Genetic & Epigenetic alterations in Gliomas with special reference to age related differences:Indian experience 

This study was undertaken to evaluate age-related differences in histopathologic and molecular profile of glioblastomas(GBMs) at various age groups,with special...
中国抗癌协会神经肿瘤专业委员会第八届学术会议论文集  2011-05-01 下载次数(1)| 被引次数(0)

Identification of a novel genetic locus on chromosome 8p21.1-q11.23 for IBGC disease 

Idiopathic basal ganglia calcification(IBGC) is a neurodegenerative syndrome that is characterized by basal ganglia and extrabasal ganglia calcifications,and...
基因开启未来:新时代的遗传学与科技进步——湖北省遗传…  2009-11-07 下载次数(5)| 被引次数(0)

Activity-dependent genetic feedback in brain circuits and disorders 

Mental functions involve coordinated activities among specific groups of neurons, or neuronal ensembles, which are embedded in complex brain circuits. To identi...
中国神经科学学会第十二届全国学术会议论文集  2017-10-12 下载次数(5)| 被引次数()

Clinical,pathologic and genetic studies on mitochondrial myopathy,encephalopathy,lactic acidosis and stroke-like episodes 

Clinical,pathologicandgeneticstudiesonmitochondrialmyopathy,encephalopathy,lacticacidosisandstroke┐likeepisodesGuoYupu郭玉璞,Guo...
《Chinese Medical Journal》  1997年 第11期 下载次数(10)| 被引次数(0)

Genetic diagnosis and prenatal diagnosis of Duchenne/Becker muscular dystrophies family 

Objective Duchenne muscular dystrophy(DMD; OMIN#310200) and Becker muscular dystrophy(BMD; OMIN#3003376) are both caused by mutations in the DMD gene(OMIN#30037...
中华医学会第十五次全国医学遗传学学术会议暨中国医师协…  2016-11-05 下载次数(3)| 被引次数()

Genetic analysis of Parkinson's disease gene Pink1 in Drosophila 

Parkinson s Disease(PD) is a common neurodegenerative disorder caused by selective loss of dopaminergic neurons in the substantia nigra.Genetic studies on fa...
Proceedings of the 7th Biennial Meeting and the 5th …  2007-10-24 下载次数(8)| 被引次数(0)

Genetic dissection of autophagy and neurodegeneration 

At adulthood,neurons have to maintaining cell integrity in response to genetic and environment insults to sustain nerve system function and prevent degenerat...
2012全国发育生物学大会摘要集  2012-10-21 下载次数(7)| 被引次数(0)

The expression and C3435T genetic polymorphism analysis of MDR1 gene in peripheral blood of patients with intractable epilepsy 

Objective To investigate the roles of antiepileptic drugs and seizures in multidrug resistance of intractable epilepsy,and to analyze the genetic polymorphis...
第九次全国神经病学学术大会论文汇编  2006-09-01 下载次数(14)| 被引次数(0)

Editor's Choice——Application of genetic engineering for the treatment of neurodegenerative diseases 

Gene therapy has been shown to be an effective m ethod for protecting neural functions in the substantia nigra,as well as for treating Parkinson s disease.Th...
《Neural Regeneration Research》  2011年 第26期 下载次数(25)| 被引次数(0)

Analysis of SCA2 and SCA3/MJD repeats in Parkinson's disease in mainland China,genetic,clinical,and PET findings 

Background Recent reports suggest that CAG triplet expansions of spinocerebellar ataxia type 2 and 3(SCA2 and SCA3/MJD) genes(ATXN2 and MJD1) are the cause o...
Proceedings of the 8th Biennial Conference of the Ch…  2009-11-07 下载次数(5)| 被引次数(0)

Analysis of SCA2 and SCA3/MJD Repeats in Parkinson's Disease in Mainland China,Genetic,Clinical,and PET Findings 

Background Recent reports suggest that CAG triplet expansions of spinocerebellar ataxia type 2 and 3(SCA2 and SCA3/MJD)genes(ATXN2 and MJD1)are the cause of ...
第八次全国医学遗传学学术会议(中华医学会2009年医学遗…  2009-07-11 下载次数(13)| 被引次数(0)

Evaluation of the correlation between the genetic alterations and clinical features in Glioblastoma with oligodendroglial component 

【Background & Purpose】 Glioblastoma with oligodendroglial component (GBMO) is pathologically defined as anaplastic oligo-astrocytoma with necrosis, however, ...
中国抗癌协会神经肿瘤专业委员会第八届学术会议论文集  2011-05-01 下载次数(1)| 被引次数(0)

Biophysics and neurobiological mechanism of genetic epilepsy led by KCNT1 channel mutations 

So far, 23 sodium-activated potassium channel(KCNT1, Slack) genetic mutants have been reported are associated with severe early-onset epilepsy patients. The cha...
第十一届全国钙信号和细胞功能研讨会摘要集  2016-07-21 下载次数(6)| 被引次数(0)

Calcium/Calmodulin-dependent Protein Kinase Ⅱ Inhibition Induces Neuronal Death in a Rat Model of Genetic Epilepsy 

Abnormal Calcium/calmodulin(Ca M)-dependent kinase Ⅱ(Ca MKII) change has been involved in many epileptic models. However, the mechanisms basing on Ca MKII inhib...
第十一届全国钙信号和细胞功能研讨会摘要集  2016-07-21 下载次数(1)| 被引次数(0)

Clinical and genetic analysis on 4 Chinese patients with Canavan Disease 

Objective To clarify clinical and genetic features of 4 Chinese patients with Canavan Disease. Methods Clinical information including medical history, physical ...
中国神经科学学会第十二届全国学术会议论文集  2017-10-12 下载次数(6)| 被引次数()

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