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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.
https://web.expasy.org/cellosaurus/CVCL_N207
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: African American., Part of: Human variation panel.
Proper citation: Coriell Cat# GM17174, RRID:CVCL_N207 Copy
https://web.expasy.org/cellosaurus/CVCL_0N24
Organism: Homo sapiens (Human)
Disease: Cystic fibrosis
Category: Transformed cell line
Proper citation: RRID:CVCL_0N24 Copy
https://web.expasy.org/cellosaurus/CVCL_JF49
Organism: Homo sapiens (Human)
Disease: 5' 10' methylenetetrahydrofolate reductase deficiency
Category: Finite cell line
Comments: Population: Arab; Saudi Arabian., From: Montreal Children's Hospital cell repository; Montreal; Canada.
Proper citation: RRID:CVCL_JF49 Copy
https://web.expasy.org/cellosaurus/CVCL_AN08
Organism: Homo sapiens (Human)
Disease: Ehlers-Danlos syndrome, type VI
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_AN08 Copy
https://web.expasy.org/cellosaurus/CVCL_1K76
Organism: Homo sapiens (Human)
Disease: Glycogen storage disease type II
Category: Transformed cell line
Proper citation: RRID:CVCL_1K76 Copy
https://web.expasy.org/cellosaurus/CVCL_N208
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Human variation panel.
Proper citation: RRID:CVCL_N208 Copy
https://web.expasy.org/cellosaurus/CVCL_CX13
Organism: Homo sapiens (Human)
Disease: Glycine encephalopathy
Category: Finite cell line
Comments: Population: Jordanian.
Proper citation: Coriell Cat# GM13440, RRID:CVCL_CX13 Copy
https://web.expasy.org/cellosaurus/CVCL_1K75
Organism: Homo sapiens (Human)
Disease: Glycogen storage disease type II
Category: Transformed cell line
Proper citation: RRID:CVCL_1K75 Copy
https://web.expasy.org/cellosaurus/CVCL_4F11
Organism: Homo sapiens (Human)
Disease: Ellis-Van Creveld syndrome
Category: Transformed cell line
Comments: Population: Caucasian; Amish.
Proper citation: RRID:CVCL_4F11 Copy
https://web.expasy.org/cellosaurus/CVCL_N208
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Human variation panel.
Proper citation: Coriell Cat# GM13418, RRID:CVCL_N208 Copy
https://web.expasy.org/cellosaurus/CVCL_0I46
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Part of: CEPH/Venezuelan pedigree cell line collection.
Proper citation: Coriell Cat# GM13356, RRID:CVCL_0I46 Copy
https://web.expasy.org/cellosaurus/CVCL_2Y99
Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_2Y99 Copy
https://web.expasy.org/cellosaurus/CVCL_CX13
Organism: Homo sapiens (Human)
Disease: Glycine encephalopathy
Category: Finite cell line
Comments: Population: Jordanian.
Proper citation: RRID:CVCL_CX13 Copy
https://web.expasy.org/cellosaurus/CVCL_IJ40
Organism: Homo sapiens (Human)
Disease: MASA syndrome
Category: Transformed cell line
Proper citation: RRID:CVCL_IJ40 Copy
https://web.expasy.org/cellosaurus/CVCL_5P88
Organism: Homo sapiens (Human)
Disease: Williams syndrome
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM13468, RRID:CVCL_5P88 Copy
https://web.expasy.org/cellosaurus/CVCL_5P91
Organism: Homo sapiens (Human)
Disease: Williams syndrome
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_5P91 Copy
https://web.expasy.org/cellosaurus/CVCL_1J79
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Proper citation: RRID:CVCL_1J79 Copy
https://web.expasy.org/cellosaurus/CVCL_5P88
Organism: Homo sapiens (Human)
Disease: Williams syndrome
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_5P88 Copy
https://web.expasy.org/cellosaurus/CVCL_5P82
Organism: Homo sapiens (Human)
Disease: Williams syndrome
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM13461, RRID:CVCL_5P82 Copy
https://web.expasy.org/cellosaurus/CVCL_DE55
Organism: Homo sapiens (Human)
Category: Hybrid cell line
Comments: Group: Human/rodent somatic cell hybrid.
Proper citation: Coriell Cat# GM13502, RRID:CVCL_DE55 Copy
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