Zobrazeno 1 - 10
of 98
pro vyhledávání: '"Elif Funda, Sener"'
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:
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:
Reyhan Tahtasakal, Elif Funda Sener, Nesrin Delibasi, Zuhal Hamurcu, Ecmel Mehmetbeyoglu, Keziban Korkmaz Bayram, Isin Gunes, Dincer Goksuluk, Omer Naci Emirogullari
Publikováno v:
Arquivos Brasileiros de Cardiologia, Vol 120, Iss 4 (2023)
Resumo Fundamento: A doença arterial coronariana é um distúrbio complexo que causa morte em todo o mundo. Um dos genes envolvidos no desenvolvimento dessa doença pode ser o PTEN. Objetivos: Nosso objetivo foi investigar a expressão gênica e pro
Externí odkaz:
https://doaj.org/article/7c7801a24d5e4ea496f9731d0e4d7e14
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:
Ismail Kocyigit, Serpil Taheri, Elif Funda Sener, Eray Eroglu, Fahir Ozturk, Aydin Unal, Kezban Korkmaz, Gokmen Zararsiz, Murat Hayri Sipahioglu, Yusuf Ozkul, Bulent Tokgoz, Oktay Oymak, Tevfik Ecder, Jonas Axelsson
Publikováno v:
BMC Nephrology, Vol 18, Iss 1, Pp 1-10 (2017)
Abstract Background Autosomal dominant polycystic kidney disease (ADPKD) is a common hereditary disorder with unclear disease mechanism. Currently, overt hypertension and increased renal volume are the best predictors of renal function. In this study
Externí odkaz:
https://doaj.org/article/5d9670bcad294b82b0c04ec1bb84a0a6
Autor:
Elif Funda Sener, Mustafa Caglar Sahin, Serpil Taheri, Keziban Korkmaz Bayramov, Mert Kahraman Marasli, Gokmen Zararsiz, Mehmet Canpolat, Nilfer Sahin, Didem Behice Oztop
Publikováno v:
Psychiatry and Clinical Psychopharmacology, Vol 27, Iss 1, Pp 24-29 (2017)
Objective: Autism spectrum disorders (ASDs) is a heterogeneous neuropsychiatric disorder with widespread abnormalities of social interaction and communication, showing severely restricted interests and extreme repetitive behavior. The relationship be
Externí odkaz:
https://doaj.org/article/ac1f75ba080448f087e613ecb5b921e8
Publikováno v:
European Journal of Clinical Pharmacology. 78:1095-1104
© 2022, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.Objective: Although several genes have previously been studied about the treatment of Attention Deficit Hyperactivity Disorder (ADHD), the number
Autor:
Elif Funda Sener, Halime Dana, Reyhan Tahtasakal, Zuhal Hamurcu, Serpil Taheri, Nesrin Delibasi, Ecmel Mehmetbeyoglu, Zeynep Yilmaz Sukranli, Fatma Dal, Esra Tufan, Asli Okan Oflamaz, Zuleyha Doganyigit, Yusuf Ozkul, Minoo Rassoulzadegan
Publikováno v:
Progress in Neuro-Psychopharmacology and Biological Psychiatry. 125:110764
Autism Spectrum Disorders (ASD) are a group of neurodevelopmental disorders characterized by repetitive behaviors, lack of social interaction and communication. CC2D1A is identified in patients as an autism risk gene. Recently, we suggested that hete
Autor:
Elif Funda Sener, Halime Dana, Reyhan Tahtasakal, Zuhal Hamurcu, Ahsen Guler, Esra Tufan, Zuleyha Doganyigit, Minoo Rassoulzadegan
Publikováno v:
Metabolic brain disease.
Alterations in the apoptosis pathway have been linked to changes in serotonin levels seen in autistic patients. Cc2d1a is a repressor of the HTR1A gene involved in the serotonin pathway. The hippocampus and hypothalamus of Cc2d1a ± mice were analyze
Autor:
Mukaddes Karaca, Reyhan Tahtasakal, Halime Dana, Murside Sahin, Seyda Nur Pirencioglu, Emre Tughan, Fatma Dal, Esra Demirci, Elif Funda Sener
Publikováno v:
Brain Research. :148410