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The GIGYF2 variants are not associated with Parkinson's disease in the mainland Chinese populationq
期刊名称:Parkinsonism and Related Disorders
时间:0
页码:294-297
语言:英文
相关项目:汉族人群中特有的LRRK2基因G2385R突变致帕金森病的分子机理
作者:
陈生弟|
同期刊论文项目
汉族人群中特有的LRRK2基因G2385R突变致帕金森病的分子机理
期刊论文 16
同项目期刊论文
Microglia in the aging brain: relevance to neurodegeneration
Four Novel Mutations in the GCH1 Gene of Chinese Patients with Dopa-Responsive Dystonia
GIGYF2 Asn56Ser mutation is rare in Chinese Parkinson’s disease patients
Modulation of the activity of dopaminergic neurons by SK channels: a potential target for the treatm
The iPS Technique Provides Hope for Parkinson’s Disease Treatment
Lack of association between ATP13A2 Ala746Thr variant and Parkinson’s disease in Han populatio
Altered Regulation of CD200 Receptor in Monocyte-Derived Macrophages from Individuals with Parkinson
Identification of glial-cell-line-derived neurotrophic factor-regulated proteins of striatum in mous
CD200-CD200R dysfunction exacerbates microglial activation and dopaminergic neurodegeneration in a r
DJ-1 can inhibit microtubule associated protein 1 B formed aggregates
Novel mutations in the CYP7B1 gene cause hereditary spastic paraplegia.
帕金森病发病机制与治疗研究十年进展
从制定指南和共识着手规范运动障碍疾病的诊疗与管理