Results 71 to 80 of about 1,131,860 (291)
Loss of eIF5A rewires thapsigargin‐mediated endoplasmic reticulum stress responses in multiple myeloma cells by selective translation of mRNA transcripts, consequently dampening thapsigargin‐induced unfolded protein response (UPR) activation and shifting the balance from induction of apoptosis toward cell survival and proliferation.
Demi Both +7 more
wiley +1 more source
UiO‐66(Zr) metal–organic frameworks are chemically stable, biocompatible, and highly tunable nanomaterials. Their modular structure enables controlled drug delivery, multimodal bioimaging, and light‐activated photodynamic therapy, supporting integrated diagnostic and therapeutic (theranostic) applications in cancer and biomedical research.
Veronika Huntošová +2 more
wiley +1 more source
Non-covalent surface modification of cellulose nanocrystals by polyethyleneimine [PDF]
: Cellulose nanocrystals (CNCs) are bio-derived, natively hydrophilic nanomaterials that disperse well in water according to their surface chemistry upon extraction.
Khandal, Dhriti +6 more
core +1 more source
Deciphering the phosphorylation of chitosan through complementary 1H and 31P{1H} DOSY NMR
Chemical modification of chitosan through phosphorylation has gained significant attention for expanding its applications. However, confirming whether phosphorylating agents form covalent bonds with the chitosan backbone or remain as non-covalently ...
Souhaib Abouricha +8 more
doaj +1 more source
Molecular characterization of covRS mutations in M1UK Streptococcus pyogenes
Group A Streptococcus (GAS) acquires covRS mutations driving a hypervirulent bacterial state, frequently associated with invasive disease‐like necrotizing fasciitis. We demonstrate that the newly emerged M1UK GAS lineage can also acquire these mutations.
Jarrad Pritchard +12 more
wiley +1 more source
Attenuation of sensory receptor signaling by covalent modification. [PDF]
The Tar receptor is a transmembrane protein that regulates bacterial chemotaxis in response to changes in the level of aspartic acid in the medium. The extracellular portion of the protein can bind aspartate, and the cytoplasmic portion modulates CheA kinase activity. The receptor can either activate or inhibit the kinase.
Borkovich, Katherine A. +2 more
openaire +4 more sources
Covalent sizing surface modification as a route to improved interfacial adhesion in carbon fibre-epoxy ...
DJ Eyckens (14451150) +6 more
core
The cytoskeleton‐mediated transport of mitochondria via tunnelling nanotubes restores respiration, increases ATP production, rescues cells from apoptosis, activates the AKT/mTOR signalling pathway, promotes cell migration and invasiveness, contributes to cancer progression and treatment resistance.
Stanislava Martínková, Jan Trnka
wiley +1 more source
Rho GTPase regulation by miRNAs and covalent modifications [PDF]
To date, most studies of Rho GTPase regulation have focused on the classic GTPase cycle - GTP binding and hydrolysis - controlled by guanine nucleotide exchange factors (GEFs), GTPase-activating proteins (GAPs) and GDP-dissociation inhibitors (GDIs).
Ming, Liu +3 more
openaire +2 more sources
Targeted anticancer pre-vinylsulfone covalent inhibitors of carbonic anhydrase IX
We designed novel pre-drug compounds that transform into an active form that covalently modifies particular His residue in the active site, a difficult task to achieve, and applied to carbonic anhydrase (CAIX), a transmembrane protein, highly ...
Aivaras Vaškevičius +21 more
doaj +1 more source

