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Cellosaurus is database indexing available cell lines from various collections: American Type Culture Collection (ATCC), Bioresource Collection and Research Center, Taiwan (BCRC), Banco de Células do Rio de Janeiro (BCRJ), CellBank Australia (CBA), Collection of Cell Lines in Veterinary Medicine (CCLV), Cell Lines Service (CLS), Coriell, Drosophila Genomics Resource Center (DGRC), Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH (DSMZ), European Bank for induced pluripotent Stem Cells (EBiSC), European Collection of Authenticated Cell Cultures (ECACC), Interlab Cell Line Collection (ICLC), Institute for Fermentation Osaka (IFO), Istituto Zooprofilattico Sperimentale della Lombardia e dell'Emilia Romagna (IZSLER) biobank, Japanese Collection of Research Bioresources (JCRB) Cell Bank, Kunming Cell Bank of Type Culture Collection (KCB), Korean Cell Line Bank (KCLB), Millipore, National Cell Bank of Iran (NCBI_Iran), National Cancer Institute - Developmental Therapeutics Program (NCI-DTP), NINDS Human Cell and Data Repository (NHCDR), NIH AIDS Reagent Program (NIH-ARP), NISES, RIKEN Bioresource Center Cell Bank (RCB), Royan Stem Cell Bank (RSCB), Tick Cell Biobank (TCB), Tohoku University cell line catalog (TKG), and Ximbio.

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  • References:pmid:23665875 (facet)

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1,669 Results - per page

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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 2026-09-19 05:32:22 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 2026-09-19 05:32:22 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 2026-09-19 05:32:22 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 2026-09-19 05:32:22 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 2026-09-19 05:32:22 0
GM22972
 
Resource Report
Resource Website 		RRID:CVCL_5S44 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM22972,
Wikidata:Q54852846		 CVCL_5S44 2026-09-19 05:32:22 0
GM21496
 
Resource Report
Resource Website 		RRID:CVCL_5U27 Homo sapiens (Human) Mayer-Rokitansky-Kuster-Hauser syndrome PMID:23665875 Transformed cell line Male CLO:CLO_0014050,
Coriell:GM21496,
Wikidata:Q54851944		 CVCL_5U27 2026-09-19 05:32:01 0
GM21681
 
Resource Report
Resource Website 		RRID:CVCL_5R35 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM21681,
Wikidata:Q54852080		 CVCL_5R35 2026-09-19 05:32:05 0
GM21729
 
Resource Report
Resource Website 		RRID:CVCL_5R38 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM21729,
Wikidata:Q54852104		 CVCL_5R38 2026-09-19 05:32:05 0
GM21729
 
Resource Report
Resource Website 		Coriell Cat# GM21729, RRID:CVCL_5R38 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM21729 Coriell:GM21729,
Wikidata:Q54852104		 CVCL_5R38 2026-09-19 05:32:05 0
GM21698
 
Resource Report
Resource Website 		Coriell Cat# GM21698, RRID:CVCL_4J60 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM21698 CLO:CLO_0014013,
Coriell:GM21698,
Wikidata:Q54852088		 CVCL_4J60 2026-09-19 05:32:05 0
GM21715
 
Resource Report
Resource Website 		Coriell Cat# GM21715, RRID:CVCL_5R37 Homo sapiens (Human) Autism spectrum disorder Population: African American. PMID:23495136
PMID:23665875 		Transformed cell line Male 801-002 LCL Coriell GM21715 Coriell:GM21715,
Wikidata:Q54852090		 CVCL_5R37 2026-09-19 05:32:05 0
GM21698
 
Resource Report
Resource Website 		RRID:CVCL_4J60 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0014013,
Coriell:GM21698,
Wikidata:Q54852088		 CVCL_4J60 2026-09-19 05:32:05 0
GM21699
 
Resource Report
Resource Website 		RRID:CVCL_4J61 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0014010,
Coriell:GM21699,
Wikidata:Q54852089		 CVCL_4J61 2026-09-19 05:32:05 0
GM21886
 
Resource Report
Resource Website 		RRID:CVCL_5R45 Homo sapiens (Human) Supernumerary circular chromosome PMID:23665875 Transformed cell line Male Coriell:GM21886,
Wikidata:Q54852208		 CVCL_5R45 2026-09-19 05:32:07 0
GM21890
 
Resource Report
Resource Website 		RRID:CVCL_U543 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Finite cell line Male Coriell:GM21890,
Wikidata:Q54852211		 CVCL_U543 2026-09-19 05:32:07 0
GM21889
 
Resource Report
Resource Website 		Coriell Cat# GM21889, RRID:CVCL_U542 Homo sapiens (Human) Prader-Willi syndrome Population: African American. PMID:23665875
PMID:24816254 		Finite cell line Male Coriell GM21889 Coriell:GM21889,
Wikidata:Q54852210		 CVCL_U542 2026-09-19 05:32:07 0
GM21892
 
Resource Report
Resource Website 		Coriell Cat# GM21892, RRID:CVCL_5R47 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM21892 Coriell:GM21892,
Wikidata:Q54852213		 CVCL_5R47 2026-09-19 05:32:08 0
GM21891
 
Resource Report
Resource Website 		RRID:CVCL_U544 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Male Coriell:GM21891,
Wikidata:Q54852212		 CVCL_U544 2026-09-19 05:32:07 0
GM21877
 
Resource Report
Resource Website 		Coriell Cat# GM21877, RRID:CVCL_F109 Homo sapiens (Human) PMID:23665875 Finite cell line Female Coriell GM21877 Coriell:GM21877,
Wikidata:Q54852195		 CVCL_F109 2026-09-19 05:32:07 0

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