Publications by authors named "Sai Zeng"

This Letter solves steering vector estimation under mismatch for adaptive beamforming. The proposed beamformer implements a stepwise estimation of steering vector, and zone orthogonal constraint is added first based on adaptive constraint framework from Khabbazibasmenj [IEEE Trans. Signal Process.

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Introduction: Postnatal cardiomyocytes respond to stress signals by hypertrophic growth and fetal gene reprogramming, which involves epigenetic remodeling mediated by histone methyltransferase polycomb repressive complex 2 (PRC2) and histone deacetylases (HDACs). However, it remains unclear to what extent these histone modifiers contribute to the development of cardiomyocyte hypertrophy.

Methods: Neonatal rat ventricular myocytes (NRVMs) were stimulated by phenylephrine (PE; 50μM) to induce hypertrophy in the presence or absence of the PRC2 inhibitor GSK126 or the HDACs inhibitor Trichostatin A (TSA).

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Synthetic aperture sonar (SAS) and interferometric synthetic aperture sonar (InSAS) have a range layover phenomenon during underwater observation, the AUV-mounted circular synthetic aperture sonar (CSAS) system, that insonifies targets using multiple circular scans that vary in height and can eliminate the layover phenomenon. However, this observation method is time-consuming and difficult to compensate. To solve this problem, the circular array synthetic aperture sonar (CASAS) based on the equivalent phase center was established for unmanned surface vehicles.

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Pathological growth of cardiomyocytes during hypertrophy is characterized by excess protein synthesis; however, the regulatory mechanism remains largely unknown. Using a neonatal rat ventricular myocytes (NRVMs) model, here we find that the expression of nucleosome assembly protein 1 like 5 (Nap1l5) is upregulated in phenylephrine (PE)-induced hypertrophy. Knockdown of Nap1l5 expression by siRNA significantly blocks cell size enlargement and pathological gene induction after PE treatment.

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Supported catalysts, consisting of PMo immobilized on silver nanomaterials at different recombination time and the silver nanomaterials with different template sodium citrate amount characterized by FT-IR, XRD, SEM, UV-vis and other test methods. The results show that the AgNPs are relatively uniformed with sizes between 100-300 nm when the sodium citrate addition amount is 9.0 mL.

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RNase III DROSHA is upregulated in multiple cancers and contributes to tumor progression by hitherto unclear mechanisms. Here, we demonstrate that DROSHA interacts with β-Catenin to transactivate STC1 in an RNA cleavage-independent manner, contributing to breast cancer stem-like cell (BCSC) properties. DROSHA mRNA stability is enhanced by N-methyladenosine (mA) modification which is activated by AURKA in BCSCs.

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