Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Hilal AKALIN"'
Autor:
Busra Aynekin, Hilal Akalin, I. Ipek Muderris, Gokhan Acmaz, Hulya Akgun, Izem Olcay Şahin, Nuriye Coşkun Gokce, Zahraa Alzaidi, Gözde Erturk Zararsiz, Yusuf Ozkul, Munis Dundar, Çetin Saatci
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 23, Iss 1, Pp 1-6 (2022)
Abstract Background Circulating tumor cells represent an opportunity for the assessment of early recurrent disease or for real-time tracing of cancer. Glucose Regulated Protein 78 (GRP78) is known in the literature as a stress factor in endometrial c
Externí odkaz:
https://doaj.org/article/8e2dcfbb42284ac5b9fcf6fc2d604e86
Autor:
Sercan Kenanoglu, Nefise Kandemir, Hilal Akalin, Nuriye Gokce, Mehmet F. Gol, Murat Gultekin, Emel Koseoglu, Meral Mirza, Munis Dundar
Publikováno v:
Global Medical Genetics, Vol 09, Iss 02, Pp 110-117 (2022)
Alzheimer's disease (AD) is a neurodegenerative disease that is characterized by a devastating decline in cognitive activities among all types of dementia, and it severely affects the quality of life. Late-onset AD (LOAD) occurs after the age of 65 y
Externí odkaz:
https://doaj.org/article/fea7d10320434afa9b4d38812a9f4f31
Publikováno v:
Kafkas Universitesi Veteriner Fakültesi Dergisi, Vol 26, Iss 5, Pp 595-602 (2020)
Triclosan (TCS) is a broad spectrum antimicrobial agent showing its effect by deactivating the fatty acid synthesis of bacteria. The aim of this study was to investigate the effects of TCS on in vitro embryonic development in rats and to determine th
Externí odkaz:
https://doaj.org/article/6fae9da9535443ed93809b5911a47803
Autor:
Nefise Kandemir, Sercan Kenanoglu, Murat Gultekin, Nuriye Gokce, Hilal Akalin, Nazife Taşçıoğlu, Meral Mirza, Emel Koseoglu, Munis Dundar
Publikováno v:
Universa Medicina, Vol 40, Iss 3 (2021)
Background Essential tremor (ET) is the most common movement disorder. Propranolol is a first-line medication for ET. We aimed to evaluate the effect of propranolol on the expression of poly (ADP-ribose) polymerase 1 (PARP1) and DNA polymerase beta (
Externí odkaz:
https://doaj.org/article/4c7a580095eb491e91d2519a7dbc6631
Publikováno v:
Eurasian Journal of Medicine, Vol 51, Iss 2, Pp 177-185 (2019)
Externí odkaz:
https://doaj.org/article/f15a6d34460a44db8b516b5481080a5a
Autor:
Zahra Heydari, Maria Peshkova, Zeynep Burcin Gonen, Ianos Coretchi, Ahmet Eken, Arzu Hanım Yay, Muhammet Ensar Dogan, Nuriye Gokce, Hilal Akalin, Nastasia Kosheleva, Daniela Galea-Abdusa, Mariana Ulinici, Valentina Vorojbit, Anastasia Shpichka, Stanislav Groppa, Massoud Vosough, Mihail Todiras, Denis Butnaru, Yusuf Ozkul, Peter Timashev
Publikováno v:
Journal of Molecular Medicine. 101:51-63
Extracellular vesicles (EVs) are produced by various cells and exist in most biological fluids. They play an important role in cell-cell signaling, immune response, and tumor metastasis, and also have theranostic potential. They deliver many function
Autor:
Nuriye, Gokce, Neslihan, Basgoz, Sercan, Kenanoglu, Hilal, Akalin, Yusuf, Ozkul, Mahmut Cerkez, Ergoren, Tommaso, Beccari, Matteo, Bertelli, Munis, Dundar
Hair loss is a widespread concern in dermatology clinics, affecting both men’s and women’s quality of life. Hair loss can have many different causes, which are critical to identify in order to provide appropriate treatment. Hair loss can happen d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd9fadf010c639b93f9a249bce827ee0
Publikováno v:
Cellular Reprogramming. 23:139-148
Although the molecular pathogenesis of hepatocellular carcinoma (HCC) is uncertain, it is known that the epithelial-mesenchymal transition (EMT) mechanism and epigenetic changes have an important role. This study was focused on evaluating the relatio
Autor:
Nilgun Karasu, Hamit Acer, Hilal Akalin, Mikail Demir, Izem Olcay Sahin, Nuriye Gokce, Ayten Gulec, Asli Ciplakligil, Ayse Caglar Sarilar, Isa Cuce, Hakan Gumus, Huseyin Per, Mehmet Canpolat, Munis Dundar
SMA (spinal muscular atrophy) is an autosomal recessive neuromuscular disease that causes muscle atrophy and weakness. SMA is diagnosed by homozygous deletion in exon 7 of the SMN1 gene. However, mutations in other genes in the SMA region may contrib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9a4fb5184ae8c68b181b6881a5e87eb
https://doi.org/10.21203/rs.3.rs-1442537/v1
https://doi.org/10.21203/rs.3.rs-1442537/v1
Autor:
Yakut Erdem, Aynur Aytekin, Oğuz Yildiz, Sadik Özöner, Hilal Akalin, Munis Dundar, Dicle Aslan, Özlem Canöz
Publikováno v:
Balkan Journal of Medical Genetics, Vol 23, Iss 1, Pp 33-41 (2020)
Balkan Journal of Medical Genetics : BJMG
Balkan Journal of Medical Genetics : BJMG
This retrospective study examined the prognostic significance and treatment effect of promoter methylation of O6- methyl guanine methyl transferase (MGMT) and meth-ylation of CpG 1, CpG2, CpG3 and CpG4 in glioblastoma (GB) patients received postopera