Results 101 to 110 of about 24,071 (113)
Mitochondrial variations in the MT-ND4 and MT-TL1 genes are associated with male infertility
Feng Ni+5 more
semanticscholar +1 more source
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Electro-Optical Properties in β- Tl1-xCuxInS2(0≤X≤0,015) Crystals
Key Engineering Materials, 2022The paper presents the results of experimental studies of the electro-optical properties of β-Tl1-xCuxInS2 (0 X 0,015) single crystals. It was found that in measurements of the induced birefringence, the transmission of the polarizer - crystal - analyzer
A. K. Matiyev+7 more
semanticscholar +1 more source
Genetic Testing and Molecular Biomarkers, 2020
Aim: Pathogenic variants within mitochondrial tRNA and rRNA genes negatively affect protein synthesis function and cause oxidative phosphorylation defects.
B. Bulduk+6 more
semanticscholar +1 more source
Aim: Pathogenic variants within mitochondrial tRNA and rRNA genes negatively affect protein synthesis function and cause oxidative phosphorylation defects.
B. Bulduk+6 more
semanticscholar +1 more source
Mitochondrial Retinopathy Due to MT-TL1 Mutation: The Role of Heteroplasmy. A Case Report.
Czech and Slovak OphthalmologyOBJECTIVE To report a case of mitochondrial retinopathy, highlighting its clinical and imaging findings, the importance of genetic confirmation, and the possible implications of heteroplasmy in this disease.
Mauricio Arango+4 more
semanticscholar +1 more source
Cardiovascular Research, 2019
Aims Heart failure with reduced ejection fraction (HFrEF) causes lung remodelling with myofibroblasts proliferation and fibrosis leading to a restrictive lung syndrome with pulmonary hypertension (PH) and right ventricular (RV) dysfunction. PBI-4050 is a
Q. Nguyen+11 more
semanticscholar +1 more source
Aims Heart failure with reduced ejection fraction (HFrEF) causes lung remodelling with myofibroblasts proliferation and fibrosis leading to a restrictive lung syndrome with pulmonary hypertension (PH) and right ventricular (RV) dysfunction. PBI-4050 is a
Q. Nguyen+11 more
semanticscholar +1 more source
Isolated mitochondrial myopathy due to m.3243A > G mutation in MT-TL1 gene
Acta Neurologica Belgica, 2021R. Mahale+4 more
semanticscholar +1 more source