نتایج جستجو برای: G genotyping

تعداد نتایج: 462990  

شریف, مهدی, فخار, مهدی, کیالاشکی, الهام,

Giardia lamblia (G. lamblia) is one of most common intestinal parasites that infect a wide range of vertebrates including human, farm, and wild animals. Molecular studies indicate G. lamblia as a complex species, consisting of eight genetic assemblages (A to H). Recently, giardiasis has been identified as a zoonotic parasitic disease. The goal of this narrative study was to review the epidem...

ژورنال: تحقیقات دامپزشکی 2020

زمینۀ مطالعه: روتاویروس‌های گروه A یکی از مهمترین عوامل مسبب گاستروانتریت و عامل 30 تا 50 درصد موارد اسهال نوزاد انسان و سایر حیوانات می‌باشند. ژنوتیپ G این ویروس‌ها بر اساس توالی ژن رمز کننده پروتئین سطحی این ویروس‌ها (VP7) تعیین شده که یکی از مهمترین عوامل القاء کننده ایمنی علیه ویروس است و نسبت به هر ژنوتیپ اختصاصی عمل می‌کند. هدف: در مطالعه حاضر احتمال وقوع ژنوتیپ‌های رایج روتاویروس A...

Journal: :Journal of animal science 2012
A A Boligon N Long L G Albuquerque K A Weigel D Gianola G J M Rosa

Genomewide marker information can improve the reliability of breeding value predictions for young selection candidates in genomic selection. However, the cost of genotyping limits its use to elite animals, and how such selective genotyping affects predictive ability of genomic selection models is an open question. We performed a simulation study to evaluate the quality of breeding value predict...

Journal: :iranian journal of public health 0
samaneh hajihoseini genetics division, dept. of biology, faculty of sciences, university of isfahan, isfahan, iran. majid motovali-bashi genetics division, dept. of biology, faculty of sciences, university of isfahan, isfahan, iran. mohammad amin honardoost molecular and cellular division, dept. of biology, faculty of sciences, university of isfahan, isfahan, iran. nader alerasool genetics division, dept. of biology, faculty of sciences, university of isfahan, isfahan, iran.

β-thalassemia, a monogenic autosomal recessive disorder, is prevalent in middle east, particularly in iran. in iran, near to 20 mutations in the β-globin gene are introduced as common mutations with varying incidence frequencies in each city. therefore, detection and screening for couples at high risk can help to solve the problems of this disease. in this study, optimized genotyping of two com...

Journal: :Meždunarodnyj vestnik veterinarii 2023

The study examined the effect of polymorphism fibroblast growth factor 21 gene (Bos taurus FGF21 g.940 C/T) on level and biochemical metabolic parameters in blood serum highproducing cows. DNA genotyping 148 animals Holstein cows was performed by a PCR-RFLP method. As result genotyping, two FGFC – 0.642 FGFT 0.358 alleles as well FGFCC 28.4% (42 animals) FGFTC 71.6% (106 genotypes were identifi...

2008
Cameron N. Gundry Steven F. Dobrowolski Y. Ranae Martin Thomas C. Robbins Lyle M. Nay Nathan Boyd Thomas Coyne Mikeal D. Wall Carl T. Wittwer David H.-F. Teng

Genotyping by high-resolution melting analysis of small amplicons is homogeneous and simple. However, this approach can be limited by physical and chemical components of the system that contribute to intersample melting variation. It is challenging for this method to distinguish homozygous G::C from C::G or A::T from T::A base-pair neutral variants, which comprise approximately 16% of all human...

2013
Keijiro Mizukami Akira Yabuki Hye-Sook Chang Mohammad Mejbah Uddin Mohammad Mahbubur Rahman Kazuya Kushida Moeko Kohyama Osamu Yamato

A single nucleotide substitution (c.-6-180T>G) associated with resistance to phenobarbital therapy has been found in the canine MDR1/ABCB1 gene in Border Collies with idiopathic epilepsy. In the present study, a PCR-restriction fragment length polymorphism assay was developed for genotyping this mutation, and a genotyping survey was carried out in a population of 472 Border Collies in Japan to ...

Abdul Khaliq Naveed Shakir Khan, Tausif Ahmed Rajput Zia-Ur Rehman Farooqi

Objective(s):Organic anion transporter polypeptide 1B1 (OATP1B1) encoded by solute carrier organic transporter 1B1 (SLCO1B1) gene; a transporter involved in the uptake of drugs and endogenous compounds is present in hepatocyte sinusoidal membrane. Aim of this study was to investigate the frequencies of functionally significant SNPs (388A>G and 521T>C) and their haplotypes in 6 ethnic groups of ...

Journal: :Journal of preventive medicine and hygiene 2006
T Grassi A De Donno M Guido G Gabutti

Rotaviruses are the most common agents of diarrhoeal illness in infants and young children. Gastroenteritis caused by rotaviruses is also more likely to be associated with severe dehydration compared to other viral gastroenteritis. We determined the G-genotype of rotaviruses circulating in the Salento. During 2004, 144 stool samples were collected from subjects with a positive screening test an...

Journal: :Clinical chemistry 2007
Kyriaki Glynou Petros Kastanis Sotiria Boukouvala Vassilis Tsaoussis Penelope C Ioannou Theodore K Christopoulos Joanne Traeger-Synodinos Emmanuel Kanavakis

BACKGROUND Hemoglobinopathies are the most common inherited diseases worldwide. Various methods for genotyping of hemoglobin, beta (HBB) gene mutations have been reported, but there is need for a high sample-throughput, cost-effective method for simultaneous screening of several mutations. We report a method that combines the high detectability and dynamic range of chemiluminescence with the hi...

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