• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验

Essential tremor linked TENM4 mutation found in healthy Chinese individuals.

作者信息

Chao Yin Xia, Lin Ng Ebonne Yu, Tio Murni, Kumar Prakash, Tan Louis, Au Wing Lok, Yih Yuen, Tan Eng King

机构信息

Department of Neurology, Singapore General Hospital, Singapore; National Neuroscience Institute, Singapore; Duke-NUS Medical School, Singapore.

Department of Neurology, Singapore General Hospital, Singapore; National Neuroscience Institute, Singapore.

出版信息

Parkinsonism Relat Disord. 2016 Oct;31:139-140. doi: 10.1016/j.parkreldis.2016.05.003. Epub 2016 May 3.

DOI:10.1016/j.parkreldis.2016.05.003
PMID:27569844
Abstract
摘要

相似文献

1
Essential tremor linked TENM4 mutation found in healthy Chinese individuals.在健康中国人群中发现与特发性震颤相关的TENM4突变。
Parkinsonism Relat Disord. 2016 Oct;31:139-140. doi: 10.1016/j.parkreldis.2016.05.003. Epub 2016 May 3.
2
Genetic testing of FUS, HTRA2, and TENM4 genes in Chinese patients with essential tremor.中国特发性震颤患者 FUS、HTRA2 和 TENM4 基因的遗传检测。
CNS Neurosci Ther. 2020 Aug;26(8):837-841. doi: 10.1111/cns.13305. Epub 2020 Mar 20.
3
Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremor.轴突导向和中枢髓鞘形成的调节因子TENM4中的错义突变会导致特发性震颤。
Hum Mol Genet. 2015 Oct 15;24(20):5677-86. doi: 10.1093/hmg/ddv281. Epub 2015 Jul 17.
4
Relationship between GWAS-linked three new loci in Essential tremor and risk of Parkinson's disease in Chinese population.中国人群中特发性震颤相关的三个新GWAS位点与帕金森病风险的关系
Parkinsonism Relat Disord. 2017 Oct;43:124-126. doi: 10.1016/j.parkreldis.2017.08.014. Epub 2017 Aug 10.
5
Genetic analysis of the CHCHD2 gene in Chinese patients with familial essential tremor.中国家族性特发性震颤患者CHCHD2基因的遗传分析。
Neurosci Lett. 2016 Nov 10;634:104-106. doi: 10.1016/j.neulet.2016.10.005. Epub 2016 Oct 4.
6
Movement disorders: novel FUS gene variants linked to essential tremor.运动障碍：与特发性震颤相关的新型FUS基因变异体
Nat Rev Neurol. 2013 Aug;9(8):418. doi: 10.1038/nrneurol.2013.143. Epub 2013 Jul 23.
7
Extended study of A265G variant of HS1BP3 in essential tremor and Parkinson disease.HS1BP3基因A265G变体在特发性震颤和帕金森病中的扩展研究。
Neurology. 2005 Aug 23;65(4):651-2. doi: 10.1212/01.wnl.0000173033.32535.23.
8
Mitochondrial serine protease HTRA2 gene mutation in Asians with coexistent essential tremor and Parkinson disease.亚洲人合并特发性震颤和帕金森病时线粒体丝氨酸蛋白酶HTRA2基因突变
Neurogenetics. 2015 Jul;16(3):241-2. doi: 10.1007/s10048-015-0443-3. Epub 2015 Mar 20.
9
Genetic biomarkers of essential tremor: time to think outside of the box.特发性震颤的遗传生物标志物：是时候跳出框框思考了。
Pharmacogenomics. 2013 Nov;14(14):1681-2.
10
Identification of a novel risk variant in the FUS gene in essential tremor.特发性震颤中FUS基因新型风险变异体的鉴定。
Neurology. 2014 Feb 4;82(5):461. doi: 10.1212/WNL.0000000000000073.

引用本文的文献

1
Han family with essential tremor caused by the P421L variant of the TENM4 gene in China.中国一个因TENM4基因P421L变异导致原发性震颤的韩氏家族。
Neurol Sci. 2023 Jun;44(6):2003-2015. doi: 10.1007/s10072-023-06603-4. Epub 2023 Jan 23.
2
Teneurin4 dimer structures reveal a calcium-stabilized compact conformation supporting homomeric trans-interactions.Ten-神经素4二聚体结构揭示了一种由钙稳定的紧密构象，支持同型反式相互作用。
EMBO J. 2022 May 2;41(9):e107505. doi: 10.15252/embj.2020107505. Epub 2022 Jan 31.
3
Role and Involvement of TENM4 and miR-708 in Breast Cancer Development and Therapy.
TENM4 和 miR-708 在乳腺癌发生发展和治疗中的作用及参与机制。
Cells. 2022 Jan 5;11(1):172. doi: 10.3390/cells11010172.
4
Genetic and functional analysis reveals contributes to schizophrenia.遗传和功能分析表明 对精神分裂症有影响。（注：原文句子不完整，“reveals”后缺少具体内容）
iScience. 2021 Aug 30;24(9):103063. doi: 10.1016/j.isci.2021.103063. eCollection 2021 Sep 24.
5
Genomic Markers for Essential Tremor.特发性震颤的基因组标记
Pharmaceuticals (Basel). 2021 May 27;14(6):516. doi: 10.3390/ph14060516.
6
Parkinson's Disease in Teneurin Transmembrane Protein 4 () Mutation Carriers.Ten-神经素跨膜蛋白4（）突变携带者中的帕金森病
Front Genet. 2020 Dec 22;11:598064. doi: 10.3389/fgene.2020.598064. eCollection 2020.
7
Rare variant analysis of essential tremor-associated genes in early-onset Parkinson's disease.早发性帕金森病中与特发性震颤相关基因的罕见变异分析。
Ann Clin Transl Neurol. 2021 Jan;8(1):119-125. doi: 10.1002/acn3.51248. Epub 2020 Nov 13.
8
A Han Chinese Family With Early-Onset Parkinson's Disease Carrying Novel Frameshift Mutation and Compound Heterozygous Mutation of Appearing Incompatible With MDS Clinical Diagnostic Criteria.一个携带新型移码突变和复合杂合突变的早发性帕金森病汉族家系，其表现不符合骨髓增生异常综合征的临床诊断标准。
Front Neurol. 2020 Oct 9;11:582323. doi: 10.3389/fneur.2020.582323. eCollection 2020.
9
Latrophilin's Social Protein Network.嗜乳脂蛋白的社交蛋白网络。
Front Neurosci. 2019 Jun 26;13:643. doi: 10.3389/fnins.2019.00643. eCollection 2019.
10
Assessment of Three New Loci from Genome-wide Association Study in Essential Tremor in Chinese population.中国人群原发性震颤全基因组关联研究中三个新位点的评估。
Sci Rep. 2017 Aug 11;7(1):7981. doi: 10.1038/s41598-017-08863-5.