نتایج جستجو برای: polymorphism carrier detection

تعداد نتایج: 735034  

2013
Masoumeh Rostami Zahra Kalaei Mohamad Amin Pourhoseingholi Mehdi Kadivar

AIM The aim of this study was to investigate relation between H-ras T81C polymorphism and some of the important risk factors in gastric adenocarcinoma (GA). BACKGROUND GA is one of the leading causes of cancer death in most countries. RAS gene is an important member in the PI3K-AKT signaling and the single nucleotide polymorphism at H-rasc DNA position 81 has been demonstrated has an importan...

Journal: :European Heart Journal 2021

Abstract The problem of cardiovascular comorbidity becomes particularly relevant in the context a pandemic, since it is known that diseases (especially arterial hypertension – AH and coronary heart disease CHD) significantly increase frequency hospitalizations fatal outcomes patients with COVID-19. From these positions, fundamentally important to identify group individuals high prognostic proba...

اخوان نیاکی, هاله, اسمعیلی دوکی, محمد رضا, توکلی بزاز, جواد, طبری‌پور, رضا, عزیزی, ماندانا, لاریجانی, باقر,

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2017
Muhammad Tariq Masood Khan Arshi Naz Jawad Ahmed Tahir Sultan Shamsi Abid Sohail Taj

OBJECTIVES 1: To assess the diagnostic utility of three polymorphisms (DdeI, XmnI and TaqI) and direct sequencing in haemophilia B (HB) carrier detection in Pakistani families. 2: To compare phenotypes of HB carriers with those of healthy females. METHODS The study was conducted from March 2014 till February 2016 at Khyber Medical University Peshawar and National Institute of Blood Diseases, ...

  Background: Cytochrome P450 2C19 (CYP2C19) is important in metabolism of wide range of drugs. CYP2C19*17 is a novel variant allele which increases gene transcription and therefore results in ultra-rapid metabolizer phenotype (URM). Distribution of this variant allele has not been well studied worldwide. The aim of present study was to investigate allele and genotype frequencies of CYP2C19*17 ...

ژورنال: پژوهش در پزشکی 2015

Background: Beta thalassemia is one of the autosomal recessive diseases that related to synthesis disorder of beta globin chain. It is caused by any of the more than 200 mutations in the β-globin gene. DNA sequencing and genotyping of numerous mutations at beta globin gene is timely and expensive. Therefore, the best method for screening is linkage using polymorph markers at beta globin region ...

Journal: :The Journal of the Acoustical Society of America 2005
Alexandra Stein Stephan D Ewert Lutz Wiegrebe

Recent temporal models of pitch and amplitude modulation perception converge on a relatively realistic implementation of cochlear processing followed by a temporal analysis of periodicity. However, for modulation perception, a modulation filterbank is applied whereas for pitch perception, autocorrelation is applied. Considering the large overlap in pitch and modulation perception, this is not p...

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