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Toplam kayıt 8, listelenen: 1-8
DNA methylation pattern of TM6SF2 influences NAFLD progression in genotype-dependent manner
(Elsevier Science Bv, 2019)
Background and aims: Non-alcoholic fatty liver disease (NAFLD) arises due to complex interaction of genetic and environmental factors. Evidence suggests that transmembrane 6 superfamily member 2 (TM6SF2) E167K variant is ...
The role of MYDGF in the injury of central nervous system
(Wiley, 2019)
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The investigation of genetic etiology in familial cases with congenital hypothyroidism
(Karger, 2019)
Background: Congenital hypothyroidism(CH) is the most common neonatal endocrinological disorder in the world. Although most of the CH is sporadic, some genetic defects are responsible from the etiology. The aim of this ...
A novel candidate frameshift mutation for catecholaminergic polymorphic ventricular tchycardia
(Nature Publishing Group, 2019)
...
Floresan mikroskop görüntülerinde miyelin segmentasyonu
(Institute of Electrical and Electronics Engineers Inc., 2019)
Aksonların etrafına sarılmış¸ miyelin kılıf, hızlı bir şekilde sinyal iletimini sağlar ve deformasyonu, Multipl Skleroz (MS) gibi çeşitli nörodejeneratif hastalıklara neden olur. Aday ilaç geliştirilmesi için, miyelinizasyonun ...