Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Madeline E. Simon"'
Autor:
Madeline E. Simon, Zachary C. Reuter, Michela M. Fabricius, Nicole M. Hitchcock, Robert P. Pierce
Publikováno v:
Journal of Community Health. 47:835-840
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c0773507948dc26ff8753eda0fa4ecd
https://doi.org/10.1007/s10900-022-01117-0
https://doi.org/10.1007/s10900-022-01117-0
Autor:
Robert P. Pierce, Zachary C. Reuter, Nicole M. Hitchcock, Madeline E. Simon, Michela M. Fabricius
Publikováno v:
Journal of Community Health
Student run free clinics (SRFCs) fill a void in healthcare access for many communities and have been subject to unprecedented shifts in care delivery brought about by the coronavirus disease 2019 (COVID-19) pandemic. Our single-center institution ser
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e583212467e979df7c65499133958009
http://europepmc.org/articles/PMC8456683
http://europepmc.org/articles/PMC8456683
Autor:
Madeline E, Simon, Zachary C, Reuter, Michela M, Fabricius, Nicole M, Hitchcock, Robert P, Pierce
Publikováno v:
Journal of community health. 47(5)
Student run free health clinics (SRFCs) provide medical care to vulnerable populations in communities throughout the United States. The COVID-19 pandemic had a significant impact on the delivery of healthcare services and demanded a rapid adjustment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b1769546d095253b3a9f8db55b1791dc
https://pubmed.ncbi.nlm.nih.gov/35788471
https://pubmed.ncbi.nlm.nih.gov/35788471
Autor:
Jose Marquez, Caley E. Smith, Toni I. Morcos, Eric Villalón, Abigail E. Hopkins, Kevin A. Kaifer, Christian L. Lorson, Madeline E. Simon
Publikováno v:
Biochemical and Biophysical Research Communications. 530:107-114
Spinal Muscular Atrophy (SMA) is an autosomal recessive neuromuscular disease caused by deletions or mutations in the survival motor neuron (SMN1) gene. An important hallmark of disease progression is the pathology of neuromuscular junctions (NMJs).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83cafd0656517571457d3790cccf898e
https://doi.org/10.1016/j.bbrc.2020.07.031
https://doi.org/10.1016/j.bbrc.2020.07.031
Autor:
Charles W. Washington, Erkan Y. Osman, Dalia Megiddo, Hagar Greif, Madeline E. Simon, Christian L. Lorson
Publikováno v:
Journal of Neuromuscular Diseases. 4:237-249
Background Spinal muscular atrophy (SMA) is a neurodegenerative autosomal recessive disorder characterized by the loss of α-motor neurons. A variety of molecular pathways are being investigated to elevate SMN protein expression in SMA models and in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dff6a3f35ae6ed5350b97291fa951a6a
https://doi.org/10.3233/jnd-170230
https://doi.org/10.3233/jnd-170230
Autor:
Hansjörg Rindt, Jose Marquez, Caley E. Smith, Christian L. Lorson, Samantha L Sison, Abigail E. Hopkins, Kevin A. Kaifer, Siri O’Day, Allison D. Ebert, Rachel Neff, Madeline E. Simon, Eric Villalón, Benjamin S. O’Brien
Publikováno v:
Hum Mol Genet
Spinal muscular atrophy (SMA) is a neuromuscular disease caused by deletions or mutations in survival motor neuron 1 (SMN1). The molecular mechanisms underlying motor neuron degeneration in SMA remain elusive, as global cellular dysfunction obscures
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d440ae04248a8b8e52112e21aeb5460
https://pubmed.ncbi.nlm.nih.gov/31211843
https://pubmed.ncbi.nlm.nih.gov/31211843
Autor:
Charles W. Washington, Christian L. Lorson, Kyra M Florea, Allison D. Ebert, Madeline E. Simon, Chiara Mazzasette, Teresa N. Patitucci, Chien-Ping Ko, Erkan Y. Osman, Kevin A. Kaifer
Publikováno v:
Molecular Therapy. 24:1592-1601
Loss of Survival Motor Neuron-1 ( SMN1 ) causes Spinal Muscular Atrophy, a devastating neurodegenerative disease . SMN2 is a nearly identical copy gene; however SMN2 cannot prevent disease development in the absence of SMN1 since the majority of SMN2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f10711d7ae9b1bf88f69db9eb22a1154
https://doi.org/10.1038/mt.2016.145
https://doi.org/10.1038/mt.2016.145