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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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GM22593
 
Resource Report
Resource Website 		Coriell Cat# GM22593, RRID:CVCL_5R86 Homo sapiens (Human) Autism spectrum disorder PMID:23495136
PMID:23665875 		Transformed cell line Female 801-009 LCL Coriell GM22593 Coriell:GM22593,
Wikidata:Q54852642		 CVCL_5R86 2026-02-14 08:20:16 0
GM22628
 
Resource Report
Resource Website 		Coriell Cat# GM22628, RRID:CVCL_1K41 Homo sapiens (Human) Potocki-Shaffer syndrome PMID:23665875 Transformed cell line Male Coriell GM22628 Coriell:GM22628,
Wikidata:Q54852669		 CVCL_1K41 2026-02-14 08:20:17 0
GM22625
 
Resource Report
Resource Website 		Coriell Cat# GM22625, RRID:CVCL_1K38 Homo sapiens (Human) Potocki-Shaffer syndrome PMID:23665875 Transformed cell line Female Coriell GM22625 Coriell:GM22625,
Wikidata:Q54852666		 CVCL_1K38 2026-02-14 08:20:16 0
GM22624
 
Resource Report
Resource Website 		RRID:CVCL_1K37 Homo sapiens (Human) Potocki-Shaffer syndrome PMID:23665875 Transformed cell line Female Coriell:GM22624,
Wikidata:Q54852665		 CVCL_1K37 2026-02-14 08:20:16 0
GM22633
 
Resource Report
Resource Website 		RRID:CVCL_1P95 Homo sapiens (Human) Potocki-Shaffer syndrome PMID:23665875 Transformed cell line Male Coriell:GM22633,
Wikidata:Q54852675		 CVCL_1P95 2026-02-14 08:20:17 0
GM22624
 
Resource Report
Resource Website 		Coriell Cat# GM22624, RRID:CVCL_1K37 Homo sapiens (Human) Potocki-Shaffer syndrome PMID:23665875 Transformed cell line Female Coriell GM22624 Coriell:GM22624,
Wikidata:Q54852665		 CVCL_1K37 2026-02-14 08:20:16 0
GM22632
 
Resource Report
Resource Website 		Coriell Cat# GM22632, RRID:CVCL_1K45 Homo sapiens (Human) Potocki-Shaffer syndrome PMID:23665875 Transformed cell line Male Coriell GM22632 Coriell:GM22632,
Wikidata:Q54852674		 CVCL_1K45 2026-02-14 08:20:17 0
GM22626
 
Resource Report
Resource Website 		Coriell Cat# GM22626, RRID:CVCL_1K39 Homo sapiens (Human) Potocki-Shaffer syndrome PMID:23665875 Transformed cell line Male Coriell GM22626 Coriell:GM22626,
Wikidata:Q54852667		 CVCL_1K39 2026-02-14 08:20:16 0
GM22631
 
Resource Report
Resource Website 		RRID:CVCL_1K44 Homo sapiens (Human) Potocki-Shaffer syndrome PMID:23665875 Transformed cell line Male Coriell:GM22631,
Wikidata:Q54852672		 CVCL_1K44 2026-02-14 08:20:17 0
GM22601
 
Resource Report
Resource Website 		Coriell Cat# GM22601, RRID:CVCL_V824 Homo sapiens (Human) Wolf-Hirschhorn syndrome PMID:23665875 Transformed cell line Male Coriell GM22601 Coriell:GM22601,
Wikidata:Q54852650		 CVCL_V824 2026-02-14 08:20:16 0
GM22628
 
Resource Report
Resource Website 		RRID:CVCL_1K41 Homo sapiens (Human) Potocki-Shaffer syndrome PMID:23665875 Transformed cell line Male Coriell:GM22628,
Wikidata:Q54852669		 CVCL_1K41 2026-02-14 08:20:16 0
GM22623
 
Resource Report
Resource Website 		Coriell Cat# GM22623, RRID:CVCL_1K36 Homo sapiens (Human) Karyotypic information: 46,XX,ins(13;11)(q14.1;p11.2p12).ish ins(13;11)(q14.1;p11.2p12)(wcp11+).arr(1-22,X)x2 (Coriell=GM22623). PMID:23665875 Transformed cell line Female Coriell GM22623 Coriell:GM22623,
Wikidata:Q54852664		 CVCL_1K36 2026-02-14 08:20:16 0
GM22630
 
Resource Report
Resource Website 		Coriell Cat# GM22630, RRID:CVCL_1K43 Homo sapiens (Human) Potocki-Shaffer syndrome PMID:23665875 Transformed cell line Female Coriell GM22630 Coriell:GM22630,
Wikidata:Q54852671		 CVCL_1K43 2026-02-14 08:20:17 0
GM22770
 
Resource Report
Resource Website 		RRID:CVCL_5S13 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM22770,
Wikidata:Q54852789		 CVCL_5S13 2026-02-14 08:20:19 0
GM22767
 
Resource Report
Resource Website 		RRID:CVCL_5K25 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell:GM22767,
Wikidata:Q54852786		 CVCL_5K25 2026-02-14 08:20:19 0
GM22770
 
Resource Report
Resource Website 		Coriell Cat# GM22770, RRID:CVCL_5S13 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM22770 Coriell:GM22770,
Wikidata:Q54852789		 CVCL_5S13 2026-02-14 08:20:19 0
GM22709
 
Resource Report
Resource Website 		Coriell Cat# GM22709, RRID:CVCL_5S08 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM22709 Coriell:GM22709,
Wikidata:Q54852745		 CVCL_5S08 2026-02-14 08:20:18 0
GM22711
 
Resource Report
Resource Website 		RRID:CVCL_5S10 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM22711,
Wikidata:Q54852747		 CVCL_5S10 2026-02-14 08:20:18 0
GM22976
 
Resource Report
Resource Website 		Coriell Cat# GM22976, RRID:CVCL_5S45 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Male Coriell GM22976 Coriell:GM22976,
Wikidata:Q54852847		 CVCL_5S45 2026-02-14 08:20:21 0
GM22916
 
Resource Report
Resource Website 		Coriell Cat# GM22916, RRID:CVCL_5S27 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Female Coriell GM22916 Coriell:GM22916,
Wikidata:Q54852825		 CVCL_5S27 2026-02-14 08:20:20 0

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