Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Keziban Korkmaz Bayram"'
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
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:
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:
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:
Alperen Vural, Murat Salih Güneş, Keziban Korkmaz Bayram, Yusuf Ozkul, Mehmet İlhan Şahin, Muhammet Ensar Dogan, Meltem Cerrah Gunes, Sevda Yesim Ozdemir, Fatma Aybuga, Arslan Bayram
Publikováno v:
Journal of Neurogenetics. 35:45-57
The characteristic feature of noise-induced hearing loss (NIHL) is the loss or malfunction of the outer hair cells (OHC) and the inner hair cells (IHC) of the cochlea. 90-95% of the spiral ganglion neurons, forming the cell bodies of cochlear nerve,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cae48e7780139508b4acbed61c34504b
https://doi.org/10.1080/01677063.2021.1904922
https://doi.org/10.1080/01677063.2021.1904922
Autor:
Murat ERDOĞAN, Hakan GÜMÜŞ, Didem Behice ÖZTOP, Burhan BALTA, Keziban KORKMAZ BAYRAM, Munis DÜNDAR
Publikováno v:
Volume: 44, Issue: 2 165-171
Cumhuriyet Medical Journal
Cumhuriyet Medical Journal
Cyclin-dependent kinase-like 5 (CDKL5, OMIM 300203), also known as STK9 (serine/threonine kinase 9), is a gene that is thought to play a role in the production of proteins involved in the normal development of the brain, although its function is not
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c38be2946ba162dcb0ec5c82726e667
https://dergipark.org.tr/tr/pub/cmj/issue/70991/1121531
https://dergipark.org.tr/tr/pub/cmj/issue/70991/1121531
Autor:
Yusuf Ozkul, Keziban Korkmaz Bayram, Zeynep Yilmaz, Arslan Bayram, Juliette Fitremann, Ecmel Mehmetbeyoglu, Minoo Rassoulzadegan
Publikováno v:
Processes, Vol 9, Iss 716, p 716 (2021)
Processes
Processes, 2021, 9 (4), pp.716. ⟨10.3390/pr9040716⟩
Processes, MDPI, 2021, 9 (4), pp.716. ⟨10.3390/pr9040716⟩
Volume 9
Issue 4
Processes
Processes, 2021, 9 (4), pp.716. ⟨10.3390/pr9040716⟩
Processes, MDPI, 2021, 9 (4), pp.716. ⟨10.3390/pr9040716⟩
Volume 9
Issue 4
Background: N-heptyl-D-galactonamide (GalC7) is a small synthetic carbohydrate derivative that forms a biocompatible supramolecular hydrogel. In this study, the objective was to analyze more in-depth how neural cells differentiate in contact with Gal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3fa63548c882c761c6331e8597a7bb3
https://www.mdpi.com/2227-9717/9/4/716
https://www.mdpi.com/2227-9717/9/4/716
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