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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
GM22908
 
Resource Report
Resource Website
RRID:CVCL_5S24 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Male Coriell:GM22908,
Wikidata:Q54852822
CVCL_5S24 Cellosaurus 2026-09-26 06:53:15 0
GM23054
 
Resource Report
Resource Website
RRID:CVCL_5S66 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell:GM23054,
Wikidata:Q54852875
CVCL_5S66 Cellosaurus 2026-09-26 06:53:16 0
GM22991
 
Resource Report
Resource Website
Coriell Cat# GM22991, RRID:CVCL_5S48 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Female Coriell GM22991 Coriell:GM22991,
Wikidata:Q54852856
CVCL_5S48 Cellosaurus 2026-09-26 06:53:16 0
GM22931
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM22931, RRID:CVCL_5S34 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Male Coriell GM22931 Coriell:GM22931,
Wikidata:Q54852836
CVCL_5S34 Cellosaurus 2026-09-26 06:53:15 0
GM23002
 
Resource Report
Resource Website
Coriell Cat# GM23002, RRID:CVCL_5S56 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Female Coriell GM23002 Coriell:GM23002,
Wikidata:Q54852864
CVCL_5S56 Cellosaurus 2026-09-26 06:53:16 0
GM22927
 
Resource Report
Resource Website
Coriell Cat# GM22927, RRID:CVCL_5S31 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Female Coriell GM22927 Coriell:GM22927,
Wikidata:Q54852832
CVCL_5S31 Cellosaurus 2026-09-26 06:53:15 0
GM23053
 
Resource Report
Resource Website
Coriell Cat# GM23053, RRID:CVCL_5S65 Homo sapiens (Human) Charcot-Marie-Tooth disease type 1A PMID:23665875 Transformed cell line Female Coriell GM23053 Coriell:GM23053,
Wikidata:Q54852874
CVCL_5S65 Cellosaurus 2026-09-26 06:53:16 0
GM22992
 
Resource Report
Resource Website
Coriell Cat# GM22992, RRID:CVCL_5S49 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Female Coriell GM22992 Coriell:GM22992,
Wikidata:Q54852857
CVCL_5S49 Cellosaurus 2026-09-26 06:53:16 0
GM22992
 
Resource Report
Resource Website
RRID:CVCL_5S49 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Female Coriell:GM22992,
Wikidata:Q54852857
CVCL_5S49 Cellosaurus 2026-09-26 06:53:16 0
GM22972
 
Resource Report
Resource Website
Coriell Cat# GM22972, RRID:CVCL_5S44 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM22972 Coriell:GM22972,
Wikidata:Q54852846
CVCL_5S44 Cellosaurus 2026-09-26 06:53:16 0
GM22930
 
Resource Report
Resource Website
Coriell Cat# GM22930, RRID:CVCL_5S33 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Male Coriell GM22930 Coriell:GM22930,
Wikidata:Q54852835
CVCL_5S33 Cellosaurus 2026-09-26 06:53:15 0
GM22979
 
Resource Report
Resource Website
Coriell Cat# GM22979, RRID:CVCL_5S47 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Female Coriell GM22979 Coriell:GM22979,
Wikidata:Q54852855
CVCL_5S47 Cellosaurus 2026-09-26 06:53:16 0
GM22995
 
Resource Report
Resource Website
RRID:CVCL_5S52 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Male Coriell:GM22995,
Wikidata:Q54852860
CVCL_5S52 Cellosaurus 2026-09-26 06:53:16 0
GM22972
 
Resource Report
Resource Website
RRID:CVCL_5S44 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM22972,
Wikidata:Q54852846
CVCL_5S44 Cellosaurus 2026-09-26 06:53:16 0
GM23226
 
Resource Report
Resource Website
RRID:CVCL_F170 Homo sapiens (Human) Type 1 diabetes mellitus Population: Native North American; Alaskan. PMID:23665875 Induced pluripotent stem cell Female GM23226*A Coriell:GM23226,
SKIP:SKIP000182,
SKIP:SKIP004346,
Wikidata:Q54852921
cvcl_8518 CVCL_F170 Cellosaurus 2026-09-26 06:53:17 0
GM23262
 
Resource Report
Resource Website
RRID:CVCL_F177 Homo sapiens (Human) Becker's muscular dystrophy Population: Caucasian. PMID:23665875 Induced pluripotent stem cell Male GM23262*A Coriell:GM23262,
SKIP:SKIP000187,
SKIP:SKIP004351,
Wikidata:Q54852945
cvcl_8521 CVCL_F177 Cellosaurus 2026-09-26 06:53:18 0
GM23081
 
Resource Report
Resource Website
Coriell Cat# GM23081, RRID:CVCL_5S68 Homo sapiens (Human) Autism spectrum disorder PMID:23495136
PMID:23665875
Transformed cell line Male 801-010 LCL Coriell GM23081 Coriell:GM23081,
Wikidata:Q54852886
CVCL_5S68 Cellosaurus 2026-09-26 06:53:17 0
GM23225
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_F169 Homo sapiens (Human) Huntington's disease PMID:23665875 Induced pluripotent stem cell Female GM23225*B Coriell:GM23225,
SKIP:SKIP000181,
SKIP:SKIP004345,
Wikidata:Q54852920
cvcl_8519 CVCL_F169 Cellosaurus 2026-09-26 06:53:17 1
GM23235
 
Resource Report
Resource Website
Coriell Cat# GM23235, RRID:CVCL_5S79 Homo sapiens (Human) Autism spectrum disorder PMID:23495136
PMID:23665875
Transformed cell line Male 801-013 LCL Coriell GM23235 Coriell:GM23235,
Wikidata:Q54852926
CVCL_5S79 Cellosaurus 2026-09-26 06:53:17 0
GM23232
 
Resource Report
Resource Website
RRID:CVCL_F191 Homo sapiens (Human) Adenosine deaminase deficiency Population: Caucasian. PMID:23665875 Induced pluripotent stem cell Male GM23232*A BioSample:SAMN00806683,
Coriell:GM23232,
SKIP:SKIP000184,
SKIP:SKIP004348,
Wikidata:Q54852925
cvcl_8517 CVCL_F191 Cellosaurus 2026-09-26 06:53:17 0

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