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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_4419
Organism: Homo sapiens (Human)
Disease: Cystic fibrosis
Category: Transformed cell line
Comments: Caution: Was briefly displayed in Cell Bank Australia under catalog number CBA-0044 but was never intended to be distributed.
Proper citation: RRID:CVCL_4419 Copy
https://web.expasy.org/cellosaurus/CVCL_T960
Organism: Rattus norvegicus (Rat)
Disease:
Category: Transformed cell line
Comments: Group: Patented cell line.
Proper citation: RRID:CVCL_T960 Copy
https://web.expasy.org/cellosaurus/CVCL_4423
Organism: Homo sapiens (Human)
Disease: Cystic fibrosis
Category: Transformed cell line
Comments: Caution: Was briefly displayed in Cell Bank Australia under catalog number CBA-0043 but was never intended to be distributed.
Proper citation: RRID:CVCL_4423 Copy
https://web.expasy.org/cellosaurus/CVCL_8X81
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Karyotypic information: 46,XY,fra(X)(q27) (ECACC=92012307)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92012307, RRID:CVCL_8X81 Copy
https://web.expasy.org/cellosaurus/CVCL_8X81
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Karyotypic information: 46,XY,fra(X)(q27) (ECACC=92012307)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_8X81 Copy
https://web.expasy.org/cellosaurus/CVCL_8X73
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Karyotypic information: 46,XY,fra(X)(q27.3) 10% in 70 metaphases (ECACC=91071906)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_8X73 Copy
https://web.expasy.org/cellosaurus/CVCL_8X79
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Karyotypic information: 46,XY,fra(X)(q27) (ECACC=92012304)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92012304, RRID:CVCL_8X79 Copy
https://web.expasy.org/cellosaurus/CVCL_8X77
Organism: Homo sapiens (Human)
Disease: Seckel syndrome
Category: Transformed cell line
Comments: Karyotypic information: 46,Y,r(X)(p22.3;q28) (ECACC=91102601)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 91102601, RRID:CVCL_8X77 Copy
https://web.expasy.org/cellosaurus/CVCL_8X72
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Karyotypic information: 46,XY,fra(X)(q27) (ECACC=90091401)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90091401, RRID:CVCL_8X72 Copy
https://web.expasy.org/cellosaurus/CVCL_8X80
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Population: Caucasian., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_8X80 Copy
https://web.expasy.org/cellosaurus/CVCL_8X73
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Karyotypic information: 46,XY,fra(X)(q27.3) 10% in 70 metaphases (ECACC=91071906)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 91071906, RRID:CVCL_8X73 Copy
https://web.expasy.org/cellosaurus/CVCL_8X82
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Karyotypic information: 46,XY,fra(X)(q27.3) (ECACC=92020605)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92020605, RRID:CVCL_8X82 Copy
https://web.expasy.org/cellosaurus/CVCL_8X72
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Karyotypic information: 46,XY,fra(X)(q27) (ECACC=90091401)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_8X72 Copy
https://web.expasy.org/cellosaurus/CVCL_8X88
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Karyotypic information: 46,XX,+fra(X) (ECACC=92080611)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92080611, RRID:CVCL_8X88 Copy
https://web.expasy.org/cellosaurus/CVCL_8X83
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Karyotypic information: 46,X,fra(X)(q27.3) (ECACC=92041013)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_8X83 Copy
https://web.expasy.org/cellosaurus/CVCL_8X76
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 91091106, RRID:CVCL_8X76 Copy
https://web.expasy.org/cellosaurus/CVCL_8X74
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Karyotypic information: 46,XY,fra(X)(q27) (ECACC=91080806)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 91080806, RRID:CVCL_8X74 Copy
https://web.expasy.org/cellosaurus/CVCL_8X87
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Karyotypic information: 46,XX,+fra(X) (ECACC=92080610)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92080610, RRID:CVCL_8X87 Copy
https://web.expasy.org/cellosaurus/CVCL_8X79
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Karyotypic information: 46,XY,fra(X)(q27) (ECACC=92012304)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_8X79 Copy
https://web.expasy.org/cellosaurus/CVCL_8X86
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_8X86 Copy
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