نتایج جستجو برای: gene frequency

تعداد نتایج: 1580534  

Journal: :Proceedings of the National Academy of Sciences 2003

Journal: :auditory and vestibular research 0
nariman rahbar department of audiology, school of rehabilitation sciences, iran university of medical sciences, tehran, iran

background and aim: it has been several decades since the technology of frequency lowering (fl) has been proposed. however, primary research has revealed no benefits regarding the use of this technique. currently, new methods for fl and improvement of perception of speech and fricative sounds have led to the application of these methods by numerous companies to produce hearing aids. in this stu...

Journal: :modares journal of medical sciences: pathobiology 2015
farzad soleimani mehrdad behmanesh amir hosain ahmadi bahram mohamad soltani

abstract: a pure nucleotide pool is an essential precursor of correct dna replication and prevention of mutagenesis and abnormality in a living cell. inosine triphosphatase (itpase) is a critical enzyme to remove any deaminated rough purine nucleotides such as inosine from nucleotide pool. it has been shown that the rate of substitution mutation in genomic dna increase by abnormal function and ...

اصغرزاده, محمد, مؤدب, سیدرضا, انصارین , خلیل , راشدی, جلیل , شیرازی , سمانه , میرقاسمی, زهرا ,

   Background & Aims: Tuberculosis is the second factor in the deaths caused by infectious diseases in the world. Out of every ten infected people, only in one the clinical symptoms of the disease is developed. The correct vitamin D receptor activity on the nuclei of macrophages is one of the main components of the host innate immunity against M. tuberculosis. In the present study, the relation...

باقری, مرتضی, عبدی راد, عیسی, عمرانی, میرداوود, نانبخش, فریبا,

Background & Aims: Deletion/insertion of a single guanosine in the promoter of the plasminogen activator inhibitor-1 (PAI-1) gene, resulting in two alleles containing either 4 or 5 guanosines (G). Results of recent studies showed that presence of PAI-1 4G allele may increase the risk of human disease.  The aim of present study was to determine the 4G/5G genetic variation in the promoter of PAI-...

Mansoureh Bakhtiari Mehrdad Hashemi Shirin Shahbazi

Abstract Background and Aims:‎ Von Willebrand disease is a bleeding disorder caused by quantitative or functional defects in von Willebrand factor. The disease is found in up to 1 percent of the population. The most common symptom is mucocutaneous bleeding. Recently, studies conducted on healthy people showed that the H817Q mutation that previously known to cause von Willebrand...

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