Volkan Yazar

ORCID: 0000-0003-3861-0181
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Epigenetics and DNA Methylation
  • Extracellular vesicles in disease
  • Amyotrophic Lateral Sclerosis Research
  • Retinal Development and Disorders
  • interferon and immune responses
  • Cell Adhesion Molecules Research
  • Immune responses and vaccinations
  • SARS-CoV-2 and COVID-19 Research
  • Cancer-related gene regulation
  • Immune cells in cancer
  • Mesenchymal stem cell research
  • Retinopathy of Prematurity Studies
  • Autism Spectrum Disorder Research
  • Graphene and Nanomaterials Applications
  • Renal Diseases and Glomerulopathies
  • Advanced biosensing and bioanalysis techniques
  • Peroxisome Proliferator-Activated Receptors
  • Tissue Engineering and Regenerative Medicine
  • Ubiquitin and proteasome pathways
  • Connexins and lens biology
  • Genomics and Rare Diseases
  • Bacterial Infections and Vaccines
  • Nuclear Receptors and Signaling
  • Histone Deacetylase Inhibitors Research
  • MicroRNA in disease regulation

Bilkent University
2019-2024

Johns Hopkins Medicine
2021-2023

Johns Hopkins University
2021-2023

German Center for Neurodegenerative Diseases
2023

Universität Ulm
2023

Radboud University Nijmegen
2010-2014

Radboud University Medical Center
2014

Non-healing wounds remain a major burden due to the lack of effective treatments. Mesenchymal stem cell-derived exosomes (MSC-Exo) have emerged as therapeutic options given their pro-regenerative and immunomodulatory features. Still, little is known on exact mechanisms mediated by MSC-Exo. Importantly, modulation efficacy through 3D-physiologic cultures together with loading strategies continues underexplored. To uncover MSC-Exo-mediated mechanism via proteomic analyses, use 3D-culture...

10.1016/j.jare.2022.01.013 article EN cc-by-nc-nd Journal of Advanced Research 2022-01-29

To determine the genetic defects underlying autosomal recessive retinitis pigmentosa (arRP) in Dutch population and a subset of patients originating from other countries. The hypothesis was that, because there has been little migration over past centuries certain areas Netherlands, significant fraction arRP carry their defect homozygous state.High-resolution genome-wide SNP genotyping on arrays subsequent homozygosity mapping were performed large cohort 186 mainly nonconsanguineous families...

10.1167/iovs.10-6185 article EN Investigative Ophthalmology & Visual Science 2011-01-07

Immunomodulatory commensal bacteria modify host immunity through delivery of regulatory microbial-derived products to cells. Extracellular membrane vesicles (MVs) secreted from symbiont commensals represent one such transport mechanism. How MVs exert their anti-inflammatory effects or whether tolerance-inducing potential can be used for therapeutic purposes remains poorly defined. In this study, we show that isolated the human lactic acid Pediococcus pentosaceus suppressed Ag-specific...

10.4049/jimmunol.2000731 article EN The Journal of Immunology 2020-10-07

Bietti's crystalline dystrophy (BCD) is a rare, autosomal recessive retinal degenerative disease associated with mutations in CYP4V2. In this study, we describe the genetic and clinical findings 19 unrelated BCD patients recruited from five international clinics. Patients underwent ophthalmic examinations were screened for CYP4V2 by Sanger sequencing quantitative polymerase chain reaction (qPCR) copy number variation screening. Eight found 10/19 patients, including three whom only...

10.1002/mgg3.109 article EN cc-by Molecular Genetics & Genomic Medicine 2014-09-15

Abstract Invasive meningococcal disease (IMD) is caused by Neisseria meningitidis, with the main serogroups responsible for being A, B, C, W, X, and Y. To date, several vaccines targeting N. meningitidis have been developed albeit a short-lived protection. Given that MenW MenB are most common causes of IMD in Europe, Turkey, Middle East, we aimed to develop an outer membrane vesicle (OMV) based bivalent vaccine as heterologous antigen source. Herein, compared immunogenicity, breadth serum...

10.1093/intimm/dxae016 article EN International Immunology 2024-03-27

ALS is a fatal motor neuron disease that displays broad variety of phenotypes ranging from early courses to slowly progressing and rather benign courses. Such divergence can also be seen in genetic cases with varying bearing specific mutations, suggesting epigenetic mechanisms like DNA methylation act as modifiers. However, the epigenotype dictated by, addition other mechanisms, strongly influenced by individual's genotype. Hence, we performed study using EPIC arrays on 7 monozygotic (MZ)...

10.1177/25168657231172159 article EN cc-by-nc Epigenetics Insights 2023-01-01

Abstract Epigenetic remodeling is emerging as a critical process for several neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS). Genetics alone fails to explain the etiology of ALS, investigation epigenome might therefore provide novel insights into molecular mechanisms disease. In this study, we interrogated epigenetic landscape in peripheral blood mononuclear cells (PBMCs) familial ALS (fALS) patients with either chromosome 9 open reading frame 72 ( C9orf72 ) or...

10.1038/s41598-023-38684-8 article EN cc-by Scientific Reports 2023-07-25

Doxorubicin (Dox) is one of the most widely used treatments for breast cancer, although limited by well-documented cardiotoxicity and other off-target effects. Mesenchymal stem cell (MSC) secretome has shown immunomodulatory regenerative properties, further potentiated under 3D conditions. This work aimed to uncover effect MSC-derived from (CM3D) or 2D (CM2D) cultures, in human malignant cells (MDA-MB-231), non-tumor epithelial (MCF10A) differentiated AC16 cardiomyocytes, co-treated with...

10.3390/ijms222313072 article EN International Journal of Molecular Sciences 2021-12-03

Immune-mediated inflammation must be down-regulated to facilitate tissue remodeling during homeostatic restoration of an inflammatory response. Uncontrolled or over-exuberant immune activation can cause autoimmune diseases, as well destruction. A151, the archetypal example a chemically synthesized suppressive oligodeoxynucleotide (ODN) based on repetitive telomere-derived TTAGGG sequences, was shown successfully down-regulate variety responses. However, degree, duration and breadth...

10.1093/intimm/dxz059 article EN International Immunology 2019-09-20

Abstract The transcriptional repressor called parkin interacting substrate (PARIS; ZNF746) was initially identified as a novel co-substrate of and PINK1 that leads to Parkinson’s disease (PD) by disrupting mitochondrial biogenesis through peroxisome proliferator-activated receptor gamma (PPARγ) coactivator -1α (PGC-1α) suppression. Since its initial discovery, growing evidence has linked PARIS defective observed in PD pathogenesis. Yet, dopaminergic (DA) neuron-specific mechanistic...

10.1038/s41598-021-00858-7 article EN cc-by Scientific Reports 2021-11-02

Since previous research suggests a role of circulating factor in the pathogenesis steroid-sensitive nephrotic syndrome (NS), we speculated that plasma extracellular vesicles (EVs) are candidate source such soluble mediator. Here, aimed to characterize and try delineate effects these EVs vitro. Plasma from 20 children with NS relapse remission, 10 healthy controls, 6 disease controls were obtained by serial ultracentrifugation. Characterization was performed electron microscopy, flow...

10.1152/ajprenal.00097.2021 article EN AJP Renal Physiology 2021-09-27

Homeostatic restoration of an inflammatory response requires quenching the immune system after pathogen threats vanish. A continued assault orchestrated by host defense results in tissue destruction or autoimmunity. A151 is epitome synthetic oligodeoxynucleotides (ODNs) that curb a subset white corpuscles through repetitive telomere-derived TTAGGG sequences. Currently, genuine effect on cell transcriptome remains unknown. Here, we leveraged integrative approach where weighted gene...

10.1016/j.omtn.2023.02.004 article EN cc-by-nc-nd Molecular Therapy — Nucleic Acids 2023-02-04

Abstract Epigenetic remodeling is emerging as a critical process for several neurodegenerative diseases, including Amyotrophic Lateral Sclerosis (ALS). Genetics alone fails to explain the etiology of ALS, investigation epigenome might therefore provide novel insights into molecular mechanisms disease. In this study, we interrogated epigenetic landscape in peripheral blood mononuclear cells (PBMCs) familial ALS (fALS) patients with either chromosome 9 open reading frame 72 ( C9orf72 ) or...

10.21203/rs.3.rs-2672952/v1 preprint EN cc-by Research Square (Research Square) 2023-03-14

The lower than expected number of SARS-CoV-2 cases in countries with fragile health systems is puzzling Herein, we hypothesize that BCG vaccination policies and vaccine strain preferences adopted by different might influence the transmission patterns and/or COVID-19 associated morbidity mortality We also postulate until a specific developed, vulnerable populations could be immunized vaccines to attain heterologous nonspecific protection from new coronavirus In lights our investigations most...

10.25002/tji.2020.1250 article EN Turkish Journal of Immunology 2020-01-01
Coming Soon ...