2024年12月25日 · MT-TE (Mitochondrially Encoded TRNA-Glu (GAA/G)) is an RNA Gene, and is affiliated with the tRNA class. Diseases associated with MT-TE include Mitochondrial Myopathy With Reversible Cytochrome C Oxidase Deficiency and Mitochondrial Myopathy With Diabetes.

Infantile transient mitochondrial myopathy, also known as benign COX deficiency myopathy, is a rare disease which occurs within the infantile stages of life. The myopathy is characterized by clinical manifestations such as severe muscle weakness, hypotonia (poor muscle tone), and lactic acidosis (a buildup of lactic acid in the body).

Transfer RNAs help assemble protein building blocks (amino acids) into functioning proteins. The MT-TE gene provides instructions for making a specific form of tRNA that is designated as tRNA Glu.

Transfer RNAs help assemble protein building blocks (amino acids) into functioning proteins. The MT-TE gene provides instructions for making a specific form of tRNA that is designated as tRNAGlu.

2011年4月29日 · 移动设备(me)可包括移动终端(mt)，终端适配功能(taf)和终端设备(te)等功能部件。 从上面可以看出 ME 的 概念最大，它包括 MT 和 TE 。 MT 完成无线传输 和 相关功能。

2024年9月12日 · Clinical resource with information about MT-TE, and available tests. There are links to practice guidelines and authoritative resources like GeneReviews, PubMed, MedlinePlus, PharmGKB and clinicaltrials.gov.

线粒体MT-TE基因突变致可逆性婴幼儿呼吸链缺乏症早期表现与进展型线粒体病类似,积极治疗预后良好.早期进行基因检测可明确预后,增强治疗的信心. 引用本文: 罗序峰, 刘楠, 谢惠源, 等. 线粒体MT-TE基因突变致可逆性婴幼儿呼吸链缺乏症1例并文献复习 [J/OL] . 临床儿科杂志, 2019, 37 (2) : 93-96. DOI: 10.3969/j.issn.1000-3606.2019.02.004.

关于 MT-TE. Compound Screening Libraries 实体化合物库 Virtual Screening 虚拟筛选 Customize Your Library 定制专属化合物库 Drug Screening Service 药物筛选服务 关联疾病. 疾病名称 别名; Mitochondrial Myopathy, Infantile, Transient ...

Predicted to enable triplet codon-amino acid adaptor activity. Predicted to act upstream of or within translation. Predicted to be located in mitochondrion. Orthologous to human MT-TE (mitochondrially encoded tRNA-Glu (GAA/G)). [provided …

2016年10月25日 · In a 29-year-old man with adult-onset progressive muscle weakness with exercise intolerance and diabetes mellitus (500002), Hao et al. (1995) identified a 14709T-C transition in the MTTE gene, which altered an evolutionarily conserved nucleotide in the region specifying for the anticodon loop of mitochondrial tRNA (glu).