A5046741111- Genetics and Neurodevelopmental Disorders
- Autism Spectrum Disorder Research
- MicroRNA in disease regulation
- Autophagy in Disease and Therapy
- Advanced biosensing and bioanalysis techniques
- Mechanical Circulatory Support Devices
- Parkinson's Disease Mechanisms and Treatments
- Cardiovascular Issues in Pregnancy
- Cancer-related molecular mechanisms research
- Ion channel regulation and function
- Circular RNAs in diseases
- Pancreatic function and diabetes
- Vestibular and auditory disorders
- Nitric Oxide and Endothelin Effects
- Multiple Sclerosis Research Studies
- Effects of Vibration on Health
Erciyes University
2019-2025
Abstract Background The aim of this research is to access the expression adenosine A3 receptor (ADORA3) and nitric oxide synthase 3 (NOS3) genes serum levels ADORA3 NOS3 in patients with multiple trauma hemorrhagic shock. Materials methods study was performed at Erciyes University between November 2022 March 2024, a prospective controlled manner. Patients diagnosed traumatic shock requiring transfusion emergency department were selected as group. Gene expressions analyzed using quantitative...
Autism spectrum disorder (ASD) is characterized by impairments in social interaction and the presence of stereotypy restrictive behavior. The clinical heterogeneity ASD makes it difficult to explain mechanisms underlying disease. In recent years, association between autophagy neuropsychiatric diseases has been investigated. this review, we aimed elucidate relationship autism mechanism well-known relevant animal models. Autophagy a cell-protective that allows cell survival low nutrient...
Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder, with highly variable expression of phenotypes (restricted interest or activity and repetitive behavior in communication social interactions), genes (mutation), markers (alteration transcription) pathways. Loss function the CC2D1A gene appears to primarily affect brain, leading range behavioral problems humans. In our study published 2020; we found that expressions miR-19a-3p, miR-361-5p, miR-150-5p, miR-3613-3p,...
Autism spectrum disorder (ASD) is a complex neurodevelopmental with highly variable expression of phenotypes (restricted interest or activity and repetitive behavior in communication social interactions), genes (mutation), markers (alteration transcription) pathways. Loss function the CC2D1A gene appears to primarily affect brain, leading range behavioral problems humans. In our study published 2020, we found that expressions miR-19a-3p, miR-361-5p, miR-150-5p, miR-3613-3p, miR-126-3p...
Objective: Multiple sclerosis, a demyelinating disease of the central nervous system, is characterized by weakness arms and legs, sensory symptoms, ataxia, fatigue, diplopia, memory, concentration, attention disorder, motor speech disorder. Common symptoms include epileptic seizures, cognitive impairment, hearing loss, cortical symptoms. Materials Methods: This study evaluated patients' mental functions with multiple sclerosis (MS) considering their auditory vestibular functions. A total 30...