Zobrazeno 1 - 10 of 17 pro vyhledávání: '"Reyhan, Tahtasakal"'
1
Akademický článek
Autism-Related Cc2d1a Heterozygous Mice: Increased Levels of miRNAs Retained in DNA/RNA Hybrid Profiles (R-Loop)
Autor: Elif Funda Sener, Halime Dana, Reyhan Tahtasakal, Serpil Taheri, Minoo Rassoulzadegan
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
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2
Akademický článek
Comparação de Soluções Cardioplégicas em Cirurgia de Revascularização Miocárdica sobre Mecanismos de Autofagia e Apoptose
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
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3
Akademický článek
Superexpressão Gênica PTEN em Tecidos Miocárdicos de Pacientes de Cirurgia de Revascularização Miocárdica
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
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4
Akademický článek
Blood mRNA Expression Profiles of Autophagy, Apoptosis, and Hypoxia Markers on Blood Cardioplegia and Custodiol Cardioplegia Groups
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
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5
Heterozygous Cc2d1a mice show sex-dependent changes in the Beclin-1/p62 ratio with impaired prefrontal cortex and hippocampal autophagy
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
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::809b8ad877f26ce0cde3cefa0b81af2d
https://doi.org/10.1016/j.pnpbp.2023.110764
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6
Partial changes in apoptotic pathways in hippocampus and hypothalamus of Cc2d1a heterozygous
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
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::969cf04cf8e0101b76cf1ec78aacba12
https://pubmed.ncbi.nlm.nih.gov/36454503
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7
Evaluation of the Rho-kinase gene expression and polymorphisms in adult patients with acute appendicitis: a differential impact of gender
Autor: Nahide Ekici Günay, Emre Bülbül, Elif Funda Şener, Reyhan Tahtasakal, Seniz Demiryürek, Nurullah Günay, Abdullah Tuncay Demiryürek
Publikováno v: Revista da Associação Médica Brasileira v.68 n.10 2022
Revista da Associação Médica Brasileira
Associação Médica Brasileira (AMB)
instacron:AMB
© 2022 Associacao Medica Brasileira. All rights reserved.OBJECTIVE: Acute appendicitis represents one of the most common causes of acute intra-abdominal emergencies worldwide. In this case-control study, we aimed to investigate associations of Rho-k
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b65d117312f2d3cb3f74105b74ef4a5a
https://pubmed.ncbi.nlm.nih.gov/36417654
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8
Blood mRNA Expression Profiles of Autophagy, Apoptosis, and Hypoxia Markers on Blood Cardioplegia and Custodiol Cardioplegia Groups
Autor: Aydın Tunçay, Ömer Naci Emiroğulları, Ecmel Mehmetbeyoglu, Deniz Elcik, Serpil Taheri, Işın Güneş, Elif Funda Sener, Reyhan Tahtasakal
Publikováno v: Brazilian Journal of Cardiovascular Surgery, Vol 36, Iss 3, Pp 331-337 (2021)
Brazilian Journal of Cardiovascular Surgery
Brazilian Journal of Cardiovascular Surgery v.36 n.3 2021
Sociedade Brasileira de Cirurgia Cardiovascular (SBCCV)
instacron:SBCCV
Brazilian Journal of Cardiovascular Surgery, Volume: 36, Issue: 3, Pages: 331-337, Published: 05 MAR 2021
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 between the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f8cb9becafab0a84773aca201a43029
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0102-76382021000300331&tlng=en
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10
Evaluation of the rs35996865 polymorphism of the ROCK1 gene in sepsis
Autor: Aykut Kale, Elif Funda Şener, Nahide Ekici Günay, Reyhan Tahtasakal, Seniz Demiryürek, Nurullah Günay, Abdullah Tuncay Demiryürek
Publikováno v: Revista da Associação Médica Brasileira, Volume: 68, Issue: 5, Pages: 586-590, Published: 13 MAY 2022
Revista da Associação Médica Brasileira v.68 n.5 2022
Revista da Associação Médica Brasileira
Associação Médica Brasileira (AMB)
instacron:AMB
© 2022 Associacao Medica Brasileira. All rights reserved.OBJECTIVE: Sepsis is a complex and serious medical condition resulting from the activation of an innate host response to infections. The etiology of sepsis is complex and can be influenced by
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6966e8f96b567d0baaacfb1ef214995e
https://pubmed.ncbi.nlm.nih.gov/35584479
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