Zobrazeno 1 - 10
of 446
pro vyhledávání: '"Whitley A"'
Autor:
Grant C. Hayward, Ahmad Mohammad, Emily N. Copeland, Daniela Caceres, Val A. Fajardo, Kennedy C. Whitley, Rebecca E. K. MacPherson, Bradley J. Baranowski
Publikováno v:
FEBS Open Bio
FEBS Open Bio, Vol 12, Iss 1, Pp 154-162 (2022)
FEBS Open Bio, Vol 12, Iss 1, Pp 154-162 (2022)
Duchenne muscular dystrophy (DMD) is a progressive muscle wasting disorder caused by a mutation in the dystrophin gene. In addition to muscle pathology, some patients with DMD will exhibit cognitive impairments with severity being linked to age and t
Autor:
Rita de Cássia Marquetti Durigan, Elaine Vieira, Anderson Sola Haro, Rodrigo Vanerson Passos Neves, Michel Kendy Souza, Fernando Costa, Thiago Santos Rosa, Jonato Prestes, Vinicius Fernandes Cruzat, Andrea Lucena Reis, Ivo Vieira de Sousa Neto, Whitley J. Stone, Herbert Gustavo Simões, Lysleine Alves Deus, Rosângela Vieira de Andrade, Hugo de Luca Corrêa, Claudio de Oliveira Assumpção
Publikováno v:
Oxidative Medicine and Cellular Longevity
Oxidative Medicine and Cellular Longevity, Vol 2021 (2021)
Oxidative Medicine and Cellular Longevity, Vol 2021 (2021)
Aerobic training (AT) promotes several health benefits that may attenuate the progression of obesity associated diabetes. Since AT is an important nitric oxide (NO-) inducer mediating kidney-healthy phenotype, the present study is aimed at investigat
Autor:
David Alexanderian, Frits A. Wijburg, Chester B. Whitley, Elsa G Shapiro, Serena Gasperini, Joseph Muenzer, Maureen Cleary, Caroline Sevin, Nicole Muschol, Mireia del Toro
Publikováno v:
Molecular genetics and metabolism, 134(1-2), 175-181. Academic Press Inc.
Sanfilippo syndrome type A (mucopolysaccharidosis type IIIA) is a rare autosomal recessive lysosomal disorder characterized by deficient heparan-N-sulfatase (HNS) activity, and subsequent accumulation of heparan sulfate, especially in the central ner
Autor:
Sarah Kim, Michael J. Przybilla, Chester B. Whitley, Li Ou, Mahmoud Al-Kofahi, Jeanine R. Jarnes
Publikováno v:
Molecular genetics and metabolism reports. 33
Lysosomal diseases are a group of over 70 rare genetic conditions in which a protein deficiency (most often an enzyme deficiency) leads to multi-system disease. Current therapies for lysosomal diseases are limited in their ability to treat certain ti
Autor:
Alia Ahmed, Kyle Rudser, Kelly E. King, Julie B. Eisengart, Paul J. Orchard, Elsa Shapiro, Chester B. Whitley
Publikováno v:
Mol Genet Metab
BACKGROUND: A physical symptom score (PSS) for the mucopolysaccharidosis (MPS) disorders has been developed to quantitate the somatic burden of disease across multiple organ systems. Studies have demonstrated the sensitivity and its relationship to a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cecd1169c235995e6b196c98df4179f6
https://europepmc.org/articles/PMC9261749/
https://europepmc.org/articles/PMC9261749/
Publikováno v:
Molecular Genetics and Metabolism. 138:106993
Autor:
Michael J. Przybilla, Vikash Reebye, Konstantinos Vanezis, John J. Rossi, Min-sun Song, Nagy A. Habib, Chester B. Whitley
Publikováno v:
Molecular Genetics and Metabolism. 138:107279
Autor:
Nagy Habib, Vikash Reebye, Konstantinos Vanezis, Luke Haslett, Konstantina Skourti-Stathaki, Brid Ryan, John J. Rossi, Min-Sun Song, Michael J. Przybilla, Laura Furness, Chester B. Whitley, Robert Habib, Simon Jones
Publikováno v:
Molecular Genetics and Metabolism. 138:107134
Publikováno v:
Molecular Genetics and Metabolism. 138:107272
Autor:
Jeanine R. Jarnes, Caroline A. Hastings, Can H. Ficicioglu, Debra-Lynn Day-Salvatore, Roberto Giugliani, Julien Baruteau, Chester B. Whitley, Michal Inbar-Feigenberg, Geneviève Bernard, Fatih S. Ezgü, Yan G. Ni, Michelle Miller, Michael H. Gelb, Pruthvi Nagilla, Rose Johnstone, Patricia Elsasser, Elizabeth Cunningham, Victoria Ballard, Thomas F. Haws, Mark S. Forman, David A. Weinstein
Publikováno v:
Molecular Genetics and Metabolism. 138:107169