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    Wyświetlanie 1-9 z 9
    Tytuł:
    Methodology for the identification of small molecule inhibitors of the Fanconi Anaemia ubiquitin E3 ligase complex.
    Autorzy:
    Sharp MF; St Vincent's Institute of Medical Research, Fitzroy, Victoria, 3065, Australia.
    Murphy VJ; St Vincent's Institute of Medical Research, Fitzroy, Victoria, 3065, Australia.
    Twest SV; St Vincent's Institute of Medical Research, Fitzroy, Victoria, 3065, Australia.
    Tan W; St Vincent's Institute of Medical Research, Fitzroy, Victoria, 3065, Australia.; Department of Medicine (St. Vincent's Health), The University of Melbourne, Melbourne, VIC, 3010, Australia.
    Lui J; Victorian Centre for Functional Genomics, Peter MacCallum Cancer Centre, Melbourne, VIC, 3000, Australia.
    Simpson KJ; Victorian Centre for Functional Genomics, Peter MacCallum Cancer Centre, Melbourne, VIC, 3000, Australia.; Sir Peter MacCallum Cancer Centre Department of Oncology, University of Melbourne, Melbourne, VIC, 3010, Australia.
    Deans AJ; St Vincent's Institute of Medical Research, Fitzroy, Victoria, 3065, Australia.; Department of Medicine (St. Vincent's Health), The University of Melbourne, Melbourne, VIC, 3010, Australia.
    Crismani W; St Vincent's Institute of Medical Research, Fitzroy, Victoria, 3065, Australia. .; Department of Medicine (St. Vincent's Health), The University of Melbourne, Melbourne, VIC, 3010, Australia. .
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    Źródło:
    Scientific reports [Sci Rep] 2020 May 14; Vol. 10 (1), pp. 7959. Date of Electronic Publication: 2020 May 14.
    Typ publikacji:
    Journal Article; Research Support, Non-U.S. Gov't
    MeSH Terms:
    Enzyme Inhibitors/*pharmacology
    Fanconi Anemia Complementation Group D2 Protein/*antagonists & inhibitors
    Small Molecule Libraries/*pharmacology
    Cell Line, Tumor ; Fanconi Anemia Complementation Group D2 Protein/metabolism ; Humans ; Ubiquitination/drug effects
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Preparation and purification of mono-ubiquitinated proteins using Avi-tagged ubiquitin.
    Autorzy:
    Tan W; Genome Stability Unit, St. Vincent's Institute of Medical Research, Fitzroy, Victoria, Australia.; Department of Medicine (St. Vincent's Health), The University of Melbourne, Victoria, Australia.
    Murphy VJ; Genome Stability Unit, St. Vincent's Institute of Medical Research, Fitzroy, Victoria, Australia.
    Charron A; Genome Stability Unit, St. Vincent's Institute of Medical Research, Fitzroy, Victoria, Australia.; National Graduate School of Chemistry of Montpellier (ENSCM), Montpellier, France.
    van Twest S; Genome Stability Unit, St. Vincent's Institute of Medical Research, Fitzroy, Victoria, Australia.
    Sharp M; Genome Stability Unit, St. Vincent's Institute of Medical Research, Fitzroy, Victoria, Australia.
    Constantinou A; Institute of Human Genetics (IGH), Centre National de la Recherche Scientifique (CNRS), Université de Montpellier (UM), Montpellier, France.
    Parker MW; Structural Biology Unit, St. Vincent's Institute of Medical Research, Fitzroy, Victoria, Australia.; Bio21 Institute, University of Melbourne, Parkville, Victoria, Australia.
    Crismani W; Genome Stability Unit, St. Vincent's Institute of Medical Research, Fitzroy, Victoria, Australia.; Department of Medicine (St. Vincent's Health), The University of Melbourne, Victoria, Australia.
    Bythell-Douglas R; Genome Stability Unit, St. Vincent's Institute of Medical Research, Fitzroy, Victoria, Australia.; Department of Medicine (St. Vincent's Health), The University of Melbourne, Victoria, Australia.
    Deans AJ; Genome Stability Unit, St. Vincent's Institute of Medical Research, Fitzroy, Victoria, Australia.; Department of Medicine (St. Vincent's Health), The University of Melbourne, Victoria, Australia.
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    Źródło:
    PloS one [PLoS One] 2020 Feb 24; Vol. 15 (2), pp. e0229000. Date of Electronic Publication: 2020 Feb 24 (Print Publication: 2020).
    Typ publikacji:
    Journal Article; Research Support, Non-U.S. Gov't
    MeSH Terms:
    Fanconi Anemia Complementation Group D2 Protein*/chemistry
    Fanconi Anemia Complementation Group D2 Protein*/isolation & purification
    Fanconi Anemia Complementation Group Proteins*/chemistry
    Fanconi Anemia Complementation Group Proteins*/isolation & purification
    Proliferating Cell Nuclear Antigen*/chemistry
    Proliferating Cell Nuclear Antigen*/isolation & purification
    Ubiquitin*/chemistry
    Ubiquitin*/isolation & purification
    Ubiquitin-Protein Ligases*/chemistry
    Ubiquitin-Protein Ligases*/isolation & purification
    Avidin/*chemistry
    Animals ; Humans ; Sf9 Cells ; Spodoptera ; Ubiquitinated Proteins/chemistry ; Ubiquitinated Proteins/isolation & purification
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    ALT control, delete: FANCM as an anti-cancer target in Alternative Lengthening of Telomeres.
    Autorzy:
    O'Rourke JJ; Genome Stability Unit, St. Vincent's Institute of Medical Research, Fitzroy, Australia.; Department of Medicine, (St Vincent's) University of Melbourne, Fitzroy, Australia.
    Bythell-Douglas R; Genome Stability Unit, St. Vincent's Institute of Medical Research, Fitzroy, Australia.
    Dunn EA; Genome Stability Unit, St. Vincent's Institute of Medical Research, Fitzroy, Australia.
    Deans AJ; Genome Stability Unit, St. Vincent's Institute of Medical Research, Fitzroy, Australia.; Department of Medicine, (St Vincent's) University of Melbourne, Fitzroy, Australia.
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    Źródło:
    Nucleus (Austin, Tex.) [Nucleus] 2019 Dec; Vol. 10 (1), pp. 221-230.
    Typ publikacji:
    Journal Article; Research Support, Non-U.S. Gov't; Review
    MeSH Terms:
    DNA Helicases/*antagonists & inhibitors
    DNA Helicases/*metabolism
    Neoplasms/*drug therapy
    Neoplasms/*genetics
    Telomere Homeostasis/*drug effects
    DNA Helicases/deficiency ; DNA Repair/drug effects ; DNA Replication/drug effects ; Humans ; Neoplasms/metabolism ; Neoplasms/pathology
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    ATP-dependent helicase activity is dispensable for the physiological functions of Recql4.
    Autorzy:
    Castillo-Tandazo W; St. Vincent's Institute of Medical Research, Fitzroy, VIC, Australia.; Department of Medicine, St. Vincent's Hospital, The University of Melbourne, Fitzroy, VIC, Australia.
    Smeets MF; St. Vincent's Institute of Medical Research, Fitzroy, VIC, Australia.; Department of Medicine, St. Vincent's Hospital, The University of Melbourne, Fitzroy, VIC, Australia.
    Murphy V; St. Vincent's Institute of Medical Research, Fitzroy, VIC, Australia.
    Liu R; St. Vincent's Institute of Medical Research, Fitzroy, VIC, Australia.
    Hodson C; St. Vincent's Institute of Medical Research, Fitzroy, VIC, Australia.
    Heierhorst J; St. Vincent's Institute of Medical Research, Fitzroy, VIC, Australia.; Department of Medicine, St. Vincent's Hospital, The University of Melbourne, Fitzroy, VIC, Australia.
    Deans AJ; St. Vincent's Institute of Medical Research, Fitzroy, VIC, Australia.; Department of Medicine, St. Vincent's Hospital, The University of Melbourne, Fitzroy, VIC, Australia.
    Walkley CR; St. Vincent's Institute of Medical Research, Fitzroy, VIC, Australia.; Department of Medicine, St. Vincent's Hospital, The University of Melbourne, Fitzroy, VIC, Australia.; Mary MacKillop Institute for Health Research, Australian Catholic University, Melbourne, VIC, Australia.
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    Źródło:
    PLoS genetics [PLoS Genet] 2019 Jul 05; Vol. 15 (7), pp. e1008266. Date of Electronic Publication: 2019 Jul 05 (Print Publication: 2019).
    Typ publikacji:
    Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
    MeSH Terms:
    Adenosine Triphosphate/*metabolism
    RecQ Helicases/*genetics
    RecQ Helicases/*metabolism
    Rothmund-Thomson Syndrome/*genetics
    Animals ; B-Lymphocytes/metabolism ; Binding Sites ; Body Weight ; DNA Damage ; Disease Models, Animal ; Embryonic Development ; Gene Knock-In Techniques ; Hematopoiesis ; Humans ; Mice ; Phenotype ; Protein Domains ; RecQ Helicases/chemistry ; T-Lymphocytes/metabolism
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    The PTEN phosphatase functions cooperatively with the Fanconi anemia proteins in DNA crosslink repair.
    Autorzy:
    Vuono EA; Department of Cell and Molecular Biology, University of Rhode Island, Kingston, Rhode Island, USA.
    Mukherjee A; Department of Obstetrics, Gynecology, and Reproductive Biology, Michigan State University, Grand Rapids, Michigan, USA.
    Vierra DA; Department of Cell and Molecular Biology, University of Rhode Island, Kingston, Rhode Island, USA.
    Adroved MM; Department of Cell and Molecular Biology, University of Rhode Island, Kingston, Rhode Island, USA.
    Hodson C; Genome Stability Unit, St. Vincent's Institute, Fitzroy, VIC 3065, Australia.
    Deans AJ; Genome Stability Unit, St. Vincent's Institute, Fitzroy, VIC 3065, Australia.; Department of Medicine, The University of Melbourne, Parkville, VIC 3010, Australia.
    Howlett NG; Department of Cell and Molecular Biology, University of Rhode Island, Kingston, Rhode Island, USA.
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    Źródło:
    Scientific reports [Sci Rep] 2016 Nov 07; Vol. 6, pp. 36439. Date of Electronic Publication: 2016 Nov 07.
    Typ publikacji:
    Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
    MeSH Terms:
    DNA Repair*
    Cell Cycle Proteins/*metabolism
    Fanconi Anemia Complementation Group Proteins/*metabolism
    PTEN Phosphohydrolase/*metabolism
    Protein Serine-Threonine Kinases/*metabolism
    Proto-Oncogene Proteins/*metabolism
    Cell Line, Tumor ; Chromatin/chemistry ; Chromatin/metabolism ; Chromosomal Instability/drug effects ; DNA Helicases/metabolism ; Fanconi Anemia Complementation Group D2 Protein/metabolism ; HCT116 Cells ; Histones/metabolism ; Humans ; Mitomycin/toxicity ; PTEN Phosphohydrolase/antagonists & inhibitors ; PTEN Phosphohydrolase/genetics ; Phosphorylation ; RNA Interference ; RNA, Small Interfering/metabolism ; Sumoylation ; Tumor Suppressor p53-Binding Protein 1/metabolism ; Ubiquitination ; Polo-Like Kinase 1
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
    Tytuł:
    DNA interstrand crosslink repair and cancer.
    Autorzy:
    Deans AJ; London Research Institute, Cancer Research UK, Clare Hall Laboratories, South Mimms EN63LD, UK.
    West SC
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    Źródło:
    Nature reviews. Cancer [Nat Rev Cancer] 2011 Jun 24; Vol. 11 (7), pp. 467-80. Date of Electronic Publication: 2011 Jun 24.
    Typ publikacji:
    Journal Article; Research Support, Non-U.S. Gov't; Review
    MeSH Terms:
    DNA Repair*
    Antineoplastic Agents/*pharmacology
    Cross-Linking Reagents/*pharmacology
    Neoplasms/*drug therapy
    Animals ; DNA Damage ; Drug Resistance, Neoplasm ; Fanconi Anemia/genetics ; Humans ; Neoplasms/etiology ; Neoplasms/genetics ; Recombination, Genetic
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
    Tytuł:
    Brca1 inactivation induces p27(Kip1)-dependent cell cycle arrest and delayed development in the mouse mammary gland.
    Autorzy:
    Deans AJ; Molecular Oncology Laboratory, Trescowthick Research Laboratories, Peter MacCallum Cancer Centre, St Andrew's Place, East Melbourne 3002, Australia.
    Simpson KJ
    Trivett MK
    Brown MA
    McArthur GA
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    Źródło:
    Oncogene [Oncogene] 2004 Aug 12; Vol. 23 (36), pp. 6136-45.
    Typ publikacji:
    Journal Article; Research Support, Non-U.S. Gov't
    MeSH Terms:
    Genes, BRCA1*
    Cell Cycle Proteins/*metabolism
    Mammary Glands, Human/*growth & development
    Tumor Suppressor Proteins/*metabolism
    Animals ; Cell Cycle ; Cell Cycle Proteins/genetics ; Cell Line ; Cyclin-Dependent Kinase Inhibitor p27 ; Epistasis, Genetic ; Epithelial Cells/metabolism ; Heterozygote ; Humans ; Kinetics ; Mammary Glands, Human/anatomy & histology ; Mammary Glands, Human/metabolism ; Mammary Tumor Virus, Mouse/genetics ; Mice ; Mutation ; Tumor Suppressor Proteins/genetics
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
      Wyświetlanie 1-9 z 9

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