Ines Leca

Vienna, Austria

Last Updated: 09/26/2026

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Found 10 publications

MAPping tubulin mutations.

MAPping tubulin mutations.

Journal: Frontiers in cell and developmental biology

Published: January 03, 2023

Correction: Biallelic PAX5 mutations cause hypogammaglobulinemia, sensorimotor deficits, and autism spectrum disorder.

Correction: Biallelic PAX5 mutations cause hypogammaglobulinemia, sensorimotor deficits, and autism spectrum disorder.

Journal: The Journal of experimental medicine

Published: December 08, 2022

Codon modification of Tuba1a alters mRNA levels and causes a severe neurodevelopmental phenotype in mice.

Codon modification of Tuba1a alters mRNA levels and causes a severe neurodevelopmental phenotype in mice.

Journal: Scientific reports

Published: May 19, 2022

Biallelic PAX5 mutations cause hypogammaglobulinemia, sensorimotor deficits, and autism spectrum disorder.

Biallelic PAX5 mutations cause hypogammaglobulinemia, sensorimotor deficits, and autism spectrum disorder.

Journal: The Journal of experimental medicine

Published: March 21, 2022

A proteomic survey of microtubule-associated proteins in a R402H TUBA1A mutant mouse.

A proteomic survey of microtubule-associated proteins in a R402H TUBA1A mutant mouse.

Journal: PLoS genetics

Published: April 06, 2020

Publisher Correction: Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans.

Publisher Correction: Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans.

Journal: Nature neuroscience

Published: June 08, 2018

Mutations in MAST1 Cause Mega-Corpus-Callosum Syndrome with Cerebellar Hypoplasia and Cortical Malformations.

Mutations in MAST1 Cause Mega-Corpus-Callosum Syndrome with Cerebellar Hypoplasia and Cortical Malformations.

Journal: Neuron

Published: October 11, 2017

Tubulins and brain development - The origins of functional specification.

Tubulins and brain development - The origins of functional specification.

Journal: Molecular and cellular neurosciences

Published: November 27, 2016

Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability.

Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability.

Journal: Human molecular genetics

Published: September 12, 2016

Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans.

Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans.

Journal: Nature neuroscience

Published: August 04, 2016

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Last Updated: 09/26/2026