• 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

The tissue-specific and developmental regulation of expression of rat medium-chain acyl-CoA dehydrogenase mRNA.

作者信息

Kelly D P, Strauss A W

机构信息

Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110.

出版信息

Prog Clin Biol Res. 1990;321:599-608.

PMID:2326314
Abstract
摘要

相似文献

1
The tissue-specific and developmental regulation of expression of rat medium-chain acyl-CoA dehydrogenase mRNA.
Prog Clin Biol Res. 1990;321:599-608.
2
Tissue specific and developmental expression of rat long-and medium-chain acyl-CoA dehydrogenases.大鼠长链和中链酰基辅酶A脱氢酶的组织特异性及发育表达
Biochim Biophys Acta. 1993 Dec 14;1216(3):460-8. doi: 10.1016/0167-4781(93)90015-6.
3
Cloning of a cDNA for short/branched chain acyl-Coenzyme A dehydrogenase from rat and characterization of its tissue expression and substrate specificity.大鼠短/支链酰基辅酶A脱氢酶cDNA的克隆及其组织表达和底物特异性的表征
Arch Biochem Biophys. 1996 Jul 1;331(1):127-33. doi: 10.1006/abbi.1996.0290.
4
Expression and purification of His-tagged rat mitochondrial medium-chain acyl-CoA dehydrogenase wild-type and Arg256 mutant proteins.带有组氨酸标签的大鼠线粒体中链酰基辅酶A脱氢酶野生型和Arg256突变体蛋白的表达与纯化
Protein Expr Purif. 2004 Oct;37(2):472-8. doi: 10.1016/j.pep.2004.06.021.
5
The tissue-specific expression and developmental regulation of two nuclear genes encoding rat mitochondrial proteins. Medium chain acyl-CoA dehydrogenase and mitochondrial malate dehydrogenase.编码大鼠线粒体蛋白的两个核基因的组织特异性表达及发育调控。中链酰基辅酶A脱氢酶和线粒体苹果酸脱氢酶。
J Biol Chem. 1989 Nov 15;264(32):18921-5.
6
[Medium chain acyl-CoA dehydrogenase deficiency].[中链酰基辅酶A脱氢酶缺乏症]
Tanpakushitsu Kakusan Koso. 1988 Apr;33(5):560-3.
7
Molecular cloning and nucleotide sequence of cDNAs encoding human short chain acyl-CoA dehydrogenase and study of the molecular basis of human short chain acyl-CoA dehydrogenase deficiency.编码人短链脂酰辅酶A脱氢酶的cDNA的分子克隆及核苷酸序列分析与人短链脂酰辅酶A脱氢酶缺乏症的分子基础研究
Prog Clin Biol Res. 1990;321:625-32.
8
Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship.线粒体脂肪酸氧化缺陷的突变分析：以酰基辅酶A脱氢酶缺乏症为例，特别关注基因型与表型的关系。
Hum Mutat. 2001 Sep;18(3):169-89. doi: 10.1002/humu.1174.
9
FAD-dependent regulation of transcription, translation, post-translational processing, and post-processing stability of various mitochondrial acyl-CoA dehydrogenases and of electron transfer flavoprotein and the site of holoenzyme formation.黄素腺嘌呤二核苷酸（FAD）依赖的对各种线粒体酰基辅酶A脱氢酶、电子传递黄素蛋白的转录、翻译、翻译后加工以及加工后稳定性的调节作用，以及全酶形成位点。
J Biol Chem. 1992 Sep 5;267(25):17925-32.
10
Molecular analysis of medium chain acyl-CoA dehydrogenase deficiency.中链酰基辅酶A脱氢酶缺乏症的分子分析
Prog Clin Biol Res. 1990;321:609-23.