نتایج جستجو برای: codon

تعداد نتایج: 20648  

نمازی, محمدجواد, گل محمدی, رحیم,

Background and purpose: Malignant breast cancer is the second cause of death in women in the world. Studies revealed different controversial results regarding the carcinogenesis role of allelic polymorphism of codon V57I of AURKA gene. The present study aimed to determine the genotypic polymorphisms in codon V57I of AURKA gene in women with invasive carcinoma compared to those in healthy contro...

2003
DOLPH HATFIELD MARY RICE CATHERINE A. HESSION

Isoacceptors of Physarum polycephalum Ala-, Arg-, Glu-, Gln-, Gly-, Ile-, Leu-, Lys-, Ser-, Thr-, and Val-tRNAs were resolved by reverse-phase chromatography and isolated, and their codon recognition properties were determined in a ribosomal binding assay. Codon assignments were made to most isoacceptors, and they are summarized along with those determined in other studies from Escherichia coli...

Journal: :مجله بین المللی زیست و زیست پزشکی 0
haleh akhavan-niaki genetic laboratory of amirkola children's hospital, babol university of medical sciences, babol, iran reza youssefi kamangari genetic laboratory of amirkola children's hospital, babol university of medical sciences, babol, iran ali banihashemi genetic laboratory of amirkola children's hospital, babol university of medical sciences, babol, iran mandana azizi genetic laboratory of amirkola children's hospital, babol university of medical sciences, babol, iran

beta thalassemia is the  most common autosomal recessive disorder. the present study reports a rare β globin gene mutation, hbb: c.180g>a: codon 59 (aag/aaa), in a patient from gilan province, northern iran. nucleotide sequencing of amplified dna belonging to a 35 years old man presenting mild hypochromia revealed a synonymous mutation due to a g>a conversion at the third position of codon 59 o...

Journal: :journal of physical & theoretical chemistry 2008
s. irani m. monajjemi s.m atyabi m. sadegizadeh m. heshmat

p53 is one of the gene that has important role in human cell cycle and in the human cancers too.models of codon substitution make it possible to separate mutational biases in the dna fromselective constraints on the protein, and offer a great advantage over amino acid models forunderstanding the evolutionary process of proteins and protein-coding dna sequences. in thiswork, we investigated abou...

آذر فام, پروین, اصغرزاده, محمد, امین بخش, محمد, حسینپورفیضی, عباسعلی, حسینپورفیضی, محمدعلی, پولادی, ناصر,

Introduction: β –Thalassaemia was first explained by Thomas Cooly as Cooly’s anaemia in 1925. The β- thalassaemias are hereditary autosomal disorders with decreased or absent β-globin chain synthesis. The most common genetic defects in β-thalassaemias are caused by point mutations, micro deletions or insertions within the β-globin gene. Material and Methods: In this research , 142 blood sampl...

2010
James J. Davis Gary J. Olsen

Most genomes are heterogeneous in codon usage, so a codon usage study should start by defining the codon usage that is typical to the genome. Although this is commonly taken to be the genomewide average, we propose that the mode-the codon usage that matches the most genes-provides a more useful approximation of the typical codon usage of a genome. We provide a method for estimating the modal co...

2018
Sudeesh Karumathil Nimal T Raveendran Doss Ganesh Sampath Kumar NS Rahul R Nair Vijaya R Dirisala

The evolution of bias in synonymous codon usage in chosen monkeypox viral genomes and the factors influencing its diversification have not been reported so far. In this study, various trends associated with synonymous codon usage in chosen monkeypox viral genomes were investigated, and the results are reported. Identification of factors that influence codon usage in chosen monkeypox viral genom...

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