Evaluation of cardiovascular system and determination of cardiometabolic risk using novel biomarkers in childhood obesity

Autor: Deniz, Melis, Doğan, Mustafa, Gül, Özlem, Özhan, Bayram, Agladıoğlu, Sebahat Yılmaz, Enli, Yaşar, Şenol, Hande

Publikováno v: In Progress in Pediatric Cardiology March 2023 68

The effects of edaravone, a free-radical scavenger in lung injury induced by valproic acid demonstrated via different biochemical parameters

Autor: Neziha Hacihasanoglu Cakmak, Refiye Yanardag, Bertan Boran Bayrak, Sebahat Yilmaz

In this study, we aimed to evaluate whether edaravone (EDA) has a protective role against valproic acid (VPA)-induced lung damage via its antioxidative activity. Male Sprague-Dawley rats were split into four groups. Control (n = 8) rats; rats given E

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48ffccd167644b4f303938d0a8b200cc
https://hdl.handle.net/20.500.12511/8506

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Functional assessment of variants associated with Wolfram syndrome

Autor: Nanna Dahl Rendtorff, Detlef Bockenhauer, Semra Çetinkaya, Sebahat Yilmaz, Erdal Kurnaz, Zehra Aycan, Maria Bitner-Glindzicz, Melissa Riachi, Lisbeth Tranebjærg, Khalid Hussain

Publikováno v: Riachi, M, Yilmaz, S, Kurnaz, E, Aycan, Z, Çetinkaya, S, Tranebjærg, L, Rendtorff, N D, Bitner-Glindzicz, M, Bockenhauer, D & Hussain, K 2019, ' Functional assessment of variants associated with Wolfram syndrome ', Human Molecular Genetics, vol. 28, no. 22, pp. 3815-3824 . https://doi.org/10.1093/hmg/ddz212

Wolfram syndrome (WS) is a heterogeneous multisystem neurodegenerative disorder with two allelic variations in addition to a separate subtype known as WS type 2. The wide phenotypic spectrum of WS includes diabetes mellitus and optic atrophy which is

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f7556741dfe0d19403f3eaeccc1e633
https://curis.ku.dk/portal/da/publications/functional-assessment-of-variants-associated-with-wolfram-syndrome(cc03cf53-8d48-4ace-80a1-e6d515b75243).html

MODY Sendromlarından Sorumlu GCK, HNF1A VE HNF1B Genleri Mutasyon Spektrumu ve 40 Yeni Mutasyon

Autor: ABACI, AYHAN, BÖBER, ECE, ONAY, HÜSEYİN, TEMİZ, FATİH, Korkmaz, Hüseyin Anıl, ARSLANOĞLU, İLKNUR, SANGÜN, ÖZLEM, DOĞAN, MURAT, AĞLADIOĞLU, SEBAHAT YILMAZ, İŞGÜVEN, ŞÜKRİYE PINAR, YILDIRIM, RUKEN, ÇAKIR, ESRA PAPATYA, KARA, CENGİZ, ÇETİNKALP, ŞEVKİ, BÜYÜKİNAN, MUAMMER, ERSOY, BETÜL, KIREL, BİRGÜL, Özbek, Mehmet Nuri, EREN, ERDAL, TÜTÜNCÜLER, FİLİZ, ANIK, AHMET, ÜLKÜ, GÜL, KARTAL, EMİNE, SAYGILI, FİSUN, ATİK, TAHİR, BOLAT, HİLMİ, ÖZEN, SAMİM, KARACA, EMİN, AYKUT, AYÇA, GÖKŞEN ŞİMŞEK, RUHSAR DAMLA, IŞIK, ESRA, ÖZKINAY, FERİŞTAH FERDA

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2605::a3c4d0b3b2ff5345ef6901bfdcb7835f
https://avesis.deu.edu.tr/publication/details/dc0b4d19-5b90-4510-8672-ac1fbf9304fd/oai