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Michel Simonneau

Showing results (31-40 of 40) with videos related to

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Nature Genetics|March 18, 2003
Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndromeJeanne Amiel, Béatrice Laudier, Tania Attié-Bitach, et al.
Human Molecular Genetics|May 22, 2008
Convergent evidence identifying MAP/microtubule affinity-regulating kinase 1 (MARK1) as a susceptibility gene for autismGilles Maussion, Jérôme Carayol, Aude-Marie Lepagnol-Bestel, et al.
Psychiatric Genetics|November 20, 2008
Polymorphisms of coding trinucleotide repeats of homeogenes in neurodevelopmental psychiatric disordersFabrice Laroche, Nicolas Ramoz, Sophie Leroy, et al.
Scientific Data|August 16, 2019
HENA, heterogeneous network-based data set for Alzheimer's diseaseElena Sügis, Jerome Dauvillier, Anna Leontjeva, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 4, 2011
Altered axonal targeting and short-term plasticity in the hippocampus of Disc1 mutant miceMirna Kvajo, Heather McKellar, Liam J Drew, et al.
Human Molecular Genetics|October 9, 2003
Noradrenergic neuronal development is impaired by mutation of the proneural HASH-1 gene in congenital central hypoventilation syndrome (Ondine's curse)Loïc de Pontual, Virginie Népote, Tania Attié-Bitach, et al.
Life Science Alliance|August 1, 2022
Chr21 protein-protein interactions: enrichment in proteins involved in intellectual disability, autism, and late-onset Alzheimer's diseaseJulia Viard, Yann Loe-Mie, Rachel Daudin, et al.
Nature Nanotechnology|November 29, 2016
Fluorescent nanodiamond tracking reveals intraneuronal transport abnormalities induced by brain-disease-related genetic risk factorsSimon Haziza, Nitin Mohan, Yann Loe-Mie, et al.
Human Molecular Genetics|February 17, 2009
DYRK1A interacts with the REST/NRSF-SWI/SNF chromatin remodelling complex to deregulate gene clusters involved in the neuronal phenotypic traits of Down syndromeAude-Marie Lepagnol-Bestel, Agnes Zvara, Gilles Maussion, et al.
Nature Methods|April 17, 2023
BigNeuron: a resource to benchmark and predict performance of algorithms for automated tracing of neurons in light microscopy datasetsLinus Manubens-Gil, Zhi Zhou, Hanbo Chen, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
Nature Genetics|March 18, 2003
Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndromeJeanne Amiel, Béatrice Laudier, Tania Attié-Bitach, et al.
Human Molecular Genetics|May 22, 2008
Convergent evidence identifying MAP/microtubule affinity-regulating kinase 1 (MARK1) as a susceptibility gene for autismGilles Maussion, Jérôme Carayol, Aude-Marie Lepagnol-Bestel, et al.
Psychiatric Genetics|November 20, 2008
Polymorphisms of coding trinucleotide repeats of homeogenes in neurodevelopmental psychiatric disordersFabrice Laroche, Nicolas Ramoz, Sophie Leroy, et al.
Scientific Data|August 16, 2019
HENA, heterogeneous network-based data set for Alzheimer's diseaseElena Sügis, Jerome Dauvillier, Anna Leontjeva, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 4, 2011
Altered axonal targeting and short-term plasticity in the hippocampus of Disc1 mutant miceMirna Kvajo, Heather McKellar, Liam J Drew, et al.
Human Molecular Genetics|October 9, 2003
Noradrenergic neuronal development is impaired by mutation of the proneural HASH-1 gene in congenital central hypoventilation syndrome (Ondine's curse)Loïc de Pontual, Virginie Népote, Tania Attié-Bitach, et al.
Life Science Alliance|August 1, 2022
Chr21 protein-protein interactions: enrichment in proteins involved in intellectual disability, autism, and late-onset Alzheimer's diseaseJulia Viard, Yann Loe-Mie, Rachel Daudin, et al.
Nature Nanotechnology|November 29, 2016
Fluorescent nanodiamond tracking reveals intraneuronal transport abnormalities induced by brain-disease-related genetic risk factorsSimon Haziza, Nitin Mohan, Yann Loe-Mie, et al.
Human Molecular Genetics|February 17, 2009
DYRK1A interacts with the REST/NRSF-SWI/SNF chromatin remodelling complex to deregulate gene clusters involved in the neuronal phenotypic traits of Down syndromeAude-Marie Lepagnol-Bestel, Agnes Zvara, Gilles Maussion, et al.
Nature Methods|April 17, 2023
BigNeuron: a resource to benchmark and predict performance of algorithms for automated tracing of neurons in light microscopy datasetsLinus Manubens-Gil, Zhi Zhou, Hanbo Chen, et al.
Pageof 4