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Sökning: WFRF:(Wang Yimeng)

  • Resultat 1-6 av 6
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1.
  • Cheng, Ye, et al. (författare)
  • Genetic variants in the HLA region contribute to the risk of cerebral palsy
  • 2024
  • Ingår i: BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE. - 0925-4439 .- 1879-260X. ; 1870:3
  • Tidskriftsartikel (refereegranskat)abstract
    • Cerebral palsy (CP) is the most common physical disability in childhood, and genetic factors play an important role in its pathogenesis. However, the genetic contributions remain incompletely elucidated. Here, we conducted a two-stage association study between 1090 CP cases and 1100 healthy controls after whole exome sequencing. The human leukocyte antigen (HLA) allelic predispositions were further analyzed in overall CP and subgroups using multivariate logistic regression. We found a strong signal in the HLA region on chromosome 6, where rs3131787 harbored the most significant association with CP (P = 2.05 x 10-14, OR = 2.22). In comparison to controls, the carrier frequencies of HLA-B*13:02 were significantly higher in children with CP (9.82 % in control vs 19.27 % in CP, P = 1.03 x 10-4, OR = 2.17). Furthermore, the effect of HLA-B*13:02 on increasing the risk of CP mainly existed in cryptogenic CP without exposure to premature birth, low birth weight, birth asphyxia, or periventricular leukomalacia. This study indicated a strong association of HLA variants with CP, which implied that immune dysregulation resulting from immunogenetic variants might underlie the pathogenesis of CP. Our findings provide genetic evidence that an immunomodulator may serve as a promising therapeutic intervention for patients with CP by reinstating the neuroinflammation hemostasis.
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2.
  • Wang, Yangong, et al. (författare)
  • TEP1 is a risk gene for sporadic cerebral palsy
  • 2021
  • Ingår i: Journal of genetics and genomics. - : Elsevier BV. - 1673-8527. ; 48:12, s. 1134-1138
  • Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)
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3.
  • Xu, Weidong, et al. (författare)
  • Iodomethane-Mediated Organometal Halide Perovskite with Record Photoluminescence Lifetime
  • 2016
  • Ingår i: ACS Applied Materials and Interfaces. - : AMER CHEMICAL SOC. - 1944-8244 .- 1944-8252. ; 8:35, s. 23181-23189
  • Tidskriftsartikel (refereegranskat)abstract
    • Organometallic lead halide perovskites are excellent light harvesters for high-efficiency photovoltaic devices. However, as the key component in these devices, a perovskite thin film with good morphology and minimal trap states is still difficult to obtain. Herein we show that by incorporating a low boiling point alkyl halide such as iodomethane (CH3I) into the precursor solution, a perovskite (CH3NH3PbI3-xClx) film with improved grain size and orientation can be easily achieved. More importantly, these films exhibit a significantly reduced amount of trap states. Record photoluminescence lifetimes of more than 4 mu s are achieved; these lifetimes are significantly longer than that of pristine CH3NH3PbI3-xClx films. Planar heterojunction solar cells incorporating these CH3I-mediated perovskites have demonstrated a dramatically increased power conversion efficiency compared to the ones using pristine CH3NH3PbI3-xClx. Photoluminescence, transient absorption, and microwave detected photoconductivity measurements all provide consistent evidence that CH3I addition increases the number of excitons generated and their diffusion length, both of which assist efficient carrier transport in the photovoltaic device. The simple incorporation of alkyl halide to enhance perovskite surface passivation introduces an important direction for future progress on high efficiency perovskite optoelectronic devices.
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4.
  • Wang, Yangong, et al. (författare)
  • Exome sequencing reveals genetic heterogeneity and clinically actionable findings in children with cerebral palsy
  • 2024
  • Ingår i: NATURE MEDICINE. - 1078-8956 .- 1546-170X. ; 30, s. 1395-1405
  • Tidskriftsartikel (refereegranskat)abstract
    • Cerebral palsy (CP) is the most common motor disability in children. To ascertain the role of major genetic variants in the etiology of CP, we conducted exome sequencing on a large-scale cohort with clinical manifestations of CP. The study cohort comprised 505 girls and 1,073 boys. Utilizing the current gold standard in genetic diagnostics, 387 of these 1,578 children (24.5%) received genetic diagnoses. We identified 412 pathogenic and likely pathogenic (P/LP) variants across 219 genes associated with neurodevelopmental disorders, and 59 P/LP copy number variants. The genetic diagnostic rate of children with CP labeled at birth with perinatal asphyxia was higher than the rate in children without asphyxia (P = 0.0033). Also, 33 children with CP manifestations (8.5%, 33 of 387) had findings that were clinically actionable. These results highlight the need for early genetic testing in children with CP, especially those with risk factors like perinatal asphyxia, to enable evidence-based medical decision-making. Using exome sequencing data from one of the largest cohorts of children with cerebral palsy, the genetic diagnostic rates of single-nucleotide and copy number variants were assessed and a sizeable fraction found to be clinically actionable.
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5.
  • Lee, Husileng, et al. (författare)
  • Hierarchical CoS2/Ni3S2/CoNiOx nanorods with favorable stability at 1 A cm(-2) for electrocatalytic water oxidation
  • 2019
  • Ingår i: Chemical Communications. - : ROYAL SOC CHEMISTRY. - 1359-7345 .- 1364-548X. ; 55:11, s. 1564-1567
  • Tidskriftsartikel (refereegranskat)abstract
    • Herein, we have reported an easily synthesized CoS2/Ni3S2/CoNiOx water oxidation catalyst with excellent catalytic activity and superior durability. The as-prepared catalyst required overpotential (eta) as low as 256 mV to exhibit a current density of 10 mA cm(-2) in 1.0 M KOH. Remarkably, it sustained a current density of 1 A cm(-2) for one week in 30% KOH solution with only 25 mV increment of eta. Thus, it is a hopeful candidate as a highly-effective water oxidation electrode in practical applications.
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6.
  • Wu, Xiujuan, et al. (författare)
  • Hollow Carbon@NiCo2O4 Core-Shell Microspheres for Efficient Electrocatalytic Oxygen Evolution
  • 2019
  • Ingår i: ENERGY TECHNOLOGY. - : Wiley. - 2194-4288 .- 2194-4296. ; 7:4
  • Tidskriftsartikel (refereegranskat)abstract
    • Earth-abundant transition metal oxides are considered one of the most promising oxygen evolution reaction (OER) catalysts. However, their intrinsically low electrical conductivity inhibits the fast kinetics for OER. To overcome this drawback, hollow carbon@NiCo2O4 core-shell microspheres (C@NiCo2O4 HSs) are synthesized with enhanced electrocatalytic activity and stability toward OER. The prepared C@NiCo2O4/Ni foam delivers a current density of 10 mA cm(-2) at a small overpotential of 268 mV and exhibits a low Tafel slope of 54 mV dec(-1). The enhanced OER performance is attributed to the enlarged specific surface area induced by the combination effect between the 1D nanosheet structure and the 3D hollow microsphere structure, and the improved electrical conductivity is ascribed to the carbon core support.
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  • Resultat 1-6 av 6

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