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    Wyświetlanie 1-9 z 9
    Tytuł:
    Arginine Is a Novel Drug Target for Arginine Decarboxylase in Human Colorectal Cancer Cells.
    Autorzy:
    Wei X; Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong, China.
    Chow HY; Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong, China.
    Chong HC; Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong, China.
    Leung SL; Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong, China.
    Ho MK; Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong, China.
    Lee MY; Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong, China.; Lo Ka Chung Research Centre for Natural Anti-Cancer Drug Development, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong, China.; State Key Laboratory of Chemical Biology and Drug Discovery, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong, China.
    Leung YC; Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong, China.; Lo Ka Chung Research Centre for Natural Anti-Cancer Drug Development, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong, China.; State Key Laboratory of Chemical Biology and Drug Discovery, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong, China.
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    Źródło:
    International journal of molecular sciences [Int J Mol Sci] 2023 Sep 06; Vol. 24 (18). Date of Electronic Publication: 2023 Sep 06.
    Typ publikacji:
    Journal Article
    MeSH Terms:
    Agmatine*
    Colonic Neoplasms*
    Humans ; Animals ; Rats ; Arginase ; Arginine
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Qualitative and quantitative assessment of Illumina's forensic STR and SNP kits on MiSeq FGx™.
    Autorzy:
    Sharma V; Department of Forensic Biology, Office of Chief Medical Examiner, New York, NY, United States of America.
    Chow HY; Department of Forensic Biology, Office of Chief Medical Examiner, New York, NY, United States of America.
    Siegel D; Department of Forensic Biology, Office of Chief Medical Examiner, New York, NY, United States of America.
    Wurmbach E; Department of Forensic Biology, Office of Chief Medical Examiner, New York, NY, United States of America.
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    Źródło:
    PloS one [PLoS One] 2017 Nov 09; Vol. 12 (11), pp. e0187932. Date of Electronic Publication: 2017 Nov 09 (Print Publication: 2017).
    Typ publikacji:
    Journal Article
    MeSH Terms:
    Microsatellite Repeats*
    Polymorphism, Single Nucleotide*
    Forensic Genetics/*methods
    High-Throughput Nucleotide Sequencing/*methods
    DNA Fingerprinting/methods ; DNA Fingerprinting/standards ; Female ; Forensic Genetics/standards ; High-Throughput Nucleotide Sequencing/standards ; Humans ; Male ; Qualitative Research ; Reagent Kits, Diagnostic ; Reproducibility of Results
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
    Tytuł:
    Proteomics analysis of co-purifying cellular proteins associated with rAAV vectors.
    Autorzy:
    Dong B; Department of Microbiology and Immunology, Sol Sherry Thrombosis Research Center, Temple University, Philadelphia, Pennsylvania, United States of America.
    Duan X; Department of Microbiology and Immunology, Sol Sherry Thrombosis Research Center, Temple University, Philadelphia, Pennsylvania, United States of America.
    Chow HY; Cancer Biology Program, Fox Chase Cancer Center, Philadelphia, Pennsylvania, United States of America.
    Chen L; Department of Microbiology and Immunology, Sol Sherry Thrombosis Research Center, Temple University, Philadelphia, Pennsylvania, United States of America.
    Lu H; Department of Microbiology and Immunology, Sol Sherry Thrombosis Research Center, Temple University, Philadelphia, Pennsylvania, United States of America.
    Wu W; Department of Microbiology and Immunology, Sol Sherry Thrombosis Research Center, Temple University, Philadelphia, Pennsylvania, United States of America.
    Hauck B; Department of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, and Center for Cellular and Molecular Therapeutics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America.
    Wright F; Department of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, and Center for Cellular and Molecular Therapeutics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America.
    Kapranov P; St. Laurent Institute, Cambridge, Massachusetts, United States of America.
    Xiao W; Department of Microbiology and Immunology, Sol Sherry Thrombosis Research Center, Temple University, Philadelphia, Pennsylvania, United States of America.
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    Źródło:
    PloS one [PLoS One] 2014 Feb 03; Vol. 9 (2), pp. e86453. Date of Electronic Publication: 2014 Feb 03 (Print Publication: 2014).
    Typ publikacji:
    Journal Article; Research Support, N.I.H., Extramural
    MeSH Terms:
    Capsid Proteins/*analysis
    Dependovirus/*metabolism
    Proteome/*analysis
    Proteomics/*methods
    Blotting, Western ; Capsid Proteins/isolation & purification ; Chromatography, Liquid ; Dependovirus/genetics ; Electrophoresis, Gel, Two-Dimensional ; Genetic Therapy/methods ; Genetic Therapy/standards ; Genetic Vectors/genetics ; Humans ; Mass Spectrometry ; Proteome/isolation & purification ; Reproducibility of Results ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
    Tytuł:
    Recombinant human arginase inhibits the in vitro and in vivo proliferation of human melanoma by inducing cell cycle arrest and apoptosis.
    Autorzy:
    Lam TL; Department of Applied Biology and Chemical Technology and Lo Ka Chung Centre for Natural Anti-Cancer Drug Development, The Hong Kong, China.
    Wong GK
    Chow HY
    Chong HC
    Chow TL
    Kwok SY
    Cheng PN
    Wheatley DN
    Lo WH
    Leung YC
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    Źródło:
    Pigment cell & melanoma research [Pigment Cell Melanoma Res] 2011 Apr; Vol. 24 (2), pp. 366-76. Date of Electronic Publication: 2010 Dec 06.
    Typ publikacji:
    Journal Article; Research Support, Non-U.S. Gov't
    MeSH Terms:
    Arginase*/genetics
    Arginase*/pharmacology
    Arginase*/therapeutic use
    Recombinant Proteins*/genetics
    Recombinant Proteins*/pharmacology
    Recombinant Proteins*/therapeutic use
    Apoptosis/*drug effects
    Cell Cycle/*drug effects
    Melanoma/*drug therapy
    Melanoma/*pathology
    Animals ; Cell Proliferation/drug effects ; Clinical Trials as Topic ; Humans ; Melanoma/physiopathology ; Mice ; Mice, Inbred BALB C ; Mice, Nude ; Skin Neoplasms/drug therapy ; Skin Neoplasms/pathology ; Skin Neoplasms/physiopathology ; Tumor Cells, Cultured ; Xenograft Model Antitumor Assays ; raf Kinases/antagonists & inhibitors
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
    Tytuł:
    p21-Activated kinases are required for transformation in a cell-based model of neurofibromatosis type 2.
    Autorzy:
    Chow HY; Cancer Biology Program, Fox Chase Cancer Center, Philadelphia, Pennsylvania, United States of America.
    Stepanova D
    Koch J
    Chernoff J
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    Źródło:
    PloS one [PLoS One] 2010 Nov 02; Vol. 5 (11), pp. e13791. Date of Electronic Publication: 2010 Nov 02.
    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:
    Cell Transformation, Neoplastic*
    Neoplasms, Experimental/*metabolism
    Neurofibromatosis 2/*metabolism
    p21-Activated Kinases/*metabolism
    Animals ; Cell Adhesion ; Cell Movement ; Cell Shape ; Gene Knockdown Techniques ; Humans ; Immunoblotting ; Mice ; Mice, Inbred BALB C ; Mice, Nude ; NIH 3T3 Cells ; Neoplasms, Experimental/genetics ; Neoplasms, Experimental/pathology ; Neurofibromatosis 2/genetics ; Neurofibromatosis 2/pathology ; Neurofibromin 2/genetics ; Neurofibromin 2/metabolism ; Signal Transduction ; Transplantation, Heterologous ; p21-Activated Kinases/genetics
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
    Tytuł:
    Development of a low-cost polymerase chain reaction-based method for studying differentially expressed genes in developing rice leaves.
    Autorzy:
    Fung YW; Faculty of Science, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China.
    Chow HY
    Law TW
    Dong B
    Kwan HS
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    Źródło:
    Journal of integrative plant biology [J Integr Plant Biol] 2009 Jun; Vol. 51 (6), pp. 614-21.
    Typ publikacji:
    Journal Article; Research Support, Non-U.S. Gov't
    MeSH Terms:
    Gene Expression Profiling/*economics
    Gene Expression Profiling/*methods
    Oryza/*genetics
    Oryza/*growth & development
    Plant Leaves/*genetics
    Polymerase Chain Reaction/*economics
    Polymerase Chain Reaction/*methods
    Blotting, Northern ; Gene Expression Regulation, Developmental ; Gene Expression Regulation, Plant ; Genes, Plant ; Plant Leaves/growth & development ; RNA, Plant/genetics ; RNA, Plant/metabolism ; Reproducibility of Results
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
      Wyświetlanie 1-9 z 9

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