Ines Leca

发表

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

Thomas M. Keane, Martin W. Breuss, D. Keays, 2018, Nature Neuroscience.

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

J. Lebbink, C. D. De Zeeuw, M. van der Burg, 2022, The Journal of experimental medicine.

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

Kiely N. James, Martin W. Breuss, D. Keays, 2016, Human molecular genetics.

MAPping tubulin mutations

D. Keays, Ines Leca, T. Cushion, 2023, Frontiers in Cell and Developmental Biology.

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

D. Keays, K. Mechtler, G. Dürnberger, 2020, PLoS genetics.

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

Martin W. Breuss, A. Reymond, A. Pagnamenta, 2018, Neuron.

Mutations in MAST 1 Caus e Mega-Corpus-Callosum Syndrome with Cerebellar Hypoplasia and Cortical Malformations Graphical

Martin W. Breuss, A. Reymond, A. Pagnamenta, 2018 .

Tubulins and brain development – The origins of functional specification

Martin W. Breuss, D. Keays, M. Breuss, 2017, Molecular and Cellular Neuroscience.

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

D. Keays, Lyubov Ushakova, Ines Leca, 2023, Scientific Reports.

Mutations in MAST1 cause mega-corpus-callosum with

Martin W. Breuss, A. Pagnamenta, D. Keays, 2019 .