Showing results (231-240 of 272) with videos related to
Sort By:
Pageof 28
Molecular Biology of the Cell|February 25, 2011
Direct binding of RalA to PKCη and its crucial role in morphological change during keratinocyte differentiationYasuhito Shirai, Shoko Morioka, Megumi Sakuma, et al.Genes to Cells : Devoted to Molecular & Cellular Mechanisms|October 6, 2004
Propagation of gammaPKC translocation along the dendrites of Purkinje cell in gammaPKC-GFP transgenic miceNorio Sakai, Hiroshi Tsubokawa, Masanori Matsuzaki, et al.Journal of Immunology (Baltimore, Md. : 1950)|September 24, 2004
Superoxide production at phagosomal cup/phagosome through beta I protein kinase C during Fc gamma R-mediated phagocytosis in microgliaTakehiko Ueyama, Michelle R Lennartz, Yukiko Noda, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 11, 2014
The role of Pak-interacting exchange factor-β phosphorylation at serines 340 and 583 by PKCγ in dopamine releaseToshihiko Shirafuji, Takehiko Ueyama, Ken-ichi Yoshino, et al.Neuroscience Letters|January 22, 2022
Pentobarbital may protect against neurogenic inflammation after surgery via inhibition of substance P release from peripheral nerves of ratsChiori Onizuka, Masahiro Irifune, Akari Mukai, et al.Nature Genetics|April 12, 2005
Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesionHugo Vega, Quinten Waisfisz, Miriam Gordillo, et al.BMC Medical Genomics|August 27, 2016
Within-pair differences of DNA methylation levels between monozygotic twins are different between male and female pairsMikio Watanabe, Chika Honda, , et al.Plos One|August 8, 2012
An overgrowth disorder associated with excessive production of cGMP due to a gain-of-function mutation of the natriuretic peptide receptor 2 geneKohji Miura, Noriyuki Namba, Makoto Fujiwara, et al.Human Genome Variation|April 10, 2019
A novel <i>PTCH1</i> mutation in basal cell nevus syndrome with rare craniofacial featuresYuka Murata, Hiroshi Kurosaka, Yasuhisa Ohata, et al.Journal of Human Genetics|June 27, 2022
Comparison of two families with and without ataxia harboring novel variants in PRKCGYui Tada, Kodai Kume, Soma Noguchi, et al.Pageof 28