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of 8
pro vyhledávání: '"Sarah Brownell"'
Autor:
Li Zheng, Sylvie Chenavas, Fabien Kieken, Andrew Trease, Sarah Brownell, Asokan Anbanandam, Paul L. Sorgen, Gaelle Spagnol
Publikováno v:
Biomolecules, Vol 10, Iss 10, p 1452 (2020)
The autosomal-dominant pleiotropic disorder called oculodentodigital dysplasia (ODDD) is caused by mutations in the gap junction protein Cx43. Of the 73 mutations identified to date, over one-third are localized in the cytoplasmic loop (Cx43CL) domai
Externí odkaz:
https://doaj.org/article/dd07bdbc63064969b5961f51ed306e92
Autor:
Helen Macpherson, Sarah Brownell, Elizabeth Harris, Rachel L. Duckham, Stella O’Connell, Barbara J. Meyer, Sam Mirzaee, Robin M. Daly
Publikováno v:
Journal of Alzheimer's Disease. 89:247-263
Background: Multidomain interventions which incorporate exercise and dietary supplementation to target both cognitive and physical health domains may be an important approach to delay cognitive decline. Objective: The Protein Omega-3 aNd vitamin D Ex
Autor:
Yevgeniya Zastavker, Abigail Fry, Holly Nguyen, Gretchen Rice, Sydney Ross, Sebastien Selarque, Bridgit Spies, Margarite Vaccaro, Jason Barrett, Sarah Brownell, Matthew Marshall, Karen Oates, David Spanagel, James Winebrake, Alison Wood
Publikováno v:
2019 ASEE Annual Conference & Exposition Proceedings.
Publikováno v:
2020 ASEE Virtual Annual Conference Content Access Proceedings.
Publikováno v:
2014 ASEE Annual Conference & Exposition Proceedings.
Autor:
Sarah Brownell, Helen Macpherson, Robin M. Daly, S. Mirzaee, Rachel L. Duckham, Barbara J. Meyer
Publikováno v:
BMJ Open
IntroductionAn increasing number of people are living with cognitive impairment and dementia. Current pharmacological therapies at best reduce Alzheimer’s disease symptomatology but do not delay dementia onset in those at high risk. Structured exer
Autor:
Sylvie Chenavas, Fabien Kieken, Sarah Brownell, Paul L. Sorgen, Asokan Anbanandam, Andrew J. Trease, Li Zheng, Gaelle Spagnol
Publikováno v:
Biomolecules
Volume 10
Issue 10
Biomolecules, Vol 10, Iss 1452, p 1452 (2020)
Volume 10
Issue 10
Biomolecules, Vol 10, Iss 1452, p 1452 (2020)
The autosomal-dominant pleiotropic disorder called oculodentodigital dysplasia (ODDD) is caused by mutations in the gap junction protein Cx43. Of the 73 mutations identified to date, over one-third are localized in the cytoplasmic loop (Cx43CL) domai
Autor:
Heidi Vitrac, Sarah Brownell, Paul L. Sorgen, Sylvie Chenavas, Admir Kellezi, Gaelle Spagnol, Vincent Forge, Denis Bouvier, Fabien Kieken
Publikováno v:
Journal of Biological Chemistry
Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2009, 284 (49), pp.34257-34271. ⟨10.1074/jbc.M109.039594⟩
Journal of Biological Chemistry, 2009, 284 (49), pp.34257-34271. ⟨10.1074/jbc.M109.039594⟩
Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2009, 284 (49), pp.34257-34271. ⟨10.1074/jbc.M109.039594⟩
Journal of Biological Chemistry, 2009, 284 (49), pp.34257-34271. ⟨10.1074/jbc.M109.039594⟩
International audience; Gap junctions are intercellular channels that allow the passage of ions, small molecules, and second messengers that are essential for the coordination of cellular function. They are formed by two hemichannels, each constitute