Novel lissencephaly‐associated DCX variants in the C‐terminal DCX domain affect microtubule binding and dynamics

Tuba8 Drives Differentiation of Cortical Radial Glia into Apical Intermediate Progenitors by Tuning Modifications of Tubulin C Termini

(2020) Susana I. Ramos et al.   DEVELOPMENTAL CELL

TUBB3 E410K syndrome: Case report and review of the clinical spectrum of TUBB3 mutations

(2020) Maria L. Dentici et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Neuronal migration in the CNS during development and disease: insights from in vivo and in vitro models

(2019) Isabel Yasmin Buchsbaum et al.   DEVELOPMENT

Subcortical heterotopic gray matter brain malformations

(2019) Renske Oegema et al.   NEUROLOGY

Multiple Functions of KBP in Neural Development Underlie Brain Anomalies in Goldberg-Shprintzen Syndrome

(2019) Hsin-Yun Chang et al.   Frontiers in Molecular Neuroscience

TUBA1A mutations identified in lissencephaly patients dominantly disrupt neuronal migration and impair dynein activity

(2018) Jayne Aiken et al.   HUMAN MOLECULAR GENETICS

Mutation of the α-tubulin Tuba1a leads to straighter microtubules and perturbs neuronal migration

(2017) Richard Belvindrah et al.   JOURNAL OF CELL BIOLOGY

A novel DCX missense mutation in a family with X-linked lissencephaly and subcortical band heterotopia syndrome inherited from a low-level somatic mosaic mother: Genetic and functional studies

(2016) Meng-Han Tsai et al.   EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

The expression oftubb2bundergoes a developmental transition in murine cortical neurons

(2015) Martin Breuss et al.   JOURNAL OF COMPARATIVE NEUROLOGY

New insights into genotype–phenotype correlations for the doublecortin-related lissencephaly spectrum

(2013) Nadia Bahi-Buisson et al.   BRAIN

CEP162 is an axoneme-recognition protein promoting ciliary transition zone assembly at the cilia base

(2013) Won-Jing Wang et al.   NATURE CELL BIOLOGY

Tuba8 Is Expressed at Low Levels in the Developing Mouse and Human Brain

(2010) Andreas Braun et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Intragenic deletions and duplications of the LIS1 and DCX genes: a major disease-causing mechanism in lissencephaly and subcortical band heterotopia

(2008) Eden V Haverfield et al.   EUROPEAN JOURNAL OF HUMAN GENETICS