MOZ directs the distal-less homeobox gene expression program during craniofacial development

Embryogenesis and Adult Life in the Absence of Intrinsic Apoptosis Effectors BAX, BAK, and BOK

(2018) Francine F.S. Ke et al.   CELL

Subtle Changes in the Levels of BCL-2 Proteins Cause Severe Craniofacial Abnormalities

(2018) Stephanie Grabow et al.   Cell Reports

Wnt6 influences the viability of mouse embryonic palatal mesenchymal cells via the β‑catenin pathway

(2017) Zheng Jiang et al.   Experimental and Therapeutic Medicine

Whole exome sequencing reveals de novo pathogenic variants inKAT6Aas a cause of a neurodevelopmental disorder

(2016) Francisca Millan et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Robust hyperparameter estimation protects against hypervariable genes and improves power to detect differential expression

(2016) Belinda Phipson et al.   Annals of Applied Statistics

MOZ (KAT6A) is essential for the maintenance of classically defined adult hematopoietic stem cells

(2016) B. N. Sheikh et al.   BLOOD

Sp7/Osterix Is Restricted to Bone-Forming Vertebrates where It Acts as a Dlx Co-factor in Osteoblast Specification

(2016) Hironori Hojo et al.   DEVELOPMENTAL CELL

Acetylation of the Cd8 Locus by KAT6A Determines Memory T Cell Diversity

(2016) Dane M. Newman et al.   Cell Reports

Dominant Mutations in KAT6A Cause Intellectual Disability with Recognizable Syndromic Features

(2015) Emma Tham et al.   AMERICAN JOURNAL OF HUMAN GENETICS

De Novo Nonsense Mutations in KAT6A, a Lysine Acetyl-Transferase Gene, Cause a Syndrome Including Microcephaly and Global Developmental Delay

(2015) Valerie A. Arboleda et al.   AMERICAN JOURNAL OF HUMAN GENETICS

MOZ regulates B-cell progenitors and, consequently, Moz haploinsufficiency dramatically retards MYC-induced lymphoma development

(2015) B. N. Sheikh et al.   BLOOD

Genetic analysis of Runx2 function during intramembranous ossification

(2015) Takeshi Takarada et al.   DEVELOPMENT

Mesodermal expression of Moz is necessary for cardiac septum development

(2015) Hannah K. Vanyai et al.   DEVELOPMENTAL BIOLOGY

DLX4is associated with orofacial clefting and abnormal jaw development

(2015) Di Wu et al.   HUMAN MOLECULAR GENETICS

limma powers differential expression analyses for RNA-sequencing and microarray studies

(2015) Matthew E. Ritchie et al.   NUCLEIC ACIDS RESEARCH

MOZ (MYST3, KAT6A) inhibits senescence via the INK4A-ARF pathway

(2015) B N Sheikh et al.   ONCOGENE

MOZ and BMI1 play opposing roles duringHoxgene activation in ES cells and in body segment identity specification in vivo

(2015) Bilal N. Sheikh et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

De novoANKRD11andKDM1Agene mutations in a male with features of KBG syndrome and Kabuki syndrome

(2014) Sanjin Tunovic et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

The chromatin remodeling protein CHD7, mutated in CHARGE syndrome, is necessary for proper craniofacial and tracheal development

(2014) Ethan D. Sperry et al.   DEVELOPMENTAL DYNAMICS

Regulation of germinal center responses and B-cell memory by the chromatin modifier MOZ

(2014) Kim L. Good-Jacobson et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

voom: precision weights unlock linear model analysis tools for RNA-seq read counts

(2014) Charity W Law et al.   GENOME BIOLOGY

featureCounts: an efficient general purpose program for assigning sequence reads to genomic features

(2013) Y. Liao et al.   BIOINFORMATICS

Haploinsufficiency of KDM6A is associated with severe psychomotor retardation, global growth restriction, seizures and cleft palate

(2013) Amelia M. Lindgren et al.   HUMAN GENETICS

The Subread aligner: fast, accurate and scalable read mapping by seed-and-vote

(2013) Yang Liao et al.   NUCLEIC ACIDS RESEARCH

Signals and Switches in Mammalian Neural Crest Cell Differentiation

(2013) S. Bhatt et al.   Cold Spring Harbor Perspectives in Biology

Mutations in KAT6B, Encoding a Histone Acetyltransferase, Cause Genitopatellar Syndrome

(2012) Philippe M. Campeau et al.   AMERICAN JOURNAL OF HUMAN GENETICS

MOZ Regulates the Tbx1 Locus, and Moz Mutation Partially Phenocopies DiGeorge Syndrome

(2012) Anne K. Voss et al.   DEVELOPMENTAL CELL

Cleft palate defect ofDlx1/2−/− mutant mice is caused by lack of vertical outgrowth in the posterior palate

(2012) Juhee Jeong et al.   DEVELOPMENTAL DYNAMICS

Whole-Exome-Sequencing Identifies Mutations in Histone Acetyltransferase Gene KAT6B in Individuals with the Say-Barber-Biesecker Variant of Ohdo Syndrome

(2011) Jill Clayton-Smith et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Downregulation of Dlx5 and Dlx6 expression by Hand2 is essential for initiation of tongue morphogenesis

(2011) F. Barron et al.   DEVELOPMENT

Palatogenesis: morphogenetic and molecular mechanisms of secondary palate development

(2011) J. O. Bush et al.   DEVELOPMENT

Histomorphological study of palatal shelf elevation during murine secondary palate formation

(2011) Kai Yu et al.   DEVELOPMENTAL DYNAMICS

Risk of Oral Clefts in Twins

(2011) Dorthe Grosen et al.   EPIDEMIOLOGY

Hierarchical Interactions of Homeodomain and Forkhead Transcription Factors in Regulating Odontogenic Gene Expression

(2011) Shankar R. Venugopalan et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Cleft lip and palate: understanding genetic and environmental influences

(2011) Michael J. Dixon et al.   NATURE REVIEWS GENETICS

A High-Resolution Anatomical Atlas of the Transcriptome in the Mouse Embryo

(2011) Graciana Diez-Roux et al.   PLOS BIOLOGY

ROAST: rotation gene set tests for complex microarray experiments

(2010) Di Wu et al.   BIOINFORMATICS

PHF8 Targets Histone Methylation and RNA Polymerase II To Activate Transcription

(2010) K. Fortschegger et al.   MOLECULAR AND CELLULAR BIOLOGY

A scaling normalization method for differential expression analysis of RNA-seq data

(2010) Mark D Robinson et al.   GENOME BIOLOGY

Collagen Structure and Stability

(2009) Matthew D. Shoulders et al.   Annual Review of Biochemistry

edgeR: a Bioconductor package for differential expression analysis of digital gene expression data

(2009) M. D. Robinson et al.   BIOINFORMATICS

Transcriptional networks controlling skeletal development

(2009) Christine Hartmann   CURRENT OPINION IN GENETICS & DEVELOPMENT

Indirect modulation of Shh signaling by Dlx5 affects the oral-nasal patterning of palate and rescues cleft palate in Msx1-null mice

(2009) J. Han et al.   DEVELOPMENT

Moz and Retinoic Acid Coordinately Regulate H3K9 Acetylation, Hox Gene Expression, and Segment Identity

(2009) Anne K. Voss et al.   DEVELOPMENTAL CELL

PHF8, a gene associated with cleft lip/palate and mental retardation, encodes for an Nε-dimethyl lysine demethylase

(2009) Christoph Loenarz et al.   HUMAN MOLECULAR GENETICS

Dlx genes pattern mammalian jaw primordium by regulating both lower jaw-specific and upper jaw-specific genetic programs

(2008) J. Jeong et al.   DEVELOPMENT