A dominant mutation etiologic for human tricho-dento-osseous syndrome impairs the ability of DLX3 to downregulate ΔNp63α

Homeodomain protein Dlx3 induces phosphorylation-dependent p63 degradation

(2010) Antonella Di Costanzo et al.   CELL CYCLE

Unkämmbare Haare und atopische Dermatitis bei tricho-dentoossärem Syndrom

(2010) Dagmara E. Y. Mayer et al.   JOURNAL DER DEUTSCHEN DERMATOLOGISCHEN GESELLSCHAFT

p300 Alters Keratinocyte Cell Growth and Differentiation through Regulation of p21Waf1/CIP1

(2010) Ping-Pui Wong et al.   PLoS One

DLX3 Mutation in a New Family and Its Phenotypic Variations

(2009) S.-K. Lee et al.   JOURNAL OF DENTAL RESEARCH

Transcriptional Network of p63 in Human Keratinocytes

(2009) Silvia Pozzi et al.   PLoS One

DLX3 c.561_562delCT mutation causes attenuated phenotype of tricho-dento-osseous syndrome

(2008) J. Timothy Wright et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Regulation of Dlx5 and Dlx6 gene expression by p63 is involved in EEC and SHFM congenital limb defects

(2008) N. Lo Iacono et al.   DEVELOPMENT

Dlx3 is a crucial regulator of hair follicle differentiation and cycling

(2008) J. Hwang et al.   DEVELOPMENT

Characterization of Ser338Phosphorylation for Raf-1 Activation

(2008) Mengwei Zang et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Molecular Consequences of a Frameshifted DLX3 Mutant Leading to Tricho-Dento-Osseous Syndrome

(2008) Olivier Duverger et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Cyclin D1 downregulation is important for permanent cell cycle exit and initiation of differentiation induced by anchorage-deprivation in human keratinocytes

(2008) Kayoko Nishi et al.   JOURNAL OF CELLULAR BIOCHEMISTRY

A 4 bp deletion mutation in DLX3 enhances osteoblastic differentiation and bone formation in vitro

(2007) Sun Jin Choi et al.   BONE