نتایج جستجو برای: nucleotide polymorphism

تعداد نتایج: 201089  

Journal: :iranian journal of radiation research 0
h. v. goutham department of radiation biology & toxicology, school of life sciences, manipal university, manipal, karnataka, india k. d. mumbrekar department of radiation biology & toxicology, school of life sciences, manipal university, manipal, karnataka, india n. hitendra department of biotechnology, school of life sciences, manipal university, manipal, karnataka india. b. m. vadhiraja department of radiation oncology, manipal hospital, bangalore, karnataka, india d. j. manipal university department of radiotherapy & oncology, shiridi saibaba cancer hospital and research centre, kasturba hospital, manipal, karnataka, india b. s. shiridi saibaba cancer hospital and research centre department of radiation biology & toxicology, school of life sciences, manipal university, manipal, karnataka, india

background: normal tissue toxicity continues to remain as a major challenge for radiation oncologists for delivering the total dose to the tumour cells in cancer patients. cellular, molecular and plasma based early biomarkers to predict the overreactions and non-overreactions of normal tissue toxicity before the initiation of radiotherapy can be valuable for personalised treatment. the aim of t...

Journal: :international journal of molecular and cellular medicine 0
maryam mafi golchin department of genetics, faculty of medicine, babol university of medical sciences, babol, iran. sayyed mohammad hossein ghaderian department of medical genetics, faculty of medicine, shahid beheshti university of medical sciences, tehran, iran. haleh akhavan-niaki department of genetics, faculty of medicine, babol university of medical sciences, babol, iran. rozita jalalian cardiovascular research center, mazandaran university of medical sciences, sari, iran. laleh hedari department of medical genetics, faculty of medicine, shahid beheshti university of medical sciences, tehran, iran. ali reza salami department of biotechnology, university of tehran, tehran, iran.

coronary artery disease (cad) including myocardial infarction (mi) as its complication, is one of the most common heart diseases worldwide and also in iran, with extremely elevated mortality. cad is a multifactorial disorder. twin and family studies at different loci have demonstrated that genetic factors have an important role in the progression of cad. many studies have reported a significant...

Journal: :caspian journal of internal medicine 0
mozhgan moazami-goudarzi stem cell research center, tabriz university of medical science, tabriz, iran majid farshdousti-hagh hematology and oncology research center, tabriz university of medical science, tabriz, iran abbasali hoseinpour-feizi hematology and oncology research center, tabriz university of medical science, tabriz, iran mehdi talebi hematology and oncology research center, tabriz university of medical science, tabriz, iran ali-akbar movassaghpour-akbari hematology and oncology research center, tabriz university of medical science, tabriz, iran karim shams-asanjan hematology and oncology research center, tabriz university of medical science, tabriz, iran

background: bcl-2 is the most important anti-apoptotic regulator and bax is a pro-apoptotic protein. the status of these parameters or the ration of bcl-2 to bax is important in malignant cell fate as well as normal cells. methods: sixty-two all patients and 62 healthy sex-and age-matched controls were studied. after genotyping, the promoter region of the bax and bcl-2 genes by rflp-pcr method ...

Journal: :international journal of fertility and sterility 0
ahamad salamian kamran ghaedi shahnaz razavi mahmud tavalaee somayeh tanhaei marzyeh tavalaee

background: single nucleotide polymorphism (snps) are considered as one of the underlying causes of male infertility. proper sperm chromatin packaging which involves replacement of histones with protamines has profound effect on male fertility. over 20 snps have been reported for the protamine 1 and 2. materials and methods: the aim of this study was to evaluate the frequency of two previously ...

Journal: :BioTechniques 1998
W Gu G D Aguirre K Ray

Identification of polymorphism is the key for genetic mapping, diagnosis and marker-assisted selection. Restriction fragment-length polymorphisms (RFLPs) and short tandem repeats (STRs), also known as microsatellites, are commonly used genetic markers. Until discovery of STRs, RFLPs were used for genetic mapping, but bi-allelic polymorphism of RFLP limited its use as a marker. Although STRs are...

A. Rafat F. Ala Noshahr,

The diacylglycerol acyltransferase 1 gene (DGAT1) was identified as a strong candidate gene affecting mutton quality traits in sheep. Single nucleotide polymorphism creates a single base mutation (C to T) in AGCT site of endonuclease AluI. DGAT1 is one of the candidate genes to improve carcass characteristics in feedlot animals. In order to study area T487C in exon 17 of the DGAT1 polymorphism,...

2014
Can Yang Cong Li Mengjie Chen Xiaowei Chen Lin Hou Hongyu Zhao

Genetic Analysis Workshop 18 provided a platform for evaluating genomic prediction power based on single-nucleotide polymorphisms from single-nucleotide polymorphism array data and sequencing data. Also, Genetic Analysis Workshop 18 provided a diverse pedigree structure to be explored in prediction. In this study, we attempted to combine pedigree information with single-nucleotide polymorphism ...

2017
Ceren Can Mehtap Yazıcıoğlu Hakan Gürkan Hilmi Tozkır Adnan Görgülü Necdet Hilmi Süt

BACKGROUND Atopic dermatitis is the most common chronic inflammatory skin disease. A complex interaction of both genetic and environmental factors is thought to contribute to the disease. AIMS To evaluate whether single nucleotide polymorphisms in the TLR2 gene c.2258C>T (R753Q) (rs5743708) and TLR2 c.-148+1614T>A (A-16934T) (rs4696480) (NM_0032643) are associated with atopic dermatitis in Tu...

Journal: :Arak Medical University Journal 2021

Background and Aim: Breast cancer is the most common type leading cause of cancer-induced deaths in women, worldwide. The Fibroblast Growth Factor Receptor 2 (FGFR2) a tyrosine kinase receptor that plays an essential role growth, invasion, movement, angiogenesis tumor cells. Several single nucleotide polymorphisms have been found intron FGFR2 gene, i.e., associated with high risk breast cancer....

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