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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.
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_CY27
Organism: Homo sapiens (Human)
Category: Finite cell line
Proper citation: Coriell Cat# GM03313, RRID:CVCL_CY27 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_CY27
Organism: Homo sapiens (Human)
Category: Finite cell line
Proper citation: RRID:CVCL_CY27 Copy
https://web.expasy.org/cellosaurus/CVCL_J655
Organism: Homo sapiens (Human)
Disease: Bloom syndrome
Category: Finite cell line
Comments: Donor information: From Bloom Syndrome Registry patient 9(EmSh) (BSR9)., Population: Jewish; Ashkenazi.
Proper citation: RRID:CVCL_J655 Copy
https://web.expasy.org/cellosaurus/CVCL_GT48
Organism: Homo sapiens (Human)
Disease: Hereditary hemorrhagic telangiectasia
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_GT48 Copy
https://web.expasy.org/cellosaurus/CVCL_V470
Organism: Homo sapiens (Human)
Disease: Down syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,XX,der(14;21)(14qter->14q10::21q10->21qter),+21 [34]; 45,XX,der(14;21)(14qter->14q10::21q10->21qter) [16] (Coriell=GM03417)., Population: Caucasian.
Proper citation: RRID:CVCL_V470 Copy
https://web.expasy.org/cellosaurus/CVCL_J998
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: African American.
Proper citation: RRID:CVCL_J998 Copy
https://web.expasy.org/cellosaurus/CVCL_5M82
Organism: Homo sapiens (Human)
Disease: Duchenne muscular dystrophy
Category: Finite cell line
Comments: From: Montreal Children's Hospital cell repository; Montreal; Canada.
Proper citation: RRID:CVCL_5M82 Copy
https://web.expasy.org/cellosaurus/CVCL_X285
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_X285 Copy
https://web.expasy.org/cellosaurus/CVCL_7385
Organism: Homo sapiens (Human)
Disease: Ataxia telangiectasia syndrome
Category: Finite cell line
Comments: Population: African American.
Proper citation: RRID:CVCL_7385 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_DS12
Organism: Homo sapiens (Human)
Disease: 46,XY sex reversal 1
Category: Finite cell line
Comments: Population: African American.
Proper citation: RRID:CVCL_DS12 Copy
https://web.expasy.org/cellosaurus/CVCL_X285
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03369, RRID:CVCL_X285 Copy
https://web.expasy.org/cellosaurus/CVCL_1F14
Organism: Homo sapiens (Human)
Disease: Glycogen storage disease type III
Category: Finite cell line
Comments: Population: Arab.
Proper citation: Coriell Cat# GM03390, RRID:CVCL_1F14 Copy
https://web.expasy.org/cellosaurus/CVCL_1F14
Organism: Homo sapiens (Human)
Disease: Glycogen storage disease type III
Category: Finite cell line
Comments: Population: Arab.
Proper citation: RRID:CVCL_1F14 Copy
https://web.expasy.org/cellosaurus/CVCL_W032
Organism: Homo sapiens (Human)
Disease: Hypophosphatasia
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_W032 Copy
https://web.expasy.org/cellosaurus/CVCL_9Z61
Organism: Homo sapiens (Human)
Disease: Neurofibromatosis type 1
Category: Transformed cell line
Proper citation: RRID:CVCL_9Z61 Copy
https://web.expasy.org/cellosaurus/CVCL_9Z62
Organism: Homo sapiens (Human)
Disease: Neurofibromatosis type 1
Category: Transformed cell line
Proper citation: Coriell Cat# GM03421, RRID:CVCL_9Z62 Copy
https://web.expasy.org/cellosaurus/CVCL_X106
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 47,XX,inv(9)(pter->p11::q13->p11::q13->qter)pat,+der(22)(22pter->22q11::11q23->11qter)mat (Coriell=GM03371)., Population: African American.
Proper citation: Coriell Cat# GM03371, RRID:CVCL_X106 Copy
https://web.expasy.org/cellosaurus/CVCL_0M20
Organism: Homo sapiens (Human)
Disease: Cystic fibrosis
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_0M20 Copy
https://web.expasy.org/cellosaurus/CVCL_GT49
Organism: Homo sapiens (Human)
Disease: Hereditary hemorrhagic telangiectasia
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_GT49 Copy
https://web.expasy.org/cellosaurus/CVCL_X105
Organism: Homo sapiens (Human)
Category: Finite cell line
Proper citation: RRID:CVCL_X105 Copy
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