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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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GM22765
 
Resource Report
Resource Website 		RRID:CVCL_5S12 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM22765,
Wikidata:Q54852784		 CVCL_5S12 2026-09-19 05:32:20 0
GM22709
 
Resource Report
Resource Website 		RRID:CVCL_5S08 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM22709,
Wikidata:Q54852745		 CVCL_5S08 2026-09-19 05:32:19 0
GM22771
 
Resource Report
Resource Website 		Coriell Cat# GM22771, RRID:CVCL_5S14 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM22771 Coriell:GM22771,
Wikidata:Q54852790		 CVCL_5S14 2026-09-19 05:32:20 0
GM22711
 
Resource Report
Resource Website 		Coriell Cat# GM22711, RRID:CVCL_5S10 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM22711 Coriell:GM22711,
Wikidata:Q54852747		 CVCL_5S10 2026-09-19 05:32:19 0
GM22766
 
Resource Report
Resource Website 		RRID:CVCL_5K24 Homo sapiens (Human) Smith-Magenis syndrome PMID:23665875 Transformed cell line Female Coriell:GM22766,
Wikidata:Q54852785		 CVCL_5K24 2026-09-19 05:32:20 0
GM22904
 
Resource Report
Resource Website 		RRID:CVCL_5S22 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Female Coriell:GM22904,
Wikidata:Q54852820		 CVCL_5S22 2026-09-19 05:32:21 0
GM22765
 
Resource Report
Resource Website 		Coriell Cat# GM22765, RRID:CVCL_5S12 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM22765 Coriell:GM22765,
Wikidata:Q54852784		 CVCL_5S12 2026-09-19 05:32:20 0
GM22894
 
Resource Report
Resource Website 		RRID:CVCL_5S18 Homo sapiens (Human) Autism spectrum disorder PMID:23495136
PMID:23665875 		Transformed cell line Female 801-008 LCL Coriell:GM22894,
Wikidata:Q54852816		 CVCL_5S18 2026-09-19 05:32:21 0
GM22771
 
Resource Report
Resource Website 		RRID:CVCL_5S14 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell:GM22771,
Wikidata:Q54852790		 CVCL_5S14 2026-09-19 05:32:20 0
GM22902
 
Resource Report
Resource Website 		Coriell Cat# GM22902, RRID:CVCL_5S20 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Female Coriell GM22902 Coriell:GM22902,
Wikidata:Q54852818		 CVCL_5S20 2026-09-19 05:32:21 0
GM22936
 
Resource Report
Resource Website 		RRID:CVCL_5S36 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Male Coriell:GM22936,
Wikidata:Q54852838		 CVCL_5S36 2026-09-19 05:32:22 0
GM22979
 
Resource Report
Resource Website 		RRID:CVCL_5S47 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Female Coriell:GM22979,
Wikidata:Q54852855		 CVCL_5S47 2026-09-19 05:32:22 0
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 2026-09-19 05:32:21 0
GM23054
 
Resource Report
Resource Website 		RRID:CVCL_5S66 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell:GM23054,
Wikidata:Q54852875		 CVCL_5S66 2026-09-19 05:32:23 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 2026-09-19 05:32:22 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 2026-09-19 05:32:22 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 2026-09-19 05:32:22 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 2026-09-19 05:32:21 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 2026-09-19 05:32:23 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 2026-09-19 05:32:22 0

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