نتایج جستجو برای: morphogenesis

تعداد نتایج: 23066  

Journal: :Microbiology and Molecular Biology Reviews 2012

Journal: :Russian Journal of Dentistry 2017

Journal: :International Journal of Architectural Computing 2009

Journal: :I.P.Pavlov Russian Medical Biological Herald 2013

Journal: :Proceedings of the National Academy of Sciences 1964

Journal: :Current opinion in biotechnology 2013
Jason P Gleghorn Sriram Manivannan Celeste M Nelson

Morphogenesis, the creation of tissue and organ architecture, is a series of complex and dynamic processes driven by genetic programs, microenvironmental cues, and intercellular interactions. Elucidating the physical mechanisms that generate tissue form is key to understanding development, disease, and the strategies needed for regenerative therapies. Advancements in imaging technologies, genet...

Journal: :Development 1999
F Agnès M Suzanne S Noselli

In Drosophila, the Jun-N-terminal Kinase-(JNK) signaling pathway is required for epithelial cell shape changes during dorsal closure of the embryo. In the absence of JNK pathway activity, as in the DJNKK/hemipterous (hep) mutant, the dorsolateral ectodermal cells fail both to elongate and move toward the dorsal midline, leading to dorsally open embryos. We show here that hep and the JNK pathway...

Journal: :Methods in molecular biology 2015
Dagmar Iber Simon Tanaka Patrick Fried Philipp Germann Denis Menshykau

During embryonic development tissue morphogenesis and signaling are tightly coupled. It is therefore important to simulate both tissue morphogenesis and signaling simultaneously in in silico models of developmental processes. The resolution of the processes depends on the questions of interest. As part of this chapter we introduce different descriptions of tissue morphogenesi s. In the simplest...

Journal: :eLife 2021

The role of compartmentalized signaling in primary cilia during tissue morphogenesis is not well understood. localized G protein-coupled receptor, Gpr161, represses hedgehog pathway via cAMP signaling. We engineered a knock-in at the Gpr161 locus mice to generate variant (Gpr161 mut1 ), which was ciliary localization defective but competent. Tissue phenotypes from depend on downstream bifunctio...

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