نتایج جستجو برای: tkd835 mutation

تعداد نتایج: 291413  

Journal: :iranian journal of basic medical sciences 0
razieh pourahmad jaktaji department of genetics, faculty of science and biotechnology center, university of shahrekord, shahrekord, iran nasim jazayeri students in genetics at university of shahrekord

objective(s): the major antibiotic efflux pump of esherichia coli is acrab-tolc. the first part of the pump, acrab, is encoded by acrab operon. the expression of this operon can be kept elevated by overexpression of an activator, mara following inactivation of marr and acrr repressors due to mutation in encoding genes, marr and acrr, respectively. the aims of this research were to use e. coli m...

Journal: :gastroenterology and hepatology from bed to bench 0
mahsa molaei royai kishani farahan mina maftouh mohammad yaghoob taleghani mahsa vahdatinia fatemeh khatami

aim : we aimed to explore the frequency of braf v600e mutation in iranian patients with colorectal cancer (crc) as well as its association with clinic pathological characteristic of patients.   background : crc is the third leading cause of cancer related death. there is a growing body of data showing the association of braf v600e mutation with malignant transformation and clinical outcome of d...

Journal: :Lecture Notes in Computer Science 2023

This work proposes Adaptive Facilitated Mutation, a self-adaptive mutation method for Structured Grammatical Evolution (SGE), biologically inspired by the theory of facilitated variation. In SGE, genotype individuals contains list each non-terminal grammar that defines search space. our proposed mutation, individual an array with different, rate non-terminal. We also propose Function Grouped Gr...

Asadpour U Hassani M, Hojati V Mohseni Meybodi A Sabbaghian M Sadighi Gilani MA

Background: Human β-defensin 126 is a small cationic glycoprotein that coats the plasma membrane of sperm during epididymal transit. It provides protection for sperms from infection-causing microbes and against the female immune system. Defensin remains on the sperm until sperm become capacitated in the female reproductive tract. DEFB126 gene is located on the subtelomeric end of 20p13 in human...

Behnam Kamalidehghan, Massoud Houshmand, Nargesossadat Nouri, Nayerossadat Nouri, Omid Aryani,

Background: Mucopolysaccharidosis type-VI (MPS-VI), which is inherited as an autosomal recessive trait, results from the deficiency of N-acetylgalactosamine 4-sulfatase (arylsulfatase B) activity and the lysosomal accumulation of dermatan sulfate. In this study, ARSB mutation analysis was performed on three unrelated patients who were originally from the West Azerbaijan province of Iran. Method...

E Fakhari , M Norouzi , SM Jazayeri ,

Background and Aims: lamivudine is amongst the antiviral for drug chronic hepatitis B treatment. During therapy with lamivudine, variants may emerge with YMDD mutation in the reverse transcriptase (RT) region of polymerase gene. This mutation might have a role in drug resistant for HBV. Materials and Methods: HBV DNA extraction from serum sample of 88 patients, were subjected to nested PCR for ...

Journal: :archives of medical laboratory sciences 0
hoorieh soleimanjahi department of virology, faculty of medical sciences, tarbiat modares university, tehran, iran taravat bamdad department of virology, faculty of medical sciences, tarbiat modares university, tehran, iran elham ahmadi department of virology, faculty of medical sciences, tarbiat modares university, tehran, iran

lots of viruses, in particular rna viruses, have high mutation rates and relatively short generation times. particle stability during infection in nature or in laboratory triggers the evolutionary event toward different mechanisms such as genome segmentation, point mutation and  recombination. the frequency of mutant genomes increase and modify  the previous distribution, which, consequently, l...

Journal: :research in molecular medicine 0
shirin farivar department of genetics, faculty of biological sciences, shahid beheshti university (gc) mahdieh hasani department of genetics, faculty of biological sciences, shahid beheshti university (gc) reza shiari division of pediatric rheumatology, mofid children’s hospital, shahid beheshti university of medical sciences

background: systemic-onset juvenile idiopathic arthritis (sojia) is an autoinflammatory disease with complex genetic trait starts in children less than 16 years of age with fever and cutaneous rash. despite, the main genetic factors that may play a role in sojia have not yet been identified. high level of interleukin-1beta in the blood of sojia patients has been reported. the production and sec...

Journal: :فصلنامه علوم پزشکی دانشگاه آزاد اسلامی واحد پزشکی تهران 0
آگاه محمدرضا agah mr research center for gastroenterology and liver diseases, shaheed beheshti university of medical sciences, tehran, iranمرکز تحقیقات بیماری های گوارش و کبد، دانشگاه علوم پزشکی شهید بهشتی ظفرقندی مریم zafarghandi m research center for gastroenterology and liver diseases, shaheed beheshti university of medical sciences, tehran, iranمرکز تحقیقات بیماری های گوارش و کبد، دانشگاه علوم پزشکی شهید بهشتی مطهری زهرا motahari z research center for gastroenterology and liver diseases, shaheed beheshti university of medical sciences, tehran, iranمرکز تحقیقات بیماری های گوارش و کبد، دانشگاه علوم پزشکی شهید بهشتی جزایری هانیه السادات jazaeri h research center for gastroenterology and liver diseases, shaheed beheshti university of medical sciences, tehran, iranمرکز تحقیقات بیماری های گوارش و کبد، دانشگاه علوم پزشکی شهید بهشتی زالی محمدرضا hajibeigi b research center of iranian blood transfusion organization, tehran, iranمرکز تحقیقات سازمان انتقال خون ایران حاجی بیگی بشیر attarchy z research center of iranian blood transfusion organization, tehran, iranمرکز تحقیقات سازمان انتقال خون ایران عطارچی زهره

background: there are no data on the frequency and biochemical expression of the hemochromatosis associated mutations, c282y and h63d, in iranian adult population. this is the first study among iranians that may advocate a screening program. materials and methods: we investigated the frequency of the c282y/h63d hfe gene mutations in a group of 1029 randomly selected iranian blood donors as well...

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