نتایج جستجو برای: ivsi 110 mutation
تعداد نتایج: 330963 فیلتر نتایج به سال:
Background: Xmn-1 polymorphism of 𝜸Gglobin gene (HBG2) is a prominent quantitative trait loci (QTL) in β-thalassemia intermediate (β-TI). In current study, we evaluated the frequency of Xmn-1 polymorphism and its association with β-globin gene (HBB) alleles and Hb F level in β-TI patients in Sistan and Balouchestan province, south-east of Iran. Subjects and Methods: 45 β-TI patients were enroll...
The mutation spectrum of 175 β-thalassemia (β-thal) carriers, identified in pilot carrier screening on 22,713 individuals from Balearic Islands (Spain), is reported. The β(0) CD39 (C>T) mutation is the most frequent (61.1%), followed by β(+) IVS-I-110 (G>A) (12.0%), β(+) IVS-I-6 (T>C) and β(0) IVS-1-1 (G>A) (3.4% both) and eight other rare mutations (2.9-0.6%); with a distinct prevalence and di...
سابقه و هدف: تالاسمی، به عنوان یکی از شایع‌ترین بیماری‌های ژنتیکی، در بسیاری از کشورهای جهان دیده شده است. دو نوع رایج از تالاسمی آلفا و بتا وجود دارد. شیوع جهش‌های مسبب تالاسمی در نقاط مختلف دنیا و حتی در درون کشور ما در نژادهای مختلف، متفاوت است. افزون بر روش‌های تشخیصی بالینی و بیوشیمیایی و هماتولوژیک، روش‌های مولکولی برای تشخیص پیش از زایمان تالاسمی نیز به کار می‌روند. بر اساس مطالعه حاضر، ...
The existence of several periodic structures (known as gliders) in the evolution space of the one-dimensional cellular automaton Rule 110, has important lines of investigation in cellular automata theory such as: complex behavior, universal computation and self-reproduction. We investigate the types of gliders, their properties and production through collisions in Rule 110 and their representat...
In this study we have characterised by oligonucleotide hybridisation and direct restriction endonuclease analysis the beta thalassaemia mutation in 494 Sardinian beta thalassaemia heterozygotes. The most prevalent mutation, accounting for 95.4% of the cases, was the nonsense mutation at codon 39. The remainder, in decreasing order of frequency, were a frameshift at codon 6 (2.2%), beta + IVS-1,...
BACKGROUND Childhood obstructive sleep apnoea (OSA) is suggested to be associated with cardiac structural abnormalities and dysfunction but existing evidence is limited and the treatment effect on echocardiographic outcome remains controversial. OBJECTIVE To examine the presence of subclinical cardiac abnormalities in childhood OSA and the effects of treatment on cardiac changes. METHODS Po...
Kabuki syndrome is a rare, multiple malformation disorder characterized by a distinctive facial appearance, cardiac anomalies, skeletal abnormalities, and mild to moderate intellectual disability. Simplex cases make up the vast majority of the reported cases with Kabuki syndrome, but parent-to-child transmission in more than a half-dozen instances indicates that it is an autosomal dominant diso...
Background Ghezel sheep are highly prolific and one of the local sheep breeds in Iran and Turkey. Growth differentiation factor-9 (GDF9) gene has been found to be essential for growth and differentiation of early ovarian follicles. Novel mutations in GDF9 have been associated with increased ovulation rates and high litter sizes in heterozygous carriers. Therefore, fecundity gene for GDF9 (FecGH...
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