Search Results - Alexis Brice

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  1. 1
    Genetics of Parkinson's disease: LRRK2 on the rise

    Genetics of Parkinson's disease: LRRK2 on the rise by Alexis Brice

    Published 2005
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  2. 2
    Mitochondrial quality control turns out to be the principal suspect in parkin and PINK1-related autosomal recessive Parkinson's disease

    Mitochondrial quality control turns out to be the principal suspect in parkin and PINK1-related autosomal recessive Parkinson's disease by Olga Corti, Alexis Brice

    Published 2012
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  3. 3
    Role of Mendelian genes in “sporadic” Parkinson's disease

    Role of Mendelian genes in “sporadic” Parkinson's disease by Suzanne Lesage, Alexis Brice

    Published 2011
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  4. 4
    Spinocerebellar ataxia 17 (SCA17) and Huntington’s disease-like 4 (HDL4)

    Spinocerebellar ataxia 17 (SCA17) and Huntington’s disease-like 4 (HDL4) by Giovanni Stévanin, Alexis Brice

    Published 2008
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  5. 5
    Parkinson's disease: from monogenic forms to genetic susceptibility factors

    Parkinson's disease: from monogenic forms to genetic susceptibility factors by Suzanne Lesage, Alexis Brice

    Published 2009
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  6. 6
    Alpha-synuclein and Parkinson's disease

    Alpha-synuclein and Parkinson's disease by C.B. Lücking, Alexis Brice

    Published 2000
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  7. 7
    Clinical and molecular advances in autosomal dominant cerebellar ataxias: from genotype to phenotype and physiopathology

    Clinical and molecular advances in autosomal dominant cerebellar ataxias: from genotype to phenotype and physiopathology by Giovanni Stévanin, Alexandra Dürr, Alexis Brice

    Published 2000
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  8. 8
    The genetic landscape of Parkinson's disease

    The genetic landscape of Parkinson's disease by Ariane Lunati, Suzanne Lesage, Alexis Brice

    Published 2018
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  9. 9
    Recent advances in understanding dominant spinocerebellar ataxias from clinical and genetic points of view

    Recent advances in understanding dominant spinocerebellar ataxias from clinical and genetic points of view by Giulia Coarelli, Alexis Brice, Alexandra Dürr

    Published 2018
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  10. 10
    Proteomic analysis of <i>parkin</i> knockout mice: alterations in energy metabolism, protein handling and synaptic function

    Proteomic analysis of <i>parkin</i> knockout mice: alterations in energy metabolism, protein handling and synaptic function by Magali Periquet, Olga Corti, Sandrine Jacquier, Alexis Brice

    Published 2005
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  11. 11
    Exploration of Neurodegenerative Diseases Using Long‐Read Sequencing and Optical Genome Mapping Technologies

    Exploration of Neurodegenerative Diseases Using Long‐Read Sequencing and Optical Genome Mapping Technologies by Guillaume Cogan, Kensuke Daida, Cornelis Blauwendraat, Kimberley J. Billingsley, Alexis Brice

    Published 2025
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  12. 12
    Molecular and Clinical Study of 18 Families with ADCA Type II: Evidence for Genetic Heterogeneity and De Novo Mutation

    Molecular and Clinical Study of 18 Families with ADCA Type II: Evidence for Genetic Heterogeneity and De Novo Mutation by Paola Giunti, Giovanni Stévanin, Paul Worth, Gilles David, Alexis Brice, Nicholas Wood

    Published 1999
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  13. 13
    cDNA cloning and complete sequence of porcine choline acetyltransferase: in vitro translation of the corresponding RNA yields an active protein.

    cDNA cloning and complete sequence of porcine choline acetyltransferase: in vitro translation of the corresponding RNA yields an active protein. by Sylvie Berrard, Alexis Brice, F. Lottspeich, Andreas Braun, Yves‐Alain Barde, Jacques Mallet

    Published 1987
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  14. 14
    Are (CTG)n expansions at the SCA8 locus rare polymorphisms?

    Are (CTG)n expansions at the SCA8 locus rare polymorphisms? by Giovanni Stévanin, Alexandra Herman, Alexandra Dürr, Carla Jodice, Marina Frontali, Y. Agid, Alexis Brice

    Published 2000
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  15. 15
    Sqstm1 knock-down causes a locomotor phenotype ameliorated by rapamycin in a zebrafish model of ALS/FTLD

    Sqstm1 knock-down causes a locomotor phenotype ameliorated by rapamycin in a zebrafish model of ALS/FTLD by Serena Lattante, Hortense de Calbiac, Isabelle Le Ber, Alexis Brice, Sorana Ciura, Edor Kabashi

    Published 2014
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  16. 16
    LRRK2 Haplotype Analyses in European and North African Families with Parkinson Disease: A Common Founder for the G2019S Mutation Dating from the 13th Century

    LRRK2 Haplotype Analyses in European and North African Families with Parkinson Disease: A Common Founder for the G2019S Mutation Dating from the 13th Century by Suzanne Lesage, Anne‐Louise Leutenegger, Pablo Ibáñez, Sabine Janin, Ebba Lohmann, Alexandra Dürr, Alexis Brice

    Published 2005
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  17. 17
    Propensity for somatic expansion increases over the course of life in Huntington disease

    Propensity for somatic expansion increases over the course of life in Huntington disease by Radhia Kacher, François‐Xavier Lejeune, Sandrine Noël, Cécile Cazeneuve, Alexis Brice, Sandrine Humbert, Alexandra Dürr

    Published 2021
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  18. 18
    Decreased choline acetyltransferase mRNA expression in the nucleus basalis of Meynert in Alzheimer disease: an in situ hybridization study.

    Decreased choline acetyltransferase mRNA expression in the nucleus basalis of Meynert in Alzheimer disease: an in situ hybridization study. by Ornella Strada, Sheela Vyas, Étienne C. Hirsch, Merle Ruberg, Alexis Brice, Y. Agid, F. Javoy‐Agid

    Published 1992
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  19. 19
    Functional interplay between Parkin and Drp1 in mitochondrial fission and clearance

    Functional interplay between Parkin and Drp1 in mitochondrial fission and clearance by Lori M. Buhlman, Maria Damiano, Giulia Bertolin, Rosa Ferrando-Miguel, Anne Lombès, Alexis Brice, Olga Corti

    Published 2014
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  20. 20
    Lentiviral vector delivery of parkin prevents dopaminergic degeneration in an α-synuclein rat model of Parkinson's disease

    Lentiviral vector delivery of parkin prevents dopaminergic degeneration in an α-synuclein rat model of Parkinson's disease by Christophe Lo Bianco, Bernard L. Schneider, Matthias Bauer, Ali Sajadi, Alexis Brice, Takeshi Iwatsubo, Patrick Aebischer

    Published 2004
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