Rezultati - François Bernier

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  1. 1
    Probiotic Bifidobacterium breve MCC1274 Protects against Oxidative Stress and Neuronal Lipid Droplet Formation via PLIN4 Gene Regulation

    Probiotic Bifidobacterium breve MCC1274 Protects against Oxidative Stress and Neuronal Lipid Droplet Formation via PLIN4 Gene Regulation od François Bernier, Tatsuya Kuhara, Jin‐zhong Xiao

    Izdano 2023
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  2. 2
    Using Biofeedback while Immersed in a Stressful Videogame Increases the Effectiveness of Stress Management Skills in Soldiers

    Using Biofeedback while Immersed in a Stressful Videogame Increases the Effectiveness of Stress Management Skills in Soldiers od Stéphane Bouchard, François Bernier, Éric Boivin, Brian Morin, Geneviève Robillard

    Izdano 2012
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  3. 3
    Identification of a new plasma biomarker of Alzheimer's disease using metabolomics technology

    Identification of a new plasma biomarker of Alzheimer's disease using metabolomics technology od Yoshiaki Sato, Ikumi Suzuki, Tatsuji Nakamura, François Bernier, Ken Aoshima, Yoshiya Oda

    Izdano 2011
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  4. 4
    Validation of an obstetric comorbidity index in an external population

    Validation of an obstetric comorbidity index in an external population od Amy Metcalfe, LM Lix, J‐A Johnson, Gillian Currie, AW Lyon, François Bernier, Suzanne Tough

    Izdano 2015
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  5. 5
    Probiotic Bifidobacterium breve in Improving Cognitive Functions of Older Adults with Suspected Mild Cognitive Impairment: A Randomized, Double-Blind, Placebo-Controlled Trial

    Probiotic Bifidobacterium breve in Improving Cognitive Functions of Older Adults with Suspected Mild Cognitive Impairment: A Randomized, Double-Blind, Placebo-Controlled Trial od Jin‐zhong Xiao, Noriko Katsumata, François Bernier, Kazuya Ohno, Yuki Yamauchi, Toshitaka Odamaki, Kenji Yoshikawa, Kumie Ito, Toshiyuki Kaneko

    Izdano 2020
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  6. 6
    Care4Rare Canada: Outcomes from a decade of network science for rare disease gene discovery

    Care4Rare Canada: Outcomes from a decade of network science for rare disease gene discovery od Kym M. Boycott, Taila Hartley, Kristin D. Kernohan, David A. Dyment, Heather Howley, A. Micheil Innes, François Bernier, Michael Brudno

    Izdano 2022
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  7. 7
    Circulating miRNA Biomarkers for Alzheimer's Disease

    Circulating miRNA Biomarkers for Alzheimer's Disease od Pavan Kumar, Zoltán Dezső, Crystal MacKenzie, Judy Oestreicher, Sergei Agoulnik, Michael Byrne, François Bernier, Mamoru Yanagimachi, Ken Aoshima, Yoshiya Oda

    Izdano 2013
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  8. 8
    Homologies between members of the germin gene family in hexaploid wheat and similarities between these wheat germins and certain Physarum spherulins

    Homologies between members of the germin gene family in hexaploid wheat and similarities between these wheat germins and certain Physarum spherulins od B. G. Lane, François Bernier, Ella Dratewka-Kos, R. Shafai, T. D. Kennedy, Caron Pyne, J.Ronald Munro, T A Vaughan, Dylan Walters, Filiberto Altomare

    Izdano 1991
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  9. 9
    The developmental-genetics of canalization

    The developmental-genetics of canalization od Benedikt Hallgrímsson, Rebecca M. Green, David C. Katz, Jennifer L. Fish, François Bernier, Charles C. Roseman, Nathan M. Young, James M. Cheverud, Ralph Marcucio

    Izdano 2018
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  10. 10
    Comparison of fluorescent single-strand conformation polymorphism analysis and denaturing high-performance liquid chromatography for detection of EXT1 and EXT2 mutations in hereditary multiple exostoses

    Comparison of fluorescent single-strand conformation polymorphism analysis and denaturing high-performance liquid chromatography for detection of EXT1 and EXT2 mutations in heredit... od Carol Dobson‐Stone, Roger Cox, Lorne Lonie, Lorraine Southam, Maria Fraser, Carol A. Wise, François Bernier, Shirley Hodgson, Daniel Porter, Hamish Simpson, Anthony P. Monaco

    Izdano 2000
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  11. 11
    The value of diagnostic testing for parents of children with rare genetic diseases

    The value of diagnostic testing for parents of children with rare genetic diseases od Deborah A. Marshall, Karen V. MacDonald, Sebastian Heidenreich, Taila Hartley, François Bernier, Meredith Gillespie, Brenda McInnes, A. Micheil Innes, Christine M. Armour, Kym M. Boycott

    Izdano 2019
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  12. 12
    GeneMatcher Aids in the Identification of a New Malformation Syndrome with Intellectual Disability, Unique Facial Dysmorphisms, and Skeletal and Connective Tissue Abnormalities Caused by De Novo Variants in<i>HNRNPK</i>

    GeneMatcher Aids in the Identification of a New Malformation Syndrome with Intellectual Disability, Unique Facial Dysmorphisms, and Skeletal and Connective Tissue Abnormalities Cau... od Ping Yee Billie Au, Jing You, Oana Caluseriu, Jeremy Schwartzentruber, Jacek Majewski, François Bernier, Marcia Ferguson, David Valle, Jillian S. Parboosingh, Nara Sobreira, A. Micheil Innes, Antonie D. Kline

    Izdano 2015
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  13. 13
    A Peroxisomal Disorder of Severe Intellectual Disability, Epilepsy, and Cataracts Due to Fatty Acyl-CoA Reductase 1 Deficiency

    A Peroxisomal Disorder of Severe Intellectual Disability, Epilepsy, and Cataracts Due to Fatty Acyl-CoA Reductase 1 Deficiency od Rebecca Buchert, Hasan Tawamie, Christopher Smith, Steffen Uebe, A. Micheil Innes, Bassam Al Hallak, Arif B. Ekici, Heinrich Sticht, Bernd Schwarze, Ryan E. Lamont, Jillian S. Parboosingh, François Bernier, Rami Abou Jamra

    Izdano 2014
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  14. 14
    Correlates of age at diagnosis of autism spectrum disorders in six Canadian regions

    Correlates of age at diagnosis of autism spectrum disorders in six Canadian regions od Helen Coo, Hélène Ouellette‐Kuntz, Miu Lam, C. T. Yu, Deborah Dewey, François Bernier, Albert E. Chudley, P.E. Hennessey, M. Breitenbach, Andrea Noonan, M. E. Suzanne Lewis, Jeanette J. A. Holden

    Izdano 2012
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  15. 15
    RTTN Mutations Cause Primary Microcephaly and Primordial Dwarfism in Humans

    RTTN Mutations Cause Primary Microcephaly and Primordial Dwarfism in Humans od Hanan E. Shamseldin, Anas M. Alazami, Melanie Manning, Amal Hashem, Oana Caluseiu, Brahim Tabarki, Edward D. Esplin, Susan Schelley, A. Micheil Innes, Jillian S. Parboosingh, Ryan E. Lamont, Jacek Majewski, François Bernier, Fowzan S. Alkuraya

    Izdano 2015
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  16. 16
    Identification of Novel Mutations Confirms<i>Pde4d</i>as a Major Gene Causing Acrodysostosis

    Identification of Novel Mutations Confirms<i>Pde4d</i>as a Major Gene Causing Acrodysostosis od Danielle C. Lynch, David A. Dyment, Lijia Huang, Sarah M. Nikkel, Didier Lacombe, Philippe M. Campeau, Brendan Lee, Carlos A. Bacino, Jacques L. Michaud, François Bernier, FORGE Canada Consortium, Jillian S. Parboosingh, A. Micheil Innes

    Izdano 2012
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  17. 17
    <i>PISD</i>is a mitochondrial disease gene causing skeletal dysplasia, cataracts, and white matter changes

    <i>PISD</i>is a mitochondrial disease gene causing skeletal dysplasia, cataracts, and white matter changes od Tian Zhao, Caitlin Goedhart, Pingdewinde N. Sam, Rasha Sabouny, Susanne Lingrell, Adam J. Cornish, Ryan E. Lamont, François Bernier, David S. Sinasac, Jillian S. Parboosingh, Jean E. Vance, Steven M. Claypool, A. Micheil Innes, Timothy E. Shutt

    Izdano 2019
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  18. 18
    Biallelic loss of function variants in COASY cause prenatal onset pontocerebellar hypoplasia, microcephaly, and arthrogryposis

    Biallelic loss of function variants in COASY cause prenatal onset pontocerebellar hypoplasia, microcephaly, and arthrogryposis od Tessa van Dijk, Sacha Ferdinandusse, Jos P.N. Ruiter, Mariëlle Alders, Inge B. Mathijssen, Jillian S. Parboosingh, A. Micheil Innes, Hanne Meijers-Heijboer, Bwee Tien Poll‐The, François Bernier, Ronald J. A. Wanders, Ryan E. Lamont, Frank Baas

    Izdano 2018
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  19. 19
    Serendipitous Discovery and X-Ray Structure of a Human Phosphate Binding Apolipoprotein

    Serendipitous Discovery and X-Ray Structure of a Human Phosphate Binding Apolipoprotein od Renaud Morales, Anne Berna, Philippe Carpentier, Carlos Contreras‐Martel, Frédérique Renault, M. Nicodeme, Marie-Laure Chesne-Seck, François Bernier, Jérôme Dupuy, Christine Schaeffer‐Reiss, Hélène Diemer, Alain Van-Dorsselaer, Juan C. Fontecilla‐Camps, Patrick Masson, Daniel Rochu, Éric Chabrière

    Izdano 2006
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  20. 20
    Effect of Probiotic Bifidobacterium breve in Improving Cognitive Function and Preventing Brain Atrophy in Older Patients with Suspected Mild Cognitive Impairment: Results of a 24-Week Randomized, Double-Blind, Placebo-Controlled Trial

    Effect of Probiotic Bifidobacterium breve in Improving Cognitive Function and Preventing Brain Atrophy in Older Patients with Suspected Mild Cognitive Impairment: Results of a 24-W... od Daisuke Asaoka, Jin‐zhong Xiao, Tsutomu Takeda, Naotake Yanagisawa, Takahiro Yamazaki, Yoichiro Matsubara, Hideki Sugiyama, Noemi Endo, Motoyuki Higa, Koji Kasanuki, Yosuke Ichimiya, Shigeo Koido, Kazuya Ohno, François Bernier, Noriko Katsumata, Akihito Nagahara, Heii Arai, Toshifumi� Ohkusa, Nobuhiro Sato

    Izdano 2022
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