Results 131 to 140 of about 9,423,140 (336)

Escape from TGF‐β‐induced senescence promotes aggressive hallmarks in epithelial hepatocellular carcinoma cells

open access: yesMolecular Oncology, EarlyView.
Chronic TGF‐β exposure drives epithelial HCC cells from a senescent state to a TGF‐β resistant mesenchymal phenotype. This transition is characterized by the loss of Smad3‐mediated signaling, escape from senescence, enhanced invasiveness and metastatic potential, and upregulation of key resistance modulators such as MARK1 and GRM8, ultimately promoting
Minenur Kalyoncu   +11 more
wiley   +1 more source

The domination number of K_{n}^3

open access: yesDiscussiones Mathematicae Graph Theory, 2014
Let K3n denote the Cartesian product Kn□Kn□Kn, where Kn is the complete graph on n vertices.
David W. Mauro   +2 more
openaire   +3 more sources

Inhibitor of DNA binding‐1 is a key regulator of cancer cell vasculogenic mimicry

open access: yesMolecular Oncology, EarlyView.
Elevated expression of transcriptional regulator inhibitor of DNA binding 1 (ID1) promoted cancer cell‐mediated vasculogenic mimicry (VM) through regulation of pro‐angiogenic and pro‐cancerous genes (e.g. VE‐cadherin (CDH5), TIE2, MMP9, DKK1). Higher ID1 expression also increased metastases to the lung and the liver.
Emma J. Thompson   +11 more
wiley   +1 more source

MET and NF2 alterations confer primary and early resistance to first‐line alectinib treatment in ALK‐positive non‐small‐cell lung cancer

open access: yesMolecular Oncology, EarlyView.
Alectinib resistance in ALK+ NSCLC depends on treatment sequence and EML4‐ALK variants. Variant 1 exhibited off‐target resistance after first‐line treatment, while variant 3 and later lines favored on‐target mutations. Early resistance involved off‐target alterations, like MET and NF2, while on‐target mutations emerged with prolonged therapy.
Jie Hu   +11 more
wiley   +1 more source

On domination number and distance in graphs

open access: yesDiscrete Applied Mathematics, 2016
A vertex set $S$ of a graph $G$ is a \emph{dominating set} if each vertex of $G$ either belongs to $S$ or is adjacent to a vertex in $S$. The \emph{domination number} $ (G)$ of $G$ is the minimum cardinality of $S$ as $S$ varies over all dominating sets of $G$.
openaire   +3 more sources

Chemoresistome mapping in individual breast cancer patients unravels diversity in dynamic transcriptional adaptation

open access: yesMolecular Oncology, EarlyView.
This study used longitudinal transcriptomics and gene‐pattern classification to uncover patient‐specific mechanisms of chemotherapy resistance in breast cancer. Findings reveal preexisting drug‐tolerant states in primary tumors and diverse gene rewiring patterns across patients, converging on a few dysregulated functional modules. Despite receiving the
Maya Dadiani   +14 more
wiley   +1 more source

Total Domination Multisubdivision Number of a Graph

open access: yesDiscussiones Mathematicae Graph Theory, 2015
The domination multisubdivision number of a nonempty graph G was defined in [3] as the minimum positive integer k such that there exists an edge which must be subdivided k times to increase the domination number of G.
Avella-Alaminos Diana   +3 more
doaj   +1 more source

On the r-domination number of a graph

open access: yesDiscrete Mathematics, 1992
AbstractFor r > 0, let the r-domination number of a graph, dr, be the size of a smallest set of vertices such that every vertex of the graph is within distance r of a vertex in that set. This paper contains proofs that every graph with a spanning tree with at least n/2 leaves has dr ⩽ n/(2r); this compares with the easy upper bound of ⌈n/(2r + 1)⌉ for ...
Jerrold R. Griggs, Joan P. Hutchinson
openaire   +2 more sources

Determination of ADP/ATP translocase isoform ratios in malignancy and cellular senescence

open access: yesMolecular Oncology, EarlyView.
The individual functions of three isoforms exchanging ADP and ATP (ADP/ATP translocases; ANTs) on the mitochondrial membrane remain unclear. We developed a method for quantitatively differentiating highly similar human ANT1, ANT2, and ANT3 using parallel reaction monitoring. This method allowed us to assess changes in translocase levels during cellular
Zuzana Liblova   +18 more
wiley   +1 more source

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