Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Joseph P. Salisbury"'
Autor:
Ned T. Sahin, Rafiq Abdus-Sabur, Neha U. Keshav, Runpeng Liu, Joseph P. Salisbury, Arshya Vahabzadeh
Publikováno v:
Frontiers in Education, Vol 3 (2018)
Background: Impairment in social communication is the primary deficit in school-aged children with autism spectrum disorder (ASD). Research has shown that there are efficacious interventions to address social communication deficits, yet their deliver
Externí odkaz:
https://doaj.org/article/9fed17d245a94c699b1cdf61ae52a34d
Publikováno v:
Frontiers in Pediatrics, Vol 5 (2017)
BackgroundAutism spectrum disorder (ASD) is a childhood-onset neurodevelopmental disorder with a rapidly rising prevalence, currently affecting 1 in 68 children, and over 3.5 million people in the United States. Current ASD interventions are primaril
Externí odkaz:
https://doaj.org/article/74ff426675534d808716b02b8a7202eb
Autor:
Neha U. Keshav, Arshya Vahabzadeh, Rafiq Abdus-Sabur, Krystal Huey, Joseph P. Salisbury, Runpeng Liu, Ned Sahin
Publikováno v:
Education Sciences, Vol 8, Iss 3, p 107 (2018)
There is considerable demand for special education services for the over half a million students with autism in the United States. While assistive technology may augment educational services, its implementation is often prevented by a number of pract
Externí odkaz:
https://doaj.org/article/a2bb69bd039741ae8c3d230cbc51ac78
Autor:
Md Amin Hossain, Richa Sarin, Daniel P Donnelly, Brandon C Miller, Alexandra Weiss, Luke McAlary, Svetlana V Antonyuk, Joseph P Salisbury, Jakal Amin, Jeremy B Conway, Samantha S Watson, Jenifer N Winters, Yu Xu, Novera Alam, Rutali R Brahme, Haneyeh Shahbazian, Durgalakshmi Sivasankar, Swathi Padmakumar, Aziza Sattarova, Aparna C Ponmudiyan, Tanvi Gawde, David E Verrill, Wensheng Yang, Sunanda Kannapadi, Leigh D Plant, Jared R Auclair, Lee Makowski, Gregory A Petsko, Dagmar Ringe, Nathalie Y R Agar, David J Greenblatt, Mary Jo Ondrechen, Yunqiu Chen, Justin J Yerbury, Roman Manetsch, S Samar Hasnain, Robert H Brown, Jeffrey N Agar
Publikováno v:
PLoS Biology, Vol 22, Iss 1, p e3002462 (2024)
Mutations in the gene encoding Cu-Zn superoxide dismutase 1 (SOD1) cause a subset of familial amyotrophic lateral sclerosis (fALS) cases. A shared effect of these mutations is that SOD1, which is normally a stable dimer, dissociates into toxic monome
Externí odkaz:
https://doaj.org/article/ae0b075acaa84b09a950667731983ac1
Autor:
Jack H. Prior, Matthew D. Campbell, Matthew Dawkins, Paul F. Mickle, Robert J. Moorhead, Simegnew Y. Alaba, Chiranjibi Shah, Joseph R. Salisbury, Kevin R. Rademacher, A. Paul Felts, Farron Wallace
Publikováno v:
Frontiers in Marine Science, Vol 10 (2023)
Increased necessity to monitor vital fish habitat has resulted in proliferation of camera-based observation methods and advancements in camera and processing technology. Automated image analysis through computer vision algorithms has emerged as a too
Externí odkaz:
https://doaj.org/article/cd4eb2ad64594485a9d9b9ee2c5296c1
Publikováno v:
Companion of the 2023 ACM/IEEE International Conference on Human-Robot Interaction.
Publikováno v:
Journal of World-Systems Research, Vol 2, Iss 1, Pp 479-505 (2015)
This paper extends the theoretical arguments of the world-systems perspective to the emerging post-industrial society. Using survey data gathered by AT&T and published in the World's Telephones (1978-1990) and data gathered by the International Insti
Externí odkaz:
https://doaj.org/article/99548b573191416a8b0167d6bcb95831
Publikováno v:
World Congress on Electrical Engineering and Computer Systems and Science.
Autor:
Ross L. Bobb, Jeffry A. Coady, Virgil O. Barnard, Matthew A. Mueller, William D. Casebeer, Joseph P. Salisbury
Publikováno v:
Virtual, Augmented, and Mixed Reality (XR) Technology for Multi-Domain Operations III.
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-13 (2020)
Scientific Reports
Scientific Reports
0.5–1% of ALS (Amyotrophic Lateral Sclerosis) and Parkinson's disease (PD) are associated with mutations in the angiogenin (ANG). These mutations are thought to cause disease through a loss of ANG function, but this hypothesis has not been evaluate