Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Nuriye, Gokce"'
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
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
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
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:
Hilal Akalin, Abdulbaki Yildirim, Munis Dundar, Nilgun Karasu, Mikail Demir, Hande Kulak, Muzaffer Keklik, Serhat Çelik, Nuriye Gokce
Publikováno v:
Medical Oncology. 38
Imatinib mesylate, a tyrosine kinase inhibitor, is the first choice in chronic myeloid leukemia treatment. However, resistance to imatinib may develop with time and in some cases, patients may not respond at all to imatinib. Progressive resistance to
Autor:
Hilal Akalin, Yakut Erdem, Munis Dundar, Muhammet Ensar Dogan, Nuriye Gokce, Sevgi Ozmen, Yusuf Ozkul
Background: In this study, expression level analysis of genes associated with Attention Deficit Hyperactivity Disorder (ADHD) (SLC6A3, SLC6A4, SLC1A2, VMAT2, MAOA, COMT, GLYAT, GRM5, DRD4, TPH1, and ADRA2C) by pre-treatment and post-treatment with At
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8670ad4dd0e7eae5dc5a4baaaf7402a
https://doi.org/10.21203/rs.3.rs-440720/v1
https://doi.org/10.21203/rs.3.rs-440720/v1