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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_9B72
Organism: Homo sapiens (Human)
Disease: Klinefelter syndrome
Category: Transformed cell line
Comments: Karyotypic information: 46,Y,inv(X)(?q11;q21.2) (ECACC=92043034)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92043034, RRID:CVCL_9B72 Copy
https://web.expasy.org/cellosaurus/CVCL_9C02
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92052813, RRID:CVCL_9C02 Copy
https://web.expasy.org/cellosaurus/CVCL_9B97
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92052211, RRID:CVCL_9B97 Copy
https://web.expasy.org/cellosaurus/CVCL_9B62
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92042410, RRID:CVCL_9B62 Copy
https://web.expasy.org/cellosaurus/CVCL_9B88
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92051804, RRID:CVCL_9B88 Copy
https://web.expasy.org/cellosaurus/CVCL_9B99
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92052213, RRID:CVCL_9B99 Copy
https://web.expasy.org/cellosaurus/CVCL_9B74
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92043036, RRID:CVCL_9B74 Copy
https://web.expasy.org/cellosaurus/CVCL_9C22
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92061217, RRID:CVCL_9C22 Copy
https://web.expasy.org/cellosaurus/CVCL_9C28
Organism: Homo sapiens (Human)
Disease: 47,XYY syndrome
Category: Transformed cell line
Comments: Karyotypic information: 46,XY; 47,XYY (ECACC=92061505)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92061505, RRID:CVCL_9C28 Copy
https://web.expasy.org/cellosaurus/CVCL_9C06
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92060310, RRID:CVCL_9C06 Copy
https://web.expasy.org/cellosaurus/CVCL_9C13
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 47,XX,+dic(15)(pter->q11::q11->pter) (ECACC=92060527)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92060527, RRID:CVCL_9C13 Copy
https://web.expasy.org/cellosaurus/CVCL_9C11
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92060502, RRID:CVCL_9C11 Copy
https://web.expasy.org/cellosaurus/CVCL_9C09
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92060313, RRID:CVCL_9C09 Copy
https://web.expasy.org/cellosaurus/CVCL_9C45
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92062583, RRID:CVCL_9C45 Copy
https://web.expasy.org/cellosaurus/CVCL_9C44
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92062582, RRID:CVCL_9C44 Copy
https://web.expasy.org/cellosaurus/CVCL_9C07
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92060311, RRID:CVCL_9C07 Copy
https://web.expasy.org/cellosaurus/CVCL_9C37
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,XY,t(9;15)(q22;q13)(?O) (ECACC=92062575)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92062575, RRID:CVCL_9C37 Copy
https://web.expasy.org/cellosaurus/CVCL_9C33
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,XY,19q+ (ECACC=92062318)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92062318, RRID:CVCL_9C33 Copy
https://web.expasy.org/cellosaurus/CVCL_9C21
Organism: Homo sapiens (Human)
Disease: Klinefelter syndrome
Category: Transformed cell line
Comments: Karyotypic information: 47,XXY (ECACC=92061216)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92061216, RRID:CVCL_9C21 Copy
https://web.expasy.org/cellosaurus/CVCL_9C50
Organism: Homo sapiens (Human)
Disease: Trisomy 18
Category: Finite cell line
Comments: Karyotypic information: 47,XY,+18 (ECACC=92070113)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92070113, RRID:CVCL_9C50 Copy
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