نتایج جستجو برای: beta globin introns

تعداد نتایج: 201054  

Journal: :iranian biomedical journal 0
مریم آیت الهی maryam ayatollahi احمد مرات ahmad merat منصور حق شناس mansour haghshenas

the restriction enzyme ava ii detects the base change of the intervening sequence ii (ivs ii) which is used as one of the markers of β-globin gene polymorphism. this study was conducted to determine the frequency of the ava ii site on the β-globin gene among normal people and patients with sickle cell syndrome (scs) in iran. dna fragments containing the ivs ii region of the β-globin gene from 3...

Alihossein Saberi, Gholamreza Shariati, Hamid Galehdari, Ladan Dawoody Nejad, Marziye Mohammadi-Anaei, Mohammad Hamid,

Background: β-thalassemia is one of the most widespread disease in the world, including Iran. In this study, we reported, for the first time, A 290-bp β-globin gene deletion in the south of Iran. Methods: Four individuals from three unrelated families with Arabic ethnic background were studied in Khuzestan Province. Red blood cell indices and hemoglobin analysis were carried out accor...

Journal: :Nucleic Acids Research 2005
Shouhong Guang Janet E. Mertz

Most mRNA-encoding genes require introns for efficient expression in high eukaryotes. However, mRNAs can efficiently accumulate in the cytoplasm without intron excision if they contain cis-acting elements such as the post-transcriptional regulatory element (PRE) of hepatitis B virus (HBV), the constitutive transport element (CTE) of Mason-Pfizer monkey virus (MPMV), or the pre-mRNA processing e...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه علوم بهزیستی و توانبخشی - پژوهشکده علوم بهزیستی 1390

چکیده ناحیه ی 5`hs4 beta globin lcr در 86 بیمار تالاسمی که ژنوتیپ بتا گلوبین هموزیگوت و یا هتروزیگوت مرکب داشتند بررسی شد. با مقایسه ی داده های بدست آمده از این مطالعه و داده های موجود از سایر نواحی مرتبط در جمعیت بیمار و 101 فرد نرمال مشخص شد که فرکانس آلل g در 5`beta globin lcr hs4 و xmn1- hbg2 مثبت در بیماران تالاسمی نسبت به جمعیت نرمال بالاتر است. ناهمسنگی پیوستگی بین آلل g، xmn1- hbg2 مثب...

Background & aims: Hemophilia B is caused by either functional deficiency or lack of the human coagulation factor IX (hFIX). The current protein-based therapy with plasma-derived proteins increases, the risk of blood-borne pathogens transmission. Therefore, replacement therapy with recombinant hFIX (rhFIX) is an attractive alternative to plasma derived hFIX concentrates. In order to express and...

Journal: :Nucleic acids research 1996
X Liu J E Mertz

Most pre-mRNAs require an intron for efficient processing in higher eukaryotes. However, not all introns can provide this function. For example, transcripts synthesized from a variant of the human beta-globin gene lacking its second intervening sequence (IVS2), yet retaining its first intervening sequence (IVS1), exhibit multiple defects in mRNA biogenesis. To investigate why, we transfected in...

Background: Beta thalassemia is a common health problem in Iran especially in Northern provinces. Premarital screening for thalassemia is compulsory in Iran and identification of the carriers is based on primary CBC (Cell Blood Count) and hemoglobin electrophoresis. Silent mutations on β-globin gene have borderline or normal hematological indices that cannot be detected in premarital scree...

Journal: :مجله دانشگاه علوم پزشکی شهید صدوقی یزد 0
محمدعلی حسینپورفیضی ma hosseinpour feizi عباسعلی حسینپورفیضی aa hosseinpour feizi ناصر پولادی n pouladi مهدی حقی m haghi پروین آذرفام p azarfam

introduction: recent molecular studies on iranian β-thalassemia genes revealed the presence of eight common mutations associated with thalassemia. although these mutations are frequent, there are other rare and unknown mutations that can create large problems in designing preventive programs. we detected and explained the common mutations in north-western iran previously and detection of the ra...

ژورنال: پژوهش در پزشکی 2015

Background: Beta thalassemia is one of the autosomal recessive diseases that related to synthesis disorder of beta globin chain. It is caused by any of the more than 200 mutations in the β-globin gene. DNA sequencing and genotyping of numerous mutations at beta globin gene is timely and expensive. Therefore, the best method for screening is linkage using polymorph markers at beta globin region ...

Journal: :Blood 1996
J E Russell S A Liebhaber

Controls that act at both transcriptional and posttranscriptional levels assure that globin genes are highly expressed in developing erythroid cells. The extraordinary stabilities of alpha- and beta-globin mRNAs permit globin proteins to accumulate to substantial levels in these cells, even in the face of physiologic transcriptional silencing. Structural features that determine alpha-globin mRN...

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