Human Genetics and Cognitive Functions,
CNRS URA 2182 'Genes,
synapses and cognition',
CNRS URA 2182 'Genes, synapses and cognition'
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Immunoregulatory properties of mast cell-derived exosomes.
Molecular immunology Sep, 2002 | Pubmed ID: 12217408
Mast cell-derived exosomes induce phenotypic and functional maturation of dendritic cells and elicit specific immune responses in vivo.
Journal of immunology (Baltimore, Md. : 1950) Mar, 2003 | Pubmed ID: 12626558
Expression and genetic variability of PCDH11Y, a gene specific to Homo sapiens and candidate for susceptibility to psychiatric disorders.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics Jan, 2006 | Pubmed ID: 16331680
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.
Nature genetics Jan, 2007 | Pubmed ID: 17173049
Analysis of X chromosome inactivation in autism spectrum disorders.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics Sep, 2008 | Pubmed ID: 18361425
An investigation of ribosomal protein L10 gene in autism spectrum disorders.
BMC medical genetics , 2009 | Pubmed ID: 19166581
Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general population.
PloS one , 2010 | Pubmed ID: 20657642
Production of soluble, active acetyl serotonin methyl transferase in Leishmania tarentolae.
Protein expression and purification Jan, 2011 | Pubmed ID: 20688166
Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with intellectual disability.
BMC medical genetics , 2011 | Pubmed ID: 21251267
Dynamics in enzymatic protein complexes offer a novel principle for the regulation of melatonin synthesis in the human pineal gland.
Journal of pineal research Aug, 2011 | Pubmed ID: 21517958
Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders.
Journal of pineal research Nov, 2011 | Pubmed ID: 21615493
Genetic and functional abnormalities of the melatonin biosynthesis pathway in patients with bipolar disorder.
Human molecular genetics Sep, 2012 | Pubmed ID: 22694957
Crystal structure and functional mapping of human ASMT, the last enzyme of the melatonin synthesis pathway.
Journal of pineal research Jan, 2013 | Pubmed ID: 22775292
A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability.
European journal of human genetics : EJHG Sep, 2015 | Pubmed ID: 26395558
Laura Gouder1,2,3,
Jean-Yves Tinevez4,
Hany Goubran-Botros1,2,3,
Alexandra Benchoua5,
Thomas Bourgeron1,2,3,
Isabelle Cloëz-Tayarani1,2,3
1Human Genetics and Cognitive Functions, Institut Pasteur,
2CNRS URA 2182 'Genes, synapses and cognition', Institut Pasteur,
3Human Genetics and Cognitive Functions, Université Paris Diderot, Sorbonne Paris Cité,
4Plateforme d' Imagerie Dynamique, Imagopole, CiTech, Institut Pasteur,
5Neuroplasticity and Therapeutics, CECS, I-STEM, AFM, Evry
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