Results 221 to 230 of about 351,954 (346)
Background and Purpose Cyclic guanosine monophosphate (cGMP) is a ubiquitous second messenger involved in human (patho‐)physiology. Phosphodiesterase 5 (PDE5) is a major cGMP hydrolyzing enzyme in many cell types including vascular smooth muscle cells (VSMCs). Several highly selective PDE5 inhibitors are in clinical use. However, there are currently no
Kürsat Kirkgöz +8 more
wiley +1 more source
RPL29 as a radiotherapy-sensitive prognostic biomarker in multiple myeloma. [PDF]
Wang Y, Jia Q, Liu H, Li Z, Ma Y.
europepmc +1 more source
Unraveling the Anti-Multiple Myeloma Activity of Alisol B 23-Acetate and Its Impact on the P38MAPK Pathway Through Integrated Analysis [PDF]
Hui Zhang +4 more
openalex +1 more source
Background and Purpose Interleukin (IL)‐13 is implicated in airway hyperreactivity (AHR), a key feature of asthma. We explored the potential anti‐AHR activity of selected specialised pro‐resolving mediators (SPMs) in IL‐13‐induced AHR models, using human bronchial smooth muscle cells (BSMCs) and human isolated bronchi.
Willem Abma +9 more
wiley +1 more source
Characterization of cytogenetic abnormalities in Lebanese multiple myeloma patients. [PDF]
Najem G +12 more
europepmc +1 more source
Body mass index throughout adulthood, physical activity, and risk of multiple myeloma: A prospective analysis in three large cohorts [PDF]
Birmann, Brenda M +8 more
core +1 more source
Prognostic value of fatty acid metabolism-related signature and integrated analysis of the immune microenvironment in multiple myeloma [PDF]
Yang Yu, Feifei Che
openalex +1 more source
We identified a novel mechanism of resistance to histone deacetylase inhibitors (HDACi) in cutaneous T‐cell lymphoma (CTCL), mediated by NF‐κB activation. This finding highlights NF‐κB as a potential therapeutic target for overcoming HDACi resistance in CTCL.
Yuto Takahashi +10 more
wiley +1 more source
T Cells Dysfunction in Multiple Myeloma. [PDF]
Cai L +7 more
europepmc +1 more source
Targeting Overexpressed IDO in Stromal Cells as a Potential Therapeutic Strategy in Multiple Myeloma
IDO expression in stromal cells was upregulated by MM cells via the JAK–STAT1–NF‐κB–IRF1 signaling pathway. JAK inhibitor abolished IDO and IRF1 upregulation. ABSTRACT Stromal cells are an essential component of the tumor microenvironment (TME) in multiple myeloma (MM). Indoleamine 2,3‐dioxygenase 1 (IDO), an enzyme that metabolizes tryptophan (Trp) to
Toru Ebina +18 more
wiley +1 more source

