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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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GM23466
 
Resource Report
Resource Website 		Coriell Cat# GM23466, RRID:CVCL_U549 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Female Coriell GM23466 Coriell:GM23466,
Wikidata:Q54853102		 CVCL_U549 2026-02-14 08:20:26 0
GM23466
 
Resource Report
Resource Website 		RRID:CVCL_U549 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Female Coriell:GM23466,
Wikidata:Q54853102		 CVCL_U549 2026-02-14 08:20:26 0
GM23489
 
Resource Report
Resource Website 		Coriell Cat# GM23489, RRID:CVCL_5S91 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM23489 Coriell:GM23489,
Wikidata:Q54853109		 CVCL_5S91 2026-02-14 08:20:27 0
GM19926
 
Resource Report
Resource Website 		Coriell Cat# GM19926, RRID:CVCL_F098 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM19926 CLO:CLO_0028382,
Coriell:GM19926,
Wikidata:Q54850758		 CVCL_F098 2026-02-14 08:19:34 0
GM20125
 
Resource Report
Resource Website 		RRID:CVCL_5R03 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0027716,
Coriell:GM20125,
Wikidata:Q54850808		 CVCL_5R03 2026-02-14 08:19:35 0
GM20027
 
Resource Report
Resource Website 		RRID:CVCL_2N06 Homo sapiens (Human) Turner syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0028353,
Coriell:GM20027,
Wikidata:Q54850785		 CVCL_2N06 2026-02-14 08:19:35 0
GM19999
 
Resource Report
Resource Website 		RRID:CVCL_F105 Homo sapiens (Human) PMID:23665875 Transformed cell line Female CLO:CLO_0028367,
Coriell:GM19999,
Wikidata:Q54850769		 CVCL_F105 2026-02-14 08:19:35 0
GM20201
 
Resource Report
Resource Website 		Coriell Cat# GM20201, RRID:CVCL_5R05 Homo sapiens (Human) Autism spectrum disorder PMID:23665875 Transformed cell line Female Coriell GM20201 CLO:CLO_0027994,
Coriell:GM20201,
Wikidata:Q54850842		 CVCL_5R05 2026-02-14 08:19:36 0
GM20087
 
Resource Report
Resource Website 		Coriell Cat# GM20087, RRID:CVCL_5T66 Homo sapiens (Human) Lennox-Gastaut syndrome Population: African American. PMID:23665875 Transformed cell line Female Coriell GM20087 CLO:CLO_0028310,
Coriell:GM20087,
Wikidata:Q54850794		 CVCL_5T66 2026-02-14 08:19:35 0
GM20087
 
Resource Report
Resource Website 		RRID:CVCL_5T66 Homo sapiens (Human) Lennox-Gastaut syndrome Population: African American. PMID:23665875 Transformed cell line Female CLO:CLO_0028310,
Coriell:GM20087,
Wikidata:Q54850794		 CVCL_5T66 2026-02-14 08:19:35 0
GM20022
 
Resource Report
Resource Website 		RRID:CVCL_5R01 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0028340,
Coriell:GM20022,
Wikidata:Q54850784		 CVCL_5R01 2026-02-14 08:19:35 0
GM20304
 
Resource Report
Resource Website 		RRID:CVCL_5R07 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0027885,
Coriell:GM20304,
Wikidata:Q54850910		 CVCL_5R07 2026-02-14 08:19:37 0
GM20220
 
Resource Report
Resource Website 		RRID:CVCL_5R06 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0027966,
Coriell:GM20220,
Wikidata:Q54850851		 CVCL_5R06 2026-02-14 08:19:36 0
GM20263
 
Resource Report
Resource Website 		RRID:CVCL_2U58 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0027836,
Coriell:GM20263,
Wikidata:Q54850874		 CVCL_2U58 2026-02-14 08:19:36 0
GM20304
 
Resource Report
Resource Website 		Coriell Cat# GM20304, RRID:CVCL_5R07 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM20304 CLO:CLO_0027885,
Coriell:GM20304,
Wikidata:Q54850910		 CVCL_5R07 2026-02-14 08:19:37 0
GM20311
 
Resource Report
Resource Website 		Coriell Cat# GM20311, RRID:CVCL_2U60 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM20311 CLO:CLO_0027880,
Coriell:GM20311,
Wikidata:Q54850914		 CVCL_2U60 2026-02-14 08:19:37 0
GM20305
 
Resource Report
Resource Website 		Coriell Cat# GM20305, RRID:CVCL_5R08 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM20305 CLO:CLO_0027886,
Coriell:GM20305,
Wikidata:Q54850911		 CVCL_5R08 2026-02-14 08:19:37 0
GM20263
 
Resource Report
Resource Website 		Coriell Cat# GM20263, RRID:CVCL_2U58 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM20263 CLO:CLO_0027836,
Coriell:GM20263,
Wikidata:Q54850874		 CVCL_2U58 2026-02-14 08:19:36 0
GM20220
 
Resource Report
Resource Website 		Coriell Cat# GM20220, RRID:CVCL_5R06 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM20220 CLO:CLO_0027966,
Coriell:GM20220,
Wikidata:Q54850851		 CVCL_5R06 2026-02-14 08:19:36 0
GM20408
 
Resource Report
Resource Website 		Coriell Cat# GM20408, RRID:CVCL_U541 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Female Coriell GM20408 CLO:CLO_0029517,
Coriell:GM20408,
Wikidata:Q54851010		 CVCL_U541 2026-02-14 08:19:39 0

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