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_X222
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: African American.
Proper citation: Coriell Cat# GM00017, RRID:CVCL_X222 Copy
https://web.expasy.org/cellosaurus/CVCL_7267
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: African American.
Proper citation: RRID:CVCL_7267 Copy
https://web.expasy.org/cellosaurus/CVCL_X224
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,X,i(X)(p11.21) (PubMed=10377420)., Population: Caucasian.
Proper citation: Coriell Cat# GM00088, RRID:CVCL_X224 Copy
https://web.expasy.org/cellosaurus/CVCL_V746
Organism: Homo sapiens (Human)
Disease: Wolf-Hirschhorn syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM00072, RRID:CVCL_V746 Copy
https://web.expasy.org/cellosaurus/CVCL_H959
Organism: Homo sapiens (Human)
Disease: Nephropathic cystinosis
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_H959 Copy
https://web.expasy.org/cellosaurus/CVCL_X225
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM00137, RRID:CVCL_X225 Copy
https://web.expasy.org/cellosaurus/CVCL_H959
Organism: Homo sapiens (Human)
Disease: Nephropathic cystinosis
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM00090, RRID:CVCL_H959 Copy
https://web.expasy.org/cellosaurus/CVCL_X224
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,X,i(X)(p11.21) (PubMed=10377420)., Population: Caucasian.
Proper citation: RRID:CVCL_X224 Copy
https://web.expasy.org/cellosaurus/CVCL_V756
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM00214, RRID:CVCL_V756 Copy
https://web.expasy.org/cellosaurus/CVCL_V753
Organism: Homo sapiens (Human)
Disease: 49,XXXXY syndrome
Category: Finite cell line
Comments: Karyotypic information: 49,XXXXY,t(4;11)(q35;q23).arr(X)x4,(Y)x1 (Coriell=GM00157)., Population: Caucasian.
Proper citation: RRID:CVCL_V753 Copy
https://web.expasy.org/cellosaurus/CVCL_V756
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_V756 Copy
https://web.expasy.org/cellosaurus/CVCL_V766
Organism: Homo sapiens (Human)
Disease: Wolf-Hirschhorn syndrome
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM00343, RRID:CVCL_V766 Copy
https://web.expasy.org/cellosaurus/CVCL_V766
Organism: Homo sapiens (Human)
Disease: Wolf-Hirschhorn syndrome
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_V766 Copy
https://web.expasy.org/cellosaurus/CVCL_V774
Organism: Homo sapiens (Human)
Disease: Intellectual developmental disorder
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM00501, RRID:CVCL_V774 Copy
https://web.expasy.org/cellosaurus/CVCL_0P86
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;9)(q13.1;p24) (PubMed=10377420)., Population: Caucasian.
Proper citation: RRID:CVCL_0P86 Copy
https://web.expasy.org/cellosaurus/CVCL_0P86
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;9)(q13.1;p24) (PubMed=10377420)., Population: Caucasian.
Proper citation: Coriell Cat# GM00705, RRID:CVCL_0P86 Copy
https://web.expasy.org/cellosaurus/CVCL_X235
Organism: Homo sapiens (Human)
Disease: Intellectual developmental disorder
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM00692, RRID:CVCL_X235 Copy
https://web.expasy.org/cellosaurus/CVCL_X076
Organism: Homo sapiens (Human)
Disease: Isodicentric chromosome
Category: Finite cell line
Comments: Karyotypic information: 46,X,i(X)(p11) (PubMed=10377420)., Population: Caucasian.
Proper citation: RRID:CVCL_X076 Copy
https://web.expasy.org/cellosaurus/CVCL_4E27
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM00782, RRID:CVCL_4E27 Copy
https://web.expasy.org/cellosaurus/CVCL_V784
Organism: Homo sapiens (Human)
Disease: Intellectual developmental disorder
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_V784 Copy
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