TRANSCRIPTION FACTORS INVOLVED IN CRANIOFACIAL AND LIMB CONGENITAL DISORDERS: IN-VIVO FUNCTIONAL STUDIES OF DLX AND T-BOX GENE FAMILIES
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Pubblicazioni Scientifiche
- DEVELOPMENT
Regulation of Dlx5 and Dlx6 gene expression by p63 is involved in EEC and SHFM congenital limb defects
- DEVELOPMENTAL BIOLOGY
The Dlx5 homeobox gene is essential for vestibular morphogenesis in the mouse embryo through a BMP4-mediated pathway
- EUROPEAN JOURNAL OF MEDICAL GENETICS
Novel TBX3 mutation data in families with Ulnar-Mammary syndrome indicate a genotype-phenotype relationship:: mutations that do not disrupt the T-domain are associated with less severe limb defects
- GENES & DEVELOPMENT
Role of Dlx6 in regulation of an endothelin-1-dependent, dHAND branchial arch enhancer
- GENESIS
Mouse model of split hand/foot malformation type I
- GENESIS
Jaw transformation with gain of symmetry after Dlx5/Dlx6 inactivation:: Mirror of the past?
- HUMAN MOLECULAR GENETICS
Connexin 31 (GJB3) is expressed in the peripheral and auditory nerves and causes neuropathy and hearing impairment
- INTERNATIONAL JOURNAL OF ONCOLOGY
The coding region of the human DLX6 gene contains a polymorphic CAG/CCG repeat
- JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY
A Symphony of Regulations Centered on p63 to Control Development of Ectoderm-Derived Structures
- JOURNAL OF MOLECULAR HISTOLOGY
The role of Dlx homeogenes in early development of the olfactory pathway
- JOURNAL OF MOLECULAR HISTOLOGY
The role of Dlx homeogenes in early development of the olfactory pathway (vol 38, pg 347, 2007)
- JOURNAL OF NEUROSCIENCE
Activation of the Wnt-βCatenin pathway in a cell population on the surface of the Forebrain is essential for the establishment of olfactory axon connections
- MECHANISMS OF DEVELOPMENT
Msx1 and Dlx5 act independently in development of craniofacial skeleton, but converge on the regulation of Bmp signaling in palate formation
- MOLECULAR AND CELLULAR NEUROSCIENCE
The Dlx5 homeodomain gene is essential for olfactory development and connectivity in the mouse
- MOLECULAR AND CELLULAR NEUROSCIENCE
Defective neuronogenesis in the absence of Dlx5