Zobrazeno 1 - 10
of 194
pro vyhledávání: '"Daniel G. Miller"'
Autor:
Vidya Eswaran, Anna Marie Chang, R. Gentry Wilkerson, Kelli N. O’Laughlin, Brian Chinnock, Stephanie A. Eucker, Brigitte M. Baumann, Nancy Anaya, Daniel G. Miller, Adrianne N. Haggins, Jesus R. Torres, Erik S. Anderson, Stephen C. Lim, Martina T. Caldwell, Ali S. Raja, Robert M. Rodriguez, The REVVED-UP Investigators
Publikováno v:
PLoS ONE, Vol 17, Iss 4 (2022)
Study objective Facemask use is associated with reduced transmission of SARS-CoV-2. Most surveys assessing perceptions and practices of mask use miss the most vulnerable racial, ethnic, and socio-economic populations. These same populations have suff
Externí odkaz:
https://doaj.org/article/d06ec8ae7343433a8fd2dc265dbd2ca7
Publikováno v:
Epigenetics & Chromatin, Vol 11, Iss 1, Pp 1-14 (2018)
Abstract Background Facioscapulohumeral muscular dystrophy 1 (FSHD1) has an autosomal dominant pattern of inheritance and primarily affects skeletal muscle. The genetic cause of FSHD1 is contraction of the D4Z4 macrosatellite array on chromosome 4 al
Externí odkaz:
https://doaj.org/article/0ab0f130c6d04aaa9e7ebc24650405af
Publikováno v:
Skeletal Muscle, Vol 7, Iss 1, Pp 1-13 (2017)
Abstract Background Facioscapulohumeral muscular dystrophy (FSHD) is most commonly inherited in an autosomal dominant pattern and caused by the abnormal expression of DUX4 in skeletal muscle. The DUX4 transcription factor has DNA binding domains simi
Externí odkaz:
https://doaj.org/article/fd2d9789af1b48f4a68bb5ac5f0aa470
Autor:
Leslie Caron, Devaki Kher, Kian Leong Lee, Robert McKernan, Biljana Dumevska, Alejandro Hidalgo, Jia Li, Henry Yang, Heather Main, Giulia Ferri, Lisa M. Petek, Lorenz Poellinger, Daniel G. Miller, Davide Gabellini, Uli Schmidt
Publikováno v:
Stem Cells Translational Medicine, Vol 5, Iss 9, Pp 1145-1161 (2016)
Facioscapulohumeral muscular dystrophy (FSHD) represents a major unmet clinical need arising from the progressive weakness and atrophy of skeletal muscles. The dearth of adequate experimental models has severely hampered our understanding of the dise
Externí odkaz:
https://doaj.org/article/acc0cb4ac8ae47ce9836e621e6d06fb8
Publikováno v:
Western Journal of Emergency Medicine, Vol 17, Iss 2, Pp 149-152 (2016)
Introduction: Work interruptions during patient care have been correlated with error. Task-switching is identified by the Accreditation Council for Graduate Medical Education (ACGME) as a core competency for emergency medicine (EM). Simulation has
Externí odkaz:
https://doaj.org/article/90d4bff70d0c42d48680f598841f92fa
Publikováno v:
Western Journal of Emergency Medicine, Vol 19, Iss 2 (2018)
Introduction: This study investigated whether a 9.6% decrease in the use of head computed tomography (HCT) for patients presenting to the emergency department (ED) with a chief complaint of headache was followed by an increase in proportions of death
Externí odkaz:
https://doaj.org/article/e645e086341348209f06498a531d5cb5
Autor:
Daniel G. Miller
Publikováno v:
Journal of Pain and Symptom Management. 65:e585-e586
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07eeffe408a571543fbf025fca3c1f98
https://doi.org/10.1016/j.jpainsymman.2023.02.150
https://doi.org/10.1016/j.jpainsymman.2023.02.150
Publikováno v:
Handbook of Scholarly Publications from the Air Force Institute of Technology (AFIT), Volume 1, 2000–2020 ISBN: 9781003220978
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4afb903eefcfeab847e832da46537f67
https://doi.org/10.1201/9781003220978-26
https://doi.org/10.1201/9781003220978-26
Autor:
Minseung Choi, Diane P Genereux, Jamie Goodson, Haneen Al-Azzawi, Shannon Q Allain, Noah Simon, Stan Palasek, Carol B Ware, Chris Cavanaugh, Daniel G Miller, Winslow C Johnson, Kevin D Sinclair, Reinhard Stöger, Charles D Laird
Publikováno v:
PLoS Genetics, Vol 13, Iss 11, p e1007060 (2017)
In storing and transmitting epigenetic information, organisms must balance the need to maintain information about past conditions with the capacity to respond to information in their current and future environments. Some of this information is encode
Externí odkaz:
https://doaj.org/article/b967721753764a2fae9f6e07de274387
Autor:
Margaret P. Adam, Karen W. Gripp, Kelly Kernan, Dan Doherty, George Anadiotis, Rebecca Sahraoui, Jennifer C. Dempsey, Michele G. Mehaffey, Daniel G. Miller, Carrie Fagerstrom, Yassmine Akkari, Katia Sol-Church, Heather C Mefford, Candace T. Myers, Wagner A.R. Baratela, Deborah L. Stabley, Martin Kircher, Michael B. Bober, Deborah A. Nickerson, Michael J. Bamshad, Katherine M. Robbins, Amy Lacroix, Angela L. Duker
Publikováno v:
The American Journal of Human Genetics. 104:35-44
Baratela-Scott syndrome (BSS) is a rare, autosomal-recessive disorder characterized by short stature, facial dysmorphisms, developmental delay, and skeletal dysplasia caused by pathogenic variants in XYLT1. We report clinical and molecular investigat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9942a8e9f1625712d3772d6888d5194
https://doi.org/10.1016/j.ajhg.2018.11.005
https://doi.org/10.1016/j.ajhg.2018.11.005