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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_Y966
Organism: Homo sapiens (Human)
Disease: Werdnig-Hoffmann disease
Category: Transformed cell line
Proper citation: RRID:CVCL_Y966 Copy
https://web.expasy.org/cellosaurus/CVCL_Y736
Organism: Homo sapiens (Human)
Disease: Ornithine carbamoyltransferase deficiency disease
Category: Transformed cell line
Proper citation: RRID:CVCL_Y736 Copy
https://web.expasy.org/cellosaurus/CVCL_T803
Organism: Homo sapiens (Human)
Category: Induced pluripotent stem cell
Comments: Population: African American.
Proper citation: Coriell Cat# GM23716, RRID:CVCL_T803 Copy
https://web.expasy.org/cellosaurus/CVCL_5S98
Organism: Homo sapiens (Human)
Disease: Lubs X-linked intellectual disability syndrome
Category: Transformed cell line
Comments: Part of: Genetic Testing Reference Material (GeT-RM) samples.
Proper citation: RRID:CVCL_5S98 Copy
https://web.expasy.org/cellosaurus/CVCL_5T12
Organism: Homo sapiens (Human)
Disease: Intellectual developmental disorder, autosomal dominant 1
Category: Transformed cell line
Proper citation: RRID:CVCL_5T12 Copy
https://web.expasy.org/cellosaurus/CVCL_AY81
Organism: Homo sapiens (Human)
Disease: Argininosuccinic aciduria
Category: Transformed cell line
Proper citation: RRID:CVCL_AY81 Copy
https://web.expasy.org/cellosaurus/CVCL_BW06
Organism: Homo sapiens (Human)
Disease: Amyotrophic lateral sclerosis 1
Category: Transformed cell line
Proper citation: RRID:CVCL_BW06 Copy
https://web.expasy.org/cellosaurus/CVCL_AD83
Organism: Homo sapiens (Human)
Disease: X-linked centronuclear myopathy
Category: Transformed cell line
Comments: Population: Caucasian; Dutch.
Proper citation: RRID:CVCL_AD83 Copy
https://web.expasy.org/cellosaurus/CVCL_5K26
Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_5K26 Copy
https://web.expasy.org/cellosaurus/CVCL_BW13
Organism: Homo sapiens (Human)
Disease: Inclusion body myositis
Category: Transformed cell line
Proper citation: Coriell Cat# GM23771, RRID:CVCL_BW13 Copy
https://web.expasy.org/cellosaurus/CVCL_AD84
Organism: Homo sapiens (Human)
Category: Transformed cell line
Proper citation: Coriell Cat# GM23806, RRID:CVCL_AD84 Copy
https://web.expasy.org/cellosaurus/CVCL_Y744
Organism: Homo sapiens (Human)
Disease: Ornithine carbamoyltransferase deficiency disease
Category: Transformed cell line
Proper citation: RRID:CVCL_Y744 Copy
https://web.expasy.org/cellosaurus/CVCL_AD80
Organism: Homo sapiens (Human)
Category: Transformed cell line
Proper citation: RRID:CVCL_AD80 Copy
https://web.expasy.org/cellosaurus/CVCL_T807
Organism: Homo sapiens (Human)
Disease: Schizophrenia
Category: Induced pluripotent stem cell
Comments: Population: Jewish and Caucasian; Scandinavian.
Proper citation: RRID:CVCL_T807 Copy
https://web.expasy.org/cellosaurus/CVCL_AY86
Organism: Homo sapiens (Human)
Category: Transformed cell line
Proper citation: Coriell Cat# GM23794, RRID:CVCL_AY86 Copy
https://web.expasy.org/cellosaurus/CVCL_4T50
Organism: Homo sapiens (Human)
Disease: Ullrich congenital muscular dystrophy
Category: Transformed cell line
Proper citation: RRID:CVCL_4T50 Copy
https://web.expasy.org/cellosaurus/CVCL_Y750
Organism: Homo sapiens (Human)
Disease: Ornithine carbamoyltransferase deficiency disease
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM23752, RRID:CVCL_Y750 Copy
https://web.expasy.org/cellosaurus/CVCL_Y754
Organism: Homo sapiens (Human)
Disease: Ornithine carbamoyltransferase deficiency disease
Category: Transformed cell line
Proper citation: Coriell Cat# GM23788, RRID:CVCL_Y754 Copy
https://web.expasy.org/cellosaurus/CVCL_Y745
Organism: Homo sapiens (Human)
Disease: Ornithine carbamoyltransferase deficiency disease
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_Y745 Copy
https://web.expasy.org/cellosaurus/CVCL_4T50
Organism: Homo sapiens (Human)
Disease: Ullrich congenital muscular dystrophy
Category: Transformed cell line
Proper citation: Coriell Cat# GM23728, RRID:CVCL_4T50 Copy
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