Results 41 to 50 of about 1,179,204 (384)
Neutrinoless $ββ$-decay nuclear matrix elements from two-neutrino $ββ$-decay data [PDF]
, 2022 We study two-neutrino ($2\nu\beta\beta$) and neutrinoless double-$\beta$ ($0\nu\beta\beta$) decays in the nuclear shell model and proton-neutron quasiparticle random-phase approximation (pnQRPA) frameworks. Calculating the decay half-life of several dozens of nuclei ranging from calcium to xenon with the shell model, and of $\beta\beta$ emitters with a
arxiv +1 more source
Beta-catenin cleavage enhances transcriptional activation [PDF]
Scientific Reports, 2018 AbstractNuclear activation of Wnt/β-catenin signaling is required for cell proliferation in inflammation and cancer. Studies from our group indicate that β-catenin activation in colitis and colorectal cancer (CRC) correlates with increased nuclear levels of β-catenin phosphorylated at serine 552 (pβ-Cat552).
Tatiana Goretsky +12 more
openaire +3 more sources
Expression of dickkopf-1 and beta-catenin related to the prognosis of breast cancer patients with triple negative phenotype. [PDF]
PLoS ONE, 2012 BACKGROUND AND AIM: We investigated the prognostic importance of dickkopf-1(DKK1) and beta-catenin expression in triple negative breast cancers. METHODS: The expression of DKK1 and beta-catenin was evaluated in breast cell lines using RT-PCR and western ...
Wen-Huan Xu +4 more
doaj +1 more source
OSTM1 regulates beta-catenin/Lef1 interaction and is required for Wnt/beta-catenin signaling [PDF]
, 2008 The Wnt/beta-catenin signaling pathway controls key aspects of embryonic development and adult tissue homeostasis, including the formation and maintenance of bone.
Feigin, M. E., Malbon, C. C.
core +1 more source
A Reaction-Diffusion Model of the Cadherin-Catenin System: A Possible Mechanism for Contact Inhibition and Implications for Tumorigenesis [PDF]
Biophys. J. 98 (12), 2770-2779 (2010), 2015 Contact inhibition is the process by which cells switch from a motile growing state to a passive and stabilized state upon touching their neighbors. When two cells touch, an adhesion link is created between them by means of transmembrane E-cadherin proteins.
arxiv +1 more source
Subshifts of finite type and matching for intermediate $β$-transformations [PDF]
, 2022 We focus on the relationships between matching and subshift of finite type for intermediate $\beta$-transformations $T_{\beta,\alpha}(x)=\beta x+\alpha $ ($\bmod$ 1), where $x\in[0,1]$ and $(\beta,\alpha) \in \Delta:= \{ (\beta, \alpha) \in \mathbb{R}^{2}:\beta \in (1, 2) \; \rm{and} \; 0 < \alpha <2 - \beta\}$.
arxiv +1 more source
PPAR Research, 2017 In both colon cancer and type 2 diabetes, metabolic changes induced by upregulation of the Wnt/beta-catenin signaling and downregulation of peroxisome proliferator-activated receptor gamma (PPAR gamma) may help account for the frequent association of ...
Y. Lecarpentier +3 more
semanticscholar +1 more source
$γγ$ decay as a probe of neutrinoless $ββ$ decay nuclear matrix elements [PDF]
Physics Letters B 827 (2022) 136965, 2021 We study double gamma ($\gamma\gamma$) decay nuclear matrix elements (NMEs) for a wide range of nuclei from titanium to xenon, and explore their relation to neutrinoless double-beta ($0\nu\beta\beta$) NMEs. To favor the comparison, we focus on double-magnetic dipole transitions in the final $\beta\beta$ nuclei, in particular the $\gamma\gamma$ decay of
arxiv +1 more source
OncoTarget, 2017 The underlying mechanism of Fusobacterium nucleatum (Fn) in the carcinogenesis of colorectal cancer (CRC) is poorly understood. Here, we examined Fn abundance in CRC tissues, as well as β-catenin, TLR4 and PAK1 protein abundance in Fn positive and Fn ...
Yongyu Chen +8 more
semanticscholar +1 more source
eLife, 2019 Beta-catenin (i.e., canonical Wnt) signaling controls CNS angiogenesis and the blood-brain and blood-retina barriers. To explore the role of the Discs large/membrane-associated guanylate kinase (Dlg/MAGUK) family of scaffolding proteins in beta-catenin ...
Chris Cho +4 more
doaj +1 more source