Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Ryan W Johnson"'
Autor:
Ryan W Johnson, Kay W P Ng, Alexander R Dietz, Mary E Hartman, Jack D Baty, Nausheen Hasan, Craig M Zaidman, Michael Shoykhet
Publikováno v:
PLoS ONE, Vol 13, Iss 12, p e0207720 (2018)
IMPORTANCE:ICU-acquired muscle atrophy occurs commonly and worsens outcomes in adults. The incidence and severity of muscle atrophy in critically ill children are poorly characterized. OBJECTIVE:To determine incidence, severity and risk factors for m
Externí odkaz:
https://doaj.org/article/a1c12ae16db14c6382b328f15e4d50dc
Autor:
Amy L. Baxter, Kyle R. Schwartz, Ryan W. Johnson, Ann-Marie Kuchinski, Kevin M. Swartout, Arni S. R. Srinivasa Rao, Robert W. Gibson, Erica Cherian, Taylor Giller, Houlton Boomer, Matthew Lyon, Richard Schwartz
ImportanceSARS-CoV-2 enters the nasopharynx to replicate; nasal irrigation soon after diagnosis could reduce viral load and inhibit furin cleavage necessary for cell entry, thereby reducing morbidity and mortality.ObjectiveTo determine whether initia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::48c78378fa095215a51fbd87333df088
https://doi.org/10.1101/2021.08.16.21262044
https://doi.org/10.1101/2021.08.16.21262044
Autor:
Amy L Baxter, Kyle R Schwartz, Ryan W Johnson, Ann-Marie Kuchinski, Kevin M Swartout, Arni S R Srinivasa Rao, Robert W Gibson, Erica Cherian, Taylor Giller, Houlton Boomer, Matthew Lyon, Richard Schwartz
Publikováno v:
Ear, Nose & Throat Journal. :014556132211237
Objective To determine whether initiating saline nasal irrigation after COVID-19 diagnosis reduces hospitalization and death in high-risk outpatients compared with observational controls, and if irrigant composition impacts severity. Methods Particip
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55ae2142a8718dc617a53d2492cbc2a6
https://doi.org/10.1177/01455613221123737
https://doi.org/10.1177/01455613221123737
Autor:
Danielle A. Griffin, Kristin N. Heller, Ellyn Peterson, Hillarie P. Windish, Kimmo Lehtimäki, Jerry R. Mendell, Louise R. Rodino-Klapac, Ryan W. Johnson, Rachael A. Potter, Plavi Mittal, Douglas E. Albrecht, Patricia C. Sondergaard, Eric R. Pozsgai
Publikováno v:
Human Gene Therapy
Dysferlinopathies comprise a family of disorders caused by mutations in the dysferlin (DYSF) gene, leading to a progressive dystrophy characterized by chronic muscle fiber loss, fat replacement, and fibrosis. To correct the underlying histopathology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b64859cd95ff95665c26c75a27390977
http://europepmc.org/articles/PMC6066196
http://europepmc.org/articles/PMC6066196
Publikováno v:
Mech Dev
Paired box (Pax) proteins function as regulators of coordinated development in organogenesis by controlling factors such as cell growth and differentiation necessary to organize multiple cell types into a single, cohesive organ. Previous work has sug
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5d06cb336b76f6549324633a42ae704
https://pubmed.ncbi.nlm.nih.gov/31398431
https://pubmed.ncbi.nlm.nih.gov/31398431
Autor:
Danielle A. Griffin, Kristin N. Heller, Zarife Sahenk, W. David Arnold, William E. Grose, Jarred M. Whitlock, Ryan W. Johnson, Eric R. Pozsgai, H. Criss Hartzell, Louise R. Rodino-Klapac
Publikováno v:
Human Molecular Genetics. 25:1900-1911
Limb-girdle muscular dystrophies are a genetically diverse group of diseases characterized by chronic muscle wasting and weakness. Recessive mutations in ANO5 (TMEM16E) have been directly linked to several clinical phenotypes including limb-girdle mu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc1fcad43251b5be423892f6b29e32af
https://doi.org/10.1093/hmg/ddw063
https://doi.org/10.1093/hmg/ddw063
Publikováno v:
Vaccine. 29:1211-1221
The pneumococcal polysaccharide conjugate vaccine which includes a nonacylated protein D carrier from Haemophilus influenzae has been recently licensed for use in many countries. While this vaccine is protective against nontypeable Haemophilus influe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fee166c8ff7d20ce5c2086bf3be638f
https://doi.org/10.1016/j.vaccine.2010.12.003
https://doi.org/10.1016/j.vaccine.2010.12.003
Autor:
Ryan W. Johnson, Helen M. Chamberlin
Publikováno v:
Mechanisms of Development. 125(5-6):486-497
The Pax-6 gene encodes a transcription factor essential for the development of eyes and other sensory organs in species ranging from planaria to mice. Because Pax-6 activity can be both necessary and sufficient for eye organogenesis, much work has fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f518bc9ca7ee9d1e03dc374d503065f3
Autor:
Danielle A. Griffin, William E. Grose, Patricia C. Sondergaard, Chrystal L. Montgomery, Louise R. Rodino-Klapac, Ryan W Johnson, Jerry R. Mendell, Zarife Sahenk, Eric R. Pozsgai, Kelly Reed Clark, Kristin Heller, Joseph Liu, Kim Shontz
Publikováno v:
Annals of Clinical and Translational Neurology
Objective Dysferlinopathies are a family of untreatable muscle disorders caused by mutations in the dysferlin gene. Lack of dysferlin protein results in progressive dystrophy with chronic muscle fiber loss, inflammation, fat replacement, and fibrosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cd920df1872e2b0a5eace2d3d996f80
https://pubmed.ncbi.nlm.nih.gov/25815352
https://pubmed.ncbi.nlm.nih.gov/25815352
Autor:
Patricia C. Sondergaard, Louise R. Rodino-Klapac, Jerry R. Mendell, Eric Pozsgai, Danielle A. Griffin, Ryan W Johnson
Publikováno v:
Neuromuscular Disorders. 24:851-852
There is no cure for dysferlinopathies, a group of related disorders caused by absent or mutant dysferlin (DYSF). Lack of dysferlin leads to progressive dystrophy with chronic muscle fiber loss, inflammation, fat replacement and fibrosis leading to d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::804a20b28b0ebd77fab8d5d371fb7e89
https://doi.org/10.1016/j.nmd.2014.06.197
https://doi.org/10.1016/j.nmd.2014.06.197