Zobrazeno 1 - 10
of 68
pro vyhledávání: '"Maya Ando"'
Autor:
Maya Ando, Fabienne C. Fiesel, Roman Hudec, Thomas R. Caulfield, Kotaro Ogaki, Paulina Górka-Skoczylas, Dariusz Koziorowski, Andrzej Friedman, Li Chen, Valina L. Dawson, Ted M. Dawson, Guojun Bu, Owen A. Ross, Zbigniew K. Wszolek, Wolfdieter Springer
Publikováno v:
Molecular Neurodegeneration, Vol 12, Iss 1, Pp 1-19 (2017)
Abstract Background Mutations in PINK1 and PARKIN are the most common causes of recessive early-onset Parkinson’s disease (EOPD). Together, the mitochondrial ubiquitin (Ub) kinase PINK1 and the cytosolic E3 Ub ligase PARKIN direct a complex regulat
Externí odkaz:
https://doaj.org/article/07b3182c73d040928dfc3a6ee1edd32c
Autor:
Bettina Balint, Takashi Ogawa, Kotaro Ogaki, Kensuke Daida, Takayasu Nishimaki, Maya Ando, Sumihiro Kawajiri, Ryo Wada, Kazuyuki Noda, Nobutaka Hattori, Yasuyuki Okuma, Orlando Barsottini
Publikováno v:
Mov Disord Clin Pract
Autor:
Maya Ando, Kazuyuki Noda, Takashi Ogawa, Kotaro Ogaki, Yasuyuki Okuma, Nobutaka Hattori, Mayu Ishiguro, Tomokatsu Yoshida
Publikováno v:
Mov Disord Clin Pract
Autor:
Guojun Bu, Paulina Górka-Skoczylas, Owen A. Ross, Maya Ando, Zbigniew K. Wszolek, Roman Hudec, Thomas R. Caulfield, Ted M. Dawson, Fabienne C. Fiesel, Li Chen, Valina L. Dawson, Dariusz Koziorowski, Andrzej Friedman, Kotaro Ogaki, Wolfdieter Springer
Publikováno v:
Juntendo Medical Journal. 64:17-30
Autor:
Y Sanotsky, Magdalena Boczarska-Jedynak, Ted M. Dawson, Matthew J. Farrer, Li Chen, Owen A. Ross, Fabienne C. Fiesel, Maya Ando, Thomas R. Caulfield, Roman Hudec, Monika Rudzińska-Bar, Joanna Siuda, Oskar Hansson, Kotaro Ogaki, Timothy Lynch, Grzegorz Opala, Andrzej Friedman, Peter A. Silburn, Valina L. Dawson, Dominika Truban, Elle D. James, Megha Mohan, Dariusz Koziorowski, Maria Swanberg, Michael G. Heckman, George D. Mellick, Itzia Jimenez-Ferrer, Carles Vilariño-Güell, Xu Hou, Wolfdieter Springer, Andreas Puschmann, Jan O. Aasly, Zbigniew K. Wszolek
Publikováno v:
Brain. 140:98-117
SEE GANDHI AND PLUN-FAVREAU DOI101093/AWW320 FOR A SCIENTIFIC COMMENTARY ON THIS ARTICLE: It has been postulated that heterozygous mutations in recessive Parkinson's genes may increase the risk of developing the disease. In particular, the PTEN-induc
Autor:
Maya Ando, Arisa Hayashida, Kotaro Ogaki, Kazumasa Yokoyama, Nobutaka Hattori, Kazuyuki Noda, Yasuyuki Okuma, Takashi Kanbayashi, Kensuke Daida
Publikováno v:
Internal Medicine
A 67-year-old woman with neuromyelitis optica spectrum disorder (NMOSD) developed severe somnolence. Ten days after admission, fluid-attenuated inversion-recovery magnetic resonance imaging (MRI) revealed hyperintense areas around the bilateral hypot
Autor:
Joanna Siuda, Megha Mohan, Grzegorz Opala, Y Sanotsky, Timothy Lynch, Ted M. Dawson, Jan O. Aasly, Michael G. Heckman, Kotaro Ogaki, Andreas Puschmann, Fabienne C. Fiesel, Peter A. Silburn, Zbigniew K. Wszolek, Dariusz Koziorowski, Owen A. Ross, Andrzej Friedman, Roman Hudec, Maya Ando, Thomas R. Caulfield, Carles Vilariño-Güell, Wolfdieter Springer, George D. Mellick, Magdalena Boczarska-Jedynak, M. Farrer, Elle D. James
Publikováno v:
Movement Disorders. 31:S1-S697
Objective: To investigate the possible disease-association and pathogenic mechanisms of heterozygous PINK1 mutations from a genetic, functional, and structural perspective. Background: It has been postulated that heterozygous mutations in recessive P
Autor:
Maya Ando, Takayuki Jo, Kazuyuki Noda, Kotaro Ogaki, Anri Hattori, Nobutaka Hattori, Mizuho Sugiyama, Yasuyuki Okuma
Publikováno v:
Journal of Stroke and Cerebrovascular Diseases. 29:104882
Pisa syndrome is usually seen in patients with Alzheimer's disease treated with a cholinesterase inhibitor, dementia with Lewy bodies, Parkinson's disease, or atypical parkinsonism including multiple system atrophy. An 86-year-old woman presented wit
Autor:
Saiko Kazuno, Norihiko Furuya, Maya Ando, Shinji Saiki, Katsuhiko Sumiyoshi, Risa Nonaka, Soichiro Kakuta, Ayami Suzuki, Nobutaka Hattori
Publikováno v:
EMBO reports. 19
Parkin‐mediated mitophagy is a quality control pathway that selectively removes damaged mitochondria via the autophagic machinery. Autophagic receptors, which interact with ubiquitin and Atg8 family proteins, contribute to the recognition of damage
Autor:
Jeannette N. Stankowski, Li Chen, Wolfdieter Springer, Anneliese R. Hill, Joanna Siuda, Maya Ando, Thomas R. Caulfield, Ted M. Dawson, Zbigniew K. Wszolek, Peter O. Bauer, Fabienne C. Fiesel, Dennis W. Dickson, Valina L. Dawson, Oswaldo Lorenzo-Betancor, Owen A. Ross, Roman Hudec, Monica Castanedes-Casey, Elisabeth L. Moussaud-Lamodière, Isidre Ferrer, José Matías Arbelo
Publikováno v:
EMBO reports. 16:1114-1130
Mutations in PINK1 and PARKIN cause recessive, early-onset Parkinson's disease (PD). Together, these two proteins orchestrate a protective mitophagic response that ensures the safe disposal of damaged mitochondria. The kinase PINK1 phosphorylates ubi