نتایج جستجو برای: deletion of copular verbs

تعداد نتایج: 21169266  

Background and Aim: A peptic ulcer is a breach in the gastric or duodenal mucosa down to the submucosa. There is evidence concerning the role of Reactive Oxygen Species (ROS) in the genesis of such ulcers production of intracellular ROS along mitochondria oxidative phosphorylation (OXPHOS) predisposes the deletion of 4977 bp mtDNA. The aim of the present study was to evaluate the association of...

The current study aims at exploring the role of causativization as one of the causes stated in the literature for overpassivization of English unaccusatives in an Iranian context.The study was conducted using three data collection procedures, an Oxford Placement Test, a Grammaticality Judgment Task, and a Production Task. The results revealed that causativization errors with non-alternating una...

Kamran Ghaedi, Marziyeh Tavalaee Mohammad Hossein Nasr-Esfahani, Mohammad Reza Deemeh Parastoo Modarres Somayeh Tanhaei

Objective Globozoospermia is a rare syndrome with an incidence of less than 0.1% among infertile men. Researchers have recently identified a large deletion, about 200 kbp, encompassing the whole length of DPY19L2 or mutations in SPATA16 and PICK1 genes associated with globozoospermia. The aim of this study was to analyze the DPY19L2 gene deletion using polymerase chain reaction technique for th...

Deemeh MR Ghaedi K Javadi GhR Modarres P, Nasr Esfahani MH, Tanhaei S

Background: Male infertility is a Multifactorial syndrome encompassing a wide variety of disorders. In more than half of infertile men, the cause of their infertility is unknown (idiopathic) and could be congenital or acquired. Globozoospermia, also called round-headed spermatozoa, is a rare disease with incidence< 0.1% among male infertile patients. The most prominent feature of globozoospermi...

عباسی, مختارعلی,

In order to study the effect of incomplete sire's pedigree on genetic trend (bBv,y) and gain (R) of quantitative trait, two population were simulated with the heritability 0.15 and 0.30. For each population, information resulted from ten years of selection were saved in different files. In generated data files, the sire numbers were eliminated from pedigree file with 0, 10, 20, …, 100 percentag...

Journal: :Annual Meeting of the Berkeley Linguistics Society 2014

Journal: :iranian red crescent medical journal 0
ziba soltani genomic research center, shahid beheshti university of medical sciences, tehran, ir iran fatemeh karami department of medical genetics, school of medicine, tehran university of medical sciences, tehran, ir iran vahidreza yassaee genomic research center, shahid beheshti university of medical sciences, tehran, ir iran feyzollah hashemi gorji genomic research center, shahid beheshti university of medical sciences, tehran, ir iran mahdieh talebzadeh genomic research center, shahid beheshti university of medical sciences, tehran, ir iran mohammad miryounesi genomic research center, shahid beheshti university of medical sciences, tehran, ir iran; genomic research center, shahid beheshti university of medical sciences, tehran, ir iran. tel: +98-2122439959, fax: +98-2122439961

conclusions this finding may help improve early detection, differential diagnosis, genetic counseling, and even treatment of patients with pku. introduction phenylketonuria (pku) is an autosomal recessive inborn error of phenylalanine metabolism, which is caused by mutation in phenylalanine hydroxylase (pah) gene. most of the pah mutations are missense mutations (67%), which are followed by sma...

Journal: :international journal of molecular and cellular medicine 0
maryam rezaei cellular and molecular research center, zahedan university of medical sciences, zahedan, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی زاهدان (zahedan university of medical sciences) mohammad hashemi cellular and molecular research center, zahedan university of medical sciences, zahedan, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی زاهدان (zahedan university of medical sciences) seyed mehdi hashemi department of internal medicine, school of medicine, zahedan university of medical sciences, zahedan, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی زاهدان (zahedan university of medical sciences) mohammad ali mashhadi department of internal medicine, school of medicine, zahedan university of medical sciences, zahedan, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی زاهدان (zahedan university of medical sciences) mohsen taheri genetics of non-communicable diseases research center, zahedan university of medical sciences, zahedan, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی زاهدان (zahedan university of medical sciences)

breast cancer (bc) is considered as one of the most important causes of death worldwide. previous studies showed that apolipoprotein b mrna- editing catalytic polypeptide-like 3 (apobec3) gene deletion significantly increased the risk of bc risk in chinese and european women. the present study aimed to assess the possible impact of apobec3 deletion and the risk of bc in a sample of iranian popu...

Journal: :ادب فارسی 0
زهر ابوالحسنی چیمه فارغ التحصیل دکتری دانشگاه تهران

the current paper is an outlook toward lexical aspect and its types exist as a semantic parameter in verb and indicate trend of doing task of verb in terms of continuance, iteration, duration etc. although discourse aspect is considered as independent factor in verb morphology, but the resultant syntactic reflection does not solely corresponds to grammatical aspect; instead, it includes lexical...

Ghasemi N, Jahaninejad T Pashaiefar H Varghaiean Y Zaimy MA

Background: Successful IVF process is limited by factors such as oocyte quality. Oocyte quality can be defined as its abilities to be fertilized, mature and give rise to normal offspring and it is dependent on nuclear maturation and cytoplasm maturation. Damage to mitochondrial DNA (mtDNA) has been described in oocytes in IVF failure women that decrease cytoplasmic quality because Mitochondria ...

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