Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Y Çetin, Kocaefe"'
Autor:
Goknur Haliloglu, Can Ebru Bekircan-Kurt, Y. Çetin Kocaefe, Haluk Topaloglu, Hasan Basri Kiliç, Sevim Erdem Özdamar, Bengisu Kevser Bulduk
Publikováno v:
Genetic Testing and Molecular Biomarkers. 24:165-170
Aim: Pathogenic variants within mitochondrial tRNA and rRNA genes negatively affect protein synthesis function and cause oxidative phosphorylation defects. The majority of mitochondrial cytopathies are caused by pathogenic point variants within the m
Publikováno v:
Turkish Journal of Biochemistry. 44:769-777
Objective Detection of mtDNA copy number is required for diagnosis of mtDNA depletion. Multiplex quantification of mtDNA in blood samples was claimed via normalizing to a nuclear single copy gene using qPCR. This is not possible in high mtDNA samples
Autor:
Bengisu Kevser, Bulduk, Hasan Basri, Kiliç, Can Ebru, Bekircan-Kurt, Göknur, Haliloğlu, Sevim, Erdem Özdamar, Haluk, Topaloğlu, Y Çetin, Kocaefe
Publikováno v:
Genetic testing and molecular biomarkers. 24(3)
Publikováno v:
Physiological genomics. 48(6)
The pathological endpoint of congenital and senile myopathies is chronic muscle degeneration characterized by the atrophy of contractile elements, accompanied by fibrosis and fatty infiltration of the interstitium. Tenotomy is the release of preload
Autor:
Meral Özgüç, Turgay Dalkara, Yasemin Gursoy-Ozdemir, Hulya Karatas, Serap Saygi, Figen Soylemezoglu, Ayse Yuzbasioglu, Y. Çetin Kocaefe, Nejat Akalan
Publikováno v:
Cellular and Molecular Neurobiology. 29:1223-1231
Selenoproteins are enzymes containing selenium in their structure and are involved in cellular processes such as defense against oxidative stress and cell survival. The aim of this study is to investigate the expression of four selenoproteins (GPX1,
Publikováno v:
Shock. 26:37-40
Interleukin 10 (IL-10) has been considered to alleviate the inflammatory cytokine response in various models of sepsis. Although being regarded as a key immunomodulator molecule to be beneficial for the treatment of sepsis, recombinant IL-10 treatmen
Publikováno v:
European Journal of Human Genetics. 11:102-104
Mitochondrial neurogastrointestinal encephalomyopathy syndrome (MNGIE) is a rare autosomal recessive neurologic disorder characterised by multiple mitochondrial DNA deletions. In this study, five Turkish IVINGIE patients are investigated for mtDNA de
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