نتایج جستجو برای: ii gene

تعداد نتایج: 1650532  

انصاری پیرسرایی, زربخت, بی‌ پروا, پوریا, دیرنده, عیسی, سربزی فرح آباد, افسانه,

   One of the problems of the poultry industry is a lack of flocks in broiler farms Although it in the factories of hatchery broiler chickens and turkey, often Sexing chickens to are selling commercial growers, because sex differences in growth rate and feed efficiency, separating males and females to the necessary recurrence needs of uniform and specified market in terms of production carcasse...

Ghorbanali Nematzadeh, Hossein Askari, Saeed Ghahary, Seyyed Hamidreza Hashemi-Petroudi

DNA methylation as epigenetic mark plays a key role in normal differential and developmental processes as well as in dynamic gene regulation at the genomic level. To assess DNA methylation pattern in different developmental stages of Aeluropus littoralis, methylation sensitive amplified polymorphism (MSAP) was used. Methylation and demethylation status at the CCGG recognition site were...

Journal: :Journal of Biological Chemistry 1995

Abbas Ghaderi, Mehrdad Lotfazar Shirin Farjadian,

Background: Papillon-Lefevre syndrome (PLS) is a rare autosomal recessive disorder characterized by palmoplantar hyperkeratosis and early development of aggressive pe-riodontitis. Although cathepsin C (CTSC) gene mutations have been established in about 70-80% of PLS patients, it is assumed that the patients may have dysfunctioning of immune defense mechanisms. Objective: To assess the associat...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه شهید باهنر کرمان - پژوهشکده علوم 1391

پنج کمپلکس جدید،از ترکیب لیگاند dpptبا نمک های کلرید، استات و نیترات از فلزات دو ظرفیتی کادمیم، مس، منگنز وکبالت ، تهیه گردیده وبا اسپکتروسکوپی های جرمی، الکترونی، مادون قرمز،آنالیز عنصری و کریستالوگرافی ایکس- ری مورد بررسی قرار گرفته اند.تحقیقات اسپکتروسکوپی برای تمامی این ترکیبات تک هسته ای ،عدد کوئوردیناسیون شش با ساختار هندسی اکتاهدرال را پیشنهاد میدهد.

برزگر, محمد, جبارپور بنیادی, مرتضی, عمرانی, امید,

Background and Objectives: The neuromuscular degenerative disorder, known as spinal muscular atrophy (SMA), is a common fatal disease in neonates. In most patients with SMA, exon 7 and/or exon 8 of SMN1 gene is deleted. It is reported that the deletion of exon 5 from NAIP gene may be involved in the severity of SMA disease. The present study was aimed to evaluate the genotype- phenotype correla...

Journal: :گوارش 0
saeid latifinavid farideh siavoshi hafez fakheri afsaneh sharifian hossein nobakht ramin tavafzadeh

background:â there is a relationship between specific genotypes of helicobacter pylori caga and vaca genes and the increased risk of peptic ulcer diseases and gastric cancer. these genes also possess strong patterns of geographical differentiation. the present study aims to determine the patterns of variation of the virulence genes in iran and their association with clinical status. materials a...

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