Results 241 to 250 of about 723,610 (311)
An electrosynthesized protein‐imprinted polymer (poly(azo‐BBY)) enables probe‐free, real‐capacitance detection of human serum albumin at 0.02 ng mL−1 within a 0.25–3.0 ng mL−1 window. The device uses a redox‐mediator‐free architecture and maintains selectivity against common interferents, illustrating a simple, scalable route to high‐sensitivity ...
Heitor F. Trevizan +4 more
wiley +1 more source
N3A motifs in RIβ mediate allosteric crosstalk between cAMP and ATP in PKA activation. [PDF]
Wu J +6 more
europepmc +1 more source
Cyclodextrin nanoparticle containing both Ga(NO3)3 and GaPP is synthesized and tested against non‐tuberculous mycobacteria (NTM). The in vivo efficacy of the nanoparticle therapy is additionally tested by treating pulmonary NTM infections in mice and observed much greater effectiveness in bacterial clearance and survival of mice.
Seoung‐ryoung Choi +2 more
wiley +1 more source
Structural characterization of an extracellular contractile injection system from Photorhabdus luminescens in extended and contracted states. [PDF]
Marín-Arraiza L +7 more
europepmc +1 more source
LRRC8A Regulates Outer Hair Cell Volume and Electromotility and is Required for Hearing
This study identifies LRRC8A‐dependent volume‐regulated anion channels (VRACs) as essential for cochlear outer hair cells' electromotility and auditory signal amplification. LRRC8A deficiency disrupts cell volume control, impairs auditory sensitivity, and causes deafness, while targeted LRRC8A re‐expression restores auditory function.
Shengnan Wang +15 more
wiley +1 more source
Properties of Heterochannels Kv(1.1-1.2)<sub>2</sub> with Mutation T226R in the Kv1.1 Subunit. [PDF]
Ignatova AA +7 more
europepmc +1 more source
Neural tube defects (NTDs) are among the most common congenital malformations. However, the underlying etiology and mechanism remain elusive. Here, the role of DNA double‐strand breaks (DSBs) in 3D genome organization within the NTDs with folate deficiency is reported.
Ting Zhang +12 more
wiley +1 more source
Correction: Role of the YWHAG gene mutations in developmental and epileptic encephalopathy. [PDF]
Vilmont V, Nowakowski RS, Zhou Y.
europepmc +1 more source

