نتایج جستجو برای: fok1 polymorphism

تعداد نتایج: 107356  

Journal: :archives of clinical infectious diseases 0
mohsen taheri genetics of non-communicable diseases research center, zahedan university of medical sciences, zahedan, ir iran; department of genetics, school of medicine, zahedan university of medical sciences, zahedan, ir iran; department of genetics, school of medicine, zahedan university of medical sciences, zahedan, ir iran. tel: +98-5413425793, fax: +98-5413425796 hamid reza kouhpayeh research center for infectious diseases and tropical medicine, zahedan university of medical sciences, zahedan, ir iran toraj hosseinalizadeh research center for infectious diseases and tropical medicine, zahedan university of medical sciences, zahedan, ir iran mohammad naderi research center for infectious diseases and tropical medicine, zahedan university of medical sciences, zahedan, ir iran gholamreza bahari department of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, ir iran mohammad hashemi department of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, ir iran

background: genetic variation influences susceptibility/resistance to tuberculosis. cxcl10 is involved in t-cell migration and stimulation of natural killer cells in mycobacterium tuberculosis infection. objectives: we aimed to investigate the genetic polymorphisms in promoter of the cxcl10 gene in patients with pulmonary tuberculosis (ptb) and healthy controls, to clarify whether polymorphisms...

Journal: :international journal of molecular and cellular medicine 0
negin dasar pardis international unit, university of guilan, rasht, iran.سازمان اصلی تایید شده: دانشگاه گیلان (guilan university) sayyed mohammad hossein ghaderian department of medical genetics, faculty of medicine, shahid beheshti university of medical sciences and health services, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) eznollah azargashb department of health & community medical, faculty of medicine, shahid beheshti university of medical sciences and health services, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences)

one of the most striking features in autosomal dominant polycystic kidney disease (adpkd) is the difference at onset age of end-stage renal disease (esrd). modifier genes may play a role in this phenotypic variability. the mutated nitric oxide synthase 3 gene (nos3), have a modifier effect on the severity of adpkd by impairment of nos3 activity and decreasing of renal vascular nitric oxide prod...

Journal: :research in molecular medicine 0
mahboobeh nasiri department of natural sciences, arsanjan branch, islamic azad university, arsanjan, iran. ali roostaei department of microbiology, science and research branch, islamic azad university, fars, iran zeinab ehsanian department of microbiology, science and research branch, islamic azad university, fars, iran

background: the association between methylene tetrahydrofolate reductase polymorphism and coronary artery diseases risk has been both confirmed and refuted in a number of published studies. the aim of this study was to investigate whether genetic polymorphisms of mthfr (c677t, a1298c) contributed to the development of myocardial infarction (mi). materials and methods: the present case-control s...

Journal: :CoRR 2017
Evgeniy Vodolazskiy

Second order conservative languages with a Maltsev polymorphism also have a majority polymorphism. Abstract The paper proves that for any second order conservative constraint language with a Maltsev polymorphism there is a majority polymor-phism. Moreover, the majority polymorphism can be defined by the Maltsev polymorphism.

Journal: :iranian journal of allergy, asthma and immunology 0
ebrahim nadi mehrdad hajilooi fatemeh zeraati mostafa ansari sasan tavana sayed hamid hashemi

the e-selectin mediates the interaction of activated endothelial cells with leukocytes and plays a fundamental role in the pathogenesis of asthma. it has been suggested that an s/r (serine128arginine) polymorphism of e-selectin alters ligand binding function. our purpose in this study was to determine whether this serine128arginine polymorphism influences the risk of asthma and also to analyze ...

Journal: :iranian journal of psychiatry 0
seyed masoud arzaghi psychosomatic research group, endocrinology and metabolism research center, tehran university of medical sciences, tehran, iran arash hossein-nezhad endocrinology and metabolism research center, tehran university of medical sciences, tehran, iran seyed vahid shariat mental health research center, tehran university of medical sciences, tehran, iran alireza ghodsipour endocrinology and metabolism research center, tehran university of medical sciences, tehran, iran jamal shams neuroscience research center, national neuroscience research network, shaheed beheshti university of medical sciences, tehran, iran bagher larijani endocrinology and metabolism research center, tehran university of medical sciences, tehran, iran

objective: the methylenetetrahydrofolate reductase (mthfr) gene polymorphism c677t is suspected to be a risk factor for psychiatric disorders, but it remains inconclusive whether the mthfr polymorphism c677t is imputed to vulnerability to schizophrenia and bipolar disorder. method: we prompted impetus to appraise this polymorphism in an iranian population. therefore, 90 patients with bipolar di...

Journal: :middle east journal of digestive diseases 0
haniyeh rahbar kafshboran mortaza bonyadi hamidreza miri mehdi haghi abbas nikravesh reza abdolmohammadi

background inflammatory bowel disease (ibd) is a chronic, relapsing, inflammatory disorder of the gastrointestinal tract that includes two entities, crohn`s disease (cd) and ulcerative colitis (uc). as with other complex diseases, both genetic susceptibility and environmental factors play role in the pathogenesis of these diseases. the tumor necrosis factor α (tnf-α) gene is located in the ibd3...

Journal: :Theoretical Computer Science 1993

Journal: :Journal of Medical Genetics 1977

Journal: :The Professional Medical Journal 2019

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