List of works - Martin Breuss

Autosomal-Recessive Mutations in the tRNA Splicing Endonuclease Subunit TSEN15 Cause Pontocerebellar Hypoplasia and Progressive Microcephaly

scientific article published on July 2016

Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration

scientific article published on 16 July 2018

Brain-specific knockin of the pathogenic Tubb5 E401K allele causes defects in motor coordination and prepulse inhibition

scientific article published on 24 January 2017

Clusters of iron-rich cells in the upper beak of pigeons are macrophages not magnetosensitive neurons

scientific article

Cytoarchitectural disruption of the superior colliculus and an enlarged acoustic startle response in the Tuba1a mutant mouse.

scientific article

Microtubules and neurodevelopmental disease: the movers and the makers

scientific article published on January 2014

Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze Type

scientific article

Mutations in LNPK, Encoding the Endoplasmic Reticulum Junction Stabilizer Lunapark, Cause a Recessive Neurodevelopmental Syndrome

publication published on 19 July 2018

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

scientific article published on 15 November 2018

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

scientific article published on 8 January 2018

Mutations in the murine homologue of TUBB5 cause microcephaly by perturbing cell cycle progression and inducing p53-associated apoptosis

scientific article published on 22 February 2016

Mutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalities

scientific article

Recurrent homozygous damaging mutation in TMX2, encoding a protein disulfide isomerase, in four families with microlissencephaly

scientific article published on 05 October 2019

TUBB5 and its disease-associated mutations influence the terminal differentiation and dendritic spine densities of cerebral cortical neurons

scientific article published on 15 May 2014

Tuba8 is expressed at low levels in the developing mouse and human brain

scientific article published on May 2010

Tubulins and brain development - The origins of functional specification

scientific article published on 24 March 2017

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

scientific journal article

List of works by Martin Breuss

Autosomal-Recessive Mutations in the tRNA Splicing Endonuclease Subunit TSEN15 Cause Pontocerebellar Hypoplasia and Progressive Microcephaly

Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration

Brain-specific knockin of the pathogenic Tubb5 E401K allele causes defects in motor coordination and prepulse inhibition

Clusters of iron-rich cells in the upper beak of pigeons are macrophages not magnetosensitive neurons

Cytoarchitectural disruption of the superior colliculus and an enlarged acoustic startle response in the Tuba1a mutant mouse.

Microtubules and neurodevelopmental disease: the movers and the makers

Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze Type

Mutations in LNPK, Encoding the Endoplasmic Reticulum Junction Stabilizer Lunapark, Cause a Recessive Neurodevelopmental Syndrome

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

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

Mutations in the murine homologue of TUBB5 cause microcephaly by perturbing cell cycle progression and inducing p53-associated apoptosis

Mutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalities

Recurrent homozygous damaging mutation in TMX2, encoding a protein disulfide isomerase, in four families with microlissencephaly

TUBB5 and its disease-associated mutations influence the terminal differentiation and dendritic spine densities of cerebral cortical neurons

Tuba8 is expressed at low levels in the developing mouse and human brain

Tubulins and brain development - The origins of functional specification

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