Loss-of-function variants inZEB1cause dominant anomalies of the corpus callosum with favourable cognitive prognosis

Abnormalities of the corpus callosum. Can prenatal imaging predict the genetic status? Correlations between imaging phenotype and genotype

(2023) Toan Nguyen et al.   PRENATAL DIAGNOSIS

Posterior Polymorphous Corneal Dystrophy in a Patient with a Novel ZEB1 Gene Mutation

(2022) Eva Fernández-Gutiérrez et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Non-Penetrance for Ocular Phenotype in Two Individuals Carrying Heterozygous Loss-of-Function ZEB1 Alleles

(2021) Lubica Dudakova et al.   Genes

Expression and Function of ZEB1 in the Cornea

(2021) Yingnan Zhang et al.   Cells

Prenatal exome sequencing in 65 fetuses with abnormality of the corpus callosum: contribution to further diagnostic delineation

(2020) Solveig Heide et al.   GENETICS IN MEDICINE

The utility of massively parallel sequencing for posterior polymorphous corneal dystrophy type 3 molecular diagnosis

(2019) Lubica Dudakova et al.   EXPERIMENTAL EYE RESEARCH

Zeb1 is important for proper cleavage plane orientation of dividing progenitors and neuronal migration in the mouse neocortex

(2019) Jie Liu et al.   CELL DEATH AND DIFFERENTIATION

ZEB1 Represses Neural Differentiation and Cooperates with CTBP2 to Dynamically Regulate Cell Migration during Neocortex Development

(2019) Huanhuan Wang et al.   Cell Reports

PAK3 mutations responsible for severe intellectual disability and callosal agenesis inhibit cell migration

(2019) Kévin Duarte et al.   NEUROBIOLOGY OF DISEASE

Metformin inhibits TGF-β1-induced epithelial-to-mesenchymal transition-like process and stem-like properties in GBM via AKT/mTOR/ZEB1 pathway

(2018) Yang Song et al.   Oncotarget

DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome

(2017) Ashley P. L. Marsh et al.   HUMAN MUTATION

Copy Number Variations Found in Patients with a Corpus Callosum Abnormality and Intellectual Disability

(2017) Solveig Heide et al.   JOURNAL OF PEDIATRICS

ARID1Bmutations are the major genetic cause of corpus callosum anomalies in patients with intellectual disability

(2016) Cyril Mignot et al.   BRAIN

Zeb1 controls neuron differentiation and germinal zone exit by a mesenchymal-epithelial-like transition

(2016) Shalini Singh et al.   eLife

ZEB1 Promotes Invasion in Human Fetal Neural Stem Cells and Hypoxic Glioma Neurospheres

(2015) Ulf D. Kahlert et al.   BRAIN PATHOLOGY

Heterozygous deletions at the ZEB1 locus verify haploinsufficiency as the mechanism of disease for posterior polymorphous corneal dystrophy type 3

(2015) Petra Liskova et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Clinical, genetic and imaging findings identify new causes for corpus callosum development syndromes

(2014) Timothy J. Edwards et al.   BRAIN

Posterior polymorphous corneal dystrophy 3 is associated with agenesis and hypoplasia of the corpus callosum

(2014) Michelle S. Jang et al.   VISION RESEARCH

Neurodevelopment after prenatal diagnosis of isolated agenesis of the corpus callosum: an integrative review

(2011) Alexandros Sotiriadis et al.   AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY

Genomic and clinical characteristics of six patients with partially overlapping interstitial deletions at 10p12p11

(2011) Christian Wentzel et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Agenesis of the corpus callosum in California 1983-2003: A population-based study

(2008) Hannah C. Glass et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A