Zobrazeno 1 - 10
of 9 785
pro vyhledávání: '"Tansey"'
Autor:
Tansey, Isabel
Background: Rural maternity care in Canada is in crisis, with many communities losing local services. This forces rural women and families to travel for care, leading to heightened stress, expenses, and adverse outcomes. Family physicians, often the
Externí odkaz:
http://hdl.handle.net/11375/29690
Publikováno v:
Applied Bionics and Biomechanics, Vol 2021 (2021)
The present study is aimed at investigating the mechanical behaviour of fabricated synthetic midthoracic paediatric spine based on range of motion (ROM) as compared to porcine spine as the biological specimen. The main interest was to ensure that the
Externí odkaz:
https://doaj.org/article/8e36c17db5974fafb9d4de12e4877e86
Controlling false positives (Type I errors) through statistical hypothesis testing is a foundation of modern scientific data analysis. Existing causal structure discovery algorithms either do not provide Type I error control or cannot scale to the si
Externí odkaz:
http://arxiv.org/abs/2310.16626
Autor:
Hannah A. Staley, Janna E. Jernigan, MacKenzie L. Bolen, Ann M. Titus, Noelle Neighbarger, Cassandra Cole, Kelly B. Menees, Rebecca L. Wallings, Malú Gámez Tansey
Publikováno v:
Journal of Neuroinflammation, Vol 21, Iss 1, Pp 1-16 (2024)
Abstract Genome-wide association studies have identified a protective mutation in the phospholipase C gamma 2 (PLCG2) gene which confers protection against Alzheimer’s disease (AD)-associated cognitive decline. Therefore, PLCG2, which is primarily
Externí odkaz:
https://doaj.org/article/2fe3c49932fc460e96040f55471113e1
Autor:
Amy D. Harper, Haluk Topaloglu, Eugenio Mercuri, Vasiliy Suslov, Liwen Wu, Cigdem Y. Ayanoglu, Michael Tansey, Michelle L. Previtera, Robert A. Crozier, Leslie Magnus, Paula R. Clemens
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-9 (2024)
Abstract Duchenne muscular dystrophy (DMD) is an X-linked recessive disease characterized by mutations in the dystrophin gene, causing motor and pulmonary function decline. Viltolarsen is indicated for patients with dystrophin gene mutations amenable
Externí odkaz:
https://doaj.org/article/9968d3b7d6514a56bdbd3bf8f3a6e367
Autor:
Valerie Joers, Benjamin C Murray, Caroline McLaughlin, Danielle Oliver, Hannah E. Staley, Jazmyn Coronado, Cindy Achat-Mendes, Sanam Golshani, Sean D. Kelly, Matthew Goodson, Danica Lee, Fredric P. Manfredsson, Bob M. Moore II, Malú Gámez Tansey
Publikováno v:
Journal of Neuroinflammation, Vol 21, Iss 1, Pp 1-20 (2024)
Abstract Research into the disequilibrium of microglial phenotypes has become an area of intense focus in neurodegenerative disease as a potential mechanism that contributes to chronic neuroinflammation and neuronal loss in Parkinson’s disease (PD)
Externí odkaz:
https://doaj.org/article/dae8f1cd186941429aefb572745115d0