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Reply: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease.
Sylvie Bannwarth
,
Samira Ait-El-Mkadem
,
Annabelle Chaussenot
,
Emmanuelle C Genin
,
Sandra Lacas-Gervais
et al.
Journal articles
hal-01060685v1
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EFA6A, an exchange factor for Arf6, regulates early steps in ciliogenesis
Mariagrazia Partisani
,
Carole L Baron
,
Rania Ghossoub
,
Racha Fayad
,
Sophie Pagnotta
et al.
Journal articles
hal-03120586v1
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A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement.
Sylvie Bannwarth
,
Samira Ait-El-Mkadem
,
Annabelle Chaussenot
,
Emmanuelle C Genin
,
Sandra Lacas-Gervais
et al.
Journal articles
hal-01059178v1
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Reply: High prevalence of CHCHD10 mutations in patients with frontotemporal dementia from China.
Sylvie Bannwarth
,
Samira Ait-El-Mkadem
,
Annabelle Chaussenot
,
Emmanuelle C. Genin
,
Sandra Lacas-Gervais
et al.
Journal articles
hal-01336629v1
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CHCHD10 and SLP2 control the stability of the PHB complex: a key factor for motor neuron viability
Emmanuelle C Genin
,
Sylvie Bannwarth
,
Baptiste Ropert
,
Françoise Lespinasse
,
Alessandra Mauri-Crouzet
et al.
Journal articles
pasteur-03853884v1
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Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis
Sylvie Bannwarth
,
Samira Ait-El-Mkadem
,
Annabelle Chaussenot
,
Emmanuelle Génin
,
Sandra Lacas-Gervais
et al.
Journal articles
hal-02108988v1
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Identification of adipocytes as target cells for Leishmania infantum parasites
Aurélie Schwing
,
Didier Pisani
,
Christelle Pomares
,
Alissa Majoor
,
Sandra Lacas-Gervais
et al.
Journal articles
pasteur-03744940v1
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Reply: CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis
Sylvie Bannwarth
,
Samira Ait-El-Mkadem
,
Annabelle Chaussenot
,
Emmanuelle Génin
,
Sandra Lacas-Gervais
et al.
Journal articles
hal-02108961v1
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Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation.
Sylvie Bannwarth
,
Samira Ait-El-Mkadem
,
Annabelle Chaussenot
,
Emmanuelle C Genin
,
Sandra Lacas-Gervais
et al.
Brain - A Journal of Neurology , 2015, 138 (Pt 9), pp.e377
Journal articles
hal-01218555v1
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Reply: Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?
Sylvie Bannwarth
,
Samira Ait-El-Mkadem
,
Annabelle Chaussenot
,
Emmanuelle C Genin
,
Sandra Lacas-Gervais
et al.
Journal articles
hal-01272635v1
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Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?
Sylvie Bannwarth
,
Samira Ait-El-Mkadem
,
Annabelle Chaussenot
,
Emmanuelle C Genin
,
Sandra Lacas-Gervais
et al.
Journal articles
hal-01135688v1
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Aminopeptidase A contributes to biochemical, anatomical and cognitive defects in Alzheimer’s disease (AD) mouse model and is increased at early stage in sporadic AD brain
Audrey Valverde
,
Julie Dunys
,
Thomas Lorivel
,
Delphine Debayle
,
Anne-Sophie Gay
et al.
Journal articles
hal-03239400v1
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