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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_6B40
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM01016, RRID:CVCL_6B40 Copy
https://web.expasy.org/cellosaurus/CVCL_V531
Organism: Homo sapiens (Human)
Disease: Hurler syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_V531 Copy
https://web.expasy.org/cellosaurus/CVCL_V036
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_V036 Copy
https://web.expasy.org/cellosaurus/CVCL_M982
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Latino or Hispanic; Dominican., Part of: Human variation panel.
Proper citation: RRID:CVCL_M982 Copy
https://web.expasy.org/cellosaurus/CVCL_V799
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 49,XXXXY (Coriell=GM01202)., Population: Caucasian.
Proper citation: RRID:CVCL_V799 Copy
https://web.expasy.org/cellosaurus/CVCL_4J28
Organism: Homo sapiens (Human)
Disease: Porphyria cutanea tarda
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM01179, RRID:CVCL_4J28 Copy
https://web.expasy.org/cellosaurus/CVCL_4J20
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM01150, RRID:CVCL_4J20 Copy
https://web.expasy.org/cellosaurus/CVCL_4J29
Organism: Homo sapiens (Human)
Disease: Glucose-6-phosphate dehydrogenase deficiency
Category: Finite cell line
Comments: Karyotypic information: 46,XY,inv(9) (Coriell=GM01188)., Population: Caucasian; Sardinian.
Proper citation: RRID:CVCL_4J29 Copy
https://web.expasy.org/cellosaurus/CVCL_4J23
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM01153, RRID:CVCL_4J23 Copy
https://web.expasy.org/cellosaurus/CVCL_CV40
Organism: Homo sapiens (Human)
Disease: Progeria
Category: Finite cell line
Comments: From: Montreal Children's Hospital cell repository; Montreal; Canada.
Proper citation: RRID:CVCL_CV40 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_CX14
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM01159, RRID:CVCL_CX14 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_JB92
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_JB92 Copy
https://web.expasy.org/cellosaurus/CVCL_8516
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM01187, RRID:CVCL_8516 Copy
https://web.expasy.org/cellosaurus/CVCL_H142
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_H142 Copy
https://web.expasy.org/cellosaurus/CVCL_4J21
Organism: Homo sapiens (Human)
Disease: Glucose-6-phosphate dehydrogenase deficiency
Category: Finite cell line
Comments: Population: Caucasian; Sardinian.
Proper citation: RRID:CVCL_4J21 Copy
https://web.expasy.org/cellosaurus/CVCL_V798
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: African American.
Proper citation: RRID:CVCL_V798 Copy
https://web.expasy.org/cellosaurus/CVCL_CX03
Organism: Homo sapiens (Human)
Disease: Glycine encephalopathy
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_CX03 Copy
https://web.expasy.org/cellosaurus/CVCL_1Y23
Organism: Homo sapiens (Human)
Disease: Galactosemia
Category: Finite cell line
Comments: Donor information: Established from monozygotic twin of GM01210 (Cellosaurus=CVCL_1Y24)., Population: Latino or Hispanic; Dominican.
Proper citation: RRID:CVCL_1Y23 Copy
https://web.expasy.org/cellosaurus/CVCL_H142
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM01206, RRID:CVCL_H142 Copy
https://web.expasy.org/cellosaurus/CVCL_H967
Organism: Homo sapiens (Human)
Disease: Hepatocyte nuclear factor 4-alpha associated monogenic diabetes
Category: Finite cell line
Comments: Population: Caucasian., Part of: R-W pedigree MODY cell line collection.
Proper citation: RRID:CVCL_H967 Copy
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