【問題】Mutation in aminoacyl-tRNA synthetase ?推薦回答
關於「Mutation in aminoacyl-tRNA synthetase」標籤,搜尋引擎有相關的訊息討論:
Disease-associated mutations in a bifunctional aminoacyl-tRNA ...。
10 小時前 · The human EPRS gene encodes a bifunctional glutamyl-prolyl-tRNA synthetase (EPRS) with two catalytic cores and appended domains that contribute ...。
Aminoacyl-tRNA synthetase deficiencies in search of common themes。
2018年6月6日 · The mutational spectrum in a cohort of Charcot-Marie-Tooth disease type 2 among the Han Chinese in Taiwan.PLoS One. 2011;6:e29393. CAS PubMed ...。
Charcot–Marie–Tooth mutation in glycyl-tRNA synthetase stalls ...。
2021年8月17日 · Toxic gain-of-function mutations in aminoacyl-tRNA synthetases cause a ... Reporter plasmids RL and FL have been described previously (23).。
Aminoacyl-tRNA synthetases in medicine and disease - NCBI。
2013年2月21日 · The ongoing discovery of genetic mutations in human ARSs is increasing exponentially and can be considered an important determinant of disease ...。
Aminoacyl tRNA synthetases and their connections to disease | PNAS。
2008年8月12日 · Because some disease-causing mutations do not affect aminoacylation activity or apparent enzyme stability, the mutations are believed to affect ...: tw | tw。
An editing-defective aminoacyl-tRNA synthetase is mutagenic in ...。
2007年2月6日 · A striking, statistically significant, enhancement of the mutation rate in aging bacteria was found. This enhancement comes from an increase in ...: tw | tw。
Full article: Human aminoacyl-tRNA synthetases in diseases of the ...。
CMT was the first neural disorder to be linked to mutations in genes encoding AaRSs. Antonellis and colleagues reported a causative link between the ...。
Overexpressed mitochondrial leucyl-tRNA synthetase suppresses ...。
This suppression of a tRNA gene mutation by increasing the steady-state levels of its cognate aminoacyl-tRNA synthetase is a model for potential therapies ...。
Alanyl-tRNA Synthetase Quality Control Prevents Global ...。
2019年12月17日 · These results demonstrate the essential role of aminoacyl-tRNA proofreading ... Interestingly, in vitro characterization of the mutant AlaRS ...。
Genomic analyses of aminoacyl tRNA synthetases from human ...。
2019年5月2日 · Datt M, Sharma A. Evolutionary and structural annotation of disease-associated mutations in human aminoacyl-tRNA synthetases. BMC Genomics. 2014 ...
常見Mutation in aminoacyl-tRNA synthetase問答
延伸文章資訊The nucleus- encoded mitochondrial aminoacyl-tRNA synthetases (mt-aaRSs) are key com- ponents of ...
Three mutations result in rare, well-defined leukodystrophy syndromes, namely, DARS2, caused by m...
The nucleus-encoded mitochondrial aminoacyl-tRNA synthetases (mt-aaRSs) are key components of the...
Within this process, aminoacyl transfer RNA (tRNA) synthetases ... Glycyl tRNA synthetase mutatio...
The disease is caused by autosomal recessive mutations that induce progressive cerebella ataxia. ...
Aminoacyl-tRNA synthetases (ARSs) are responsible for charging amino acids to cognate tRNA molecu...
The nucleus- encoded mitochondrial aminoacyl-tRNA synthetases (mt-aaRSs) are key com- ponents of ...
Three mutations result in rare, well-defined leukodystrophy syndromes, namely, DARS2, caused by m...
The nucleus-encoded mitochondrial aminoacyl-tRNA synthetases (mt-aaRSs) are key components of the...
Within this process, aminoacyl transfer RNA (tRNA) synthetases ... Glycyl tRNA synthetase mutatio...
The disease is caused by autosomal recessive mutations that induce progressive cerebella ataxia. ...
Aminoacyl-tRNA synthetases (ARSs) are responsible for charging amino acids to cognate tRNA molecu...