Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Nolwazi Z. Gcwensa"'
Autor:
Nolwazi Z. Gcwensa, Dreson L. Russell, Khaliah Y. Long, Charlotte F. Brzozowski, Xinran Liu, Karen L. Gamble, Rita M. Cowell, Laura A. Volpicelli-Daley
Publikováno v:
Neurobiology of Disease, Vol 199, Iss , Pp 106595- (2024)
Parkinson's disease (PD) and Dementia with Lewy bodies (DLB) are characterized by neuronal α-synuclein (α-syn) inclusions termed Lewy Pathology, which are abundant in the amygdala. The basolateral amygdala (BLA), in particular, receives projections
Externí odkaz:
https://doaj.org/article/090e4f4033cc4d278eafd11471bee7dd
Autor:
Charlotte F. Brzozowski, Baraa A. Hijaz, Vijay Singh, Nolwazi Z. Gcwensa, Kaela Kelly, Edward S. Boyden, Andrew B. West, Deblina Sarkar, Laura A. Volpicelli-Daley
Publikováno v:
Acta Neuropathologica Communications, Vol 9, Iss 1, Pp 1-18 (2021)
Abstract Pathologic inclusions composed of α-synuclein called Lewy pathology are hallmarks of Parkinson’s Disease (PD). Dominant inherited mutations in leucine rich repeat kinase 2 (LRRK2) are the most common genetic cause of PD. Lewy pathology is
Externí odkaz:
https://doaj.org/article/529d6d304c07412f8ead36c5d416d3e5
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 15 (2021)
Parkinson’s disease (PD) is a progressive neurodegenerative disease that impairs movement as well as causing multiple other symptoms such as autonomic dysfunction, rapid eye movement (REM) sleep behavior disorder, hyposmia, and cognitive changes. L
Externí odkaz:
https://doaj.org/article/d1a17e596a4543c3aded2a04905f74fa
Autor:
Nolwazi Z. Gcwensa, Edward S. Boyden, Laura A. Volpicelli-Daley, Vijay Singh, Deblina Sarkar, Kaela Kelly, Andrew B. West, Baraa A. Hijaz, Charlotte F. Brzozowski
Publikováno v:
Acta Neuropathologica Communications, Vol 9, Iss 1, Pp 1-18 (2021)
Acta Neuropathologica Communications
Acta Neuropathologica Communications
Pathologic inclusions composed of α-synuclein called Lewy pathology are hallmarks of Parkinson’s Disease (PD). Dominant inherited mutations in leucine rich repeat kinase 2 (LRRK2) are the most common genetic cause of PD. Lewy pathology is found in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88f83c404955d9677941eb3b5389dec1
https://doi.org/10.1101/2021.10.04.463043
https://doi.org/10.1101/2021.10.04.463043
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 15 (2021)
Frontiers in Cellular Neuroscience
Frontiers in Cellular Neuroscience
Parkinson’s disease (PD) is a progressive neurodegenerative disease that impairs movement as well as causing multiple other symptoms such as autonomic dysfunction, rapid eye movement (REM) sleep behavior disorder, hyposmia, and cognitive changes. L
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf3f545cd71f9d4675554163e02ab4eb
https://www.frontiersin.org/articles/10.3389/fncel.2021.626128/full
https://www.frontiersin.org/articles/10.3389/fncel.2021.626128/full