Publications by authors named "Ines Leca"

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MAPping tubulin mutations.
Thomas D Cushion, Ines Leca, David A Keays

Front Cell Dev Biol· February 2023

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Correction: Biallelic PAX5 mutations cause hypogammaglobulinemia, sensorimotor deficits, and autism spectrum disorder.
Fabian M P Kaiser, Sarah Gruenbacher, Maria Roa Oyaga, Enzo Nio, Markus Jaritz, Ines Leca

J Exp Med· January 2023

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Codon modification of Tuba1a alters mRNA levels and causes a severe neurodevelopmental phenotype in mice.
Ines Leca, Alexander William Phillips, Lyubov Ushakova, Thomas David Cushion, David Anthony Keays

Sci Rep· January 2023

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Biallelic PAX5 mutations cause hypogammaglobulinemia, sensorimotor deficits, and autism spectrum disorder.
Fabian M P Kaiser, Sarah Gruenbacher, Maria Roa Oyaga, Enzo Nio, Markus Jaritz, Ines Leca

J Exp Med· September 2022

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A proteomic survey of microtubule-associated proteins in a R402H TUBA1A mutant mouse.
Ines Leca, Alexander William Phillips, Iris Hofer, Lukas Landler, Lyubov Ushakova

PLoS Genet· November 2020

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Mutations in MAST1 Cause Mega-Corpus-Callosum Syndrome with Cerebellar Hypoplasia and Cortical Malformations.
Ratna Tripathy, Ines Leca, Tessa van Dijk, Janneke Weiss, Bregje W van Bon

Neuron· December 2018

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Publisher Correction: Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans.
Thomas Gstrein, Andrew Edwards, Anna Přistoupilová, Ines Leca, Martin Breuss

Nat Neurosci· August 2018

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Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans.
Thomas Gstrein, Andrew Edwards, Anna Přistoupilová, Ines Leca, Martin Breuss

Nat Neurosci· February 2018

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Tubulins and brain development - The origins of functional specification.
Martin W Breuss, Ines Leca, Thomas Gstrein, Andi H Hansen, David A Keays

Mol Cell Neurosci· October 2017

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Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability.
Martin W Breuss, Thai Nguyen, Anjana Srivatsan, Ines Leca, Guoling Tian

Hum Mol Genet· January 2017

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