Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Kevin J Sonnemann"'
Publikováno v:
PLoS Genetics, Vol 6, Iss 10, p e1001158 (2010)
Hair cell stereocilia structure depends on actin filaments composed of cytoplasmic β-actin and γ-actin isoforms. Mutations in either gene can lead to progressive hearing loss in humans. Since β-actin and γ-actin isoforms are 99% identical at the
Externí odkaz:
https://doaj.org/article/ea30eb6846ca4c44bfab8ce75806a2d4
Autor:
Kevin J Sonnemann, Hanke Heun-Johnson, Amy J Turner, Kristen A Baltgalvis, Dawn A Lowe, James M Ervasti
Publikováno v:
PLoS Medicine, Vol 6, Iss 5, p e1000083 (2009)
The loss of dystrophin compromises muscle cell membrane stability and causes Duchenne muscular dystrophy and/or various forms of cardiomyopathy. Increased expression of the dystrophin homolog utrophin by gene delivery or pharmacologic up-regulation h
Externí odkaz:
https://doaj.org/article/4fdad23a597c44f7b801c8d249d2427a
Publikováno v:
The FASEB Journal. 32
Autor:
Kevin J. Sonnemann, William M. Bement
Publikováno v:
Annual Review of Cell and Developmental Biology. 27:237-263
The importance of wound healing to medicine and biology has long been evident, and consequently, wound healing has been the subject of intense investigation for many years. However, several relatively recent developments have added new impetus to wou
Autor:
Karen H. Friderici, Edward J. Walsh, Mei Zhu, James M. Ervasti, Inna A. Belyantseva, Kevin J. Sonnemann, Benjamin J. Perrin, JoAnn McGee, Gregory I. Frolenkov, Ruben Stepanyan, Thomas B. Friedman
Publikováno v:
Proceedings of the National Academy of Sciences. 106:9703-9708
β cyto -Actin and γ cyto -actin are ubiquitous proteins thought to be essential building blocks of the cytoskeleton in all non-muscle cells. Despite this widely held supposition, we show that γ cyto -actin null mice ( Actg1 −/− ) are viable. H
Publikováno v:
The FASEB Journal. 23:2205-2214
We generated transgenic mice that overexpressed γ-cyto actin 2000-fold above wild-type levels in skeletal muscle. γ-cyto actin comprised 40% of total actin in transgenic skeletal muscle, with a concomitant 40% decrease in α-actin. Surprisingly, tr
Publikováno v:
Journal of Biological Chemistry. 281:9996-10001
This study was designed to define the molecular epitopes of dystrophin-actin interaction and to directly compare the actin binding properties of dystrophin and utrophin. According to our data, dystrophin and utrophin both bound alongside actin filame
Publikováno v:
FASEB journal : official publication of the Federation of American Societies for Experimental Biology. 23(7)
We generated transgenic mice that overexpressed γ-cyto actin 2000-fold above wild-type levels in skeletal muscle. γ-cyto actin comprised 40% of total actin in transgenic skeletal muscle, with a concomitant 40% decrease in α-actin. Surprisingly, tr
Autor:
Kristen A. Baltgalvis, Hanke Heun-Johnson, Kevin J. Sonnemann, Dawn A. Lowe, James M. Ervasti, Amy J. Turner
Publikováno v:
PLoS Medicine
PLoS Medicine, Vol 6, Iss 5, p e1000083 (2009)
PLoS Medicine, Vol 6, Iss 5, p e1000083 (2009)
James Ervasti and colleagues show that injection of a truncated form of utrophin transduced all tissues examined, integrated with members of the dystrophin complex, and reduced serum levels of creatine kinase in a mouse model of muscular dystrophy.
Autor:
James M, Ervasti, Kevin J, Sonnemann
Publikováno v:
International review of cytology. 265
Since its first description in 1990, the dystrophin-glycoprotein complex has emerged as a critical nexus for human muscular dystrophies arising from defects in a variety of distinct genes. Studies in mammals widely support a primary role for the dyst