Zobrazeno 1 - 10
of 81
pro vyhledávání: '"Serpil Taheri"'
Autor:
Zeynep Yilmaz Sukranli, Keziban Korkmaz Bayram, Serpil Taheri, Francois Cuzin, Yusuf Ozkul, Minoo Rassoulzadegan
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-17 (2024)
Abstract We previously identified a unique genetic feature of Autism Spectrum Disorder (ASD) in human patients and established mouse models, a low to very low level of six microRNAs, miR-19a-3p, miR-361-5p, miR-3613-3p, miR-150-5p, miR-126-3p and miR
Externí odkaz:
https://doaj.org/article/f974551c620b47448dd9fc9edfebe50e
Publikováno v:
Biomolecules, Vol 14, Iss 9, p 1183 (2024)
Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder with a highly variable expression of phenotypes (restricted interest or activity and repetitive behavior in communication and social interactions), genes (mutation), markers (alt
Externí odkaz:
https://doaj.org/article/f502455f8e884b53a31539f6bdd839ad
Autor:
Zeynep Yilmaz Sukranli, Keziban Korkmaz Bayram, Ecmel Mehmetbeyoglu, Zuleyha Doganyigit, Feyzullah Beyaz, Elif Funda Sener, Serpil Taheri, Yusuf Ozkul, Minoo Rassoulzadegan
Publikováno v:
Biomolecules, Vol 14, Iss 2, p 201 (2024)
Recently, we described the alteration of six miRNAs in the serum of autistic children, their fathers, mothers, siblings, and in the sperm of autistic mouse models. Studies in model organisms suggest that noncoding RNAs participate in transcriptional
Externí odkaz:
https://doaj.org/article/1184744af79549c988e597d18396455f
Autor:
Ecmel Mehmetbeyoglu, Claudia Chiriches, Imran Shair Mohammed, Beyza Nur Onat, Kadir Yaray, Oguz Galip Yildiz, Serpil Taheri, Martin Ruthardt
Publikováno v:
HemaSphere, Vol 7, p e69134db (2023)
Externí odkaz:
https://doaj.org/article/61ee5b602f77466f98220b3674253c2e
Autor:
Elif Funda Sener, Zuhal Hamurcu, Serpil Taheri, Reyhan Tahtasakal, Nesrin Delibasi, Deniz Elcik, Ecmel Mehmetbeyoglu, Aydin Tuncay, Fatma Dal, Keziban Korkmaz Bayram, Isın Gunes, Omer Naci Emirogullari
Publikováno v:
Arquivos Brasileiros de Cardiologia, Vol 120, Iss 7 (2023)
Resumo Fundamento A doença arterial coronariana (DAC) devido à isquemia miocárdica causa perda permanente de tecido cardíaco. Objetivos Nosso objetivo foi demonstrar o possível dano ao miocárdio em nível molecular através dos mecanismos de au
Externí odkaz:
https://doaj.org/article/a9094e18255e4b7b9cd9e73328435a17
Autor:
Deniz Elcik, Aydın Tuncay, Elif Funda Sener, Serpil Taheri, Reyhan Tahtasakal, Ecmel Mehmetbeyoğlu, Isın Gunes, Omer Naci Emirogullari
Publikováno v:
Brazilian Journal of Cardiovascular Surgery, Vol 36, Iss 3, Pp 331-337 (2021)
Abstract Introduction: Blood cardioplegia (BC) and Custodiol cardioplegia (CC) have been used for a long time in open heart surgery and are highly effective solutions. The most controversial issue among these two is whether there is any difference be
Externí odkaz:
https://doaj.org/article/8828ac23fb8849b8b1a678c1987d01fe
Autor:
Guzide Satir-Basaran, Leila Kianmehr, Ecmel Mehmetbeyoglu, Kezban Korkmaz Bayram, Mehmet Memis, Zeynep Yilmaz, Esra Tufan, Serpil Taheri, Fahrettin Kelestimur, Minoo Rassoulzadegan
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
A wide range of diseases result from environmental effects, and the levels of many native transcripts are altered. The alteration of non-coding RNAs (ncRNAs) and transmission of the variation to the next generation is increasingly recognized as a mar
Externí odkaz:
https://doaj.org/article/e7481cc875fd497aab6d5136f4bd2445
Autor:
Serpil Taheri, Züleyha Karaca, Ecmel Mehmetbeyoglu, Zuhal Hamurcu, Zeynep Yilmaz, Fatma Dal, Venhar Çınar, Halil Ulutabanca, Fatih Tanriverdi, Kursad Unluhizarci, Minoo Rassoulzadegan, Fahrettin Kelestimur
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 24, p 15699 (2022)
Traumatic brain injury (TBI) is a major health problem affecting millions of people worldwide and leading to death or permanent damage. TBI affects the hypothalamic–pituitary–adrenal (HPA) axis either by primary injury to the hypothalamic–hypop
Externí odkaz:
https://doaj.org/article/c4d9b10f07eb4e328e0b43a3dcca9bd3
Autor:
Ismail Kocyigit, Serpil Taheri, Cihan Uysal, Mehmet Memis, Salih Guntug Ozayturk, Gokmen Zararsiz, Minoo Rassoulzadegan
Publikováno v:
Cells, Vol 11, Iss 20, p 3300 (2022)
Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited cause of chronic kidney disease with Polycystin (PKD) 1 and 2 gene mutation. However, the intra-familial variability in symptoms further suggests a non-Mendelian contri
Externí odkaz:
https://doaj.org/article/59d91570162d4b6ba5422bad705fde20
Publikováno v:
Eurasian Journal of Medicine, Vol 51, Iss 2, Pp 177-185 (2019)
Externí odkaz:
https://doaj.org/article/f15a6d34460a44db8b516b5481080a5a