Publications by authors named "Hao Ran Geng"

Article Synopsis
  • Folic acid (FA) over-supplementation during pregnancy can lead to negative outcomes for the heart health of offspring, including impaired cardiac function and increased levels of reactive oxygen species (ROS).
  • In a study with pregnant mice, over-supplementation was linked to decreased left ventricular ejection fraction and other signs of cardiac dysfunction, as well as downregulation of genes vital for heart health.
  • Using antioxidants like N-acetylcysteine showed potential in reversing some of the cardiac damage caused by maternal FA over-supplementation, highlighting the balance needed in FA intake during pregnancy.
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Article Synopsis
  • Maternal hyperhomocysteinemia is known to independently increase the risk of congenital heart disease (CHD), but the impact of high paternal homocysteine levels on CHD is not well understood.!*
  • In a study with male mice, high homocysteine levels led to reduced sperm quality and increased ventricular septal defects (VSD) in their offspring, linked to changes in sperm DNA methylation.!*
  • Folic acid supplementation was shown to reduce the incidence of VSD in offspring from high homocysteine male mice, suggesting that lowering paternal homocysteine could be a potential strategy to prevent CHD in children.!*
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Prenatal diagnosis of congenital heart disease (CHD) relies primarily on fetal echocardiography conducted at mid-gestational age-the sensitivity of which varies among centers and practitioners. An objective method for early diagnosis is needed. Here, we conducted a case-control study recruiting 103 pregnant women with healthy offspring and 104 cases with CHD offspring, including VSD (42/104), ASD (20/104), and other CHD phenotypes.

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This work reports the refinement of nanoporous copper (NPC) ligaments by introducing the sodium dodecyl sulfate (SDS) surfactant in the dealloying process. The AlCu (at%) alloy precursor is chemically dealloyed in a mixed solution of NaOH and SDS surfactant, producing NPC with a hierarchical microstructure. Micron-scaled skeletons that build up higher level networks consist of geometrically similar nano-scaled bi-continuous ligament-pore networks at the lower level.

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Elevation in homocysteine (Hcy) level is associated with insulin resistance; however, the causality between them and the underlying mechanism remain elusive. Here, we show that Hcy induces insulin resistance and causes diabetic phenotypes by protein cysteine-homocysteinylation (C-Hcy) of the pro-insulin receptor (pro-IR). Mechanistically, Hcy reacts and modifies cysteine-825 of pro-IR in the endoplasmic reticulum (ER) and abrogates the formation of the original disulfide bond.

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A new surface molecularly imprinted polymer (MIP) based on nano-TiO2 was developed using propazine (Pro) as a template molecule, ethyleneglycol dimethacrylate (EGDMA) as a crosslinker, methacrylic acid (MAA) as a functional monomer, and 2,2'-azobis (isobutyronitrile) (AIBN) as an initiator. Structures of the newly synthesized surface MIPs were characterized by Fourier transmission infrared spectrometry (FT-IR), scanning electron microscope (SEM), transmission electron microscope (TEM), and X-ray diffraction (XRD). The MIP had a good adsorption capacity and high recognition selectivity to propazine.

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A new molecularly imprinted polymer (MIP) based on silica-gel surface was developed using Dufulin (Duf) as a template, methacrylic acid (MAA) as a functional monomer, ethyleneglycol dimethacrylate (EGDMA) as a crosslinker, and azodiisobutyronitrile (AIBN) as an initiator. The synthetic samples were characterized by the techniques of Fourier transmission infrared spectrometry (FT-IR) and scanning electron microscope (SEM). Batch experiments were performed to evaluate adsorption isotherms, adsorption kinetics and selective recognition of the MIP.

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Molecularly imprinted polymers (MIPs) are prepared on the surface of modified silica gel using prometryne as a template, methacrylic acid as the functional monomer, ethylene glycol dimethacrylate as a crosslinker, and 2,2-azobisisobutyronitrile as an initiator. The structure of the MIPs was characterized using SEM and FTIR spectroscopy. The selectivity of the MIPs for the template molecule prometryne was proven by adsorption experiments.

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