Search Results - "WYLIE, J. A"

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    Systemic Correction of the Muscle Disorder Glycogen Storage Disease Type II after Hepatic Targeting of a Modified Adenovirus Vector Encoding Human Acid α -Glucosidase by Amalfitano, A., McVie-Wylie, A. J., Hu, H., Dawson, T. L., Raben, N., Plotz, P., Chen, Y. T.

    “…This report demonstrates that a single intravenous administration of a gene therapy vector can potentially result in the correction of all affected muscles in…”
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    Journal Article
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    Long-term efficacy after [E1-, polymerase-] adenovirus-mediated transfer of human acid-alpha-glucosidase gene into glycogen storage disease type II knockout mice by Ding, E Y, Hodges, B L, Hu, H, McVie-Wylie, A J, Serra, D, Migone, F K, Pressley, D, Chen, Y T, Amalfitano, A

    Published in Human gene therapy (20-05-2001)
    “…Glycogen storage disease type II (GSD-II) is a lethal, autosomal recessive metabolic myopathy caused by a lack of acid-alpha-glucosidase (GAA) activity in the…”
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    Biochemical and pharmacological characterization of different recombinant acid α-glucosidase preparations evaluated for the treatment of Pompe disease by McVie-Wylie, A.J., Lee, K.L., Qiu, H., Jin, X., Do, H., Gotschall, R., Thurberg, B.L., Rogers, C., Raben, N., O’Callaghan, M., Canfield, W., Andrews, L., McPherson, J.M., Mattaliano, R.J.

    Published in Molecular genetics and metabolism (01-08-2008)
    “…Pompe disease results in the accumulation of lysosomal glycogen in multiple tissues due to a deficiency of acid α-glucosidase (GAA). Enzyme replacement therapy…”
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    Transcriptional response to GAA deficiency (Pompe disease) in infantile-onset patients by Palermo, A.T., Palmer, R.E., So, K.S., Oba-Shinjo, S.M., Zhang, M., Richards, B., Madhiwalla, S.T., Finn, P.F., Hasegawa, A., Ciociola, K.M., Pescatori, M., McVie-Wylie, A.J., Mattaliano, R.J., Madden, S.L., Marie, S.K.N., Klinger, K.W., Pomponio, R.J.

    Published in Molecular genetics and metabolism (01-07-2012)
    “…Pompe disease is a genetic disorder resulting from a deficiency of lysosomal acid alpha-glucosidase (GAA) that manifests as a clinical spectrum with regard to…”
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    Molecular Cloning of a Novel Member of the GLUT Family of Transporters, SLC2A10 (GLUT10), Localized on Chromosome 20q13.1: A Candidate Gene for NIDDM Susceptibility by McVie-Wylie, Alison J., Lamson, David R., Chen, Y.T.

    Published in Genomics (San Diego, Calif.) (15-02-2001)
    “…Non-insulin-dependent diabetes mellitus (NIDDM) is a multifactoral disease with both environmental and genetics causes. Genome-wide screening procedures have…”
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    The Plague of Athens: 430–428 B.C. Epidemic and Epizoötic by Wylie, J. A. H., Stubbs, H. W.

    Published in Classical quarterly (01-01-1983)
    “…In a recent re-assessment of the medical aspects of the Plague of Athens which is, to date, the most scholarly and comprehensive, Poole and Holladay have…”
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    Inhibition of Glycogen Biosynthesis via mTORC1 Suppression as an Adjunct Therapy for Pompe Disease by Ashe, K, Taylor, K.M, Chu, Q, Meyers, E, Ellis, A, Jingozyan, V, Klinger, K, Finn, P.F, Cooper, C.G.F, Chuang, W, Marshall, J, McVie-Wylie, A.J, McPherson, J.M, Mattaliano, R.J, Cheng, S.H, Scheule, R.K, Moreland, R.J

    Published in Clinical therapeutics (01-06-2011)
    “…Methods, Results We have examined the biochemical pathways regulating glycogen accumulation in muscle tissue of GAA-/- mice, and evaluated the efficacy of…”
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    Academic-Industry Liaison in the United Kingdom: Economic Perspectives by Connor, A. I., Wylie, J. A., Young, A.

    Published in Higher education (01-01-1986)
    “…In recent years, higher educational institutions (HEIs) have been under increasing pressure to liaise more closely with industry. This paper draws on some…”
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