Results 81 to 90 of about 14,669 (262)
Strong chromatic index of sparse graphs [PDF]
A coloring of the edges of a graph $G$ is strong if each color class is an induced matching of $G$. The strong chromatic index of $G$, denoted by $\chi_{s}^{\prime}(G)$, is the least number of colors in a strong edge coloring of $G$.
Dębski, Michał +2 more
core
This study indicates that Merkel cell carcinoma (MCC) does not originate from Merkel cells, and identifies gene, protein & cellular expression of immune‐linked and neuroendocrine markers in primary and metastatic Merkel cell carcinoma (MCC) tumor samples, linked to Merkel cell polyomavirus (MCPyV) status, with enrichment of B‐cell and other immune cell
Richie Jeremian +10 more
wiley +1 more source
Fuzzy Edge Chromatic Number of the Join of Fuzzy Graphs and Its Applications
Fuzzy edge coloring has proven to be a powerful tool for modeling and optimizing complex network systems, owing to its ability to effectively represent and manage the uncertainty in relational strengths and conflicts.
Jing Qu, Qian Wang, Angmo Deji
doaj +1 more source
Following high dose rate brachytherapy (HDR‐BT) for hepatocellular carcinoma (HCC), patients were classified as responders and nonresponders. Post‐therapy serum induced increased BrdU incorporation and Cyclin E expression of Huh7 and HepG2 cells in nonresponders, but decreased levels in responders.
Lukas Salvermoser +14 more
wiley +1 more source
A synthetic benzoxazine dimer derivative targets c‐Myc to inhibit colorectal cancer progression
Benzoxazine dimer derivatives bind to the bHLH‐LZ region of c‐Myc, disrupting c‐Myc/MAX complexes, which are evaluated from SAR analysis. This increases ubiquitination and reduces cellular c‐Myc. Impairing DNA repair mechanisms is shown through proteomic analysis.
Nicharat Sriratanasak +8 more
wiley +1 more source
This study integrates transcriptomic profiling of matched tumor and healthy tissues from 32 colorectal cancer patients with functional validation in patient‐derived organoids, revealing dysregulated metabolic programs driven by overexpressed xCT (SLC7A11) and SLC3A2, identifying an oncogenic cystine/glutamate transporter signature linked to ...
Marco Strecker +16 more
wiley +1 more source
Edge-coloring via fixable subgraphs [PDF]
Many graph coloring proofs proceed by showing that a minimal counterexample to the theorem being proved cannot contain certain configurations, and then showing that each graph under consideration contains at least one such configuration; these ...
Cranston, Daniel W., Rabern, Landon
core
Aggressive prostate cancer is associated with pericyte dysfunction
Tumor‐produced TGF‐β drives pericyte dysfunction in prostate cancer. This dysfunction is characterized by downregulation of some canonical pericyte markers (i.e., DES, CSPG4, and ACTA2) while maintaining the expression of others (i.e., PDGFRB, NOTCH3, and RGS5).
Anabel Martinez‐Romero +11 more
wiley +1 more source
ERRFI1, a neural crest (NC)‐associated gene, was upregulated in melanoma and negatively correlated with the expression of melanocytic differentiation markers and the susceptibility of melanoma cells toward BRAF inhibitors (BRAFi). Knocking down ERRFI1 significantly increased the sensitivity of melanoma cells to BRAFi.
Nina Wang +8 more
wiley +1 more source
Twin edge colorings of certain square graphs and product graphs
A twin edge $k\!$-coloring of a graph $G$ is a proper edge $k$-coloring of $G$ with the elements of $\mathbb{Z}_k$ so that the induced vertex $k$-coloring, in which the color of a vertex $v$ in $G$ is the sum in $\mathbb{Z}_k$ of the colors of the edges ...
R Rajarajachozhan, R. Sampathkumar
doaj +1 more source

