Holoprosencephaly PMID:7485158
PMID:23665875
Transformed cell line Male JL218 Coriell GM16586 CLO:CLO_0017390,
Coriell:GM16586,
Wikidata:Q54848646
CVCL_0G75 Cellosaurus 2026-10-17 06:17:37 0
GM16718
 
Resource Report
Resource Website
RRID:CVCL_5Q76 Homo sapiens (Human) Azoospermia Population: Southeast Asian; Vietnamese. PMID:23665875 Transformed cell line Male CLO:CLO_0018424,
Coriell:GM16718,
Wikidata:Q54848711
CVCL_5Q76 Cellosaurus 2026-10-17 06:17:38 0
GM16580
 
Resource Report
Resource Website
RRID:CVCL_5Q68 Homo sapiens (Human) Deletion 18p syndrome PMID:23665875 Transformed cell line Male JL462 Coriell:GM16580,
Wikidata:Q54848641
CVCL_5Q68 Cellosaurus 2026-10-17 06:17:37 0
GM16598
 
Resource Report
Resource Website
Coriell Cat# GM16598, RRID:CVCL_5Q74 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Male JL88 Coriell GM16598 CLO:CLO_0017405,
Coriell:GM16598,
Wikidata:Q54848671
CVCL_5Q74 Cellosaurus 2026-10-17 06:17:37 0

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