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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_GS81
Organism: Homo sapiens (Human)
Disease: Juvenile myoclonic epilepsy
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_GS81 Copy
https://web.expasy.org/cellosaurus/CVCL_9Z47
Organism: Homo sapiens (Human)
Disease: Refsum disease
Category: Finite cell line
Proper citation: Coriell Cat# GM13202, RRID:CVCL_9Z47 Copy
https://web.expasy.org/cellosaurus/CVCL_N205
Organism: Homo sapiens (Human)
Disease: Hunter syndrome
Category: Finite cell line
Comments: Population: Caribbean; Haitian., Part of: Human variation panel.
Proper citation: RRID:CVCL_N205 Copy
https://web.expasy.org/cellosaurus/CVCL_H548
Organism: Homo sapiens (Human)
Category: Finite cell line
Proper citation: RRID:CVCL_H548 Copy
https://web.expasy.org/cellosaurus/CVCL_X451
Organism: Homo sapiens (Human)
Disease: Aspartylglycosaminuria
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM13201, RRID:CVCL_X451 Copy
https://web.expasy.org/cellosaurus/CVCL_U401
Organism: Homo sapiens (Human)
Disease: Tay-Sachs disease
Category: Finite cell line
Proper citation: RRID:CVCL_U401 Copy
https://web.expasy.org/cellosaurus/CVCL_9Y33
Organism: Homo sapiens (Human)
Disease: Sly syndrome
Category: Finite cell line
Comments: Population: Mexican.
Proper citation: RRID:CVCL_9Y33 Copy
https://web.expasy.org/cellosaurus/CVCL_4Z71
Organism: Homo sapiens (Human)
Disease: Trichothiodystrophy
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM13287, RRID:CVCL_4Z71 Copy
https://web.expasy.org/cellosaurus/CVCL_2U25
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_2U25 Copy
https://web.expasy.org/cellosaurus/CVCL_9R32
Organism: Homo sapiens (Human)
Disease: Neonatal adrenoleukodystrophy
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_9R32 Copy
https://web.expasy.org/cellosaurus/CVCL_4F71
Organism: Homo sapiens (Human)
Disease: Medium-chain acyl-CoA dehydrogenase deficiency
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_4F71 Copy
https://web.expasy.org/cellosaurus/CVCL_IJ39
Organism: Homo sapiens (Human)
Disease: Galactosialidosis
Category: Finite cell line
Proper citation: Coriell Cat# GM13206, RRID:CVCL_IJ39 Copy
https://web.expasy.org/cellosaurus/CVCL_4F69
Organism: Homo sapiens (Human)
Disease: Zellweger syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM13272, RRID:CVCL_4F69 Copy
https://web.expasy.org/cellosaurus/CVCL_2U24
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(1;13)(1pter->1q25::13q22->13qter;13pter->13q22::1q25->1qter) (Coriell=GM13238).
Proper citation: Coriell Cat# GM13238, RRID:CVCL_2U24 Copy
https://web.expasy.org/cellosaurus/CVCL_IJ39
Organism: Homo sapiens (Human)
Disease: Galactosialidosis
Category: Finite cell line
Proper citation: RRID:CVCL_IJ39 Copy
https://web.expasy.org/cellosaurus/CVCL_4F66
Organism: Homo sapiens (Human)
Disease: Zellweger syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM13266, RRID:CVCL_4F66 Copy
https://web.expasy.org/cellosaurus/CVCL_4Z71
Organism: Homo sapiens (Human)
Disease: Trichothiodystrophy
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_4Z71 Copy
https://web.expasy.org/cellosaurus/CVCL_BW65
Organism: Homo sapiens (Human)
Disease: D-bifunctional protein deficiency
Category: Finite cell line
Comments: Population: African American.
Proper citation: RRID:CVCL_BW65 Copy
https://web.expasy.org/cellosaurus/CVCL_4F67
Organism: Homo sapiens (Human)
Disease: Zellweger syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM13267, RRID:CVCL_4F67 Copy
https://web.expasy.org/cellosaurus/CVCL_AX25
Organism: Homo sapiens (Human)
Disease: Niemann-Pick disease, type A
Category: Finite cell line
Comments: Population: Jewish; Ashkenazi., Part of: Genetic Testing Reference Material (GeT-RM) samples.
Proper citation: RRID:CVCL_AX25 Copy
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