نتایج جستجو برای: insulin genetics

تعداد نتایج: 258304  

2014
Bertha Hidalgo M. Ryan Irvin Jin Sha Degui Zhi Stella Aslibekyan Devin Absher Hemant K. Tiwari Edmond K. Kabagambe Jose M. Ordovas Donna K. Arnett

Known genetic susceptibility loci for type 2 diabetes (T2D) explain only a small proportion of heritable T2D risk. We hypothesize that DNA methylation patterns may contribute to variation in diabetes-related risk factors, and this epigenetic variation across the genome can contribute to the missing heritability in T2D and related metabolic traits. We conducted an epigenome-wide association stud...

Journal: :International Journal of Community Medicine and Public Health 2022

Healthy lifestyle includes physical activity as the basic component however, exercises with eccentricity have been associated to a higher risk of muscle injury and slower recovery. The development exercise-induced is phenomenon that results from atypical or unaccustomed activity; intensity pain extent damage steadily deteriorate over time, when exercise session contains an eccentric component, ...

Journal: :iranian biomedical journal 0
jai prakash department of physiology, king george’s medical university, lucknow, uttar pradesh, india; balraj mittal department of genetics, sanjay gandhi postgraduate institute of medical sciences, lucknow, u.p., india apurva srivastava department of physiology, king george’s medical university, lucknow, uttar pradesh, india; shally awasthi department of pediatrics, king george’s medical university, lucknow, uttar pradesh, india pranjal srivastava darbhanga medical college and hospital near karpuri chowk benta laheriasarai darbhanga bihar 846003, india neena srivastava department of physiology, king george’s medical university, lucknow, uttar pradesh, india;

background: obesity is a very common disorder resulting from an imbalance between food intake and energy expenditure, and it has a substantial impact on the development of chronic diseases.  the aim of this study was to examine the association of insig2 (rs7566605) gene polymorphism with obesity and obesity associated phenotypes in north indian subjects. methods: the variants were investigated ...

Journal: :journal of research in health sciences 0
h pour-jafari dd farhud m hashemzadeh chaleshtori

background: the goal of the present study was to report the results of two parallel works in which the incidence of fetal deaths and also congenital malformations among the progenies of the iranian chemical victims were studied. methods: the subjects were progenies of a randomly selected population from survivors of chemical attacks during iran-iraq conflict. totally 807 male cases ranged 18-85...

Journal: :وقایع علوم کاربردی ورزش 0
korkut ulucan üsküdar univerity, haluk turksoy sok. no:14, altunizade, üsküdar, i̇stanbul, turkey. marmara university, basibuyuk yolu 9/3 maltepe saglık yerleşkesi, maltepe, istanbul, turkey betul biyik üsküdar univerity, haluk turksoy sok. no:14, altunizade, üsküdar, i̇stanbul, turkey sezgin kapici üsküdar univerity, haluk turksoy sok. no:14, altunizade, üsküdar, i̇stanbul, turkey canan sercan marmara university, basibuyuk yolu 9/3 maltepe saglık yerleşkesi, maltepe, istanbul, turkey oznur yilmaz üsküdar univerity, haluk turksoy sok. no:14, altunizade, üsküdar, i̇stanbul, turkey tunc catal üsküdar univerity, haluk turksoy sok. no:14, altunizade, üsküdar, i̇stanbul, turkey

actins are small globular filaments functioning in cell processes like muscle contraction, and stabilized to the sarcomeric z- discs by actin binding proteins (actinins). one of the important gene coding for actin binding proteins in fast twitch fibers is alpha- actinin- 3 (actn3). in this research, we have conducted a gene profile study investigating the genotype and allele distributions of ac...

Journal: :genetics in the 3rd millennium 0
sorush ghafurian

genetic basis of diffrent arrhythmias has always been an intresting subject of resesrch for scientists. here i will review in brief the most common familia arrhythmias and the new findings regarding their mode of inhetitance. this paper will mainly focus on the genetic basis of the long qt syndromes but we will also have a short review of the genetics of three other familia congenital arrhythmo...

Journal: :acta medica iranica 0
rozita jalilian research center for immunodeficiencies, children’s medical center, pediatrics center of excellence, tehran university of medical sciences, tehran, iran. nima rezaei research center for immunodeficiencies, children’s medical center, pediatrics center of excellence, tehran university of medical sciences, tehran, iran. and molecular immunology research center; and department of immunology, school of medicine, tehran university of medical sciences, tehran, iran.

no abstract

Journal: :Journal of Health Science and Medical Research (JHSMR) 2023

Obesity is described as the accumulation of excess body fat. Several health issues are caused by fat, including cancer, type 2 diabetes, and cardiovascular disease. Additionally, obesity rates among schoolchildren young adults rising globally, putting people at risk chronic diseases. Genetics, epigenetic modification, epigenomics, environmental factors influence inheritance patterns significant...

Journal: :gene, cell and tissue 0
mohammad hashemi cellular and molecular research center, zahedan university of medical sciences, zahedan, ir iran; department of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, ir iran; department of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, ir iran. tel: +98-5413235122 majid naderi genetics of non communicable disease research center, zahedan university of medical sciences, zahedan, ir iran; department of pediatrics, school of medicine, zahedan university of medical sciences, zahedan, ir iran ebrahim eskandari nasab genetics of non communicable disease research center, zahedan university of medical sciences, zahedan, ir iran seyed shahaboddin hasani department of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, ir iran simin sadeghi bojd department of pediatrics, school of medicine, zahedan university of medical sciences, zahedan, ir iran mohsen taheri genetics of non communicable disease research center, zahedan university of medical sciences, zahedan, ir iran

conclusions our findings indicated that mdm2 40-bp ins/del polymorphism was not associated with all in our iranian population. further studies with larger sample sizes and diverse ethnicities are required to verify our findings. background the human murine double minute 2 (mdm2), an oncoprotein, is the major negative regulator of p53. objectives the purpose of this study was to evaluate the imp...

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