1.
CONCLUSION These results suggest that infrasound can influence the molecular chaperone activity of α crystallin.
结论 次声可影响α-晶体蛋白的分子伴侣活性
2.
Change of α-Crystallin Acting as Molecular Chaperone Activity with Ageing
老化过程中α-晶体蛋白分子伴侣活性的变化
3.
Effects of fructose 6-phosphate and ribose on molecular chaperone activity of α-crystallin
磷酸果糖和核糖对α-晶状体蛋白分子伴侣活性的作用
4.
ConclusionThe molecular chaperone activity of α crystallin was compromised by UV B irradiation in time-dependent manner.
结论 UV B辐射可降低α 晶状体蛋白的分子伴侣活性 ,并呈时间依赖效应。
5.
The Research on ATP-ADP Exchange Activity and Molecular Chaperone Activity of Hsp70;
热休克蛋白Hsp70 ATP-ADP转换活性及分子伴侣功能研究
6.
The Impact of ATPase Activity to the Function of Chaperonin from Sulfolobus Solfataricus P2
硫矿硫化叶菌P2分子伴侣的ATPase活性对其功能影响
7.
Expression and Enzyme Activity Assay of pfu with Molecular Chaperone
应用分子伴侣共表达系统表达pfu基因及酶活性测定
8.
α Crystallin acts as a molecular chaperone to protect esterase against inactivation.
α-晶体蛋白作为分子伴侣可保护酯酶免于失活
9.
Character of α-Crystallin Molecular Chaperone Activity in Selenite Cataract
硒性白内障α-晶体蛋白的分子伴侣特性
10.
Study on Renaturation of Lysozyme with the Assistance of Artificial Chaperone;
人工分子伴侣体系辅助溶菌酶复性的研究
11.
Artificial Molecular Chaperon-Ion Exchange Chromatography Assisted Refolding of Denatured/Reduced Proteins;
人工分子伴侣—离子交换色谱法辅助还原变性蛋白质的复性
12.
The Refolding of Denatured Lysozyme Assisted by the Cooperative Effect of Artificial Chaperones and Additives;
人工伴侣与小分子添加剂协同辅助变性溶菌酶复性的研究
13.
Molecular Cloning and Expression Analysis of Calnexin in Tomato;
番茄类凝集素分子伴侣calnexin基因的克隆及表达特性分析
14.
The Expression of Endoplasmic Reticulum Molecular Chaperons in Mouse Brain during Development;
内质网分子伴侣与小鼠脑发育的关系
15.
Identification of novel partner proteins of PCBP1
PCBP1的新伴侣蛋白分子的研究(英文)
16.
Research Advances in Co-Chaperone Cdc37 Protein
辅助伴侣分子Cdc37蛋白的研究进展
17.
A Compound of Chaperone-rich Antigen Peptides with Tumour Cell Treated by Trichosanthin and Heat Stress
富伴侣分子肿瘤抗原肽复合物的制备
18.
Molecular chaperone may rescue the conformational diseases and revive the inactive enzymes in lens.
分子伴侣能解 救构象性疾病,使晶状体重要的代谢酶‘起死回生’.