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Craniosynostosis is the premature closure of one or more cranial sutures. It is a well-recognized congenital problem. It is present in 4 of 10,000 infants and is almost exclusively seen in males. The sutures most commonly involved are coronal, sagittal, metopic and lambdoid. The condition is due to several etiologies, including osseous overgrowth and connective tissue overgrowth. The intrauterine diagnosis of craniosynostosis is increasingly made. The management of craniosynostosis has also been improving with the use of cranial expanders, which make surgery easier and improve outcome.Classical homeobox gene Cseng1 regulates extraembryonic growth and yolk deposition in the early stages of embryonic development.
The paired-like homeobox gene Cseng1 has previously been isolated in Xenopus as one of six genes involved in the early embryonic patterning system. We have continued with the characterization of this gene and show that it is strongly expressed in the early cleavage stages of development. At later stages of development, Cseng1 is expressed in different tissues and its expression persists in the developing gut of larval and juvenile stages. Expression of Cseng1 has been shown to be necessary for correct embryogenesis of the head, eyes, ears, brain, dorsal midline structures, tailbud, neural tube, and lateral plate mesoderm. Analysis of Cseng1 function in development revealed that it is required for the initiation of gastrulation and for the correct extension of the yolk cell population in the ventral blastoderms, and more specifically in the activation of the yolk uptake system. Our results suggest that Cseng1 is involved in the formation of the yolk cell population and that it regulates yolk uptake by the mouth during gastrulation.Bio-analytical procedure for the bioassay-guided isolation of taxifolin derivatives from Taxus chinensis Miller.
In the present study, an accurate analytical method was developed for the simultaneous
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