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Juliette Nectoux

Showing results (11-20 of 67) with videos related to

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Neuromolecular Medicine|July 26, 2015
Astrocyte Transcriptome from the Mecp2(308)-Truncated Mouse Model of Rett SyndromeChloé Delépine, Juliette Nectoux, Franck Letourneur, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry|April 17, 2023
A systematic literature review and meta-analysis of circulating nucleic acids as biomarkers in psychiatryCamille Verebi, Juliette Nectoux, Philip Gorwood, et al.
Neurogenetics|November 27, 2008
The first missense mutation causing Rett syndrome specifically affecting the MeCP2_e1 isoformYann Fichou, Juliette Nectoux, Nadia Bahi-Buisson, et al.
Journal of Neuroscience Research|January 19, 2012
Altered microtubule dynamics in Mecp2-deficient astrocytesJuliette Nectoux, Cedrick Florian, Chloe Delepine, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 26, 2010
Cell cloning-based transcriptome analysis in cyclin-dependent kinase-like 5 mutation patients with severe epileptic encephalopathyJuliette Nectoux, Yann Fichou, Nicolas Cagnard, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|February 20, 2020
MeCP2 is involved in random mono-allelic expression for a subset of human autosomal genesMarine Brousseau, Juliette Nectoux, Benjamin Saintpierre, et al.
Pediatric Neurology|October 2, 2007
Netrin G1 mutations are an uncommon cause of atypical Rett syndrome with or without epilepsyJuliette Nectoux, Benoit Girard, Nadia Bahi-Buisson, et al.
Gastroenterology|March 4, 2003
A quantitative gene expression study suggests a role for angiopoietins in focal nodular hyperplasiaValérie Paradis, Ivan Bièche, Delphine Dargère, et al.
International Journal of Antimicrobial Agents|February 17, 2007
Update on fluoroquinolone resistance in Helicobacter pylori: new mutations leading to resistance and first description of a gyrA polymorphism associated with hypersusceptibilityVincent Cattoir, Juliette Nectoux, Christine Lascols, et al.
Neuromuscular Disorders : NMD|August 15, 2025
McLeod syndrome mimicking mitochondrial myopathy due to a novel in-frame duplication in the XK geneMaelle Garnier, Juliette Nectoux, Thomas Smol, et al.
Pageof 7

Showing results (11-20 of 67) with videos related to

Sort By:
Pageof 7
Neuromolecular Medicine|July 26, 2015
Astrocyte Transcriptome from the Mecp2(308)-Truncated Mouse Model of Rett SyndromeChloé Delépine, Juliette Nectoux, Franck Letourneur, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry|April 17, 2023
A systematic literature review and meta-analysis of circulating nucleic acids as biomarkers in psychiatryCamille Verebi, Juliette Nectoux, Philip Gorwood, et al.
Neurogenetics|November 27, 2008
The first missense mutation causing Rett syndrome specifically affecting the MeCP2_e1 isoformYann Fichou, Juliette Nectoux, Nadia Bahi-Buisson, et al.
Journal of Neuroscience Research|January 19, 2012
Altered microtubule dynamics in Mecp2-deficient astrocytesJuliette Nectoux, Cedrick Florian, Chloe Delepine, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 26, 2010
Cell cloning-based transcriptome analysis in cyclin-dependent kinase-like 5 mutation patients with severe epileptic encephalopathyJuliette Nectoux, Yann Fichou, Nicolas Cagnard, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|February 20, 2020
MeCP2 is involved in random mono-allelic expression for a subset of human autosomal genesMarine Brousseau, Juliette Nectoux, Benjamin Saintpierre, et al.
Pediatric Neurology|October 2, 2007
Netrin G1 mutations are an uncommon cause of atypical Rett syndrome with or without epilepsyJuliette Nectoux, Benoit Girard, Nadia Bahi-Buisson, et al.
Gastroenterology|March 4, 2003
A quantitative gene expression study suggests a role for angiopoietins in focal nodular hyperplasiaValérie Paradis, Ivan Bièche, Delphine Dargère, et al.
International Journal of Antimicrobial Agents|February 17, 2007
Update on fluoroquinolone resistance in Helicobacter pylori: new mutations leading to resistance and first description of a gyrA polymorphism associated with hypersusceptibilityVincent Cattoir, Juliette Nectoux, Christine Lascols, et al.
Neuromuscular Disorders : NMD|August 15, 2025
McLeod syndrome mimicking mitochondrial myopathy due to a novel in-frame duplication in the XK geneMaelle Garnier, Juliette Nectoux, Thomas Smol, et al.
Pageof 7