Результаты поиска - Guy A. Rouleau

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  1. 1
    Oculopharyngeal muscular dystrophy: Recent advances in the understanding of the molecular pathogenic mechanisms and treatment strategies

    Oculopharyngeal muscular dystrophy: Recent advances in the understanding of the molecular pathogenic mechanisms and treatment strategies по Aida Abu‐Baker, Guy A. Rouleau

    Опубликовано 2006
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  2. 2
    Genetic analysis of Factor XII and bradykinin catabolic enzymes in a family with estrogen-dependent inherited angioedema

    Genetic analysis of Factor XII and bradykinin catabolic enzymes in a family with estrogen-dependent inherited angioedema по Qing Duan, Karen Binkley, Guy A. Rouleau

    Опубликовано 2009
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    Artigo
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  3. 3
    Genetic perspective on the role of the autophagy-lysosome pathway in Parkinson disease

    Genetic perspective on the role of the autophagy-lysosome pathway in Parkinson disease по Ziv Gan‐Or, Patrick A. Dion, Guy A. Rouleau

    Опубликовано 2015
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  4. 4
    Genetics of familial and sporadic amyotrophic lateral sclerosis

    Genetics of familial and sporadic amyotrophic lateral sclerosis по François Gros‐Louis, Cláudia Gaspar, Guy A. Rouleau

    Опубликовано 2006
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  5. 5
    Genetics of Intracranial Aneurysms

    Genetics of Intracranial Aneurysms по Sirui Zhou, Patrick A. Dion, Guy A. Rouleau

    Опубликовано 2018
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  6. 6
    Linking neocortical, cognitive, and genetic variability in autism with alterations of brain plasticity: The Trigger-Threshold-Target model

    Linking neocortical, cognitive, and genetic variability in autism with alterations of brain plasticity: The Trigger-Threshold-Target model по Laurent Mottron, Sylvie Belleville, Guy A. Rouleau, Olivier Collignon

    Опубликовано 2014
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  7. 7
    Systematic review of autosomal recessive ataxias and proposal for a classification

    Systematic review of autosomal recessive ataxias and proposal for a classification по Marie Beaudin, Christopher J. Klein, Guy A. Rouleau, Nicolas Dupré

    Опубликовано 2017
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  8. 8
    Deletion of C9ORF72 Results in Motor Neuron Degeneration and Stress Sensitivity in C. elegans

    Deletion of C9ORF72 Results in Motor Neuron Degeneration and Stress Sensitivity in C. elegans по Martine Therrien, Guy A. Rouleau, Patrick A. Dion, J. Alex Parker

    Опубликовано 2013
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    Artigo
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  9. 9
    Neuron-Specific Expression of Mutant Superoxide Dismutase 1 in Transgenic Mice Does Not Lead to Motor Impairment

    Neuron-Specific Expression of Mutant Superoxide Dismutase 1 in Transgenic Mice Does Not Lead to Motor Impairment по Albéna Pramatarova, Janet Laganière, Julie Roussel, Katéri Brisebois, Guy A. Rouleau

    Опубликовано 2001
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  10. 10
    Clinical Spectrum of Amyotrophic Lateral Sclerosis (ALS)

    Clinical Spectrum of Amyotrophic Lateral Sclerosis (ALS) по Leslie I. Grad, Guy A. Rouleau, John Ravits, Neil R. Cashman

    Опубликовано 2016
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  11. 11
    Sleep disorders and Parkinson disease; lessons from genetics

    Sleep disorders and Parkinson disease; lessons from genetics по Ziv Gan‐Or, Roy N. Alcalay, Guy A. Rouleau, Ronald B. Postuma

    Опубликовано 2018
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  12. 12
    Oligomerization of polyalanine expanded PABPN1 facilitates nuclear protein aggregation that is associated with cell death

    Oligomerization of polyalanine expanded PABPN1 facilitates nuclear protein aggregation that is associated with cell death по Xueping Fan, Patrick A. Dion, Janet Laganière, Bernard Brais, Guy A. Rouleau

    Опубликовано 2001
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    Artigo
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  13. 13
    Identification of a Major Susceptibility Locus for Restless Legs Syndrome on Chromosome 12q

    Identification of a Major Susceptibility Locus for Restless Legs Syndrome on Chromosome 12q по Alex Désautels, Gustavo Turecki, Jacques Montplaisir, Adolfo Sequeira, Andrei Verner, Guy A. Rouleau

    Опубликовано 2001
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    Artigo
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  14. 14
    The Impact of Phenotypic and Genetic Heterogeneity on Results of Genome Wide Association Studies of Complex Diseases

    The Impact of Phenotypic and Genetic Heterogeneity on Results of Genome Wide Association Studies of Complex Diseases по Mirko Manchia, Jeffrey Cullis, Gustavo Turecki, Guy A. Rouleau, Rudolf Uher, Martin Alda

    Опубликовано 2013
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  15. 15
    H3K4 tri-methylation in synapsin genes leads to different expression patterns in bipolar disorder and major depression

    H3K4 tri-methylation in synapsin genes leads to different expression patterns in bipolar disorder and major depression по Cristiana Cruceanu, Martin Alda, Corina Nagy, Erika Freemantle, Guy A. Rouleau, Gustavo Turecki

    Опубликовано 2012
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  16. 16
    Human copy number variants are enriched in regions of low mappability

    Human copy number variants are enriched in regions of low mappability по Jean Monlong, Patrick Cossette, Caroline Meloche, Guy A. Rouleau, Simon Girard, Guillaume Bourque

    Опубликовано 2018
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  17. 17
    Lithium response and genetic variation in the CREB family of genes

    Lithium response and genetic variation in the CREB family of genes по Firoza Mamdani, Martin Alda, Paul Grof, L. Trevor Young, Guy A. Rouleau, Gustavo Turecki

    Опубликовано 2008
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  18. 18
    Mutant TDP-43 and FUS Cause Age-Dependent Paralysis and Neurodegeneration in C. elegans

    Mutant TDP-43 and FUS Cause Age-Dependent Paralysis and Neurodegeneration in C. elegans по Alexandra Vaccaro, Arnaud Tauffenberger, Dina Aggad, Guy A. Rouleau, Pierre Drapeau, J. Alex Parker

    Опубликовано 2012
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  19. 19
    The Neuropathology of CAG Repeat Diseases: Review and Update of Genetic and Molecular Features

    The Neuropathology of CAG Repeat Diseases: Review and Update of Genetic and Molecular Features по Yves Robitaille, Íscia Lopes‐Cendes, Mark W. Bêcher, Guy A. Rouleau, Arthur W. Clark

    Опубликовано 1997
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  20. 20
    FUS and TARDBP but Not SOD1 Interact in Genetic Models of Amyotrophic Lateral Sclerosis

    FUS and TARDBP but Not SOD1 Interact in Genetic Models of Amyotrophic Lateral Sclerosis по Edor Kabashi, Valérie Bercier, Alexandra Lissouba, Meijiang Liao, Edna Brustein, Guy A. Rouleau, Pierre Drapeau

    Опубликовано 2011
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