fulya tuzcu gurkan

Dr. fulya tuzcu gurkan

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Research Focus & Metrics

Academic Career Length

9Years (2018-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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16 April 2018 in Journal of Biochemical and Molecular Toxicology
Verified
Journal Article
Closed access
PDF file
OEOytun Erbaş
Oytun Erbaş
MEMumin Alper Erdogan
Mumin Alper Erdogan
AKAsghar Khalilnezhad
Asghar Khalilnezhad
VSVolkan Solmaz
Volkan Solmaz
FGfulya tuzcu gurkan
fulya tuzcu gurkan
DTDilek Taskiran
Dilek Taskiran

9 July 2018 in International Journal of Developmental Neuroscience
Verified
Journal Article
Closed access
OEOytun Erbas
Oytun Erbas
MEMumin Alper Erdogan
Mumin Alper Erdogan
AKAsghar Khalilnezhad
Asghar Khalilnezhad
FGfulya tuzcu gurkan
fulya tuzcu gurkan
GYGürkan Yiğittürk
Gürkan Yiğittürk
DTDilek Taskiran
Dilek Taskiran

8 April 2019 in Molecules
Verified
Journal Article
Open access
PDF file
ARMAGAN GÜLİZARMAGAN GÜLİZ
ARMAGAN GÜLİZ
ESElvin Sevgili
Elvin Sevgili
FGfulya tuzcu gurkan
fulya tuzcu gurkan
FKFadime Aydin Kose
Fadime Aydin Kose
TBTuğçe Bilgiç
Tuğçe Bilgiç
Luciano SasoLuciano Saso
Luciano Saso
Recently, nuclear translocation and stability of nuclear factor erythroid 2 (NF-E2)-related factor 2 (Nrf2) have gained increasing attention in the prevention of oxidative stress. The present study was aimed to evaluate the regulatory role of glycogen synthase kinase-3β (GSK-3β) inhibition by tideglusib through the Nrf2 pathway in a cellular damage model. Gene silencing (siRNA-mediated) was performed to examine the responses of Nrf2-target genes (i.e., heme oxygenase-1, NAD(P)H:quinone oxidoreductase1) to siRNA depletion of Nrf2 in MPP+-induced dopaminergic cell death. Nrf2 and its downstream regulated genes/proteins were analyzed using Real-time PCR and Western Blotting techniques, respectively. Moreover, free radical production, the changes in mitochondrial membrane potential, total glutathione, and glutathione-S-transferase were examined. The possible contribution of peroxisome proliferator-activated receptor gamma (PPARγ) to tideglusib-mediated neuroprotection was evaluated. The number of viable cells and mitochondrial membrane potential were increased following GSK-3β enzyme inhibition against MPP+. HO-1, NQO1 mRNA/protein expressions and Nrf2 nuclear translocation significantly triggered by tideglusib. Moreover, the neuroprotection by tideglusib was not observed in the presence of siRNA Nrf2. Our study supports the idea that GSK-3β enzyme inhibition may modulate the Nrf2/ARE pathway in cellular damage and the inhibitory role of tideglusib on GSK-3β along with PPARγ activation may be responsible for neuroprotection.

1 January 2018 in Archives of Neuropsychiatry
Verified
Journal Article
Closed access
MGMuharrem Anil Gurkan
Muharrem Anil Gurkan
FGfulya tuzcu gurkan
fulya tuzcu gurkan
Life is pain. It is important to determine the features and the measurement of pain. Common types of pain are described in multiple sclerosis. One-dimensional and multi-dimensional pain scales, which are also used in different painful diseases, are used in the measurement of these pain. Scoring and recording in one-dimensional pain scales are easy and a better measurement is achieved in acute pain. However, the disadvantage of these scales is that they do not give detailed information about the nature of the pain. Multidimensional pain scales are used in chronic and complex pain. Multidimensional scales have some disadvantage about application by patients because of complexity. The development of specific scales for the better measurement of pain in multiple sclerosis is important for the effective treatment of pain in patients.