نتایج جستجو برای: پروتئین msx2
تعداد نتایج: 18187 فیلتر نتایج به سال:
We describe the clinical characterization, molecular analyses, and genetic mapping of a distinct genetic condition characterized by craniosynostosis, delayed closure of the fontanel, cranial defects, clavicular hypoplasia, anal and genitourinary malformations, and skin eruption. We have identified seven patients with this phenotype in four families from different geographic regions and ethnic b...
Mutations in transcription factors with homeobox domains have been identified in a number of developmental disorders, for instance, mutations in PAX6 have been identified in patients with aniridia, mutations in HOX13 in patients with synpolydactyly, and mutations in MSX2 in patients with Boston-type craniosynostosis. The mouse GSH2 gene, like the related GSH1 gene, encodes a homeodomain contain...
TGF-β mediated Msx2 expression controls occipital somites-derived caudal region of skull development
The Mexican axolotl, Ambystoma mexicanum, is a unique vertebrate species which has amazing powers of limb regeneration. In the present study we have used a Subtractive Amplification approach to identify genes which are activated and overexpressed during the limb regeneration process. In our initial studies, we have found that levels of expression of 11 genes are increased during the limb regene...
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