نتایج جستجو برای: single mutation

تعداد نتایج: 1124173  

Journal: :Proceedings of the National Academy of Sciences 1996

Journal: :Nucleic Acids Research 2009

A. Mahallati Rayeni, H. Ghohani Arab, M. R. Ghasemi,

This paper presents an improved multi-objective evolutionary algorithm (IMOEA) for the design of planar steel frames. By considering constraints as a new objective function, single objective optimization problems turned to multi objective optimization problems. To increase efficiency of IMOEA different Crossover and Mutation are employed. Also to avoid local optima dynamic interference of mutat...

 Abstract Background: Investigators were suspicious of tyrosine-methionine-aspartate-aspartate (YMDD) mutations occurred only in patients who were treated by lamivudine. However, YMDD mutations of hepatitis B virus gene (HBV DNA) in patients with chronic hepatitis B (CHB) untreated with antiviral medicines was reported in some studies. The aim of this study was to evaluate YMDD mutations in Ira...

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 Background: Breast cancer is one of the most common cancer of women in the world.  Although different genetic alteration has been reported in this malignancy, but P 53 gene  mutations has more frequency. P 53 gene is one of the most important suppressor genes and it  play a central role in breast cancer and detecting of mutations in this gene would be very helpful in understanding of genetic m...

2009
PAMELA VALVA PABLO D. BECKER PATRICIA STREITEMBERGER MERCEDES GARCIA LOMBARDI GUADALUPE REY CARLOS A. GUZMAN MARIA VICTORIA PRECIADO

Mutations in the gene TP53, which codifies the tumor suppressor protein p53, are found in about 50% of tumors. These mutations can occur not only at somatic level, but also in germline. Pediatric cancer patients, mostly with additional family history of malignancy, should be considered as potential TP53 germline mutation carriers. Germline TP53 mutations and polymorphisms have been widely studi...

ابراهیم زاده وصال, رضا, درخشنده پیکر, پوپک, شاهقلی, الهام,

Background and Aim: Thalassemia is one of the most common worldwide single-gene diseases. On the molecular level, it is a heterogeneous disease. So far, beside large deletions, more than fifty point mutations have been identified for this disease around the world. Four to ten percent of Iranians are carriers of thalassemia-affected genes. In this study we determined the relationship between the...

Journal: :hepatitis monthly 0
bo qin shaoxing centre for disease control and prevention, shaoxing, china; state key lab of virology, wuhan institute of virology, chinese academy of sciences, wuhan, china; shaoxing center for disease control and prevention, shaoxing, china. tel: +86-57588137362, fax: +86-57588137333 bo zhang state key lab of virology, wuhan institute of virology, chinese academy of sciences, wuhan, china xiaodong zhang college of life science, shaoxing university, shaoxing, china tingting he shaoxing centre for disease control and prevention, shaoxing, china wenying xu shaoxing centre for disease control and prevention, shaoxing, china lijun fu shaoxing centre for disease control and prevention, shaoxing, china

background nucleus(t)ide analogs (nas), containing lamivudine (lmv), adefovir dipivoxil (adv), endeavor (etv), telbivudine (ldt), and tenofovir (tdf) are widely used for the treatment of chronic hepatitis b (chb), but long term anti-hepatitis b virus (hbv) therapy with nas may give rise to the emergence of drug-resistant viral mutants. objectives this study aimed to find and identify some new r...

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