نتایج جستجو برای: nucleotide polymorphisms

تعداد نتایج: 172638  

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2008
Parveen Bhatti Michele M Doody Bruce H Alexander Jeff Yuenger Steven L Simon Robert M Weinstock Marvin Rosenstein Marilyn Stovall Michael Abend Dale L Preston Paul Pharoah Jeffery P Struewing Alice J Sigurdson

Genome-wide association studies are discovering relationships between single-nucleotide polymorphisms and breast cancer, but the functions of these single-nucleotide polymorphisms are unknown and environmental exposures are likely to be important. We assessed whether breast cancer risk single-nucleotide polymorphisms interacted with ionizing radiation, a known breast carcinogen, among 859 cases...

Journal: :Anesthesiology 2005
Michael Zaugg Marcus C Schaub

The adrenergic system provides the primary control for cardiac, vascular, pulmonal, and metabolic functions. Seven of the nine adrenergic receptor subtypes display mutations that affect their function. Results from transgenic mouse models and from association studies in human populations allow to link protein dysfunctions to cardiovascular diseases or to risk for disease development. The diseas...

2017
Yoshiji Yamada Jun Sakuma Ichiro Takeuchi Yoshiki Yasukochi Kimihiko Kato Mitsutoshi Oguri Tetsuo Fujimaki Hideki Horibe Masaaki Muramatsu Motoji Sawabe Yoshinori Fujiwara Yu Taniguchi Shuichi Obuchi Hisashi Kawai Shoji Shinkai Seijiro Mori Tomio Arai Masashi Tanaka

We have performed exome-wide association studies to identify genetic variants that influence body mass index or confer susceptibility to obesity or metabolic syndrome in Japanese. The exome-wide association study for body mass index included 12,890 subjects, and those for obesity and metabolic syndrome included 12,968 subjects (3954 individuals with obesity, 9014 controls) and 6817 subjects (39...

Journal: :Turkish Journal of Fisheries and Aquatic Sciences 2022

The whole genome resequencing was used to develop single nucleotide polymorphisms (SNP) markers for the yellow catfish (Tachysurus fulvidraco). A total of 46 SNP from 129 individuals were selected 5550676 genotyping which distributed on 26 chromosomes. Of SNPs analyzed, 35 conformed Hardy-Weinberg equilibrium. observed and expected heterozygosity these ranged 0.2519 0.771 0.265 0.5018, respecti...

Abbas Shirdel, Abdol Rahim Rezaee Akram Beyk yazdi Hassan Rahimi Houshang Rafatpanah Ian V Hutchinson Mahmoud Reza Azarpajooh

Introduction Genetic background has known to be associated with the outcome of human T cell lymphotropic virus (HTLV) type I infection. In The present study we investigate the association between GM-CSF gene polymorphisms with the outcome of HTLV-I infection. Materials and Methods We analyzed 3 single-nucleotide polymorphisms in the promter region of granulocyte macrophage colony stimulating...

Journal: :The Journal of heredity 2014
Beatrice Coizet Letizia Nicoloso Donata Marletta Alessandra Tamiozzo-Calligarich Giulio Pagnacco Paola Crepaldi

The dietary demand of the modern horse relies on high-cereal feeding and limited forage compared with natural grazing conditions, predisposing the horse to several important diseases. Salivary and pancreatic alpha-amylases (coded by AMY1 and AMY2 genes, respectively) play a crucial role in carbohydrate digestion in nonruminants, but little is known about these 2 genes in the horse. Aim of this ...

اسعدی طهرانی, گلناز, بینشیان, فرحناز, زمانیان, مهسا, سلیمانی, سعیده, شریفی, زهره, فردوسیان, فرشته, پاز, زهرا,

Background and Objective: Genetic factors greatly impact the response to treatment in patients. Recent studies on rs10853728 single nucleotide polymorphisms in the promoter area, determined the IL-28B gene as a host factor affecting the treatment of hepatitis C infection. The aim of this study was to evaluate this polymorphism among Iranian patients Materials and Methods: This cross-sectiona...

Journal: :genetics in the 3rd millennium 0
اشرف احمدی شادمهری ashraf ahmadi shadmehri science and research center, islamic azad university, tehran, iranدانشگاه آزاد اسلامی، واحدعلوم و تحقیقات، تهران، ایران علی اکبر امیرزرگر ali akbar amirzargar department of immunogenetic, science faculty, tehran university of medical science, tehran, iranبخش ایمونوژنتیک، دانشکده علوم، دانشگاه علوم پزشکی تهران، تهران، ایران ، محمد حسین نیکنام mohammad hossein niknam department of immunogenetic, science faculty, tehran university of medical science, tehran, iranبخش ایمونوژنتیک، دانشکده علوم، دانشگاه علوم پزشکی تهران، تهران، ایران اعظم احمدی شادمهری azam ahmadi shadmehri genetic counseling centre, welfare organization of southern khorasan, iranسازمان بهزیستی، مرکز مشاوره ژنتیک خراسان جنوبی، ایران

the immunoreceptor programmed cell death-1 (pd-1) is a cell surface molecule that is reported to play an important role in the regulation of peripheral tolerance. it has been shown that pd-1 gene is associated with susceptibility to the autoimmune disease systemic lupus erythematosus (sle) in humans. however, there are no reports on the association between this gene and multiple sclerosis (ms)....

2016
Ting Wang Yuting Liang Hong Li Haibo Li Quanze He Ying Xue Cong Shen Chunhua Zhang Jingjing Xiang Jie Ding Longwei Qiao Qiping Zheng

Osteoarthritis (OA) is a complex disorder characterized by degenerative articular cartilage and is largely attributed to genetic risk factors. Single nucleotide polymorphisms (SNPs) are common DNA variants that have shown promising and efficiency, compared with positional cloning, to map candidate genes of complex diseases, including OA. In this study, we aim to provide an overview of multiple ...

Journal: :Psychiatric genetics 2006
Yu-Li Liu Cathy Shen-Jang Fann Chih-Min Liu Jer-Yuarn Wu Shuen-Iu Hung Hung-Yu Chan Jiahn-Jyh Chen Chia-Ching Pan Shih-Kai Liu Ming H Hsieh Tzung-Jeng Hwang Wen-Chen Ouyang Chun-Ying Chen Jin-Jia Lin Frank Huang-Chih Chou Ching-Mo Chueh Wei-Ming Liu Ming-Ming Tsuang Stephen V Faraone Ming T Tsuang Wei J Chen Hai-Gwo Hwu

AKT1 (V-akt murine thymoma viral oncogene homolog 1) is a protein kinase isoform of AKT. Five single-nucleotide polymorphisms, rs3803300, rs1130214, rs3730358, rs2498799 and rs2494732, at the genomic region of AKT1 have been reported to be significantly associated with schizophrenia. We tested for the presence of these five single-nucleotide polymorphisms in a Taiwanese population by genotyping...

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