Results 31 to 40 of about 112,737 (278)
Variation of DNA copies number in etiology of congenital heart defects
Российский кардиологический журнал, 2018 Past decade, there is a remarkable evidence of that the variation of DNA copies number (copy number variation, CNV) is related with onset of inborn heart defects (IHD). The review is focused on an impact of CNV in IHD development.
A. A. Slepukhina +2 more
doaj +1 more source
Frontiers in Genetics, 2021 Copy number variations (CNVs) are important structural variations that can cause significant phenotypic diversity. Reliable CNVs mapping can be achieved by identification of CNVs from different genetic backgrounds.
Zhipeng Wang +6 more
doaj +1 more source
Abnormal proactive and reactive cognitive control during conflict processing in major depression [PDF]
, 2014 According to the Dual Mechanisms of Control framework, cognitive control consists of two complementary components: proactive control refers to anticipatory maintenance of goal-relevant information, whereas reactive control acts as a correction mechanism ...
Aarts, Kristien +6 more
core +2 more sources
STRUCTURAL VARIABLITY OF LEUCOCYTE GENOME AND ARTERIAL CELLS IN HUMAN ATHEROSCLEROSIS
Российский кардиологический журнал, 2017 The review is focused on current views on the structural variation of genome of somatic cells as components related to atherosclerosis. The original data presented on the variation spectrum of DNA areas copies in peripheral blood leucocytes and arterial ...
А. A. Sleptsov +2 more
doaj +1 more source
Soluble Epoxide Hydrolase Inhibition for Ocular Diseases: Vision for the Future [PDF]
, 2019 Ocular diseases cause visual impairment and blindness, imposing a devastating impact on quality of life and a substantial societal economic burden. Many such diseases lack universally effective pharmacotherapies.
Corson, Timothy W., Park, Bomina
core +1 more source
Gender differences in CNV burden do not confound schizophrenia CNV associations [PDF]
Scientific Reports, 2016 AbstractCompared with the general population, an excess of rare copy number variants (CNVs) has been identified in people with schizophrenia. Females with neurodevelopmental disorders and in the general population have been reported to carry more large, rare CNVs than males.
Jun Han +8 more
openaire +3 more sources
Functional Genomics Profiling of Bladder Urothelial Carcinoma MicroRNAome as a Potential Biomarker. [PDF]
, 2018 Though bladder urothelial carcinoma is the most common form of bladder cancer, advances in its diagnosis and treatment have been modest in the past few decades.
Li, Wei Tse +4 more
core +2 more sources
Biology Open, 2020 Vascular endothelial growth factor (VEGF) is a crucial stimulator for choroidal neovascularization (CNV). Our aim was to develop a reproducible and valid treatment-naive quiescent CNV (i.e.
Shan Liu +5 more
doaj +1 more source
A backward procedure for change-point detection with applications to copy number variation detection
, 2019 Change-point detection regains much attention recently for analyzing array or sequencing data for copy number variation (CNV) detection. In such applications, the true signals are typically very short and buried in the long data sequence, which makes it ...
Hao, Ning, Shin, Seung Jun, Wu, Yichao
core +1 more source