نتایج جستجو برای: lack gene
تعداد نتایج: 1385843 فیلتر نتایج به سال:
Introduction: Congenital long QT syndrome (LQTS) is a cardiac disorder characterized by QT interval prolongation at basal ECG. Different LQTS genes encode ion channel subunits or proteins involved in regulating cardiac ionic currents. Long QT syndrome type 6 (LQT6) is caused by mutation in the KCNE2 gene. Our research aimed to analyze genetic variants of KCNE2 gene causing the disease in Irania...
Detection of Lack Function Mutation p.Q879X Affecting Abortion in APAF1 Gene Holstein Cattle
Fit testing of tight-fitting respiratory protective facepieces has been in use for some years, but there are still widespread misconceptions and misunderstandings about what a fit test pass actually signifies. Various aspects frequently generate research papers, and there are three relevant ones in this issue (Han and Lee, 2005; Kuo et al., 2005; Vaughan and RajanSithamparanadarajah, 2005). In ...
Reporter gene expression vectors have streamlined the dissection of promoters and the analysis of their regulatory elements. It is generally assumed that the vector has no influence on the activity of the promoter. This is a dangerous assumption because any 6-bp recognition sequence will occur on average approximately once every 4 kb, and more frequently, if as little as one deviation from a pe...
تنش دمای پایین یکی از مهم ترین عوامل محیطی است که عملکرد گیاهان را محدود می نماید. شبکه وسیعی از ژن های مختلف در تنظیم تحمل گیاه به این تنش نقش ایفا می نمایند. در این تحقیق، نخست 921 عدد از ژن های مذکور از تحقیقات و مقالات معتبر علمی استخراج گردید و سپس به منظور شناسایی ژن های مشابه با آنها در ژنوم کامل دو گیاه سیب (malus domestica)و انگور (vitis vinifera)، توالی آمینو اسیدی این ژن ها در گیاه م...
Because of two 3σ anomalies, the Standard Model (SM) fit of the precision electroweak data has a poor confidence level, CL = 0.02. Since both anomalies involve challenging systematic issues, it might appear that the SM could still be valid if the anomalies resulted from underestimated systematic error. Indeed the CL of the global fit could then increase to 0.71, but that fit predicts a small Hi...
BACKGROUND Coronary artery disease (CAD) and myocardial infarction (MI) are caused in part by genetic factors. Recently, the MEF2A gene was linked to MI/CAD in a single pedigree with autosomal-dominant pattern of inheritance. In addition, genetic variants within the gene have been associated with MI in case-control settings, producing inconsistent results. METHODS AND RESULTS The MEF2A gene w...
The APC gene at human chromosome 5q21 is responsible for familial adenomatous polyposis coli. Furthermore, sporadic cancers of not only colon but also other digestive organs often contain mutations in the APC gene. A dominant mouse mutation Min that was generated by chemical mutagenesis and causes polyposis in the digestive tract is in the mouse homologue of the human APC gene. The APC mRNA is ...
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