نتایج جستجو برای: mas pcr

تعداد نتایج: 193504  

2016
Eun-Kyung Cho Jinsup Kim Aram Yang Chang-Seok Ki Ji-Eun Lee Sung Yoon Cho Dong-Kyu Jin

BACKGROUND McCune-Albright syndrome (MAS) is a rare disease defined by the triad of fibrous dysplasia (FD), café au lait spots, and peripheral precocious puberty (PP). Because of the rarity of this disease, only a few individuals with MAS have been reported in Korea. We describe the various clinical and endocrine manifestations and genetic analysis of 14 patients with MAS in Korea. METHODS Pa...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه زنجان - دانشکده کشاورزی 1390

در تحقیق حاضر اقدام به تولید نرم افزار mas گردید. این نرم افزار برای پیش بینی ارزش ارثی از تلفیق اطلاعات کمی و مولکولی استفاده می نماید. بعضی از ژن هایی که یک صفت را کنترل می کنند، می توانند نسبت به بقیه دارای اثرات بزرگی باشند. این قبیل ژن ها، ژن های با اثر بزرگ نامیده می شوند که در -qtl ها (جایگاه صفت کمی) مکان یابی می شوند. دنبال کردن الگوی توارث این قبیل qtl ها می تواند برای کمک به انتخاب م...

Journal: :cell journal 0

objective: global surveillance has shown that drug resistant (dr) tuberculosis (tb) is widespread. prompt detection of mycobacterium tuberculosis drug resistance is essential for effective control of tb. the most frequent mutations associated with isoniazid (inh) resistance in mycobacterium are substitutions at codons 315 in the katg gene and the maba-inha promoter region (−15). this survey eva...

Ahmad Reza Bahrmand, Elham Safarpour, Mahnaz Saifi, Morteza Masoumi, Somayeh Bahrami,

  Tuberculosis is a serious global public health problem and its high prevalence is stron gly associated with the enhancement of drug resistance. In this study we demonstrate a multiplex allele-specific polymerase chain reaction (MAS)-PCR assay to simultaneously detect mutations in the first and third bases of the embB gene codon 306 ATG in ethambutol (EMB) resistant isolates of Mycobacterium t...

مسجدی, محمد رضا , بیگلری , علیرضا , دین محمدی , فریده , رمضان زاده, رشید , فرنیا, پریسا , ولایتی , علی اکبر , کاظم پور , مهدی ,

چکیده زمینه و هدف: ایزونیازید یکی از داروهای مهم خط اول درمان سل می‌باشد. مقاومت به این دارو در بسیاری از نقاط جهان رو به افزایش است. جهش‌های ایجاد شده در ژنKatG و inhA در اغلب موارد عامل مقاومت به ایزونیازید می‌باشند. هدف از این مطالعه ارائه روشی مناسب و سریع برای شناسایی موتاسیونهای مرتبط با مقاومت به ایزونیازید در مایکوباکتریوم توبرکلوزیس می‌باشد. روش بررسی: در این مطالعه وجود جهش در نوا...

2011
Ainong Shi Richard Vierling Richard Grazzini Pengyin Chen Homer Caton Dilip Panthee

Tomato spotted wilt virus (TSWV) is one of the most destructive viral diseases that threaten worldwide tomato (Solanuum lycopersicum L. syn Lycopersicon esculentum Mill.) production. Use of host resistance appears to be the best way to control the disease. Marker assisted selection (MAS) has become very important and useful in the selection of TSWV resistance genes. The objective of this resear...

2011
Kimia Taghavi Parissa Farnia Mohammad Varahram Fatemeh Maryam Sheikhoslami Mojtaba Ahmadi Mehdi Kazempoor Mohammad Reza Masjedi Ali Akbar Velayati

OBJECTIVE Global surveillance has shown that drug resistant (DR) tuberculosis (TB) is widespread. Prompt detection of Mycobacterium tuberculosis drug resistance is essential for effective control of TB. The most frequent mutations associated with Isoniazid (INH) resistance in Mycobacterium are substitutions at codons 315 in the katG gene and the mabA-inhA promoter region (-15). This survey eval...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1996
A K Azad T D Sirakova L M Rogers P E Kolattukudy

A single gene (mas) encodes the multifunctional enzyme that catalyzes the synthesis of very long chain multiple methyl branched fatty acids called mycocerosic acids that are present only in slow-growing pathogenic mycobacteria and are thought to be important for pathogenesis. To achieve a targeted disruption of mas, an internal 2-kb segment of this gene was replaced with approximately the same ...

Journal: :Clinica chimica acta; international journal of clinical chemistry 2010
Rui Bi A-Mei Zhang Dandan Yu Diana Chen Yong-Gang Yao

BACKGROUND Leber hereditary optic neuropathy (LHON) is one of the most common mitochondrial diseases, which is mainly caused by three mitochondrial DNA (mtDNA) mutations (m.3460G>A, m.11778G>A and m.14484T>C). Incomplete penetrance suggests that there might be asymptomatic carriers in general populations. These asymptomatic carriers are clinically important as they are potential future patients...

Journal: :journal of medical microbiology and infectious diseases 0
somayeh bahrami department of microbiology, science and research branch, islamic azad university, tehran, iran ahmad reza bahrmand department of mycobacteriology, pasteur institute of iran, tehran, iran elham safarpour department of mycobacteriology, pasteur institute of iran, tehran, iran morteza masoumi department of mycobacteriology, pasteur institute of iran, tehran, iran mahnaz saifi department of mycobacteriology, pasteur institute of iran, tehran, iran

tuberculosis is a serious global public health problem and its high prevalence is stron gly associated with the enhancement of drug resistance. in this study we demonstrate a multiplex allele-specific polymerase chain reaction (mas)-pcr assay to simultaneously detect mutations in the first and third bases of the embb gene codon 306 atg in ethambutol (emb) resistant isolates of mycobacterium tub...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید