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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_7371
Organism: Homo sapiens (Human)
Disease: Smith-Lemli-Opitz syndrome
Category: Finite cell line
Comments: Karyotypic information: 45,XY,der(13;14)(13qter->13q10::14q10->14qter) (Coriell=GM03044)., Population: Caucasian.
Proper citation: RRID:CVCL_7371 Copy
https://web.expasy.org/cellosaurus/CVCL_7375
Organism: Homo sapiens (Human)
Disease: Niemann-Pick disease, type C1
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_7375 Copy
https://web.expasy.org/cellosaurus/CVCL_4N36
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Jewish; Ashkenazi.
Proper citation: RRID:CVCL_4N36 Copy
https://web.expasy.org/cellosaurus/CVCL_X278
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XY,rec(3)(qter->p25::q21->qter)pat (Coriell=GM03085)., Population: Caucasian; French Canadian.
Proper citation: Coriell Cat# GM03085, RRID:CVCL_X278 Copy
https://web.expasy.org/cellosaurus/CVCL_EF92
Organism: Homo sapiens (Human)
Disease: Congenital sucrase-isomaltase deficiency
Category: Transformed cell line
Proper citation: Coriell Cat# GM03070, RRID:CVCL_EF92 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_UR78
Organism: Homo sapiens (Human)
Category: Finite cell line
Proper citation: Coriell Cat# GM03081, RRID:CVCL_UR78 Copy
https://web.expasy.org/cellosaurus/CVCL_EF92
Organism: Homo sapiens (Human)
Disease: Congenital sucrase-isomaltase deficiency
Category: Transformed cell line
Proper citation: RRID:CVCL_EF92 Copy
https://web.expasy.org/cellosaurus/CVCL_X061
Organism: Homo sapiens (Human)
Disease: Glycogen storage disease type VII
Category: Transformed cell line
Proper citation: Coriell Cat# GM03128, RRID:CVCL_X061 Copy
https://web.expasy.org/cellosaurus/CVCL_X102
Organism: Homo sapiens (Human)
Disease: Tetralogy of Fallot
Category: Finite cell line
Comments: Karyotypic information: 46,XX,der(1)(pter->p13.1::q21.1->p13.1::q21.1->q42.3) (Coriell=GM03126)., Population: African American.
Proper citation: Coriell Cat# GM03126, RRID:CVCL_X102 Copy
https://web.expasy.org/cellosaurus/CVCL_4Z82
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian; Sardinian.
Proper citation: Coriell Cat# GM03031, RRID:CVCL_4Z82 Copy
https://web.expasy.org/cellosaurus/CVCL_X054
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 45,X,-Y,inv(9)(p11;q13) [13]; 46,XY,inv(9)(p11;q13) [7] (Coriell=GM03120).
Proper citation: RRID:CVCL_X054 Copy
https://web.expasy.org/cellosaurus/CVCL_M934
Organism: Homo sapiens (Human)
Disease: Alpha thalassemia
Category: Finite cell line
Comments: Population: Southeast Asian; Vietnamese., Part of: Human variation panel.
Proper citation: Coriell Cat# GM03037, RRID:CVCL_M934 Copy
https://web.expasy.org/cellosaurus/CVCL_M936
Organism: Homo sapiens (Human)
Disease: Myopathy due to myoadenylate deaminase deficiency
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_M936 Copy
https://web.expasy.org/cellosaurus/CVCL_1F11
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_1F11 Copy
https://web.expasy.org/cellosaurus/CVCL_X428
Organism: Homo sapiens (Human)
Disease: X-linked ichthyosis
Category: Finite cell line
Comments: Population: Caucasian; Sardinian.
Proper citation: RRID:CVCL_X428 Copy
https://web.expasy.org/cellosaurus/CVCL_JM08
Organism: Homo sapiens (Human)
Disease: Anetoderma
Category: Finite cell line
Proper citation: Coriell Cat# GM03129, RRID:CVCL_JM08 Copy
https://web.expasy.org/cellosaurus/CVCL_X440
Organism: Homo sapiens (Human)
Disease: Type 1 diabetes mellitus
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03236, RRID:CVCL_X440 Copy
https://web.expasy.org/cellosaurus/CVCL_X047
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Karyotypic information: 46,XX,inv(5)(pter->p13::q13->p13::q13->qter),t(17;22)(17qter->17p13::22q11->22qter;22pter->22q11::17p13->17pter) (Coriell=GM03197)., Population: Caucasian.
Proper citation: Coriell Cat# GM03197, RRID:CVCL_X047 Copy
https://web.expasy.org/cellosaurus/CVCL_DD74
Organism: Homo sapiens (Human)
Disease: Osteogenesis imperfecta
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_DD74 Copy
https://web.expasy.org/cellosaurus/CVCL_AX76
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Proper citation: RRID:CVCL_AX76 Copy
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