Results 201 to 210 of about 175,201 (271)
The A3 adenosine receptors (A3ARs) are overexpressed in prostate cancer. AR 292 and AR 357, as A3AR antagonists, are capable of blocking proliferation, modulating the expression of drug transporter genes involved in chemoresistance, ferroptosis, and the hypoxia response, and inducing cell death.
Maria Beatrice Morelli+15 more
wiley +1 more source
SEDATION FOR ENDOSCOPY: MIDAZOLAM OR DIAZEPAM AND PETHIDINE?
D.A.R. Boldy+4 more
openalex +1 more source
Use of sedative drugs in specialist palliative care (iSedPall): a multi-modal intervention pilot study protocol. [PDF]
Ostgathe C+13 more
europepmc +1 more source
Etoposide, a topoisomerase II inhibitor, reduces O‐GlcNAcylation in HepG2 liver cancer cells. Further inhibition of O‐GlcNAc transferase by OSMI‐1 enhanced etoposide‐induced apoptosis, lowering the IC50 for viability and increasing the EC50 for cytotoxicity.
Jaehoon Lee+5 more
wiley +1 more source
Alfentanil and fentanyl sedation in infants and small children during cardiac catheterization [PDF]
Olli A. Meretoja, Paula Rautiainen
openalex +1 more source
Isoflurane vs. Propofol Sedation in Patients with Severe Stroke: A Clinical Proof-of-Concept-Study. [PDF]
Worm A+12 more
europepmc +1 more source
ICP34.5 is one of the most important antihost response proteins. The saRNA‐encoding HSV‐1 neurovirulence protein ICP34.5 clearly mediated the eukaryotic initiation factor 2 alpha subunit (eIF2α) dephosphorylation and significant suppression of innate immune responses in vitro, leading to enhanced expression of the saRNA‐encoded gene.
Xuemin Lu+6 more
wiley +1 more source
A comparison of morphine-perphenazine and midazolam on preoperative sedation and arterial oxygen saturation [PDF]
Elliot T. Hudes+4 more
openalex +1 more source