1,951 research outputs found
Nonextensive effects on QCD chiral phase diagram and baryon-number fluctuations within Polyakov-Nambu-Jona-Lasinio model
In this paper, a version of the Polyakov-Nambu-Jona-Lasinio (PNJL) model
based on nonextensive statistical mechanics is presented. This new statistics
summarizes all possible factors that violate the assumptions of the
Boltzmann-Gibbs (BG) statistics to a dimensionless nonextensivity parameter
, and when tends to 1, it returns to the BG case. Within the
nonextensive PNJL model, we found that as increases, the location of the
critical end point (CEP) exhibits non-monotonic behavior. That is, for
, CEP moves in the direction of lower temperature and larger quark
chemical potential. But for , CEP turns to move in the direction of
lower temperature and lower quark chemical potential. In addition, we studied
the moments of the net-baryon number distribution, that is, the variance
(), skewness (S), and kurtosis (). Our results are
generally consistent with the latest experimental data, especially for
, when is set to
Nonsurjective zero product preservers between matrices over an arbitrary field
In this paper, we give concrete descriptions of additive or linear
disjointness preservers between matrix algebras over an arbitrary field
of different sizes. In particular, we show that a linear map
preserving zero products
carries the form for some invertible matrices in
, in and a zero product preserving
linear map with
range consisting of nilpotent matrices. Here, either or can be
vacuous. The structure of could be quite arbitrary. We classify
with some additional assumption. When has a zero nilpotent
part, especially when is diagonalizable, we have
for all in , and we give more
information about in this case. Similar results for double zero
product preservers and orthogonality preservers are obtained.Comment: 29 page
DNA Repair Pathways in Cancer Therapy and Resistance
DNA repair pathways are triggered to maintain genetic stability and integrity when mammalian cells are exposed to endogenous or exogenous DNA-damaging agents. The deregulation of DNA repair pathways is associated with the initiation and progression of cancer. As the primary anti-cancer therapies, ionizing radiation and chemotherapeutic agents induce cell death by directly or indirectly causing DNA damage, dysregulation of the DNA damage response may contribute to hypersensitivity or resistance of cancer cells to genotoxic agents and targeting DNA repair pathway can increase the tumor sensitivity to cancer therapies. Therefore, targeting DNA repair pathways may be a potential therapeutic approach for cancer treatment. A better understanding of the biology and the regulatory mechanisms of DNA repair pathways has the potential to facilitate the development of inhibitors of nuclear and mitochondria DNA repair pathways for enhancing anticancer effect of DNA damage-based therapy
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