Results 31 to 40 of about 282,884 (301)

An Insight into Ocular Genetics

open access: yesDelhi Journal of Ophthalmology, 2017
Over the past decade, there has been an exponential increase in the database of heritable eye disorders. More than 100,000 germline mutations reported in more than 3,700 different human nuclear genes are associated with inherited diseases.
Shilpa Bisht   +3 more
doaj   +1 more source

Unique and conserved MicroRNAs in wheat chromosome 5D revealed by next-generation sequencing [PDF]

open access: yes, 2013
MicroRNAs are a class of short, non-coding, single-stranded RNAs that act as post-transcriptional regulators in gene expression. miRNA analysis of Triticum aestivum chromosome 5D was performed on 454 GS FLX Titanium sequences of flow sorted chromosome 5D
Hikmet Budak (150694)   +15 more
core   +2 more sources

Amniotic fetal stem cells – derived endothelial progenitors, a support for personalized cardiovascular regenerative medicine [PDF]

open access: yesArchives of the Balkan Medical Union, 2022
Introduction. Worldwide, cardiovascular diseases represent the first cause of morbidity and mortality. The genetic contribution in this pathology is heterogenous, and the microenvironment-genes interactions (mediated by epigenetic mechanisms) influence ...
Cosmin A. BUZILA, Florin IORDACHE
doaj   +1 more source

Predicting the possible effect of miR-203a-3p and miR-29a-3p on DNMT3B and GAS7 genes expression

open access: yesJournal of Integrative Bioinformatics, 2021
Aberrant expression of genes involved in methylation, including DNA methyltransferase 3 Beta (DNMT3B), can cause hypermethylation of various tumor suppressor genes.
Ali Afgar   +3 more
doaj   +1 more source

Regulation of gene expression by micrornas : targeting specificity, kinetics and function [PDF]

open access: yes, 2011
Summary: Understanding gene regulation is a central question of molecular biology. For decades, gene expression was thought to be controlled by a complex network of proteins called transcription factors.
Hausser, Jean Albert René
core   +1 more source

Establishment and Analysis of MicroRNA Prognostic Risk Model of Papillary Thyroid Carcinoma Based on TCGA Database

open access: yesZhongliu Fangzhi Yanjiu, 2020
Objective To construct a risk model for predicting the prognosis of papillary thyroid carcinoma (PTC) patients based on the expression of microRNAs (miRNA).
JIAO Zhaoshuang, ZHANG Huainian
doaj   +1 more source

Circulating microRNA, secreted microRNA and exogenous plant microRNA [PDF]

open access: yesJournal of Translational Medicine, 2012
Dysregulated expression of microRNAs (miRNAs) in various tissues has been associated with a variety of diseases, including cancers. Here we demonstrate that miRNAs are present in the serum and plasma of humans and other animals such as mice, rats, bovine fetuses, calves and horses.
openaire   +1 more source

MicroRNAs in cardiac arrhythmia: DNA sequence variation of MiR-1 and MiR-133A in long QT syndrome. [PDF]

open access: yes, 2014
Long QT syndrome (LQTS) is a genetic cardiac condition associated with prolonged ventricular repolarization, primarily a result of perturbations in cardiac ion channels, which predisposes individuals to life-threatening arrhythmias.
Corfield, VA   +13 more
core   +1 more source

MicroRNA-145-5p Regulates the Epithelial-Mesenchymal Transition in Nasal Polyps by Targeting Smad3 [PDF]

open access: yesClinical and Experimental Otorhinolaryngology
Objectives. The annual prevalence of chronic rhinosinusitis (CRS) is increasing, and the lack of effective treatments imposes a substantial burden on both patients and society.
Mengyu Zhang   +8 more
doaj   +1 more source

miRNAs as Interconnectors between Obesity and Cancer

open access: yesNon-Coding RNA
Obesity and cancer are a concern of global interest. It is proven that obesity may trigger the development or progression of some types of cancer; however, the connection by non-coding RNAs has not been totally explored. In the present review, we discuss
Grecia Denisse González-Sánchez   +4 more
doaj   +1 more source

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