Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Neşe Vardar Acar"'
Autor:
Neşe Vardar Acar, Riza Köksal Özgül
Publikováno v:
EXCLI Journal : Experimental and Clinical Sciences, Vol 22, Pp 520-555 (2023)
As a requirement of aerobic metabolism, regulation of redox homeostasis is indispensable for the continuity of living homeostasis and life. Since the stability of the redox state is necessary for the maintenance of the biological functions of the cel
Externí odkaz:
https://doaj.org/article/1b26475eed4b406a93fe801fd77f432f
Autor:
Neşe Vardar Acar, Ali Dursun, Damla Aygün, H. Esra Gürses Cila, İncilay Lay, Basri Gülbakan, R.Köksal Özgül
Publikováno v:
Free radical biologymedicine. 179
Oxidative stress is associated with various disease pathologies including Inborn Errors of Metabolism (IEMs), among the most important causes of childhood morbidity and mortality. At least as much as oxidative stress in cells, reductive stress poses
Autor:
Ebru Arik Yilmaz, Betul Buyuktiryaki, Cagatay Karaaslan, Ozlem Cavkaytar, Neşe Vardar Acar, Ozge Soyer, Bulent Enis Sekerel, Umit Murat Sahiner, Cansin Sackesen
Publikováno v:
Turkish Journal of Medical Sciences
Background/aim: filaggrin is a protein complex involved in epidermal differentiation and skin barrier formation. Mutations of the filaggrin gene (FLG) arc associated with allergen sensitization and allergic diseases like atopic dermatitis (AD), aller
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5333bfb13c9661e550d399c546c0eee
https://hdl.handle.net/11499/37528
https://hdl.handle.net/11499/37528
Autor:
Yilmaz Yildiz, Can Kosukcu, Kader Karli Oguz, Ceren Günbey, Neşe Vardar Acar, Dilek Yalnizoglu, Ali Dursun, Halil Tuna Akar, Basri Gülbakan, Didem Yücel Yılmaz, R. Köksal Özgül, Ayça Burcu Kahraman
Publikováno v:
European Journal of Medical Genetics. 64:104340
ELFN1, a transmembrane leucine rich repeat protein, is involved in signal transduction in both neural cells and ROD ON-bipolar synaptogenesis. We present three siblings with developmental and epileptic encephalopathy and co-morbidities due to ELFN1 g