Role of rare-earth metals (R) in the appearance of relaxation processes in AL-Ni-R metal melts.

The temperature and time dependences of the viscosity of liquid ternary alloys AlNiY, AlNiLa, AlNiCe, AlNiCo, AlNiCoand binary melts Al(Y/Ni/Co)have been studied after different temperature-time treatment of the melt. It is shown that long-time relaxations in the Al-TM-R melts occur only after the phase transition 'crystal-liquid' due to the melt transition from the non-equilibrium to equilibrium state. The non-equilibrium state of the melt appears due to inheriting non-equilibrium atomic groups during melting; the atomic groups have ordering characteristic of chemical compounds of the AlRtype present in solid-state alloys.

[Ankylosing hyperostosis Forestier, simulating a neoplasm of the larynx].

Relevance: Forestier syndrome, despite its appearance as an independent disease in the 60s of the last century, remains as difficult to diagnose. This is due to a number of factors: age group, late treatment, insufficient knowledge of pathology. The timely detection of pathology is complicated by the similarity of the clinical picture in the early stages of its manifestation with a number of orthopedic diseases.

Clinical significance of molecular subtypes of gastrointestinal tract adenocarcinoma.

Adenocarcinomas of the gastrointestinal tract (esophagus, stomach, and colon) represent a heterogeneous group of diseases with distinct etiology, clinical features, treatment approaches, and prognosis. Studies are ongoing to isolate molecular genetic subtypes, perform complete biological characterization of the tumor, determine prognostic groups, and find predictive markers to the effectiveness of therapy. Separate molecular genetic classifications were created for esophageal adenocarcinoma [The Cancer Genome Atlas (TCGA)], stomach cancer (TCGA, Asian Cancer Research Group), and colon cancer (Colorectal Cancer Subtyping Consortium).

Platinum-based chemotherapy for pancreatic cancer: impact of mutations in the homologous recombination repair and Fanconi anemia genes.

Background: Mutations in homologous recombination (HR) and Fanconi anemia (FA) genes may predispose to pancreatic cancer (PC) and enable the prediction of sensitivity to platinum-based chemotherapy. FOLFIRINOX is a standard treatment option for non-selected PC patients and could be effective due to undiagnosed DNA repair deficiency. Here, we aimed to determine the frequency of mutations in genes involved in the HR and FA pathways, evaluate their clinical implications, and determine the objective response rate (ORR), progression-free survival (PFS), and overall survival (OS) of PC patients treated with platinum.