Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Sandeep K. Barodia"'
Publikováno v:
Acta Neuropathologica Communications, Vol 10, Iss 1, Pp 1-19 (2022)
Abstract Genetic and neuropathological evidence strongly implicates aberrant forms of α-synuclein in neurodegeneration. Antibodies specific for α-synuclein phosphorylated at serine 129 (pS129) are selective for the pathological protein aggregates t
Externí odkaz:
https://doaj.org/article/32492b2590f04bc79c6937d8dab78d2f
Publikováno v:
Neurobiology of Disease, Vol 98, Iss , Pp 122-136 (2017)
Dominantly inherited mutations in leucine-rich repeat kinase 2 (LRRK2) are the most common causes of familial Parkinson's disease (PD) and LRRK2 polymorphisms are associated with increased risk for idiopathic PD. However, the molecular mechanisms by
Externí odkaz:
https://doaj.org/article/468c4088f8f14fbea1e63a68bc53eac9