نتایج جستجو برای: genetics

تعداد نتایج: 76572  

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: :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...

Journal: :iranian journal of neurology 0
jon andoni urtizberea school of myology, institute of myology, paris and gnmh neuromuscular reference center, marine hospital, hendaye, france.

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Journal: :acta medica iranica 0
reza shirkoohi cancer research center, cancer institute of iran, tehran university of medical sciences, tehran, iran. cyrus azimi cancer research center, cancer institute of iran, tehran university of medical sciences, tehran, iran.

cancer is a genetic-epigenetic based disease which contains a complex of alterations that cause irreversible transformation of cells with a new anarchic behavior. tumor suppressor inactivation and/or oncogene activation will lead to tumorigenesis. based on the genetic alteration in germ or somatic cells, the affected person will have a different fate of cancer incidence or inheritable cancer su...

Journal: :iranian journal of public health 0
dd farhud m mahmoudi p derakhshandeh p s stengel-rutkowski

the photoanthropometric method was used to study the facial features in 136 iranian children with down syndrome, aged 4 to 14 years. nineteen parameters were investigated and compared to an age related control group of 100 normal iranian children. the obtained measurements were related to reference values in the same faces. the normal range was defined by age related index values between the 20...

Background: Vitiligo is an acquired, idiopathic, and common depigmentation disorder of the skin that affects people of all ages and both sexes equally in the worldwide. Although etiology of the disease is unknown, there are theories such as environment and genetic factors. Methods: In this article, we collected and summarized the appropriate manuscripts regarding the epidemiology and gene...

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