Results 191 to 200 of about 679,279 (310)
SARS-CoV-2 and Microbiologists
Nikunja Kumar Das +3 more
openaire +2 more sources
Characterization and immunogenicity of nanoparticle vaccines displaying embecovirus spike proteins
Virus‐like particle vaccines displaying spike proteins from OC43, HKU1 A, and HKU1 B were evaluated in mice for their ability to elicit antibodies against the spike proteins from OC43, HKU1 A, HKU1 B, and HKU1 C. Abstract Endemic human coronaviruses OC43 and HKU1 cause widespread respiratory infections and can be associated with severe illness in ...
Peter J. Halfmann +6 more
wiley +1 more source
SARS-CoV-2 and reproductive system: a scientometric study. [PDF]
Zhang L, Wang M, Zhang H, Mao G.
europepmc +1 more source
Humoral epitope dominance and immune imprinting by SARS-CoV-1 and SARS-CoV-2 vaccines. [PDF]
Burnett DL +17 more
europepmc +1 more source
Why add another catalyst when the product itself holds the power to catalyze its own formation? Autocatalysis in synthetic chemistry enhances reaction efficiency and uncovers novel catalytic behavior across both closed‐shell and open‐shell systems, expanding reactivity and enabling innovative design strategies.
Jaspreet Kaur, Joshua P. Barham
wiley +1 more source
Bilateral subscapular hematoma following SARS‐CoV‐2 vaccination
Osamu Imataki, Makiko Uemura
doaj +1 more source
SARS-CoV-2 Evolution and Its Implications for RT-PCR Diagnostic Performance. [PDF]
Gupta S, Chaudhary A, Bhatnagar S.
europepmc +1 more source
Favipiravir (T‐705) and the non‐fluorinated counterpart (T‐1106) are antiviral agents that inhibit the RNA‐dependent RNA polymerase (RdRp) of various RNA viruses. The antiviral efficacy of nucleoside analogues is strongly dependent on their intracellular activation by cellular kinases to produce their corresponding triphosphate metabolites (T‐705‐RTP ...
Chris Meier +7 more
wiley +1 more source
Functional and structural characterization of the SARS-CoV-2 spike N481K mutation. [PDF]
Smatti MK +7 more
europepmc +1 more source
The SARS‐CoV‐2 papain‐like protease (PLpro) is a medicinal chemistry target. Here we report mass spectrometry assays employing oligopeptide substrates based on the sequences of the viral polyproteins 1a/1ab and on an ISG15‐modified human protein, which enabled the identification of substrate‐selective PLpro inhibitors.
Sakshi Sharma +13 more
wiley +1 more source

