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Norway

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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GM21681
 
Resource Report
Resource Website 		Coriell Cat# GM21681, RRID:CVCL_5R35 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM21681 Coriell:GM21681,
Wikidata:Q54852080		 CVCL_5R35 2026-02-07 08:10:35 0
GM21715
 
Resource Report
Resource Website 		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,
Wikidata:Q54852090		 CVCL_5R37 2026-02-07 08:10:24 0
GM21699
 
Resource Report
Resource Website 		Coriell Cat# GM21699, RRID:CVCL_4J61 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM21699 CLO:CLO_0014010,
Coriell:GM21699,
Wikidata:Q54852089		 CVCL_4J61 2026-02-07 08:10:35 0
GM21889
 
Resource Report
Resource Website 		RRID:CVCL_U542 Homo sapiens (Human) Prader-Willi syndrome Population: African American. PMID:23665875
PMID:24816254 		Finite cell line Male Coriell:GM21889,
Wikidata:Q54852210		 CVCL_U542 2026-02-07 08:10:38 0
GM21893
 
Resource Report
Resource Website 		Coriell Cat# GM21893, RRID:CVCL_5R48 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM21893 Coriell:GM21893,
Wikidata:Q54852214		 CVCL_5R48 2026-02-07 08:10:38 0
GM21878
 
Resource Report
Resource Website 		RRID:CVCL_5R41 Homo sapiens (Human) PMID:23665875 Finite cell line Female Coriell:GM21878,
Wikidata:Q54852196		 CVCL_5R41 2026-02-07 08:10:38 0
GM21890
 
Resource Report
Resource Website 		Coriell Cat# GM21890, RRID:CVCL_U543 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Finite cell line Male Coriell GM21890 Coriell:GM21890,
Wikidata:Q54852211		 CVCL_U543 2026-02-07 08:10:38 0
GM21877
 
Resource Report
Resource Website 		RRID:CVCL_F109 Homo sapiens (Human) PMID:23665875 Finite cell line Female Coriell:GM21877,
Wikidata:Q54852195		 CVCL_F109 2026-02-07 08:10:27 0
GM21887
 
Resource Report
Resource Website 		Coriell Cat# GM21887, RRID:CVCL_5R46 Homo sapiens (Human) Angelman syndrome PMID:23665875 Transformed cell line Female Coriell GM21887 Coriell:GM21887,
Wikidata:Q54852209		 CVCL_5R46 2026-02-07 08:10:27 0
GM21884
 
Resource Report
Resource Website 		Coriell Cat# GM21884, RRID:CVCL_5R43 Homo sapiens (Human) Supernumerary circular chromosome PMID:23665875 Transformed cell line Female Coriell GM21884 Coriell:GM21884,
Wikidata:Q54852206		 CVCL_5R43 2026-02-07 08:10:27 0
GM21874
 
Resource Report
Resource Website 		Coriell Cat# GM21874, RRID:CVCL_5R40 Homo sapiens (Human) PMID:23665875 Finite cell line Male Coriell GM21874 Coriell:GM21874,
Wikidata:Q54852194		 CVCL_5R40 2026-02-07 08:10:38 0
GM21874
 
Resource Report
Resource Website 		RRID:CVCL_5R40 Homo sapiens (Human) PMID:23665875 Finite cell line Male Coriell:GM21874,
Wikidata:Q54852194		 CVCL_5R40 2026-02-07 08:10:27 0
GM21885
 
Resource Report
Resource Website 		RRID:CVCL_5R44 Homo sapiens (Human) Supernumerary circular chromosome PMID:23665875 Transformed cell line Male Coriell:GM21885,
Wikidata:Q54852207		 CVCL_5R44 2026-02-07 08:10:38 0
GM21893
 
Resource Report
Resource Website 		RRID:CVCL_5R48 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell:GM21893,
Wikidata:Q54852214		 CVCL_5R48 2026-02-07 08:10:28 0
GM21885
 
Resource Report
Resource Website 		Coriell Cat# GM21885, RRID:CVCL_5R44 Homo sapiens (Human) Supernumerary circular chromosome PMID:23665875 Transformed cell line Male Coriell GM21885 Coriell:GM21885,
Wikidata:Q54852207		 CVCL_5R44 2026-02-07 08:10:27 0
GM21884
 
Resource Report
Resource Website 		RRID:CVCL_5R43 Homo sapiens (Human) Supernumerary circular chromosome PMID:23665875 Transformed cell line Female Coriell:GM21884,
Wikidata:Q54852206		 CVCL_5R43 2026-02-07 08:10:27 0
GM21892
 
Resource Report
Resource Website 		RRID:CVCL_5R47 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell:GM21892,
Wikidata:Q54852213		 CVCL_5R47 2026-02-07 08:10:38 0
GM21891
 
Resource Report
Resource Website 		Coriell Cat# GM21891, RRID:CVCL_U544 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Male Coriell GM21891 Coriell:GM21891,
Wikidata:Q54852212		 CVCL_U544 2026-02-07 08:10:28 0
GM21883
 
Resource Report
Resource Website 		RRID:CVCL_5R42 Homo sapiens (Human) Supernumerary circular chromosome PMID:23665875 Transformed cell line Male Coriell:GM21883,
Wikidata:Q54852205		 CVCL_5R42 2026-02-07 08:10:27 0
GM22049
 
Resource Report
Resource Website 		Coriell Cat# GM22049, RRID:CVCL_5R51 Homo sapiens (Human) Isodicentric chromosome PMID:23665875 Transformed cell line Male Coriell GM22049 Coriell:GM22049,
Wikidata:Q54852314		 CVCL_5R51 2026-02-07 08:10:39 0

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