Results 211 to 220 of about 134,815 (339)
Charge‐transfer assisted ligation (CTAL) enables ultrafast CuAAC and SPAAC conjugation of a tetra‐DiAlkoxyNaphthalene (DAN4)‐azide and a noncomplementary tetraNaphthaleneDiImide (NDI4)‐alkyne oligonucleotide under dilute conditions, and the reaction can be carried out tracelessly by subsequently removing the tags.
Laura Nicollet +4 more
wiley +1 more source
Uridine as a hub in cancer metabolism and RNA biology. [PDF]
Choi KM, Berard BA, Yoon JH, Kim D.
europepmc +1 more source
ABSTRACT Background Nonsmall cell lung cancer (NSCLC) with mesenchymal‐epithelial transition exon 14 skipping mutation (METex14) represents a distinct molecular subtype with limited therapeutic options. Selective MET tyrosine kinase inhibitors (MET‐TKIs) such as tepotinib, capmatinib, and gumarontinib have improved outcomes, but toxicities frequently ...
Akina Nigi +5 more
wiley +1 more source
Discovery of α-glucosidase inhibitors from Paenibacillus sp. JNUCC 31 via genome mining, fatty acid profiling, and in silico analysis. [PDF]
Xu Y, Liang X, Hyun CG.
europepmc +1 more source
Abstract SGR‐1505 is a novel small‐molecule inhibitor of MALT1, a key mediator of NF‐κB signaling implicated in the pathogenesis of B‐cell malignancies. This study evaluated the safety, tolerability, pharmacokinetics, and pharmacodynamics of SGR‐1505 in healthy volunteers. In this four‐part, open‐label study, 73 participants received single or multiple
Vipul K. Gupta +16 more
wiley +1 more source
Potentiometric and spectroscopic characterization of uridine and its derivatives complexes. [PDF]
Stachowiak K +3 more
europepmc +1 more source
The wobble hypothesis revisited: Uridine-5-oxyacetic acid is critical for reading of G-ending codons [PDF]
Joakim Näsvall +2 more
openalex +1 more source
RYR‐stabilizers such as S107, JTV‐519, ARM 036, and ARM 210 are emerging doping‐relevant compounds due to their performance‐enhancing effects on leaky skeletal muscle Ca2+ channels. To support proactive antidoping efforts, all four compounds were synthesized and their in vitro metabolism was systematically investigated.
Tristan Möller +2 more
wiley +1 more source

