Results 201 to 210 of about 591,025 (333)

Theranostic Toolbox for Neutrophil Functionalization

open access: yesAdvanced Science, EarlyView.
Here, neutrophil‐specific fluorine nanoparticles additionally equipped with either activating or inhibiting peptides for a background‐free 19F MRI‐based nanotheranostic approach are engineered. It is demonstrated that this approach is suitable to visualize and concomitantly direct neutrophil functionality depending on the specific requirements to ...
Pascal Bouvain   +11 more
wiley   +1 more source

Correction: Produced water treatment by semi-continuous sequential bioreactor and microalgae photobioreactor. [PDF]

open access: yesBioresour Bioprocess
Khairuddin NFM   +5 more
europepmc   +1 more source

NADPH Oxidase Inhibition Promotes Brain Resilience by Attenuating Tauopathy and Neuroinflammation in Alzheimer's Disease

open access: yesAdvanced Science, EarlyView.
CRB‐2131, as a novel Nox inhibitor, suppresses brain oxidation, tauopathy, and neuro‐inflammation, thereby preventing death of mature neurons and promoting regeneration of immature neurons. Ultimately, this fosters a resilient brain and protects cognition.
Jihyeon Lee   +13 more
wiley   +1 more source

Pulsed Laser Synthesis of Carbon Nanostructures from Organic Molecular Liquids: Structure, Kinetics and Photophysical Properties

open access: yesAdvanced Science, EarlyView.
The non‐focused nanosecond pulsed laser irradiation of aromatic liquids produces amorphous carbon nanodots (CNDs) or curved‐graphene quantum dots (c‐GQDs) by surface‐catalyzed 0‐order reactions under kinetic control. C hybridization partially changes from sp2 to sp3. O‐based groups passivate the surface.
Antonio Ribeiro‐González   +8 more
wiley   +1 more source

Structurally Constrained Cyclic (Diacyloxyiodo)Arenes as an Enabling Platform for Hypervalent Iodine(III) Chemistry

open access: yesAdvanced Science, EarlyView.
We developed cyclic (diacyloxyiodo)arenes to overcome the reactivity/selectivity paradox in iodine chemistry. This new platform enables simple, one‐pot synthesis of diverse hypervalent iodine(III) reagents. The method is sustainable, catalytic, works for asymmetric reactions, and is biocompatible (e.g., modifying peptides).
Shengyu Zhong   +4 more
wiley   +1 more source

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