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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_BV37
Organism: Homo sapiens (Human)
Disease: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
Category: Finite cell line
Proper citation: RRID:CVCL_BV37 Copy
https://web.expasy.org/cellosaurus/CVCL_JF24
Organism: Homo sapiens (Human)
Disease: Muscular dystrophy-dystroglycanopathy (limb-girdle) type C, 1
Category: Finite cell line
Proper citation: RRID:CVCL_JF24 Copy
https://web.expasy.org/cellosaurus/CVCL_BV32
Organism: Homo sapiens (Human)
Disease: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
Category: Finite cell line
Proper citation: RRID:CVCL_BV32 Copy
https://web.expasy.org/cellosaurus/CVCL_4T47
Organism: Homo sapiens (Human)
Disease: Ullrich congenital muscular dystrophy
Category: Finite cell line
Proper citation: RRID:CVCL_4T47 Copy
https://web.expasy.org/cellosaurus/CVCL_F196
Organism: Homo sapiens (Human)
Disease: Merosin-deficient congenital muscular dystrophy type 1A
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_F196 Copy
https://web.expasy.org/cellosaurus/CVCL_AZ46
Organism: Homo sapiens (Human)
Disease: Bethlem myopathy 1
Category: Finite cell line
Proper citation: RRID:CVCL_AZ46 Copy
https://web.expasy.org/cellosaurus/CVCL_4T45
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Korean.
Proper citation: Coriell Cat# GM23307, RRID:CVCL_4T45 Copy
https://web.expasy.org/cellosaurus/CVCL_4T45
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Korean.
Proper citation: RRID:CVCL_4T45 Copy
https://web.expasy.org/cellosaurus/CVCL_BV58
Organism: Homo sapiens (Human)
Disease: Renal agenesis
Category: Finite cell line
Proper citation: Coriell Cat# GM23377, RRID:CVCL_BV58 Copy
https://web.expasy.org/cellosaurus/CVCL_1N00
Organism: Homo sapiens (Human)
Disease: Hardcastle's syndrome
Category: Finite cell line
Proper citation: Coriell Cat# GM23468, RRID:CVCL_1N00 Copy
https://web.expasy.org/cellosaurus/CVCL_BV62
Organism: Homo sapiens (Human)
Disease: Long QT syndrome 2
Category: Finite cell line
Proper citation: RRID:CVCL_BV62 Copy
https://web.expasy.org/cellosaurus/CVCL_BV58
Organism: Homo sapiens (Human)
Disease: Renal agenesis
Category: Finite cell line
Proper citation: RRID:CVCL_BV58 Copy
https://web.expasy.org/cellosaurus/CVCL_BV94
Organism: Homo sapiens (Human)
Disease: Facioscapulohumeral muscular dystrophy
Category: Finite cell line
Proper citation: RRID:CVCL_BV94 Copy
https://web.expasy.org/cellosaurus/CVCL_1N06
Organism: Homo sapiens (Human)
Disease: Hardcastle's syndrome
Category: Finite cell line
Proper citation: Coriell Cat# GM23623, RRID:CVCL_1N06 Copy
https://web.expasy.org/cellosaurus/CVCL_M919
Organism: Homo sapiens (Human)
Disease: Hardcastle's syndrome
Category: Finite cell line
Proper citation: RRID:CVCL_M919 Copy
https://web.expasy.org/cellosaurus/CVCL_M919
Organism: Homo sapiens (Human)
Disease: Hardcastle's syndrome
Category: Finite cell line
Proper citation: Coriell Cat# GM23613, RRID:CVCL_M919 Copy
https://web.expasy.org/cellosaurus/CVCL_1N02
Organism: Homo sapiens (Human)
Disease: Hardcastle's syndrome
Category: Finite cell line
Proper citation: Coriell Cat# GM23611, RRID:CVCL_1N02 Copy
https://web.expasy.org/cellosaurus/CVCL_BV94
Organism: Homo sapiens (Human)
Disease: Facioscapulohumeral muscular dystrophy
Category: Finite cell line
Proper citation: Coriell Cat# GM23642, RRID:CVCL_BV94 Copy
https://web.expasy.org/cellosaurus/CVCL_BX05
Organism: Homo sapiens (Human)
Disease: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type A, 6
Category: Finite cell line
Proper citation: RRID:CVCL_BX05 Copy
https://web.expasy.org/cellosaurus/CVCL_AZ47
Organism: Homo sapiens (Human)
Disease: Rigid spine muscular dystrophy 1
Category: Finite cell line
Comments: Population: Jewish; Ashkenazi.
Proper citation: RRID:CVCL_AZ47 Copy
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