Publications by authors named "F Hanisch"

Article Synopsis
  • The study investigates the processes e^{+}e^{-}→D_{s}^{+}D_{s1}(2536)^{-} and e^{+}e^{-}→D_{s}^{+}D_{s2}^{*}(2573)^{-} using data from the BESIII detector, focusing on a range of center-of-mass energies.
  • For the first time, the absolute branching fractions of the decay processes for D_{s1}(2536)^{-} and D_{s2}^{*}(2573)^{-} are measured, revealing values of 35.9% and 37.4% respectively.
  • The research identifies a resonant structure around 4.6 Ge
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Article Synopsis
  • The study investigates the J/ψ and ψ(3686) decays into Σ^{0}Σ[over ¯]^{0} processes using data from the BESIII detector, which has extensive datasets.
  • It presents the first measurements of parity-violating decay parameters for Σ^{0} and Σ[over ¯]^{0}, suggesting implications for strong CP symmetry through their asymmetries.
  • The findings include the observation of opposite transverse polarizations of Σ^{0} hyperons in these decays and the ratio of S-wave to D-wave contributions, contributing valuable insights into charmonium state dynamics.
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Using data samples collected with the BESIII detector operating at the BEPCII storage ring, the cross section of the inclusive process e^{+}e^{-}→η+X, normalized by the total cross section of e^{+}e^{-}→hadrons, is measured at eight center-of-mass energy points from 2.0000 to 3.6710 GeV.

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The world-wide COVID-19 pandemic has promoted a series of alternative vaccination strategies aiming to elicit neutralizing adaptive immunity in the human host. However, restricted efficacies of these vaccines targeting epitopes on the spike (S) protein that is involved in primary viral entry were observed and putatively assigned to viral glycosylation as an effective escape mechanism. Besides the well-recognized N-glycan shield covering SARS-CoV-2 spike (S) proteins, immunization strategies may be hampered by heavy O-glycosylation and variable O-glycosites fluctuating depending on the organ sites of primary infection and those involved in immunization.

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Fucoidans are discussed as antiviral agents, and fucoidan from Undaria pinnatifida (UpF), in particular has gained interest as potential food additive in antinoroviral strategies. As the competitive blocking activity of antinoroviral agents increases with the valency of terminal nonreducing fucose on the competitor, an effective processing of fucoidans to inhibitory oligosaccharides will depend on basic structural features of the polysaccharide. We demonstrate increased antiviral binding activity of processed low-mass UpF generated by hydrothermal degradation contrasting with decreased efficacy of low-mass fucoidan from Fucus vesiculosus.

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