Publications by authors named "Xavier Jaglin"

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Nova proteins direct synaptic integration of somatostatin interneurons through activity-dependent alternative splicing.
Leena Ali Ibrahim, Brie Wamsley, Norah Alghamdi, Nusrath Yusuf, Elaine Sevier, Xavier Hubert Jaglin

Elife· June 2023

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Rbfox1 Mediates Cell-type-Specific Splicing in Cortical Interneurons.
Brie Wamsley, Xavier Hubert Jaglin, Emilia Favuzzi, Giulia Quattrocolo, Maximiliano José Nigro

Neuron· November 2018

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Developmental diversification of cortical inhibitory interneurons.
Christian Mayer, Christoph Hafemeister, Rachel C Bandler, Robert Machold, Renata Batista Brito, Xavier Jaglin

Nature· March 2018

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Activity Regulates Cell Death within Cortical Interneurons through a Calcineurin-Dependent Mechanism.
Rashi Priya, Mercedes Francisca Paredes, Theofanis Karayannis, Nusrath Yusuf, Xingchen Liu, Xavier Jaglin

Cell Rep· February 2018

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Mutation of the α-tubulin Tuba1a leads to straighter microtubules and perturbs neuronal migration.
Richard Belvindrah, Kathiresan Natarajan, Preety Shabajee, Elodie Bruel-Jungerman, Jennifer Bernard, Xavier H Jaglin

J Cell Biol· August 2017

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Tracking the Fragile X Mental Retardation Protein in a Highly Ordered Neuronal RiboNucleoParticles Population: A Link between Stalled Polyribosomes and RNA Granules.
Rachid El Fatimy, Laetitia Davidovic, Sandra Tremblay, Xavier Jaglin, Alain Dury

PLoS Genet· July 2016

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Clonally Related Forebrain Interneurons Disperse Broadly across Both Functional Areas and Structural Boundaries.
Christian Mayer, Xavier H Jaglin, Lucy V Cobbs, Rachel C Bandler, Carmen Streicher

Neuron· September 2015

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A foot in the door: how the chromatin modifier Brg1 and Pax6 jointly potentiate adult neurogenesis.
Xavier H Jaglin, Gord Fishell

Cell Stem Cell· October 2013

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Mutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalities.
Martin Breuss, Julian Ik-Tsen Heng, Karine Poirier, Guoling Tian, Xavier Hubert Jaglin

Cell Rep· December 2012

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The origin of neocortical nitric oxide synthase-expressing inhibitory neurons.
Xavier H Jaglin, Jens Hjerling-Leffler, Gord Fishell, Renata Batista-Brito

Front Neural Circuits· October 2012

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Mutations in the neuronal ß-tubulin subunit TUBB3 result in malformation of cortical development and neuronal migration defects.
Karine Poirier, Yoann Saillour, Nadia Bahi-Buisson, Xavier H Jaglin, Catherine Fallet-Bianco

Hum Mol Genet· November 2010

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Disease-associated mutations in TUBA1A result in a spectrum of defects in the tubulin folding and heterodimer assembly pathway.
Guoling Tian, Xavier H Jaglin, David A Keays, Fiona Francis, Jamel Chelly

Hum Mol Genet· September 2010

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Human lissencephaly with cerebellar hypoplasia due to mutations in TUBA1A: expansion of the foetal neuropathological phenotype.
Magalie Lecourtois, Karine Poirier, Gaëlle Friocourt, Xavier Jaglin, Alice Goldenberg

Acta Neuropathol· June 2010

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Tubulin-related cortical dysgeneses: microtubule dysfunction underlying neuronal migration defects.
Xavier H Jaglin, Jamel Chelly

Trends Genet· December 2009

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Mutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyria.
Xavier Hubert Jaglin, Karine Poirier, Yoann Saillour, Emmanuelle Buhler, Guoling Tian

Nat Genet· June 2009

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A pachygyria-causing alpha-tubulin mutation results in inefficient cycling with CCT and a deficient interaction with TBCB.
Guoling Tian, Xiang-Peng Kong, Xavier H Jaglin, Jamel Chelly, David Keays

Mol Biol Cell· March 2008

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The fragile X mental retardation protein is a molecular adaptor between the neurospecific KIF3C kinesin and dendritic RNA granules.
Laetitia Davidovic, Xavier H Jaglin, Aude-Marie Lepagnol-Bestel, Sandra Tremblay, Michel Simonneau

Hum Mol Genet· December 2007

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The nuclear microspherule protein 58 is a novel RNA-binding protein that interacts with fragile X mental retardation protein in polyribosomal mRNPs from neurons.
Laetitia Davidovic, Elias Bechara, Maud Gravel, Xavier H Jaglin, Sandra Tremblay

Hum Mol Genet· May 2006

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