16 results match your criteria: "United Arab University[Affiliation]"

Effect of acetylcholinesterase inhibition on immune cells in the murine intestinal mucosa.

Heliyon

July 2024

Department of Biochemistry and Molecular Biology, College of Medicine and Health Sciences, United Arab University, Al-Ain, United Arab Emirates.

The gastrointestinal tract (GI) is the largest immune organ whose function is controlled by a complex network of neurons from the enteric nervous system (ENS) as well as the sympathetic and parasympathetic system. Evolving evidence indicates that cross-communication between gut-innervating neurons and immune cells regulates many essential physiological functions including protection against mucosal infections. We previously demonstrated that following paraoxon treatment, 70 % of the mice were able to survive an oral infection with , a virulent strain of serovar Typhimurium.

View Article and Find Full Text PDF

Terahertz frequency has promising applications in communication, security scanning, medical imaging, and industry. THz absorbers are one of the required components for future THz applications. However, nowadays, obtaining a high absorption, simple structure, and ultrathin absorber is a challenge.

View Article and Find Full Text PDF

Introduction: Vitamin D deficiency and insufficiency are highly prevalent among several populations across the globe. Numerous studies have shown a significant correlation between body-mass-index (BMI) and Vitamin D status, however, some results differed according to ethnicity. Despite the abundance of sunshine throughout the year, vitamin D deficiency is prominent in the United Arab Emirates (UAE).

View Article and Find Full Text PDF

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes the cytokine release syndrome (CRS) and leads to multiorgan dysfunction. Mitochondrial dynamics are fundamental to protect against environmental insults, but they are highly susceptible to viral infections. Defective mitochondria are potential sources of reactive oxygen species (ROS).

View Article and Find Full Text PDF

β2-microglobulin (β2-m), a 11.8 kDa protein, pairs non-covalently with the α3 domain of the major histocompatibility class (MHC) I α-chain and is essential for the conformation of the MHC class I protein complex. Shed β2-m is measurable in circulation, and various disorders are accompanied by increases in β2-m levels, including several viral infections.

View Article and Find Full Text PDF

Calcium-induced calcium release in astroglia-a view "from the inside".

Pflugers Arch

April 2020

Department of Physiology, College of Medicine and Health Sciences, United Arab University, Al Ain, UAE.

View Article and Find Full Text PDF

Correction: A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome.

Genet Med

May 2020

Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine, and Health, The University of Manchester, Manchester, UK.

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

View Article and Find Full Text PDF

A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome.

Genet Med

May 2020

Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine, and Health, The University of Manchester, Manchester, UK.

Purpose: To investigate if specific exon 38 or 39 KMT2D missense variants (MVs) cause a condition distinct from Kabuki syndrome type 1 (KS1).

Methods: Multiple individuals, with MVs in exons 38 or 39 of KMT2D that encode a highly conserved region of 54 amino acids flanked by Val3527 and Lys3583, were identified and phenotyped. Functional tests were performed to study their pathogenicity and understand the disease mechanism.

View Article and Find Full Text PDF
Article Synopsis
  • The original article had a typo in the Results section where Subject 17 was mistakenly referred to as Subject 1.
  • This Correction article provides the accurate statement regarding the subjects.
  • The original article has since been updated to reflect this correction.
View Article and Find Full Text PDF
Article Synopsis
  • Neurodevelopmental disorders are diverse and can involve developmental delay, intellectual disability, and autism spectrum disorders, with a few mutations linked to the TCF20 gene potentially causing these issues.
  • Using exome sequencing and microarray analysis, researchers identified numerous damaging variants in the TCF20 gene within affected individuals and families.
  • The study found 25 unique pathogenic variants in TCF20 across 32 patients, with common symptoms like developmental delay, intellectual disability, and hypotonia, suggesting a new syndrome similar to Smith-Magenis syndrome.
View Article and Find Full Text PDF

Inflammation is a crucial defense mechanism that protects the body from the devastating effects of invading pathogens. However, an unrestrained inflammatory reaction may result in systemic manifestations with dire consequences to the host. The extent of activation of the inflammatory response is tightly regulated through immunological and neural pathways.

View Article and Find Full Text PDF

Clinical, immunologic, and genetic spectrum of 696 patients with combined immunodeficiency.

J Allergy Clin Immunol

April 2018

Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children's Medical Center, Tehran, and the University of Medical Science, Tehran, Iran; Primary Immunodeficiency Diseases Network (PIDNet), Universal Scientific Education and Research Network (USERN), Tehran, Iran. Electronic address:

Background: Combined immunodeficiencies (CIDs) are diseases of defective adaptive immunity with diverse clinical phenotypes. Although CIDs are more prevalent in the Middle East than Western countries, the resources for genetic diagnosis are limited.

Objectives: This study aims to characterize the categories of patients with CIDs in Iran clinically and genetically.

View Article and Find Full Text PDF

Type I diabetes (T1D) results from T cell-mediated damage of pancreatic β-cells and loss of insulin production. The cholinergic anti-inflammatory pathway represents a physiological link connecting the central nervous and immune systems vagus nerve, and functions to control the release of proinflammatory cytokines. Using the multiple low-dose streptozotocin (MLD-STZ) model to induce experimental autoimmune diabetes, we investigated the potential of regulating the development of hyperglycemia through administration of paraoxon, a highly specific acetylcholinesterase inhibitor (AChEI).

View Article and Find Full Text PDF
Article Synopsis
  • Aging increases the risk of neurodegenerative diseases by disrupting proteostasis, leading to harmful protein aggregates like α-synuclein, which is linked to Parkinson's disease.
  • Research using C. elegans models showed that aging-related genetic variations speed up the spread of these aggregates and worsen disease symptoms, including nerve damage and shorter lifespan.
  • Anti-aging treatments improved lysosomal function and slowed both aggregate transmission and the progression of related health issues, highlighting a connection between aging, proteostasis, and neurodegenerative disease progression.*
View Article and Find Full Text PDF

Distribution of AGG interruption patterns within nine world populations.

Intractable Rare Dis Res

November 2014

Department of Biochemistry and Molecular Medicine, University of California Davis, School of Medicine, Davis, CA, USA; ; M.I.N.D. Institute, University of California Davis Medical Center, Davis, CA, USA.

The CGG trinucleotide repeat within the FMR1 gene is associated with multiple clinical disorders, including fragile X-associated tremor/ataxia syndrome, fragile X-associated primary ovarian insufficiency, and fragile X syndrome. Differences in the distribution and prevalence of CGG repeat length and of AGG interruption patterns have been reported among different populations and ethnicities. In this study we characterized the AGG interruption patterns within 3,065 normal CGG repeat alleles from nine world populations including Australia, Chile, United Arab Emirates, Guatemala, Indonesia, Italy, Mexico, Spain, and United States.

View Article and Find Full Text PDF