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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
GM20087
 
Resource Report
Resource Website
Coriell Cat# GM20087, RRID:CVCL_5T66 Homo sapiens (Human) Lennox-Gastaut syndrome Population: African American. PMID:23665875 Transformed cell line Female Coriell GM20087 CLO:CLO_0028310,
Coriell:GM20087,
Wikidata:Q54850794
CVCL_5T66 2026-02-14 08:19:35 0
GM20087
 
Resource Report
Resource Website
RRID:CVCL_5T66 Homo sapiens (Human) Lennox-Gastaut syndrome Population: African American. PMID:23665875 Transformed cell line Female CLO:CLO_0028310,
Coriell:GM20087,
Wikidata:Q54850794
CVCL_5T66 2026-02-14 08:19:35 0
GM20022
 
Resource Report
Resource Website
RRID:CVCL_5R01 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0028340,
Coriell:GM20022,
Wikidata:Q54850784
CVCL_5R01 2026-02-14 08:19:35 0
GM20304
 
Resource Report
Resource Website
RRID:CVCL_5R07 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0027885,
Coriell:GM20304,
Wikidata:Q54850910
CVCL_5R07 2026-02-14 08:19:37 0
GM20220
 
Resource Report
Resource Website
RRID:CVCL_5R06 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0027966,
Coriell:GM20220,
Wikidata:Q54850851
CVCL_5R06 2026-02-14 08:19:36 0
GM20263
 
Resource Report
Resource Website
RRID:CVCL_2U58 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0027836,
Coriell:GM20263,
Wikidata:Q54850874
CVCL_2U58 2026-02-14 08:19:36 0
GM20304
 
Resource Report
Resource Website
Coriell Cat# GM20304, RRID:CVCL_5R07 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM20304 CLO:CLO_0027885,
Coriell:GM20304,
Wikidata:Q54850910
CVCL_5R07 2026-02-14 08:19:37 0
GM20311
 
Resource Report
Resource Website
Coriell Cat# GM20311, RRID:CVCL_2U60 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM20311 CLO:CLO_0027880,
Coriell:GM20311,
Wikidata:Q54850914
CVCL_2U60 2026-02-14 08:19:37 0
GM20305
 
Resource Report
Resource Website
Coriell Cat# GM20305, RRID:CVCL_5R08 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM20305 CLO:CLO_0027886,
Coriell:GM20305,
Wikidata:Q54850911
CVCL_5R08 2026-02-14 08:19:37 0
GM20263
 
Resource Report
Resource Website
Coriell Cat# GM20263, RRID:CVCL_2U58 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM20263 CLO:CLO_0027836,
Coriell:GM20263,
Wikidata:Q54850874
CVCL_2U58 2026-02-14 08:19:36 0
GM20220
 
Resource Report
Resource Website
Coriell Cat# GM20220, RRID:CVCL_5R06 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM20220 CLO:CLO_0027966,
Coriell:GM20220,
Wikidata:Q54850851
CVCL_5R06 2026-02-14 08:19:36 0
GM20408
 
Resource Report
Resource Website
Coriell Cat# GM20408, RRID:CVCL_U541 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Female Coriell GM20408 CLO:CLO_0029517,
Coriell:GM20408,
Wikidata:Q54851010
CVCL_U541 2026-02-14 08:19:39 0
GM20366
 
Resource Report
Resource Website
Coriell Cat# GM20366, RRID:CVCL_5R09 Homo sapiens (Human) Isodicentric chromosome PMID:23665875 Transformed cell line Male Coriell GM20366 CLO:CLO_0029625,
Coriell:GM20366,
Wikidata:Q54850985
CVCL_5R09 2026-02-14 08:19:39 0
GM20406
 
Resource Report
Resource Website
RRID:CVCL_U540 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Male CLO:CLO_0029518,
Coriell:GM20406,
Wikidata:Q54851009
CVCL_U540 2026-02-14 08:19:39 0
GM20406
 
Resource Report
Resource Website
Coriell Cat# GM20406, RRID:CVCL_U540 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Male Coriell GM20406 CLO:CLO_0029518,
Coriell:GM20406,
Wikidata:Q54851009
CVCL_U540 2026-02-14 08:19:39 0
GM20501
 
Resource Report
Resource Website
RRID:CVCL_5R19 Homo sapiens (Human) PMID:23665875 Transformed cell line Female CLO:CLO_0029528,
Coriell:GM20501,
Wikidata:Q54851048
CVCL_5R19 2026-02-14 08:19:40 0
GM20419
 
Resource Report
Resource Website
Coriell Cat# GM20419, RRID:CVCL_5R15 Homo sapiens (Human) Attention deficit hyperactivity disorder Population: Caucasian. PMID:23665875 Transformed cell line Male Coriell GM20419 CLO:CLO_0029508,
Coriell:GM20419,
Wikidata:Q54851020
CVCL_5R15 2026-02-14 08:19:39 0
GM20418
 
Resource Report
Resource Website
RRID:CVCL_5R14 Homo sapiens (Human) Isodicentric chromosome PMID:23665875 Transformed cell line Female CLO:CLO_0029509,
Coriell:GM20418,
Wikidata:Q54851019
CVCL_5R14 2026-02-14 08:19:39 0
GM20411
 
Resource Report
Resource Website
Coriell Cat# GM20411, RRID:CVCL_5R13 Homo sapiens (Human) Angelman syndrome PMID:23665875 Transformed cell line Female Coriell GM20411 CLO:CLO_0029511,
Coriell:GM20411,
Wikidata:Q54851013
CVCL_5R13 2026-02-14 08:19:39 0
GM20435
 
Resource Report
Resource Website
RRID:CVCL_5R17 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM20435,
Wikidata:Q54851025
CVCL_5R17 2026-02-14 08:19:39 0

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