Výsledky vyhledávání - Patrick M. Abou‐Sleiman

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  1. 1
    Hereditary motor and autonomic neuronopathy 1 maps to chromosome 20q13.2-13.3

    Hereditary motor and autonomic neuronopathy 1 maps to chromosome 20q13.2-13.3 Autor Wilson Marques, Mary B. Davis, Patrick M. Abou‐Sleiman, Vanessa Daccach Marques, Wilson A. Silva, Marco A. Zago, Cláudia Sobreira, Amilton Antunes Barreira

    Vydáno 2004
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  2. 2
    Transcriptional repression of p53 by parkin and impairment by mutations associated with autosomal recessive juvenile Parkinson's disease

    Transcriptional repression of p53 by parkin and impairment by mutations associated with autosomal recessive juvenile Parkinson's disease Autor Cristine Alvès da Costa, Claire Sunyach, Emilie Giaime, Andrew B. West, Olga Corti, Alexis Brice, Stephen Safe, Patrick M. Abou‐Sleiman, Nicholas Wood, Hitoshi Takahashi, Matthew S. Goldberg, Jie Shen, Frédéric Checler

    Vydáno 2009
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  3. 3
    Mitochondrial function and morphology are impaired in <i>parkin</i>‐mutant fibroblasts

    Mitochondrial function and morphology are impaired in <i>parkin</i>‐mutant fibroblasts Autor Heather Mortiboys, Kelly Jean Thomas Craig, Werner J.H. Koopman, Stefanie Klaffke, Patrick M. Abou‐Sleiman, S. E. Olpin, Nicholas Wood, Peter H.G.M. Willems, Jan Smeitink, Mark Cookson, Oliver Bandmann

    Vydáno 2008
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  4. 4
    Mitochondrial ND5 Gene Variation Associated with Encephalomyopathy and Mitochondrial ATP Consumption

    Mitochondrial ND5 Gene Variation Associated with Encephalomyopathy and Mitochondrial ATP Consumption Autor Matthew McKenzie, Danae Liolitsa, Natalya Akinshina, Michelangelo Campanella, Sanjay M. Sisodiya, I. Hargreaves, Niranjanan Nirmalananthan, Mary G. Sweeney, Patrick M. Abou‐Sleiman, Nicholas Wood, Michael G. Hanna, Michael R. Duchen

    Vydáno 2007
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  5. 5
    Age group and sex differences in performance on a computerized neurocognitive battery in children age 8−21.

    Age group and sex differences in performance on a computerized neurocognitive battery in children age 8−21. Autor Ruben C. Gur, Jan Richard, Monica E. Calkins, Rosetta Chiavacci, John A. Hansen, Warren B. Bilker, James Loughead, John J. Connolly, Haijun Qiu, Frank Mentch, Patrick M. Abou‐Sleiman, Hákon Hákonarson, Raquel E. Gur

    Vydáno 2012
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  6. 6
    PINK1 protein in normal human brain and Parkinson's disease

    PINK1 protein in normal human brain and Parkinson's disease Autor Sonia Gandhi, Miratul M. K. Muqit, Lee Stanyer, D. G. Healy, Patrick M. Abou‐Sleiman, Iain P. Hargreaves, Simon Heales, Milan Ganguly, Lauren Parsons, Andrew Lees, D.S. Latchman, Janice L. Holton, Nicholas Wood, T. Révész

    Vydáno 2006
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  7. 7
    Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration

    Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration Autor Alan Pittman, A. J. W. Myers, Patrick M. Abou‐Sleiman, Hon‐Chung Fung, M. Kaleem, Lauren Marlowe, Jaime Duckworth, Doris G. Leung, David R. Williams, Linda Kilford, Natalie Thomas, Christopher M. Morris, Dennis W. Dickson, Nicholas Wood, John Hardy, Andrew Lees, R. De Silva

    Vydáno 2005
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  8. 8
    Altered cleavage and localization of PINK1 to aggresomes in the presence of proteasomal stress

    Altered cleavage and localization of PINK1 to aggresomes in the presence of proteasomal stress Autor Miratul M. K. Muqit, Patrick M. Abou‐Sleiman, Adrian T. Saurin, Kirsten Harvey, Sonia Gandhi, Emma Deas, Simon Eaton, Martin Smith, Kerrie Venner, Antoni Matilla‐Dueñas, Daniel G. Healy, William P. Gilks, Andrew J. Lees, Janice L. Holton, Tamás Révész, Peter J. Parker, Victoria L. Harvey, Nicholas Wood, David S. Latchman

    Vydáno 2006
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  9. 9
    Hereditary Early-Onset Parkinson's Disease Caused by Mutations in <i>PINK1</i>

    Hereditary Early-Onset Parkinson's Disease Caused by Mutations in <i>PINK1</i> Autor Enza Maria Valente, Patrick M. Abou‐Sleiman, Viviana Caputo, Miratul M. K. Muqit, Kirsten Harvey, Suzana Gispert, Zeeshan Ali, Domenico Del Turco, Anna Rita Bentivoglio, Daniel G. Healy, Alberto Albanese, Robert Nussbaum, Rafael González-Maldonado, Thomas Deller, Sergio Salvi, Pietro Cortelli, William P. Gilks, David S. Latchman, Victoria L. Harvey, Bruno Dallapiccola, Georg Auburger, Nicholas Wood

    Vydáno 2004
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  10. 10
    Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data

    Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data Autor Naheed L. Khan, Shushant Jain, John Lynch, Nicola Pavese, Patrick M. Abou‐Sleiman, Janice L. Holton, Daniel G. Healy, William P. Gilks, Mary G. Sweeney, Milan Ganguly, Vaneesha Gibbons, Sonia Gandhi, Jenny Vaughan, L. H. Eunson, Regina Katzenschlager, Juliet Gayton, Graham Lennox, Tamás Révész, David Nicholl, Kailash P. Bhatia, Niall Quinn, David J. Brooks, Andrew J. Lees, Mary B. Davis, Paola Piccini, Andrew Singleton, Nicholas Wood

    Vydáno 2005
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