The role of gene variants in the pathogenesis of neurodegenerative disorders as revealed by next generation sequencing studies: a review-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

The role of gene variants in the pathogenesis of neurodegenerative disorders as revealed by next generation sequencing studies: a review

Published:2017-10-06 Issue:1 Volume:6 Page:
ISSN:2047-9158
Container-title:Translational Neurodegeneration
language:en
Short-container-title:Transl Neurodegener

Author:

Pang Shirley Yin-Yu,Teo Kay-Cheong,Hsu Jacob Shujui,Chang Richard Shek-Kwan,Li Miaoxin,Sham Pak-Chung,Ho Shu-Leong

Funder

Liu Po Shan/Dr Vincent Liu Endowment Fund for Motor Neurone Disease

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience,Clinical Neurology

Link

http://link.springer.com/content/pdf/10.1186/s40035-017-0098-0.pdf

Reference54 articles.

1. Rajput AH, Rajput A. Accuracy of Parkinson disease diagnosis unchanged in 2 decades. Neurology. 2014;83:386–7.

2. Sun YM, Ly C, Wu ZY. Spinocerebellar ataxia: relationship between phenotype and genotype – a review. Clin Genet. 2016;90:305–14.

3. Klebe S, Stevanin G, Depienne C. Clinical and genetic heterogeneity in hereditary spastic paraplegias: from SPG1 to SPG72 and still counting. Rev Neurol (Paris). 2015;171:505–30.

4. Pedroso JL, de Souza PV, Pinto WB, Braga-Neto P, Albuquerque MV, Saraiva-Pereira ML, et al. SCA1 patients may present as hereditary spastic paraplegia and must be included in spastic-ataxias group. Parkinsonism Relat Disord. 2015;21:1243–6.

5. Finsterer J, Loscher W, Quasthoff S, Wanschitz J, Auer-Grumbach M, Stevanin G. Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance. J Neurol Sci. 2012;318:1–18.

Cited by 30 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Trends in drug development for rare and intractable diseases based on the KEGG NETWORK;NAR Molecular Medicine;2024-07

2. The Neurodegenerative Disease Knowledge Portal: Propelling Discovery Through the Sharing of Neurodegenerative Disease Genomic Resources;2024-05-28

3. Effects of Carvacrol on Cognitive Function and Apoptotic Gene Expression in Trimethyltin-Induced Hippocampal Injury in Rats;CELL J;2024

4. Genomic Insights into Dementia: Precision Medicine and the Impact of Gene-Environment Interaction;Aging and disease;2024

5. Application of Proteomics in Alzheimer’s Disease: A Mini Review;SEPTEMBER 2023;2023-09-11

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3