Results 161 to 170 of about 5,161 (208)

Exploring the Quantum: Atoms, Cavities, and Photons [PDF]

open access: yes, 2006
Haroche, Serge, Raimond, Jean Michel
core   +1 more source

Identification of a Selective Cell‐Active Inhibitor of Protein Arginine Methyltransferase 5 (PRMT5) for the Treatment of Prostate Cancer by Structure‐Based Virtual Screening

open access: yesChemical Biology &Drug Design, Volume 105, Issue 6, June 2025.
Combining previous research, compound SJL2‐1 was identified through virtual screening based on molecular docking. By reducing the expression levels of PRMT5 and AR, it exhibits anti‐proliferative effects, inhibits cell migration and invasion abilities, blocks the cell cycle, and induces apoptosis in AR‐sensitive prostate cancer and CRPC.
TongXiang Diao   +6 more
wiley   +1 more source

Junctional Internal Carotid Artery Aneurysms: The Schrödinger's Cat of Vascular Neurosurgery. [PDF]

open access: yesJ Neurol Surg B Skull Base, 2015
Carlson AP   +3 more
europepmc   +1 more source

Schrödinger's Worker: Are They Positive or Negative for SARS-CoV-2? [PDF]

open access: yesInt J Environ Res Public Health, 2020
Meloni F   +3 more
europepmc   +1 more source

Flavodiiron proteins associate pH‐dependently with the thylakoid membrane for ferredoxin‐1‐powered O2 photoreduction

open access: yesNew Phytologist, Volume 246, Issue 5, Page 2084-2101, June 2025.
Summary Flavodiiron proteins (FDPs) catalyse light‐dependent reduction of oxygen to water in photosynthetic organisms, creating an electron sink on the acceptor side of Photosystem I that protects the photosynthetic apparatus. However, ambiguity about the electron donor(s) remains, and the molecular mechanisms regulating FDP activity have remained ...
Lauri Nikkanen   +9 more
wiley   +1 more source

Entangling Schrödinger's cat states by bridging discrete- and continuous-variable encoding. [PDF]

open access: yesNat Commun
Hoshi D   +11 more
europepmc   +1 more source

Design and Evaluation of Bivalent K‐Ras Inhibitors That Target the CAAX Binding Site and the Acidic Surface of Farnesyltransferase and Geranylgeranyltransferase I

open access: yesChemistry – A European Journal, Volume 31, Issue 27, May 14, 2025.
Chemical inhibition of K‐Ras posttranslational prenylation represents a promising strategy against aggressive cancers. A structure‐based design produces piperidine‐based peptidomimetics conjugated to cationic modules, effectively inhibiting FTase and GGTase I at single‐digit nanomolar concentrations.
Naomi Horiuchi   +8 more
wiley   +1 more source

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