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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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1,669 Results - per page

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GM22910
 
Resource Report
Resource Website 		Coriell Cat# GM22910, RRID:CVCL_5S26 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Male Coriell GM22910 Coriell:GM22910,
Wikidata:Q54852824		 CVCL_5S26 2026-02-14 08:20:20 0
GM23264
 
Resource Report
Resource Website 		RRID:CVCL_5S85 Homo sapiens (Human) Chromosome 15q11-q13 duplication syndrome PMID:23495136
PMID:23665875 		Transformed cell line Female 801-015 LCL Coriell:GM23264,
Wikidata:Q54852947		 CVCL_5S85 2026-02-14 08:20:23 0
GM23161
 
Resource Report
Resource Website 		RRID:CVCL_5S78 Homo sapiens (Human) Autism spectrum disorder PMID:23665875 Transformed cell line Male Coriell:GM23161,
Wikidata:Q54852913		 CVCL_5S78 2026-02-14 08:20:22 0
GM23161
 
Resource Report
Resource Website 		Coriell Cat# GM23161, RRID:CVCL_5S78 Homo sapiens (Human) Autism spectrum disorder PMID:23665875 Transformed cell line Male Coriell GM23161 Coriell:GM23161,
Wikidata:Q54852913		 CVCL_5S78 2026-02-14 08:20:22 0
GM23263
 
Resource Report
Resource Website 		RRID:CVCL_5S84 Homo sapiens (Human) Autism spectrum disorder PMID:23495136
PMID:23665875 		Transformed cell line Male 801-014 LCL Coriell:GM23263,
Wikidata:Q54852946		 CVCL_5S84 2026-02-14 08:20:23 0
GM23263
 
Resource Report
Resource Website 		Coriell Cat# GM23263, RRID:CVCL_5S84 Homo sapiens (Human) Autism spectrum disorder PMID:23495136
PMID:23665875 		Transformed cell line Male 801-014 LCL Coriell GM23263 Coriell:GM23263,
Wikidata:Q54852946		 CVCL_5S84 2026-02-14 08:20:23 0
GM23255
 
Resource Report
Resource Website 		RRID:CVCL_5S83 Homo sapiens (Human) Spinal muscular atrophy type 3 PMID:23665875
PMID:26247043
PMID:28284873
PMID:33197628 		Transformed cell line Male Coriell:GM23255,
Wikidata:Q54852940		 CVCL_5S83 2026-02-14 08:20:23 0
GM23081
 
Resource Report
Resource Website 		RRID:CVCL_5S68 Homo sapiens (Human) Autism spectrum disorder PMID:23495136
PMID:23665875 		Transformed cell line Male 801-010 LCL Coriell:GM23081,
Wikidata:Q54852886		 CVCL_5S68 2026-02-14 08:20:22 0
GM23125
 
Resource Report
Resource Website 		RRID:CVCL_5S75 Homo sapiens (Human) Autism spectrum disorder PMID:23495136
PMID:23665875 		Transformed cell line Female 801-011 LCL Coriell:GM23125,
Wikidata:Q54852899		 CVCL_5S75 2026-02-14 08:20:22 0
GM23270
 
Resource Report
Resource Website 		Coriell Cat# GM23270, RRID:CVCL_5S86 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM23270 Coriell:GM23270,
Wikidata:Q54852957		 CVCL_5S86 2026-02-14 08:20:23 0
GM23235
 
Resource Report
Resource Website 		RRID:CVCL_5S79 Homo sapiens (Human) Autism spectrum disorder PMID:23495136
PMID:23665875 		Transformed cell line Male 801-013 LCL Coriell:GM23235,
Wikidata:Q54852926		 CVCL_5S79 2026-02-14 08:20:22 0
GM23336
 
Resource Report
Resource Website 		RRID:CVCL_U546 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Female Coriell:GM23336,
Wikidata:Q54853009		 CVCL_U546 2026-02-14 08:20:24 0
GM23354
 
Resource Report
Resource Website 		Coriell Cat# GM23354, RRID:CVCL_HK74 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Male Coriell GM23354 Coriell:GM23354,
Wikidata:Q54853016		 CVCL_HK74 2026-02-14 08:20:24 0
GM23302
 
Resource Report
Resource Website 		RRID:CVCL_5S87 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM23302,
Wikidata:Q54852981		 CVCL_5S87 2026-02-14 08:20:24 0
GM23356
 
Resource Report
Resource Website 		Coriell Cat# GM23356, RRID:CVCL_HK75 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Male Coriell GM23356 Coriell:GM23356,
Wikidata:Q54853018		 CVCL_HK75 2026-02-14 08:20:25 0
GM23337
 
Resource Report
Resource Website 		Coriell Cat# GM23337, RRID:CVCL_BV43 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Male Coriell GM23337 Coriell:GM23337,
Wikidata:Q54853010		 CVCL_BV43 2026-02-14 08:20:24 0
GM23356
 
Resource Report
Resource Website 		RRID:CVCL_HK75 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Male Coriell:GM23356,
Wikidata:Q54853018		 CVCL_HK75 2026-02-14 08:20:25 0
GM23392
 
Resource Report
Resource Website 		RRID:CVCL_F167 Homo sapiens (Human) Population: African American. PMID:23665875 Induced pluripotent stem cell Male GM23392*B Coriell:GM23392,
SKIP:SKIP000175,
SKIP:SKIP004358,
Wikidata:Q54853043		 cvcl_7449 CVCL_F167 2026-02-14 08:20:25 0
GM23392
 
Resource Report
Resource Website 		Coriell Cat# GM23392, RRID:CVCL_F167 Homo sapiens (Human) Population: African American. PMID:23665875 Induced pluripotent stem cell Male GM23392*B Coriell GM23392 Coriell:GM23392,
SKIP:SKIP000175,
SKIP:SKIP004358,
Wikidata:Q54853043		 cvcl_7449 CVCL_F167 2026-02-14 08:20:25 0
GM23489
 
Resource Report
Resource Website 		RRID:CVCL_5S91 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM23489,
Wikidata:Q54853109		 CVCL_5S91 2026-02-14 08:20:26 0

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