نتایج جستجو برای: ژن gnb3
تعداد نتایج: 15934 فیلتر نتایج به سال:
Objective: to evaluate the association of essential arterial hypertension (EAH) and its severity with genes polymorphism NOS3 (rs2070744) GNB3 (rs5443) in West-Ukrainian population.
 Materials methods. One-hundred EAH patients (48 – healthy control) participated cohort case-control study. Blood pressure (BP), Creatinine, glucose, lipids panel were studied. genotyping performed by TaqMan pr...
Aim: Irritable bowel syndrome (IBS) defined by chronic or recurrent abdominal pain discomfort and changes in habits, is the most common functional gastrointestinal disorder. Studies proved that polymorphisms genes were one of key roles underlying IBS. This study aimed to investigate genotypes allele frequencies IBS-associated single nucleotide polymorphism (SNP) from GNB3 (rs54443) SCN5A (rs801...
Abstract Background: The burden of erectile dysfunction (ED) is rising worldwide due to unresponsiveness some affected individuals existing drugs and treatment strategies. Fortunately, improvement in biological techniques has led the understanding that cases disorder may have a genetic etiology, which, when fully understood, lead improved treatment. Objective: This review articulated establishe...
زمینه و هدف: کم‌تحرکی در مقابل آن تمرین جزء عوامل مرتبط با شاخص‌های آسیب کبدی به‌شمار می‌روند. وجود این هنوز نقش بسیاری از تمرین‌های ورزشی به‌ویژه تمرینات تناوبی مقاومتی مصرف برخی مکمل‌های غذایی جمله اسپیرولینا بر ایمنی التهابی کاملاٌ شناخته نشده است؛ بنابراین هدف پژوهش تعیین اثر هشت هفته مکمل‌دهی هوازی فعالیت بافت کبد بیان ژن CXCL1 عضلة موش‌های صحرایی نر بود.مواد روش‌ها: نیمه‌تجربی، 60 سر موش ن...
Major depressive disorder is a highly prevalent disease that is challenging to treat, often requiring medication and dose adjustments. Genetic factors play an important role in psychotropic medication responses. However, the translation of pharmacogenetics findings to clinical recommendations with regards to antidepressant responses is still in its early stages. We reviewed recent primary resea...
Hypertension is a leading cause of stroke, heart disease, and kidney failure. The genetic basis of blood pressure variation is largely unknown but is likely to involve genes that influence renal salt handling and arterial vessel tone. Here we argue that susceptibility to hypertension is ancestral and that differential susceptibility to hypertension is due to differential exposure to selection p...
Metabolic syndrome (MetS) is characterized by a cluster of cardiovascular risk factors that include: abdominal obesity, dyslipidaemia, hypertension, insulin resistance and impaired glucose tolerance. Recent genome wide association studies have identified several susceptibility regions involved in lipid metabolism that are also associated with MetS. We have explored the association of 9 genetic ...
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