Результати пошуку - Sankar Surendran

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  1. 1
    Arginine Stimulates cdx2-Transformed Intestinal Epithelial Cell Migration via a Mechanism Requiring Both Nitric Oxide and Phosphorylation of p70 S6 Kinase1,

    Arginine Stimulates cdx2-Transformed Intestinal Epithelial Cell Migration via a Mechanism Requiring Both Nitric Oxide and Phosphorylation of p70 S6 Kinase1, за авторством J. Marc Rhoads, Yuying Liu, Xiaomei Niu, Sankar Surendran, Guoyao Wu

    Опубліковано 2008
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  2. 2
    A Novel Role for ATM in Regulating Proteasome-Mediated Protein Degradation through Suppression of the ISG15 Conjugation Pathway

    A Novel Role for ATM in Regulating Proteasome-Mediated Protein Degradation through Suppression of the ISG15 Conjugation Pathway за авторством Laurence M. Wood, Sankar Surendran, Ryan Reed, Arthur L. Haas, Leroy F. Liu, Peter J. McKinnon, Shyamal D. Desai

    Опубліковано 2011
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  3. 3
    A Novel Role for ATM in Regulating Proteasome-Mediated Protein Degradation through Suppression of the ISG15 Conjugation Pathway

    A Novel Role for ATM in Regulating Proteasome-Mediated Protein Degradation through Suppression of the ISG15 Conjugation Pathway за авторством Wood, Laurence M., Sankar, Surendran, Reed, Ryan E., Haas, Arthur L., Liu, Leroy F., McKinnon, Peter, Desai, Shyamal D.

    Опубліковано 2011
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  4. 4
    Defective N-acetylaspartate catabolism reduces brain acetate levels and myelin lipid synthesis in Canavan's disease

    Defective N-acetylaspartate catabolism reduces brain acetate levels and myelin lipid synthesis in Canavan's disease за авторством Chikkathur N. Madhavarao, Peethambaran Arun, John R. Moffett, Sylvia Szucs, Sankar Surendran, Reuben Matalon, James Garbern, Diana Hristova, Toby Johnson, Wei Jiang, M.A.A. Namboodiri

    Опубліковано 2005
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  5. 5
    Correction of kinetic and stability defects by tetrahydrobiopterin in phenylketonuria patients with certain phenylalanine hydroxylase mutations

    Correction of kinetic and stability defects by tetrahydrobiopterin in phenylketonuria patients with certain phenylalanine hydroxylase mutations за авторством Heidi Erlandsen, Ángel L. Pey, Alejandra Gámez, Belén Pérez, Lourdes R. Desviat, Cristina Aguado, Richard Koch, Sankar Surendran, Stephen K. Tyring, Reuben Matalon, Charles R. Scriver, Magdalena Ugarte, Aurora Martı́nez, Raymond C. Stevens

    Опубліковано 2004
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