Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Keiko Saisho"'
Autor:
Katherine C M Chew, Noriyuki Matsuda, Keiko Saisho, Grace G Y Lim, Chou Chai, Hui-Mei Tan, Keiji Tanaka, Kah-Leong Lim
Publikováno v:
PLoS ONE, Vol 6, Iss 5, p e19720 (2011)
Mutations in the parkin gene, which encodes a ubiquitin ligase (E3), are a major cause of autosomal recessive parkinsonism. Although parkin-mediated ubiquitination was initially linked to protein degradation, accumulating evidence suggests that the e
Externí odkaz:
https://doaj.org/article/4987a5e223204bd09706a72f5e91c936
Autor:
Masaaki Komatsu, Shigeto Sato, Keiko Saisho, Yu-shin Sou, Mayumi Kimura, Kei Okatsu, Noriyuki Matsuda, Midori Shimanuki, Hiroshi Shitara, Nobutaka Hattori, Kazuto Nakada, Keiji Tanaka
Publikováno v:
Genes to Cells.
PINK1 and Parkin were first identified as the causal genes responsible for familial forms of early-onset Parkinson’s disease (PD), a prevalent neurodegenerative disorder. PINK1 encodes a mitochondrial serine/threonine protein kinase, whereas Parkin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfee54f7e959392878a5d4fbd5793593
https://doi.org/10.1111/j.1365-2443.2010.01426.x
https://doi.org/10.1111/j.1365-2443.2010.01426.x
Autor:
Sumihiro Kawajiri, Kei Okatsu, Masaaki Komatsu, Shigeto Sato, Keiko Saisho, Shinji Saiki, Nobutaka Hattori, Fumiaki Sato, Yu-shin Sou, Mayumi Kimura, Kahori Shiba, Keiji Tanaka, Noriyuki Matsuda, Clement A. Gautier
Publikováno v:
The Journal of Cell Biology
Defective mitochondrial quality control is shown to be a mechanism for neurodegeneration in some forms of Parkinson's disease.
Parkinson's disease (PD) is a prevalent neurodegenerative disorder. Recent identification of genes linked to familial
Parkinson's disease (PD) is a prevalent neurodegenerative disorder. Recent identification of genes linked to familial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67cdde66d3d35bbbfae5e9d531e4916a
https://pubmed.ncbi.nlm.nih.gov/20404107
https://pubmed.ncbi.nlm.nih.gov/20404107
Autor:
Keiko Saisho, Kah-Leong Lim, Hui-Mei Tan, Noriyuki Matsuda, Keiji Tanaka, Katherine C. M. Chew, Grace G. Y. Lim, Chou Chai
Publikováno v:
PLoS ONE, Vol 6, Iss 5, p e19720 (2011)
PLoS ONE
PLoS ONE
Background Mutations in the parkin gene, which encodes a ubiquitin ligase (E3), are a major cause of autosomal recessive parkinsonism. Although parkin-mediated ubiquitination was initially linked to protein degradation, accumulating evidence suggests
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f23e378607c24afc9ce68de5a994b3b5
https://doi.org/10.1371/journal.pone.0019720
https://doi.org/10.1371/journal.pone.0019720
Autor:
Lowell T. Duncan
This volume contains eleven chapters that detail advances in health and disease. Chapter One discusses the use and benefits of photobiomodulation across various applications within restorative dentistry. Chapter Two details the physicochemical and ph
