Neurohypophysial dysmorphogenesis in mice lacking the homeobox gene Uncx4•1
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چکیده
منابع مشابه
Neurohypophysial dysmorphogenesis in mice lacking the homeobox gene Uncx4.1.
A number of transcription factors have been implicated in the development of the hypothalamo-neurohypophysial system (HNS). Null mutations for these factors caused severe defects in proliferation, migration and survival during early embryogenesis. While they have informed about early events of HNS developments no insights in mechanisms of late development and maturation of this major peptidergi...
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Dlx3 is a homeodomain transcription factor and a member of the vertebrate Distal-less family. Targeted deletion of the mouse Dlx3 gene results in embryonic death between day 9.5 and day 10 because of placental defects that alter the development of the labyrinthine layer. In situ hybridization reveals that the Dlx3 gene is initially expressed in ectoplacental cone cells and chorionic plate, and ...
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Heterozygous mutations in the cardiac homeobox gene, NKX2-5, underlie familial cases of atrial septal defect (ASD) with severe atrioventricular conduction block. In this study, mice heterozygous for Nkx2-5-null alleles were assessed for analogous defects. Although ASD occurred only rarely, atrial septal dysmorphogenesis was evident as increased frequencies of patent foramen ovale and septal ane...
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ژورنال
عنوان ژورنال: Journal of Molecular Endocrinology
سال: 2006
ISSN: 0952-5041,1479-6813
DOI: 10.1677/jme.1.01831