نتایج جستجو برای: trnaleu (cun) gene

تعداد نتایج: 1141765  

Journal: :Nucleic Acids Research 2005
Rui Hao Ming-Wei Zhao Zhan-Xi Hao Yong-Neng Yao En-Duo Wang

The human mitochondrial tRNALeu(CUN) [hmtRNALeu(CUN)] corresponds to the most abundant codon for leucine in human mitochondrial protein genes. Here, in vitro studies reveal that the U48C substitution in hmtRNALeu(CUN), which corresponds to the pathological T12311C gene mutation, improved the aminoacylation efficiency of hmtRNALeu(CUN). Enzymatic probing suggested a more flexible secondary struc...

Journal: :Human molecular genetics 1998
A El Meziane S K Lehtinen I J Holt H T Jacobs

We have investigated the representation of structural isoforms of the two mitochondrial leucyl tRNAs in lung carcinoma cybrid cell lines containing the np 3243 (MELAS) mtDNA mutation, alone or in combination with the np 12300 suppressor mutation. The mutant tRNALeu(UUR) is aminoacylated very poorly or not at all, whereas the suppressor tRNALeu(CUN) is efficiently aminoacylated. Deacylated mitoc...

Journal: :iranian journal of child neurology 0
mohammad medhi heidari phd, assistant professor of molecular genetics, department of biology,sciences school,yazd university of medical sciences, yazd,iran mehri khatami phd, assistant professor of molecular genetics, department of biology,sciences school,yazd university of medical sciences, yazd,iran massoud houshmand phd, assistant professor of human molecular genetics,department of medical genetic,national institute of genetic engineering and biotechnology,tehran,iran eisa mahmoudi phd, assitant professor of mathematical statistic,department of statistics,yazd university, yazd,iran shahriar nafissi md, associate professor of neurology, neurology department, tehran university of medical sciences, tehran,iran

how to cite this article: heidari mm, khatami m, houshmand m, mahmoudi e, nafissi sh .increased prevalence 12308 a > g mutation in mitochondrialtrnaleu (cun) gene associated with earlier age of onset in friedreich ataxia. iranian journal of child neurology 2011;5(4):25-31. objective friedreich ataxia (frda) is an inherited recessive disorder. mitochondrial dna is a candidate modifying factor fo...

2015
Fawziah MA Mohammed Ali Reza Rezaee khorasany Elaheh Mosaieby Massoud Houshmand

BACKGROUND Colorectal cancer is the third most common type of cancer in men and women and the second leading cause of cancer-related deaths in the United States and UK. Colorectal cancer is strongly related to age, with almost three-quarters of cases occurring in people aged 65 or over. Pre-symptomatic screening is one of the most powerful tools for preventing colorectal cancer. Recently, the u...

2012
Qian Huang Peng Yao Gilbert Eriani En-Duo Wang

The fidelity of protein biosynthesis requires the aminoacylation of tRNA with its cognate amino acid catalyzed by aminoacyl-tRNA synthetase with high levels of accuracy and efficiency. Crucial bases in tRNALeu to aminoacylation or editing functions of leucyl-tRNA synthetase have been extensively studied mainly by in vitro methods. In the present study, we constructed two Saccharomyces cerevisia...

Journal: :Nucleic acids research 1984
A Rosen S Sarid V Daniel

A 13.4 kb rat genomic DNA fragment containing two related tRNA gene clusters was isolated from a rat lambda recombinant and analyzed for gene arrangement and nucleotide sequence. One cluster was found to contain a tRNALeuCUG gene while the second contained a tRNALeuCUA pseudogene with multiple base substitutions. The tRNALeu gene was found to possess an intact coding region and a functional tra...

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