نتایج جستجو برای: nucleotide polymorphism

تعداد نتایج: 201089  

Journal: :International Journal of Health Sciences (IJHS) 2022

The present study aims to examine the genetic variation of ATP1B1 gene concerning hypertension and chronic kidney disease CKD. (120 ) blood samples from participants were obtained divided into three groups: a first group representing hypertensive patients (hyper), second Hypertensive CKD (hyper with CKD), third control group. DNA was extracted all then converted cDNA ARMS-PCR technique used inv...

Journal: :Baltic Journal of Sport and Health Sciences 2022

Background: The ACSL A/G single nucleotide polymorphism is associated with endurance trainability. It was previously demonstrated that AA carriers had a reduced maximal oxygen consumption (VO2 max) in response to training compared GG carriers, and this explained 6.1% of the variance VO2 max training. aim present study determine prevalence among soccer players. Methods: One hundred sixty-seven m...

Journal: :KnE Life Sciences 2022

Melanocortin-4 Receptor (MC4R) expressed in hypothalamus which is part of the brain that are involved regulation appetite, metabolism and bodyweight. This study aimed to identify MC4R gene diversity second cross generation Belgian Blue, Wagyu, Brahman crossbred its relationship with body weight size birth. Polymerase Chain Reaction (PCR) DNA sequencing were used Single Nucleotide Polymorphism (...

ابراهیمی, احمد , خلیلی, آزاده , عرب‌نژاد, محدثه , مقدم, محمد , نصیری, محبوبه , کریمی, مهران ,

Background: There are many genetic and non-hereditary risk factors that are known to causes venous thromboembolic (VTE) disorders, Cardiovascular diseases and types of cancer. One of these is the Prothrombin G20210A mutation. Prothrombin mutation (guanine to adenine G→A) at nucleotide position 20210, which is present in the 3′ untranslated region of the prothrombin gene. Prothrombin G20210A mut...

Journal: :Haematologica 2008
Thomas Ernst Jana Hoffmann Philipp Erben Benjamin Hanfstein Armin Leitner Rüdiger Hehlmann Andreas Hochhaus Martin C Müller

The BCR-ABL K247R change is based on a rare single nucleotide polymorphism occurring likewise in healthy controls and non-hematologic cell types. Despite its juxtaposition to the P-loop, functional analysis showed no alteration compared to non-mutated BCR-ABL. We sought to investigate if other changes in the BCR-ABL kinase domain should be considered as single nucleotide polymorphisms rather th...

Journal: :Circulation. Cardiovascular genetics 2014
John M Hartney Timothy Stidham David A Goldstrohm Rebecca E Oberley-Deegan Michael R Weaver Zuzana Valnickova-Hansen Carsten Scavenius Richard K P Benninger Katelyn F Leahy Richard Johnson Fabienne Gally Beata Kosmider Angela K Zimmermann Jan J Enghild Eva Nozik-Grayck Russell P Bowler

BACKGROUND The enzyme extracellular superoxide dismutase (EC-SOD; SOD3) is a major antioxidant defense in lung and vasculature. A nonsynonomous single-nucleotide polymorphism in EC-SOD (rs1799895) leads to an arginine to glycine amino acid substitution at position 213 (R213G) in the heparin-binding domain. In recent human genetic association studies, this single-nucleotide polymorphism attenuat...

P48 protein of Mycoplasma agalactiae is used to diagnose infection and was identified as potential vaccine candidate. According to the genetic nature of mycoplasma and variable sensitivity in P48-based serological diagnosis tests, intra species variation of P48 nucleotide sequence investigated in 13 field isolates of difference province of Iran along with three vaccine strains. Samples were col...

Journal: :Heliyon 2023

BackgroundIt has been confirmed that the connective tissue growth factor (CTGF) gene rs9402373 polymorphism is associated with fibrotic and inflammatory diseases. However, studies on relationship between polymorphisms in CTGF bowel disease (IBD) remain rare. Therefore, aim of this study was to assess association IBD susceptibility a Chinese population.Materials methodsTo establish an amplificat...

برزگر, علی, میرمجیدی, سیده حبیبه, نیک بخش, نوین,

Background and purpose: Gastric cancer is the fourth most common cancer and the second leading cause of cancer death worldwide. North of Iran is a high risk area for gastric cancer. Bcl2 family is the most important regulator of apoptosis and -938C>A single nucleotide polymorphism of bcl2 gene promoter has been demonstrated to influence gastric cancer susceptibility. In this research we studied...

Journal: :Genetics 2007
Jay F Storz Monica Baze Jessica L Waite Federico G Hoffmann Juan C Opazo Jack P Hayes

Results of electrophoretic surveys have suggested that hemoglobin polymorphism may be maintained by balancing selection in natural populations of house mice, Mus musculus. Here we report a survey of nucleotide variation in the adult globin genes of house mice from South America. We surveyed nucleotide polymorphism in two closely linked alpha-globin paralogs and two closely linked beta-globin pa...

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