Zobrazeno 1 - 10
of 502
pro vyhledávání: '"Familial Parkinsons-Disease"'
Akademický článek
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Akademický článek
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Publikováno v:
Biochemical Society Transactions, 44(6), 1611-1616. PORTLAND PRESS LTD
Mutations in the human leucine-rich repeat kinase 2 (LRRK2) are the most frequent cause of hereditary Parkinson's disease (PD). LRRK2 belongs to the Roco family of proteins, which are characterized by the presence of a Ras of complex proteins domain
Autor:
JHA, NN, RANGANATHAN, S, KUMAR, R, MEHRA, S, PANIGRAHI, R, NAVALKAR, A, GHOSH, D, KUMAR, A, PADINHATEERI, R, MAJI, SK
Publikováno v:
IndraStra Global.
Aggregation of alpha-synuclein (alpha-Syn) into neurotoxic oligomers and amyloid fibrils is suggested to be the pathogenic mechanism for Parkinson's disease (PD). Recent studies'have indicated that oligomeric species of alpha-Syn are more cytotoxic t
Autor:
Mensch, Carl, Konijnenberg, Albert, Van Elzen, Roos, Lambeir, Anne-Marie, Sobott, Frank, Johannessen, Christian
Publikováno v:
Journal of Raman spectroscopy
JOURNAL OF RAMAN SPECTROSCOPY
JOURNAL OF RAMAN SPECTROSCOPY
Alpha-synuclein (α-syn) is a 140 residue protein that plays a central role in Parkinsons disease and other neurological disorders. The precise function and pathological properties of α-syn remain however poorly understood. While α-syn is considere
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2f56ff53702a943ca65ac50015576a62
Publikováno v:
IndraStra Global.
Parkinson's disease (PD) is a neurological disorder marked by the presence of cytoplasmic inclusions, Lewy bodies (LBs) and Lewy neurites (LNs) as well as the degeneration of dopamine producing neurons in the substantia nigra region of the brain. The
Akademický článek
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Autor:
Wojciech Bobela, Safa Mohanna, Patrick Aebischer, Marco Cantoni, Bernard L. Schneider, Graham Knott, Meret Nora Gaugler, Ralf Schneggenburger, Mustafa T. Ardah, Özgür Genç, Omar El-Agnaf, Jean-Charles Bensadoun
Publikováno v:
Acta Neuropathologica; Vol 123
Acta neuropathologica
Acta neuropathologica
alpha-Synuclein (alpha-syn) is a presynaptic protein present at most nerve terminals, but its function remains largely unknown. The familial forms of Parkinson's disease associated with multiplications of the alpha-syn gene locus indicate that overab
Autor:
Michiko Minegishi, Omi Katsuse, Heii Arai, Kiyoshi Sato, Keiji Wada, Darren J. Moore, Takashi Togo, Hiroshige Fujishiro, Kenji Kosaka, Yoshiko Furukawa, Eizo Iseki, Shinji Higashi, Koji Kasanuki, Hirotake Uchikado, Tomohiro Kabuta, Hiroaki Hino
Publikováno v:
Journal of Neuropathology & Experimental Neurology. 70:264-280
There is emerging evidence implicating a role for the autophagy-lysosome pathway in the pathogenesis of Lewy body disease. We investigated potential neuropathologic and biochemical alterations of autophagy-lysosome pathway-related proteins in the bra
Autor:
Silke Nuber, Rejko Krüger, K. Gierga, Abdelhaq Rami, Dennis W. Dickson, Elisabeth Petrasch-Parwez, Wilfried F. A. Den Dunnen, Wei P. Gai, Zbigniew K. Wszolek, Thomas Deller, Kay Seidel, Udo Rüb, Ludger Schöls, Antje Bornemann, Olaf Riess
Publikováno v:
Annals of Neurology, 67(5), 684-689. Wiley
Familial Parkinson disease (PD) due to the A30P mutation in the SNCA gene encoding alpha-synuclein is clinically associated with PD symptoms. In this first pathoanatomical study of the brain of an A30P mutation carrier, we observed neuronal loss in t