Systematic analysis of genetic variants in Han Chinese patients with sporadic Parkinson’s disease
出版年份 2016 全文链接
标题
Systematic analysis of genetic variants in Han Chinese patients with sporadic Parkinson’s disease
作者
关键词
-
出版物
Scientific Reports
Volume 6, Issue 1, Pages -
出版商
Springer Nature
发表日期
2016-09-22
DOI
10.1038/srep33850
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
- (2016) Suzanne Lesage et al. AMERICAN JOURNAL OF HUMAN GENETICS
- D NAJC 6 Mutations Associated With Early-Onset Parkinson's Disease
- (2016) Simone Olgiati et al. ANNALS OF NEUROLOGY
- ER stress and Parkinson's disease: Pathological inputs that converge into the secretory pathway
- (2016) Gabriela Mercado et al. BRAIN RESEARCH
- Association of the MTHFR rs1801131 and rs1801133 variants in sporadic Parkinson’s disease patients
- (2016) Lamei Yuan et al. NEUROSCIENCE LETTERS
- Genetic analysis of TREM2 variants in Chinese Han patients with sporadic Parkinson’s disease
- (2016) Ting Tan et al. NEUROSCIENCE LETTERS
- TheEIF4G1gene and Parkinson's disease
- (2015) H. Deng et al. ACTA NEUROLOGICA SCANDINAVICA
- Alpha-synuclein (SNCA) polymorphisms and susceptibility to Parkinson's disease: A meta-analysis
- (2015) Wei Han et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
- Candidate genes for Parkinson disease: Lessons from pathogenesis
- (2015) Priscilla De Rosa et al. CLINICA CHIMICA ACTA
- Modulation of endoplasmic reticulum stress in Parkinson's disease
- (2015) Saori Tsujii et al. EUROPEAN JOURNAL OF PHARMACOLOGY
- Association analysis revealed one susceptibility locus for vitiligo with immune-related diseases in the Chinese Han population
- (2015) Shu Li et al. IMMUNOGENETICS
- Glucocerebrosidase deficiency and mitochondrial impairment in experimental Parkinson disease
- (2015) Carmen Noelker et al. JOURNAL OF THE NEUROLOGICAL SCIENCES
- Insights from late-onset familial parkinsonism on the pathogenesis of idiopathic Parkinson's disease
- (2015) Mattia Volta et al. LANCET NEUROLOGY
- CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study
- (2015) Manabu Funayama et al. LANCET NEUROLOGY
- Basic science breaks through: New therapeutic advances in Parkinson's disease
- (2015) Patrik Brundin et al. MOVEMENT DISORDERS
- The contribution of rare variation to prostate cancer heritability
- (2015) Nicholas Mancuso et al. NATURE GENETICS
- TCEANC2 rs10788972 and rs12046178 variants in the PARK10 region in Chinese Han patients with sporadic Parkinson's disease
- (2015) Yi Guo et al. NEUROBIOLOGY OF AGING
- Genetic analysis of the RAB39B gene in Chinese Han patients with Parkinson's disease
- (2015) Lamei Yuan et al. NEUROBIOLOGY OF AGING
- Polygenic determinants of Parkinson's disease in a Chinese population
- (2015) Ji-Feng Guo et al. NEUROBIOLOGY OF AGING
- Aldehyde dehydrogenase 2 genetic variations may increase susceptibility to Parkinson's disease in Han Chinese population
- (2015) Xiong Zhang et al. NEUROBIOLOGY OF AGING
- The RIT2 and STX1B polymorphisms are associated with Parkinson's disease
- (2015) Jian-Yong Wang et al. PARKINSONISM & RELATED DISORDERS
- Nuclear receptor Nurr1 agonists enhance its dual functions and improve behavioral deficits in an animal model of Parkinson’s disease
- (2015) Chun-Hyung Kim et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- The epigenetics of aging and neurodegeneration
- (2015) Roy Lardenoije et al. PROGRESS IN NEUROBIOLOGY
- Therapeutic strategies in Parkinson's disease: what we have learned from animal models
- (2014) Jorge S. Valadas et al. Annals of the New York Academy of Sciences
- A Mitocentric View of Parkinson's Disease
- (2014) Nele A. Haelterman et al. Annual Review of Neuroscience
- Analysis of non-synonymous-coding variants of Parkinson's disease-related pathogenic and susceptibility genes in East Asian populations
- (2014) J. N. Foo et al. HUMAN MOLECULAR GENETICS
- Endothelin-1: A potential pathological factor in Parkinson's disease? —From endoplasmic reticulum stress to beyond
- (2014) Arjun Jain JOURNAL OF THE NEUROLOGICAL SCIENCES
- Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
- (2014) Mike A Nalls et al. NATURE GENETICS
- MutationTaster2: mutation prediction for the deep-sequencing age
- (2014) Jana Marie Schwarz et al. NATURE METHODS
- Fibroblast growth factor 20 (FGF20) gene polymorphism and risk of Parkinson’s disease: a meta-analysis
- (2014) Ruixia Zhu et al. NEUROLOGICAL SCIENCES
- Protective Role of DNJ-27/ERdj5 in Caenorhabditis elegans Models of Human Neurodegenerative Diseases
- (2013) Fernando Muñoz-Lobato et al. ANTIOXIDANTS & REDOX SIGNALING
- DNAJC13 mutations in Parkinson disease
- (2013) Carles Vilariño-Güell et al. HUMAN MOLECULAR GENETICS
- ERdj5 Is the ER Reductase that Catalyzes the Removal of Non-Native Disulfides and Correct Folding of the LDL Receptor
- (2013) Ojore Benedict Valentine Oka et al. MOLECULAR CELL
- DNAJ mutations are rare in Chinese Parkinson's disease patients and controls
- (2013) Jia Nee Foo et al. NEUROBIOLOGY OF AGING
- EIF4G1 Ala502Val and Arg1205His variants in Chinese patients with Parkinson disease
- (2013) Lamei Yuan et al. NEUROSCIENCE LETTERS
- F-Box Only Protein 7 Gene in Parkinsonian-Pyramidal Disease
- (2013) Hao Deng et al. JAMA Neurology
- Single nucleotide polymorphisms in thymic stromal lymphopoietin gene are not associated with allergic rhinitis susceptibility in Chinese subjects
- (2012) Yuan Zhang et al. BMC Medical Genetics
- Association between polymorphisms in cytokine genes IL-17A and IL-17F and development of allergic rhinitis and comorbid asthma in Chinese subjects
- (2012) Min Wang et al. HUMAN IMMUNOLOGY
- Association between polymorphisms in FOXP3 and EBI3 genes and the risk for development of allergic rhinitis in Chinese subjects
- (2012) Yuan Zhang et al. HUMAN IMMUNOLOGY
- Polymorphisms in thymic stromal lymphopoietin gene demonstrate a gender and nasal polyposis-dependent association with chronic rhinosinusitis
- (2012) Yuan Zhang et al. HUMAN IMMUNOLOGY
- A Deleterious Mutation in DNAJC6 Encoding the Neuronal-Specific Clathrin-Uncoating Co-Chaperone Auxilin, Is Associated with Juvenile Parkinsonism
- (2012) Simon Edvardson et al. PLoS One
- Mutations in DNAJC5, Encoding Cysteine-String Protein Alpha, Cause Autosomal-Dominant Adult-Onset Neuronal Ceroid Lipofuscinosis
- (2011) Lenka Nosková et al. AMERICAN JOURNAL OF HUMAN GENETICS
- A method and server for predicting damaging missense mutations
- (2010) Ivan A Adzhubei et al. NATURE METHODS
- A partition-ligation-combination-subdivision EM algorithm for haplotype inference with multiallelic markers: update of the SHEsis (http://analysis.bio-x.cn)
- (2009) Zhiqiang Li et al. CELL RESEARCH
- ERdj5 Sensitizes Neuroblastoma Cells to Endoplasmic Reticulum Stress-induced Apoptosis
- (2009) Christophoros G. Thomas et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
- (2009) Prateek Kumar et al. Nature Protocols
- Parkinson's disease: clinical features and diagnosis
- (2008) J Jankovic JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- ERdj4 and ERdj5 Are Required for Endoplasmic Reticulum-associated Protein Degradation of Misfolded Surfactant Protein C
- (2008) Mei Dong et al. MOLECULAR BIOLOGY OF THE CELL
- ERdj5 Is Required as a Disulfide Reductase for Degradation of Misfolded Proteins in the ER
- (2008) R. Ushioda et al. SCIENCE
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