CHD7 and retinoic acid signaling cooperate to regulate neural stem cell and inner ear development in mouse models of CHARGE syndrome

The Chromatin Remodeler CHD7 Regulates Adult Neurogenesis via Activation of SoxC Transcription Factors

(2013) Weijun Feng et al.   Cell Stem Cell

Retinoic Acid Deficiency Impairs the Vestibular Function

(2013) R. Romand et al.   JOURNAL OF NEUROSCIENCE

Mutation update on the CHD7 gene involved in CHARGE syndrome

(2012) Nicole Janssen et al.   HUMAN MUTATION

Antenatal spectrum of CHARGE syndrome in 40 fetuses withCHD7mutations

(2012) Marine Legendre et al.   JOURNAL OF MEDICAL GENETICS

Delayed fusion and altered gene expression contribute to semicircular canal defects in Chd7 deficient mice

(2012) Elizabeth A. Hurd et al.   MECHANISMS OF DEVELOPMENT

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

(2012) Brian J. O’Roak et al.   NATURE

Abnormal development of NG2+PDGFR-α+ neural progenitor cells leads to neonatal hydrocephalus in a ciliopathy mouse model

(2012) Calvin S Carter et al.   NATURE MEDICINE

Chromatin remodeling by the CHD7 protein is impaired by mutations that cause human developmental disorders

(2012) K. Bouazoune et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Eyes Wide Open: A Critical Review of Sphere-Formation as an Assay for Stem Cells

(2011) Erika Pastrana et al.   Cell Stem Cell

Cycling or not cycling: cell cycle regulatory molecules and adult neurogenesis

(2011) Pierre Beukelaers et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

Mature middle and inner ears express Chd7 and exhibit distinctive pathologies in a mouse model of CHARGE syndrome

(2011) Elizabeth A. Hurd et al.   HEARING RESEARCH

Reproductive dysfunction and decreased GnRH neurogenesis in a mouse model of CHARGE syndrome

(2011) W. S. Layman et al.   HUMAN MOLECULAR GENETICS

CHD7 mutations and CHARGE syndrome: the clinical implications of an expanding phenotype

(2011) J. E. H. Bergman et al.   JOURNAL OF MEDICAL GENETICS

Sox2 cooperates with Chd7 to regulate genes that are mutated in human syndromes

(2011) Erik Engelen et al.   NATURE GENETICS

The ATP-dependent chromatin remodeling enzyme CHD7 regulates pro-neural gene expression and neurogenesis in the inner ear

(2010) E. A. Hurd et al.   DEVELOPMENT

CHD7 functions in the nucleolus as a positive regulator of ribosomal RNA biogenesis

(2010) Gabriel E. Zentner et al.   HUMAN MOLECULAR GENETICS

Notch1 Is Required for Maintenance of the Reservoir of Adult Hippocampal Stem Cells

(2010) J. L. Ables et al.   JOURNAL OF NEUROSCIENCE

Study of smell and reproductive organs in a mouse model for CHARGE syndrome

(2009) Jorieke EH Bergman et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Involvement of Ngn2, Tbr and NeuroD proteins during postnatal olfactory bulb neurogenesis

(2009) Laurent Roybon et al.   EUROPEAN JOURNAL OF NEUROSCIENCE

Defects in neural stem cell proliferation and olfaction in Chd7 deficient mice indicate a mechanism for hyposmia in human CHARGE syndrome

(2009) W.S. Layman et al.   HUMAN MOLECULAR GENETICS

Origin and function of olfactory bulb interneuron diversity

(2008) Pierre-Marie Lledo et al.   TRENDS IN NEUROSCIENCES