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16.796  Articles
1 of 1.681 pages  |  10  records  |  more records»
Genetic variability of 19 isolates of Grapevine leafroll-associated virus 2 (GLRaV-2) from Portuguese grapevine cultivars was characterized by sequencing the entire capsid protein (CP) gene of the virus. Global phylogenetic analysis of the CP gene, which ... see more

The interaction between genetic factors, blood glucose and hypertension plays a role in the onset of diabetic kidney disease (DKD) in type II diabetes mellitus (T2DM). Genetic variation of TGF-ß1 is associated with renal complication in T2DM with varying ... see more

Current clinical genetic and genomic testing involves genome-wide evaluation of chromosomal abnormalities, copy number variants (CNVs) and gene mutations. The major challenge facing genetic laboratory directors, physicians and counselors is to distinguish... see more

Objectives: To determine the role of two genetic variants, (rs3804594) and (rs1801725), in calcium sensing receptor (CASR) gene with colorectal cancer (CRC) risk in patients visited King Abdulaziz University hospital (KAUH) in Jeddah, Saudi Arabia.Methods... see more

BACKGROUND: Acute first-ever ischemic stroke (FIS) is a heterogeneous, polygenic disorder. The contribution of vascular genetic variants as inherited causes of ischemic stroke has remained controversial.AIM: To examine the association of genetic variants ... see more

Objective. To improve the results of treatment in patients, suffering insufficiency of sutures of intestinal anastomoses, using analysis of rate in the genes polymorphous variants of the matrix metalloproteinase Type 2 (C-1306 ?T) and the tissue inhibitor... see more

The demand for tomatoes is increasing along with population growth. However, this demand needs to be supported by increasing tomato productivity. One way to increase this is the assembly of high-yielding tomato varieties. In the assembly of varieties, the... see more

In Malaysia, Sabah population constitutes the most number of ß-thalassaemia cases ranging from asymptomatic to transfusion dependent. Filipino ß°-deletion has been reported as the predominant mutation in Sabah [1]. Despite having the same primary mutation... see more

A disorder of copper metabolism at Wilson’s disease (WD), conditioned by a mutation of adenosine thriphospate P-type gene (ATP7B), results in irreversible changes in the liver and in the nervous system. Mortality is high at WD, but it is one of hereditary... see more

1 of 1.681 pages  |  10  records  |  more records»