Results 191 to 200 of about 683,642 (281)

EhC2B, a C2 domain-containing protein, promotes erythrophagocytosis in Entamoeba histolytica via actin nucleation. [PDF]

open access: yesPLoS Pathog, 2020
Tripathi A   +7 more
europepmc   +1 more source

Toxoplasma gondii C2 Domain Protein Deletion Mutant as a Promising Vaccine Against Toxoplasmosis in Mice. [PDF]

open access: yesMicrob Biotechnol
Luo Y   +8 more
europepmc   +1 more source

Synergistic Ion Transport and Spatial Confinement in Sb‐Embedded Hollow Carbon Nanofibers for Stable Na Metal Anodes

open access: yesAdvanced Science, EarlyView.
This work presents a 3D Sb‐embedded hollow carbon nanofiber (Sb@HCF) host for ultra‐stable Na metal anodes. Experimental analyses and theoretical simulations clearly uncovers that in situ formed Na‐Sb alloy guides uniform Na deposition and serves as efficient ion transport highways. The Sb@HCF‐based cells achieve exceptional cycling stability in half‐,
Feng Han   +9 more
wiley   +1 more source

Interaction between the TBC1D24 TLDc domain and the KIBRA C2 domain is disrupted by two epilepsy-associated TBC1D24 missense variants. [PDF]

open access: yesJ Biol Chem
Tona R   +10 more
europepmc   +1 more source

The 3.2 Å structure of a bioengineered variant of blood coagulation factor VIII indicates two conformations of the C2 domain. [PDF]

open access: yesJ Thromb Haemost, 2020
Smith IW   +9 more
europepmc   +1 more source

Persistently Increased Expression of PKMzeta and Unbiased Gene Expression Profiles Identify Hippocampal Molecular Traces of a Long‐Term Active Place Avoidance Memory and “Shadow” Proteins

open access: yesAdvanced Science, EarlyView.
Protein complexes like KIBRA‐PKMζ are crucial for maintaining memories, forming month‐long protein traces in memory‐tagged neurons, but conventional RNA‐seq analysis fails to detect their transcript changes, leaving memory molecules undetected in the shadows of abundantly‐expressed genes.
Jiyeon Han   +10 more
wiley   +1 more source

A Germline Mutation in the C2 Domain of PLCγ2 Associated with Gain-of-Function Expands the Phenotype for PLCG2-Related Diseases. [PDF]

open access: yesJ Clin Immunol, 2020
Novice T   +20 more
europepmc   +1 more source

Calcium signaling and pathogenesis of dysferlin C2 domains

open access: yes, 2020
Failure to repair injured sarcolemmal membranes leads to muscular dystrophy, a degenerative disorder that results in increasing weakness and gradual wasting of skeletal muscles. Mutations in the gene encoding dysferlin are causative for limb girdle muscular dystrophy type 2B (LGMD2B) and Miyoshi myopathy (MM) forms of the disease.
openaire   +1 more source

Atomic Tuning of Metal‐Support Interactions for Pathway‐Selective CO2 Photoreduction on TiO2

open access: yesAdvanced Science, EarlyView.
Single‐atom Fe and Cu catalysts anchored on TiO2 steer photocatalytic CO2 reduction toward distinct pathways. Fe sites favor rapid *CO desorption and selective CO formation, whereas Cu sites stabilize *CHO intermediates, enabling deep reduction and C─C coupling. Combined spectroscopy and DFT calculations reveal how metal–support interactions and oxygen
Dongyun Kim   +13 more
wiley   +1 more source

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