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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 Authority Record Last Update Mentions Count
GM09025
 
Resource Report
Resource Website
Coriell Cat# GM09025, RRID:CVCL_4D94 Homo sapiens (Human) Supernumerary circular chromosome PMID:23665875 Transformed cell line Male Coriell GM09025 CLO:CLO_0010836,
BioSample:SAMN00798441,
Coriell:GM09025,
Wikidata:Q54843508
CVCL_4D94 Cellosaurus 2026-10-17 06:15:25 0
GM09209
 
Resource Report
Resource Website
Coriell Cat# GM09209, RRID:CVCL_5U23 Homo sapiens (Human) Miller-Dieker syndrome PMID:23665875 Finite cell line Male Coriell GM09209 CLO:CLO_0010636,
Coriell:GM09209,
Wikidata:Q54843611
CVCL_5U23 Cellosaurus 2026-10-17 06:15:28 0
GM09102
 
Resource Report
Resource Website
RRID:CVCL_5N95 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0010656,
Coriell:GM09102,
Wikidata:Q54843587
CVCL_5N95 Cellosaurus 2026-10-17 06:15:27 0
GM09132
 
Resource Report
Resource Website
Coriell Cat# GM09132, RRID:CVCL_1P22 Homo sapiens (Human) Population: African American. PMID:1505951
PMID:23665875
Finite cell line Female GM9132 Coriell GM09132 CLO:CLO_0010622,
BioSample:SAMN00798563,
Coriell:GM09132,
Wikidata:Q54843595
CVCL_1P22 Cellosaurus 2026-10-17 06:15:27 0
GM09209
 
Resource Report
Resource Website
RRID:CVCL_5U23 Homo sapiens (Human) Miller-Dieker syndrome PMID:23665875 Finite cell line Male CLO:CLO_0010636,
Coriell:GM09209,
Wikidata:Q54843611
CVCL_5U23 Cellosaurus 2026-10-17 06:15:28 0
GM09102
 
Resource Report
Resource Website
Coriell Cat# GM09102, RRID:CVCL_5N95 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM09102 CLO:CLO_0010656,
Coriell:GM09102,
Wikidata:Q54843587
CVCL_5N95 Cellosaurus 2026-10-17 06:15:27 0
GM09133
 
Resource Report
Resource Website
RRID:CVCL_5N96 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0010629,
BioSample:SAMN00798565,
Coriell:GM09133,
Wikidata:Q54843596
CVCL_5N96 Cellosaurus 2026-10-17 06:15:27 0
GM09133
 
Resource Report
Resource Website
Coriell Cat# GM09133, RRID:CVCL_5N96 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Female Coriell GM09133 CLO:CLO_0010629,
BioSample:SAMN00798565,
Coriell:GM09133,
Wikidata:Q54843596
CVCL_5N96 Cellosaurus 2026-10-17 06:15:27 0
GM09132
 
Resource Report
Resource Website
RRID:CVCL_1P22 Homo sapiens (Human) Population: African American. PMID:1505951
PMID:23665875
Finite cell line Female GM9132 CLO:CLO_0010622,
BioSample:SAMN00798563,
Coriell:GM09132,
Wikidata:Q54843595
CVCL_1P22 Cellosaurus 2026-10-17 06:15:27 0
GM09216
 
Resource Report
Resource Website
RRID:CVCL_V823 Homo sapiens (Human) Population: African American. PMID:23665875 Transformed cell line Male CLO:CLO_0010685,
BioSample:SAMN00798587,
Coriell:GM09216,
Wikidata:Q54843618
CVCL_V823 Cellosaurus 2026-10-17 06:15:28 0
GM09332
 
Resource Report
Resource Website
Coriell Cat# GM09332, RRID:CVCL_5N98 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM09332 CLO:CLO_0011950,
Coriell:GM09332,
Wikidata:Q54843683
CVCL_5N98 Cellosaurus 2026-10-17 06:15:30 0
GM09285
 
Resource Report
Resource Website
Coriell Cat# GM09285, RRID:CVCL_2T62 Homo sapiens (Human) Population: Caucasian. PMID:23665875 Finite cell line Female Coriell GM09285 CLO:CLO_0012057,
Coriell:GM09285,
Wikidata:Q54843646
CVCL_2T62 Cellosaurus 2026-10-17 06:15:29 0
GM09332
 
Resource Report
Resource Website
RRID:CVCL_5N98 Homo sapiens (Human) PMID:23665875 Transformed cell line Female CLO:CLO_0011950,
Coriell:GM09332,
Wikidata:Q54843683
CVCL_5N98 Cellosaurus 2026-10-17 06:15:30 0
GM50168
 
Resource Report
Resource Website
Coriell Cat# GM50168, RRID:CVCL_5L31 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male JL339 Coriell GM50168 CLO:CLO_0015018,
Coriell:GM50168,
Wikidata:Q54854241
CVCL_5L31 Cellosaurus 2026-10-17 06:20:08 0
GM50160
 
Resource Report
Resource Website
RRID:CVCL_5L28 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female JL305 CLO:CLO_0014717,
Coriell:GM50160,
Wikidata:Q54854234
CVCL_5L28 Cellosaurus 2026-10-17 06:20:07 0
GM50124
 
Resource Report
Resource Website
Coriell Cat# GM50124, RRID:CVCL_1U16 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male JL208 Coriell GM50124 CLO:CLO_0014753,
Coriell:GM50124,
Wikidata:Q54854209
CVCL_1U16 Cellosaurus 2026-10-17 06:20:07 0
GM50159
 
Resource Report
Resource Website
RRID:CVCL_5T53 Homo sapiens (Human) PMID:23665875 Transformed cell line Female JL298 CLO:CLO_0014716,
Coriell:GM50159,
Wikidata:Q54854229
CVCL_5T53 Cellosaurus 2026-10-17 06:20:07 0
GM50121
 
Resource Report
Resource Website
RRID:CVCL_0G78 Homo sapiens (Human) Holoprosencephaly PMID:7485158
PMID:23665875
Transformed cell line Male JL182 CLO:CLO_0014751,
Coriell:GM50121,
Wikidata:Q54854207
CVCL_0G78 Cellosaurus 2026-10-17 06:20:06 0
GM50139
 
Resource Report
Resource Website
RRID:CVCL_0G55 Homo sapiens (Human) PMID:23665875 Transformed cell line Female JL259 CLO:CLO_0014675,
Coriell:GM50139,
Wikidata:Q54854216
CVCL_0G55 Cellosaurus 2026-10-17 06:20:07 0
GM50121
 
Resource Report
Resource Website
Coriell Cat# GM50121, RRID:CVCL_0G78 Homo sapiens (Human) Holoprosencephaly PMID:7485158
PMID:23665875
Transformed cell line Male JL182 Coriell GM50121 CLO:CLO_0014751,
Coriell:GM50121,
Wikidata:Q54854207
CVCL_0G78 Cellosaurus 2026-10-17 06:20:07 0

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