Results 171 to 180 of about 14,686,195 (254)

Development of an influenza D virus with an eight- or nine-segment genome. [PDF]

open access: yesSci Rep
Ishida H   +9 more
europepmc   +1 more source

Cattle influenza D virus in Brazil is divergent from established lineages. [PDF]

open access: yesArch Virol, 2022
da Silva MS   +9 more
europepmc   +1 more source

m6A‐Driven Pexophagy Triggers Placental Ferroptosis to Impair Fetal Growth Upon Environmental Stress

open access: yesAdvanced Science, EarlyView.
Prenatal environmental stress exposure promotes m6A modification to drive PEX2‐dependent pexophagy, thereby causing placental ferroptosis and FGR. ABSTRACT The role and underlying mechanisms of placental ferroptosis in fetal growth restriction (FGR) induced by environmental stress remain poorly understood.
Xin‐Xin Zhang   +18 more
wiley   +1 more source

First Detection and Genetic Characterization of Influenza D Virus in Cattle in Spain. [PDF]

open access: yesVet Sci
Benito AA   +5 more
europepmc   +1 more source

Influenza D virus. [PDF]

open access: yesCurr Opin Virol, 2020
Liu R, Sheng Z, Huang C, Wang D, Li F.
europepmc   +1 more source

Detection of antibodies against influenza D virus in swine veterinarians in Italy in 2004. [PDF]

open access: yesJ Med Virol, 2022
Trombetta CM   +5 more
europepmc   +1 more source

A Small‐Molecule DEPTAC Rescues Cognitive Deficits by Targeted Dephosphorylation of Pathological Tau

open access: yesAdvanced Science, EarlyView.
TP2 is a fully synthetic small‐molecule dephosphorylation‐targeting chimera that recruits endogenous PP2A‐Bα to Tau, enabling targeted removal of pathological phosphate modifications. In two tauopathy mouse models, systemic TP2 reduces Tau pathology, preserves neuronal and synaptic integrity, improves neuroimmune homeostasis, and rescues cognition ...
Fei Sun   +12 more
wiley   +1 more source

Kidney‐Targeted Cilastatin Nanoparticles Inhibit DPEP1‐Mediated Ferroptosis for Acute Kidney Injury Therapy

open access: yesAdvanced Science, EarlyView.
In this study, MPDA NPs were engineered to encapsulate CTT. To further increase renal accumulation of CTT, L‐serine was conjugated to the surface of the MPDA nanoparticles (CTT/MPDA@L‐Ser NPs). CTT/MPDA@L‐Ser NPs inhibit DPEP1 activity, thereby restoring ferroptosis defense mechanisms through upregulation of GPX4 and SLC7A11 expression, ultimately ...
Wanbing Qin   +12 more
wiley   +1 more source

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