Zobrazeno 1 - 10
of 19
pro vyhledávání: '"D'anna M. Nelson"'
Autor:
D'anna M. Nelson, Elizabeth K. Fasbender, Margurite C. Jakubiak, Angus Lindsay, Dawn A. Lowe, James M. Ervasti
Publikováno v:
Redox Biology, Vol 37, Iss , Pp 101730- (2020)
The highly ordered cortical microtubule lattice of skeletal muscle is disorganized in dystrophin-deficient mdx mice. Implicated mechanisms include loss of dystrophin binding, altered α-tubulin posttranslational modification, expression of a β-tubul
Externí odkaz:
https://doaj.org/article/1b0c4238eba7419dbdc9c554a0ef0a20
Publikováno v:
Biosensors, Vol 13, Iss 3, p 331 (2023)
Urinary chloride concentration is a valuable health metric that can aid in the early detection of serious conditions, such as acid base disorders, acute heart failure, and incidences of acute renal failure in the intensive care unit. Physiologically,
Externí odkaz:
https://doaj.org/article/cff91ecde472464fb8236010902ca572
Autor:
David Jones, Holly Caretta-Weyer, Ryanne J. Mayersak, Lalena M. Yarris, Joshua G. Kornegay, Rachel R. Bengtzen, Anna M. Nelson, Rebecca C. Tuttle
Publikováno v:
J Grad Med Educ
Autor:
D’anna M. Nelson, James M. Ervasti
Publikováno v:
Encyclopedia of Biological Chemistry III ISBN: 9780128220405
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::594089df84d9d56c8f0505ebfa255b32
https://doi.org/10.1016/b978-0-12-809633-8.21355-1
https://doi.org/10.1016/b978-0-12-809633-8.21355-1
Autor:
Angus Lindsay, D'anna M. Nelson, Dongsheng Duan, James M. Ervasti, Jeffrey S. Chamberlain, Luke M. Judge, Dawn A. Lowe
Publikováno v:
Human Molecular Genetics. 27:2090-2100
Delivery of miniaturized dystrophin genes via adeno-associated viral vectors is one leading approach in development to treat Duchenne muscular dystrophy. Here we directly compared the functionality of five mini- and micro-dystrophins via skeletal mus
Autor:
James M. Ervasti, Michael D. Tarpey, Allison R. O'Rourke, Angus Lindsay, Preston M. McCourt, Benjamin J. Perrin, Dawn A. Lowe, Samantha L. Yuen, D'anna M. Nelson, David D. Thomas, Espen E. Spangenburg
Publikováno v:
The FEBS Journal. 285:481-500
While α-actin isoforms predominate in adult striated muscle, skeletal muscle-specific knockouts (KOs) of nonmuscle cytoplasmic βcyto - or γcyto -actin each cause a mild, but progressive myopathy effected by an unknown mechanism. Using transmission
Autor:
John T. Olthoff, Dawn A. Lowe, Jackie L McCourt, Robert W. Arpke, Dana M Talsness, James M. Ervasti, Michael Kyba, Joseph J. Belanto, Angus Lindsay, D'anna M. Nelson, Christopher M. Chamberlain, Paul D Chatterton, Preston M. McCourt
Publikováno v:
Human Molecular Genetics. 27:451-462
Missense mutations in the dystrophin protein can cause Duchenne muscular dystrophy (DMD) or Becker muscular dystrophy (BMD) through an undefined pathomechanism. In vitro studies suggest that missense mutations in the N-terminal actin-binding domain (
Publikováno v:
Medical Science Educator. 27:509-514
The authors’ curricular goal was to develop, pilot, and evaluate an educational intervention designed to train incoming medical students on entrustable professional activity (EPA) 10, the recognition, and evaluation of a patient requiring emergent
Autor:
Craig D. Newgard, Dowin Boatright, Kaitlin Z. Gee, Ann M. Arens, Antonio Bueso, Deborah B. Diercks, Samuel D. Gaona, Jody A. Vogel, Ernest E. Moore, Anna M. Nelson, Jeremy J. Voros, Christopher B. Colwell, James F. Holmes, Jason S. Haukoos
Publikováno v:
Journal of the American College of Surgeons, vol 222, iss 1
Background Early recognition of trauma patients at risk for multiple organ failure (MOF) is important to reduce the morbidity and mortality associated with MOF. The objective of the study was to externally validate the Denver Emergency Department (ED
Autor:
Margurite C. Jakubiak, Angus Lindsay, James M. Ervasti, Elizabeth K. Fasbender, Dawn A. Lowe, D'anna M. Nelson
Publikováno v:
Redox Biology, Vol 37, Iss, Pp 101730-(2020)
Redox Biology
Redox Biology
The highly ordered cortical microtubule lattice of skeletal muscle is disorganized in dystrophin-deficient mdx mice. Implicated mechanisms include loss of dystrophin binding, altered α-tubulin posttranslational modification, expression of a β-tubul