![Ecmel Mehmetbeyoglu Duman](https://profiles-cardiff.imgix.net/attachments/434?w=200&h=200&auto=format&crop=faces&fit=crop&q=90")
Dr Ecmel Mehmetbeyoglu Duman
(hi/ei)
Myfyriwr ymchwil
Cyhoeddiad
2023
- Mehmetbeyoglu Duman, E., Duman, A., Taheri, S., Ozkul, Y. and Rassaulzadegan, M. 2023. From data to insights: machine learning empowers prognostic biomarker prediction in Autism. Journal of Personalized Medicine 13(12), article number: 1713. (10.3390/jpm13121713)
- Mehmetbeyoglu Duman, S. 2023. Imbalance of DNA methylation and demethylation as pathogenic mechanism of acute leukaemia. PhD Thesis, Cardiff University.
2022
- Taheri, S. et al. 2022. The role of apoptosis and autophagy in the hypothalamic-pituitary-adrenal (HPA) axis after traumatic brain injury (TBI). International Journal of Molecular Sciences 23(24), article number: 15699. (10.3390/ijms232415699)
- Taheri, S. et al. 2022. The characterization of sex dfferences in hypoglycemia-induced activation of HPA axis on the transcriptomic level. Cellular and Molecular Neurobiology 42(5), pp. 1523-1542. (10.1007/s10571-021-01043-0)
- Bayram, K. K., Fitremann, J., Bayram, A., Yilmaz, Z., Mehmetbeyoglu, E., Ozkul, Y. and Rassoulzadegan, M. 2022. Mouse neuronal cells outperform in a novel galactonamide molecular gel rather than in neurosphere; comparison of neurogenesis and neuronal differentiation mRNA markers. Presented at: 54th European Society of Human Genetics (ESHG) Conference, 28-31 August 2021European Journal of Human Genetics, Vol. 30. Vol. SUPPL. Springer Nature pp. 259-259., (10.1038/s41431-021-01026-1)
- Satir-Basaran, G. et al. 2022. Mouse paternal RNAs initiate a pattern of metabolic disorders in a line-dependent manner. Frontiers in Genetics 13, article number: 839841. (10.3389/fgene.2022.839841)
- Mehmetbeyoglu, E. et al. 2022. Decrease in RNase HII and accumulation of lncRNAs/DNA Hybrids: a causal implication in psoriasis?. Biomolecules 12(3), article number: 368. (10.3390/biom12030368)
2021
- Dursun, I. et al. 2021. Effect of elamipretide (SS-31) on inflammasom formation in mice model with oxalate nephropathy. Presented at: 53rd ESPN Annual Meeting, Amsterdam, The Netherlands, September 2021, Vol. 36. Vol. 10. Springer Verlag (Germany) pp. 3317-3318., (10.1007/s00467-021-05210-9)
- Bayram, K. K., Fitremann, J., Bayram, A., Yilmaz, Z., Mehmetbeyoglu, E., Ozkul, Y. and Rassoulzadegan, M. 2021. Gene expression of mouse hippocampal stem cells grown in a galactose-derived molecular gel compared to in vivo and neurospheres. Processes 9(4), article number: 716. (10.3390/pr9040716)
- Karaca, Z. et al. 2021. Molecular skin changes in Cushing syndrome and the effects of treatment. Journal of Endocrinological Investigation 44(1), pp. 153-163. (10.1007/s40618-020-01285-7)
- Elcik, D. et al. 2021. Blood mRNA expression profiles of autophagy, apoptosis, and hypoxia markers on blood cardioplegia and custodiol cardioplegia groups. Brazilian Journal of Cardiovascular Surgery 36(3), pp. 331-337. (10.21470/1678-9741-2020-0330)
2020
- Kocyigit, I. et al. 2020. Association of OSR-1 with vascular dysfunction and hypertension in polycystic kidney disease. Therapeutic Apheresis and Dialysis 24(1), pp. 64-71. (10.1111/1744-9987.12814)
2019
- Kocyigit, I. et al. 2019. Systemic succinate, Hypoxia-Inducible factor-1 alpha, and IL-1 beta gene expression in autosomal dominant polycystic kidney disease with and without Hypertension. Cardiorenal Medicine 9(6), pp. 370-381. (10.1159/000500478)
- Gol, M. F., Erdogan, F. F., Bayramov, K. K., Mehmetbeyoglu, E. and Ozkul, Y. 2019. Assessment of genes involved in behavior, learning, memory, and synaptic plasticity following status epilepticus in rats. Epilepsy & Behavior 98(Part A), pp. 101-109. (10.1016/j.yebeh.2019.06.023)
2018
- Eroglu, E. et al. 2018. The association of OSR-1 between vascular dysfunction and hypertension in polycystic kidney disease. Nephrology Dialysis Transplantation 33(Suppl), pp. i65-i65. (10.1093/ndt/gfy104.FP053)
Cynadleddau
- Bayram, K. K., Fitremann, J., Bayram, A., Yilmaz, Z., Mehmetbeyoglu, E., Ozkul, Y. and Rassoulzadegan, M. 2022. Mouse neuronal cells outperform in a novel galactonamide molecular gel rather than in neurosphere; comparison of neurogenesis and neuronal differentiation mRNA markers. Presented at: 54th European Society of Human Genetics (ESHG) Conference, 28-31 August 2021European Journal of Human Genetics, Vol. 30. Vol. SUPPL. Springer Nature pp. 259-259., (10.1038/s41431-021-01026-1)
- Dursun, I. et al. 2021. Effect of elamipretide (SS-31) on inflammasom formation in mice model with oxalate nephropathy. Presented at: 53rd ESPN Annual Meeting, Amsterdam, The Netherlands, September 2021, Vol. 36. Vol. 10. Springer Verlag (Germany) pp. 3317-3318., (10.1007/s00467-021-05210-9)
Erthyglau
- Mehmetbeyoglu Duman, E., Duman, A., Taheri, S., Ozkul, Y. and Rassaulzadegan, M. 2023. From data to insights: machine learning empowers prognostic biomarker prediction in Autism. Journal of Personalized Medicine 13(12), article number: 1713. (10.3390/jpm13121713)
- Taheri, S. et al. 2022. The role of apoptosis and autophagy in the hypothalamic-pituitary-adrenal (HPA) axis after traumatic brain injury (TBI). International Journal of Molecular Sciences 23(24), article number: 15699. (10.3390/ijms232415699)
- Taheri, S. et al. 2022. The characterization of sex dfferences in hypoglycemia-induced activation of HPA axis on the transcriptomic level. Cellular and Molecular Neurobiology 42(5), pp. 1523-1542. (10.1007/s10571-021-01043-0)
- Satir-Basaran, G. et al. 2022. Mouse paternal RNAs initiate a pattern of metabolic disorders in a line-dependent manner. Frontiers in Genetics 13, article number: 839841. (10.3389/fgene.2022.839841)
- Mehmetbeyoglu, E. et al. 2022. Decrease in RNase HII and accumulation of lncRNAs/DNA Hybrids: a causal implication in psoriasis?. Biomolecules 12(3), article number: 368. (10.3390/biom12030368)
- Bayram, K. K., Fitremann, J., Bayram, A., Yilmaz, Z., Mehmetbeyoglu, E., Ozkul, Y. and Rassoulzadegan, M. 2021. Gene expression of mouse hippocampal stem cells grown in a galactose-derived molecular gel compared to in vivo and neurospheres. Processes 9(4), article number: 716. (10.3390/pr9040716)
- Karaca, Z. et al. 2021. Molecular skin changes in Cushing syndrome and the effects of treatment. Journal of Endocrinological Investigation 44(1), pp. 153-163. (10.1007/s40618-020-01285-7)
- Elcik, D. et al. 2021. Blood mRNA expression profiles of autophagy, apoptosis, and hypoxia markers on blood cardioplegia and custodiol cardioplegia groups. Brazilian Journal of Cardiovascular Surgery 36(3), pp. 331-337. (10.21470/1678-9741-2020-0330)
- Kocyigit, I. et al. 2020. Association of OSR-1 with vascular dysfunction and hypertension in polycystic kidney disease. Therapeutic Apheresis and Dialysis 24(1), pp. 64-71. (10.1111/1744-9987.12814)
- Kocyigit, I. et al. 2019. Systemic succinate, Hypoxia-Inducible factor-1 alpha, and IL-1 beta gene expression in autosomal dominant polycystic kidney disease with and without Hypertension. Cardiorenal Medicine 9(6), pp. 370-381. (10.1159/000500478)
- Gol, M. F., Erdogan, F. F., Bayramov, K. K., Mehmetbeyoglu, E. and Ozkul, Y. 2019. Assessment of genes involved in behavior, learning, memory, and synaptic plasticity following status epilepticus in rats. Epilepsy & Behavior 98(Part A), pp. 101-109. (10.1016/j.yebeh.2019.06.023)
- Eroglu, E. et al. 2018. The association of OSR-1 between vascular dysfunction and hypertension in polycystic kidney disease. Nephrology Dialysis Transplantation 33(Suppl), pp. i65-i65. (10.1093/ndt/gfy104.FP053)
Gosodiad
- Mehmetbeyoglu Duman, S. 2023. Imbalance of DNA methylation and demethylation as pathogenic mechanism of acute leukaemia. PhD Thesis, Cardiff University.
- Taheri, S. et al. 2022. The characterization of sex dfferences in hypoglycemia-induced activation of HPA axis on the transcriptomic level. Cellular and Molecular Neurobiology 42(5), pp. 1523-1542. (10.1007/s10571-021-01043-0)
- Satir-Basaran, G. et al. 2022. Mouse paternal RNAs initiate a pattern of metabolic disorders in a line-dependent manner. Frontiers in Genetics 13, article number: 839841. (10.3389/fgene.2022.839841)