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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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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 2026-09-05 10:59:34 0
GM23302
 
Resource Report
Resource Website 		RRID:CVCL_5S87 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM23302,
Wikidata:Q54852981		 CVCL_5S87 2026-09-05 10:59:33 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 2026-09-05 10:59:34 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 2026-09-05 10:59:34 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 2026-09-05 10:59:34 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 2026-09-05 10:59:35 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 2026-09-05 10:59:35 0
GM23489
 
Resource Report
Resource Website 		RRID:CVCL_5S91 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM23489,
Wikidata:Q54853109		 CVCL_5S91 2026-09-05 10:59:36 0
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 2026-09-05 10:59:36 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 2026-09-05 10:59:36 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 2026-09-05 10:59:36 0
GM23504
 
Resource Report
Resource Website 		Coriell Cat# GM23504, RRID:CVCL_5S95 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM23504 Coriell:GM23504,
Wikidata:Q54853125		 CVCL_5S95 2026-09-05 10:59:36 0
GM23616
 
Resource Report
Resource Website 		RRID:CVCL_5S96 Homo sapiens (Human) Isodicentric chromosome PMID:23665875 Transformed cell line Male Coriell:GM23616,
Wikidata:Q54853154		 CVCL_5S96 2026-09-05 10:59:37 0
GM23616
 
Resource Report
Resource Website 		Coriell Cat# GM23616, RRID:CVCL_5S96 Homo sapiens (Human) Isodicentric chromosome PMID:23665875 Transformed cell line Male Coriell GM23616 Coriell:GM23616,
Wikidata:Q54853154		 CVCL_5S96 2026-09-05 10:59:37 0
GM23498
 
Resource Report
Resource Website 		RRID:CVCL_5S94 Homo sapiens (Human) Argininosuccinic aciduria PMID:23665875 Transformed cell line Female Coriell:GM23498,
Wikidata:Q54853119		 CVCL_5S94 2026-09-05 10:59:36 0
GM23697
 
Resource Report
Resource Website 		RRID:CVCL_5T03 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell:GM23697,
Wikidata:Q54853242		 CVCL_5T03 2026-09-05 10:59:38 0
GM23702
 
Resource Report
Resource Website 		Coriell Cat# GM23702, RRID:CVCL_5T08 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM23702 Coriell:GM23702,
Wikidata:Q54853247		 CVCL_5T08 2026-09-05 10:59:39 0
GM23675
 
Resource Report
Resource Website 		RRID:CVCL_5S97 Homo sapiens (Human) Lubs X-linked intellectual disability syndrome Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:23665875
PMID:24508304 		Transformed cell line Male Coriell:GM23675,
Wikidata:Q54853218		 CVCL_5S97 2026-09-05 10:59:38 0
GM23708
 
Resource Report
Resource Website 		Coriell Cat# GM23708, RRID:CVCL_5T11 Homo sapiens (Human) Chromosome 15q11-q13 duplication syndrome PMID:23665875 Transformed cell line Female Coriell GM23708 Coriell:GM23708,
Wikidata:Q54853253		 CVCL_5T11 2026-09-05 10:59:39 0
GM23698
 
Resource Report
Resource Website 		Coriell Cat# GM23698, RRID:CVCL_5T04 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM23698 Coriell:GM23698,
Wikidata:Q54853243		 CVCL_5T04 2026-09-05 10:59:39 0

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