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A novel duplication/insertion mutation of NEFL in a patient with Charcot-Marie-Tooth disease.

作者信息

Leung Conrad L, Nagan Narasimhan, Graham Thomas H, Liem Ronald K H

出版信息

Am J Med Genet A. 2006 May 1;140(9):1021-5. doi: 10.1002/ajmg.a.31242.

DOI:10.1002/ajmg.a.31242
PMID:16619203
Abstract
摘要

相似文献

1
A novel duplication/insertion mutation of NEFL in a patient with Charcot-Marie-Tooth disease.一名患有夏科-马里-图斯病的患者中发现了一种新的神经丝轻链蛋白(NEFL)重复/插入突变。
Am J Med Genet A. 2006 May 1;140(9):1021-5. doi: 10.1002/ajmg.a.31242.
2
Is a novel I214M substitution in the NEFL gene a cause of Charcot-Marie-Tooth disease? Functional analysis using cell culture models.NEFL基因中一种新的I214M替代是夏科-马里-图斯病的病因吗?使用细胞培养模型的功能分析。
J Peripher Nerv Syst. 2006 Sep;11(3):225-31. doi: 10.1111/j.1529-8027.2006.00092.x.
3
Effects of Charcot-Marie-Tooth-linked mutations of the neurofilament light subunit on intermediate filament formation.神经丝轻链亚基与夏科-马里-图思病相关的突变对中间丝形成的影响。
J Cell Sci. 2002 Dec 15;115(Pt 24):4937-46. doi: 10.1242/jcs.00148.
4
A novel out-of-frame mutation in the neurofilament light chain gene (NEFL) does not result in Charcot-Marie-Tooth disease type 2E.神经丝轻链基因(NEFL)中的一种新型移码突变不会导致2E型夏科-马里-图斯病。
Neurogenetics. 2005 Feb;6(1):49-50. doi: 10.1007/s10048-004-0202-3. Epub 2005 Jan 15.
5
NEFL Pro22Arg mutation in Charcot-Marie-Tooth disease type 1.1型遗传性运动感觉神经病中的神经丝轻链蛋白Pro22Arg突变
J Hum Genet. 2008;53(10):936-940. doi: 10.1007/s10038-008-0333-8. Epub 2008 Aug 29.
6
NEFL-related Charcot-Marie-tooth disease: an unraveling story.
Ann Neurol. 2009 Dec;66(6):714-6. doi: 10.1002/ana.21848.
7
Clinical and electrophysiological features in Charcot-Marie-Tooth disease with mutations in the NEFL gene.伴有NEFL基因突变的夏科-马里-图斯病的临床和电生理特征
Arch Neurol. 2007 Jul;64(7):966-70. doi: 10.1001/archneur.64.7.966.
8
Heterogeneity in the properties of NEFL mutants causing Charcot-Marie-Tooth disease results in differential effects on neurofilament assembly and susceptibility to intervention by the chaperone-inducer, celastrol.导致遗传性运动感觉神经病(Charcot-Marie-Tooth disease)的 NEFL 突变体在性质上存在异质性,导致对神经丝组装的影响不同,并且对伴侣蛋白诱导剂雷公藤红素的敏感性也不同。
Int J Biochem Cell Biol. 2013 Jul;45(7):1499-508. doi: 10.1016/j.biocel.2013.04.009. Epub 2013 Apr 22.
9
Further evidence that neurofilament light chain gene mutations can cause Charcot-Marie-Tooth disease type 2E.神经丝轻链基因突变可导致2E型夏科-马里-图斯病的进一步证据。
Ann Neurol. 2001 Feb;49(2):245-9. doi: 10.1002/1531-8249(20010201)49:2<245::aid-ana45>3.0.co;2-a.
10
A novel homozygous nonsense mutation in NEFL causes autosomal recessive Charcot-Marie-Tooth disease.一种新的 NEFL 纯合无义突变导致常染色体隐性遗传性腓骨肌萎缩症。
Neuromuscul Disord. 2018 Jan;28(1):44-47. doi: 10.1016/j.nmd.2017.09.018. Epub 2017 Oct 12.

引用本文的文献

1
Neurofilaments in health and Charcot-Marie-Tooth disease.健康与夏科-马里-图思病中的神经丝蛋白
Front Cell Dev Biol. 2023 Dec 18;11:1275155. doi: 10.3389/fcell.2023.1275155. eCollection 2023.
2
A review and analysis of the clinical literature on Charcot-Marie-Tooth disease caused by mutations in neurofilament protein L.神经丝蛋白 L 突变引起的夏科-马里-图什病的临床文献回顾与分析。
Cytoskeleton (Hoboken). 2021 Mar;78(3):97-110. doi: 10.1002/cm.21676. Epub 2021 Jun 3.
3
Charcot-Marie-Tooth disease Type 2E/1F mutant neurofilament proteins assemble into neurofilaments.
Charcot-Marie-Tooth 病 2E/1F 型突变神经丝蛋白组装成神经丝。
Cytoskeleton (Hoboken). 2019 Jul;76(7-8):423-439. doi: 10.1002/cm.21566. Epub 2019 Nov 6.
4
Absence of NEFL in patient-specific neurons in early-onset Charcot-Marie-Tooth neuropathy.早发性夏科-马里-图思病患者特异性神经元中无神经丝轻链蛋白。
Neurol Genet. 2018 Jun 5;4(3):e244. doi: 10.1212/NXG.0000000000000244. eCollection 2018 Jun.
5
Genetic and clinical characteristics of -related Charcot-Marie-Tooth disease.与[疾病名称未明确]相关的夏科-马里-图思病的遗传和临床特征。 (需注意,这里原文中“-related”前疾病名称缺失,翻译是根据完整语境推测补充的表述)
J Neurol Neurosurg Psychiatry. 2017 Jul;88(7):575-585. doi: 10.1136/jnnp-2016-315077. Epub 2017 May 13.
6
NEFL E396K mutation is associated with a novel dominant intermediate Charcot-Marie-Tooth disease phenotype.神经丝轻链(NEFL)E396K突变与一种新型显性中间型遗传性运动感觉神经病(Charcot-Marie-Tooth病)表型相关。
J Neurol. 2015 May;262(5):1289-300. doi: 10.1007/s00415-015-7709-4. Epub 2015 Apr 1.
7
A novel recessive Nefl mutation causes a severe, early-onset axonal neuropathy.一种新的隐性 Nefl 突变导致严重的、早发性轴索性神经病。
Ann Neurol. 2009 Dec;66(6):759-70. doi: 10.1002/ana.21728.
8
Dysfunctions of neuronal and glial intermediate filaments in disease.疾病中神经元和神经胶质中间丝的功能障碍。
J Clin Invest. 2009 Jul;119(7):1814-24. doi: 10.1172/JCI38003. Epub 2009 Jul 1.
9
Review of the multiple aspects of neurofilament functions, and their possible contribution to neurodegeneration.神经丝功能多方面的综述及其对神经退行性变的可能作用。
Mol Neurobiol. 2008 Aug;38(1):27-65. doi: 10.1007/s12035-008-8033-0. Epub 2008 Jul 23.
10
Role of phosphorylation on the structural dynamics and function of types III and IV intermediate filaments.磷酸化对III型和IV型中间丝的结构动力学及功能的作用
Exp Cell Res. 2007 Jun 10;313(10):2098-109. doi: 10.1016/j.yexcr.2007.04.010. Epub 2007 Apr 12.