نتایج جستجو برای: gnb3 gene

تعداد نتایج: 1141400  

Journal: :Circulation. Cardiovascular genetics 2016
Richard A Jensen Xueling Sim Albert Vernon Smith Xiaohui Li Jóhanna Jakobsdóttir Ching-Yu Cheng Jennifer A Brody Mary Frances Cotch Barbara Mcknight Ronald Klein Jie Jin Wang Annette Kifley Tamara B Harris Lenore J Launer Kent D Taylor Barbara E K Klein Leslie J Raffel Xiang Li M Arfan Ikram Caroline C Klaver Sven J van der Lee Unal Mutlu Albert Hofman André G Uitterlinden Chunyu Liu Aldi T Kraja Paul Mitchell Vilmundur Gudnason Jerome I Rotter Eric Boerwinkle Cornelia M van Duijn Bruce M Psaty Tien Y Wong

BACKGROUND There is increasing evidence that retinal microvascular diameters are associated with cardiovascular and cerebrovascular conditions. The shared genetic effects of these associations are currently unknown. The aim of this study was to increase our understanding of the genetic factors that mediate retinal vessel size. METHODS AND RESULTS This study extends previous genome-wide associ...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تربیت مدرس 1381

ماکروفاژها از سلولهای مهم سیستم ایمنی در پاسخ به عوامل بیماریزای مختلف از جمله ویروس هرپس سیمپلکس یک 1- ‏‎hsv0 هستند و عوامل موثر بر فعالیت آنها می توانند در سرنوشت بیماری موثر باشند. در این مطالعه اثر نوروپپتیدهای ‏‎substance p(sp)‎‏ و‏‎calcitonin gene related-peptide‎‏ (‏‎cgrp‎‏) که تحت شرایطی مثل استرس و التهاب از رشته های عصبی حسی آزاد می شوند و دارای گیرنده فعال بر روی ماکروفاژها می باشند ...

Journal: :genetics in the 3rd millennium 0
abolfazl barzegari alireza ostadrahimi vahideh ebrahimzadeh attari abolfazl gorbani

in view of the fundamental role of genetics in development of obesity, the present study aimed to investigate the single nucleotide polymorphism of some obesity-related genes among a subset of obese women living in tabriz, iran. for this purpose, 70 eligible obese women (aged 18-45 years) were genotyped for the uncoupling protein-1 (ucp-1) -3826a>g, ß3-adrenergic receptor (ß3adr) trp64arg, lept...

Journal: :Duzce Universitesi Tip Fakültesi Dergisi 2023

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...

Journal: :medical journal of islamic republic of iran 0
amir mehrgou department of medical genetics and molecular biology, school of medicine, iran university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی ایران (iran university of medical sciences) mansoureh akouchekian department of medical genetics and molecular biology, school of medicine, iran university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی ایران (iran university of medical sciences)

many factors including genetic, environmental, and acquired are involved in breast cancer development across various societies. among all of these factors in families with a history of breast cancer throughout several generations, genetics, like predisposing genes to develop this disease, should be considered more. early detection of mutation carriers in these genes, in turn, can play an import...

2013
Paola León-Mimila Hugo Villamil-Ramírez Marisela Villalobos-Comparán Teresa Villarreal-Molina Sandra Romero-Hidalgo Blanca López-Contreras Roxana Gutiérrez-Vidal Joel Vega-Badillo Leonor Jacobo-Albavera Carlos Posadas-Romeros Adrián Canizalez-Román Blanca Del Río-Navarro Francisco Campos-Pérez Victor Acuña-Alonzo Carlos Aguilar-Salinas Samuel Canizales-Quinteros

BACKGROUND Several studies have identified multiple obesity-associated loci mainly in European populations. However, their contribution to obesity in other ethnicities such as Mexicans is largely unknown. The aim of this study was to examine 26 obesity-associated single-nucleotide polymorphisms (SNP) in a sample of Mexican mestizos. METHODS 9 SNPs in biological candidate genes showing replica...

2016
Cynthia Reyes-Barron Silvina Tonarelli Andrew Delozier David F. Briones Brenda B. Su Lewis P. Rubin

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...

Journal: :PLoS Genetics 2005
J. Hunter Young Yen-Pei C Chang James Dae-Ok Kim Jean-Paul Chretien Michael J Klag Michael A Levine Christopher B Ruff Nae-Yuh Wang Aravinda Chakravarti

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...

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