Commentary: Parkinson's Disease Genes VPS35 and EIF4G1 Interact Genetically and Converge on α-Synuclein
出版年份 2016 全文链接
标题
Commentary: Parkinson's Disease Genes VPS35 and EIF4G1 Interact Genetically and Converge on α-Synuclein
作者
关键词
-
出版物
Frontiers in Neuroscience
Volume 10, Issue -, Pages -
出版商
Frontiers Media SA
发表日期
2016-04-18
DOI
10.3389/fnins.2016.00162
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Eukaryotic translation initiation factor 4-γ, 1 gene mutations are rare in Parkinson's disease among Taiwanese
- (2016) Yi Ching Weng et al. JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION
- TheEIF4G1gene and Parkinson's disease
- (2015) H. Deng et al. ACTA NEUROLOGICA SCANDINAVICA
- Retromer in Alzheimer disease, Parkinson disease and other neurological disorders
- (2015) Scott A. Small et al. NATURE REVIEWS NEUROSCIENCE
- EIF4G1 mutations do not cause Parkinson's disease
- (2015) Noah Nichols et al. NEUROBIOLOGY OF AGING
- Parkinson’s Disease Genes VPS35 and EIF4G1 Interact Genetically and Converge on α-Synuclein
- (2015) Nripesh Dhungel et al. NEURON
- Parkin is activated by PINK1-dependent phosphorylation of ubiquitin at Ser65
- (2014) Agne Kazlauskaite et al. BIOCHEMICAL JOURNAL
- EIF4G1is neither a strong nor a common risk factor for Parkinson's disease: evidence from large European cohorts: Table1
- (2014) Johanna Huttenlocher et al. JOURNAL OF MEDICAL GENETICS
- EIF4G1 gene mutations are not a common cause of Parkinson's disease in the Japanese population
- (2014) Kenya Nishioka et al. PARKINSONISM & RELATED DISORDERS
- New Perception of Mitochondrial Regulatory Pathway in Parkinsonism – Ubiquitin, PINK1, and Parkin
- (2014) Diana Angelika Olszewska et al. Frontiers in Neurology
- Mutation in theSYNJ1Gene Associated with Autosomal Recessive, Early-Onset Parkinsonism
- (2013) Marialuisa Quadri et al. HUMAN MUTATION
- VPS35 and EIF4G1 mutations are rare in Parkinson's disease among Indians
- (2013) Sumedha Sudhaman et al. NEUROBIOLOGY OF AGING
- Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease
- (2013) K. Nuytemans et al. NEUROLOGY
- Genetics of Parkinson's disease – state of the art, 2013
- (2013) Vincenzo Bonifati PARKINSONISM & RELATED DISORDERS
- The retromer complex - endosomal protein recycling and beyond
- (2012) M. N. J. Seaman JOURNAL OF CELL SCIENCE
- Vps10 Family Proteins and the Retromer Complex in Aging-Related Neurodegeneration and Diabetes
- (2012) R. F. Lane et al. JOURNAL OF NEUROSCIENCE
- Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease
- (2011) Marie-Christine Chartier-Harlin et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Retromer deficiency observed in Alzheimer's disease causes hippocampal dysfunction, neurodegeneration, and A accumulation
- (2008) A. Muhammad et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now