https://biblio.ugent.be/publication/685594/file/1130605.pdf

Review of Particle Physics

The Pythia program can be used to generate high-energy-physics ''events'', i.e. sets of outgoing particles produced in the interactions between two incoming particles. The objective is to provide as accurate as possible a representation of event properties in a wide range of reactions, within and beyond the Standard Model, with emphasis on those where strong interactions play a role, directly or indirectly, and therefore multihadronic final states are produced. The physics is then not understood well enough to give an exact description; instead the program has to be based on a combination of analytical results and various QCD-based models. This physics input is summarized here, for areas such as hard subprocesses, initial- and final-state parton showers, underlying events and beam remnants, fragmentation and decays, and much more. Furthermore, extensive information is provided on all program elements: subroutines and functions, switches and parameters, and particle and process data. This should allow the user to tailor the generation task to the topics of interest.

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PYTHIA 6.4 Physics and Manual

Missale, Cristina, S. Russel Nash, Susan W. Robinson, Mohamed Jaber, and Marc G. Caron. Dopamine Receptors: From Structure to Function. Physiol. Rev. 78: 189–225, 1998. — The diverse physiological actions of dopamine are mediated by at least five distinct G protein-coupled receptor subtypes. Two D1-like receptor subtypes (D1 and D5) couple to the G protein Gs and activate adenylyl cyclase. The other receptor subtypes belong to the D2-like subfamily (D2 , D3 , and D4) and are prototypic of G protein-coupled receptors that inhibit adenylyl cyclase and activate K+ channels. The genes for the D1 and D5 receptors are intronless, but pseudogenes of the D5 exist. The D2 and D3 receptors vary in certain tissues and species as a result of alternative splicing, and the human D4 receptor gene exhibits extensive polymorphic variation. In the central nervous system, dopamine receptors are widely expressed because they are involved in the control of locomotion, cognition, emotion, and affect as well as neuroendocrine s...

Dopamine Receptors: From Structure to Function

▪ Abstract Neurotransmitter release is mediated by exocytosis of synaptic vesicles at the presynaptic active zone of nerve terminals. To support rapid and repeated rounds of release, synaptic vesicles undergo a trafficking cycle. The focal point of the vesicle cycle is Ca2+-triggered exocytosis that is followed by different routes of endocytosis and recycling. Recycling then leads to the docking and priming of the vesicles for another round of exo- and endocytosis. Recent studies have led to a better definition than previously available of how Ca2+ triggers exocytosis and how vesicles recycle. In particular, insight into how Munc18-1 collaborates with SNARE proteins in fusion, how the vesicular Ca2+ sensor synaptotagmin 1 triggers fast release, and how the vesicular Rab3 protein regulates release by binding to the active zone proteins RIM1α and RIM2α has advanced our understanding of neurotransmitter release. The present review attempts to relate these molecular data with physiological results in an emerg...

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The synaptic vesicle cycle

This article reports world averages of measurements of b-hadron, c-hadron, and tau-lepton properties obtained by the Heavy Flavor Averaging Group (HFAG) using results available through the end of 2011. In some cases results available in the early part of 2012 are included. For the averaging, common input parameters used in the various analyses are adjusted (rescaled) to common values, and known correlations are taken into account. The averages include branching fractions, lifetimes, neutral meson mixing parameters, CP violation parameters, parameters of semileptonic decays and CKM matrix elements.

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Averages of b-hadron, c-hadron, and tau-lepton properties as of early 2012

In vitro studies have widely demonstrated that the abundance and availability of G-protein-coupled receptors (GPCRs) at the cell surface is regulated by the neuronal environment and is the result of complex intraneuronal trafficking; however, this regulation is still poorly understood in vivo. Yet, modulation of receptor availability at the neuronal membrane is a key event in the regulation of neuronal functions (e.g., neurotransmitter release or neuronal excitability in physiological, pathological or therapeutic conditions). This chapter discusses the effects of duration of receptor stimulation (acute vs. chronic) on the intraneuronal trafficking of GPCRs in vivo and we show that this trafficking of GPCRs might differ according to subcellular compartment (soma, dendrites or axon terminals). Using data obtained for different receptors, we propose here a model of GPCRs trafficking in vivo. Acute stimulation induces GPCR endocytosis, which is followed by either recycling or degradation of receptors from membranes of the soma and dendrites but not of axon terminals. Chronic stimulation induces blockade of targeting of GPCRs to membranes of the somatodendritic field and an increase in receptor density at the membrane of axonal varicosities.

Regulation of Intraneuronal Trafficking of G-Protein-Coupled Receptors by Neurotransmitters In Vivo

We investigate threshold pion photoproduction in the framework of heavy baryon chiral perturbation theory. We give the expansion of the electric dipole amplitude $E_{0+}$ to three orders in $\mu$, the ratio of the pion to nucleon mass, and show that it is slowly converging. We argue that this observable is not a good testing ground for the chiral dynamics of QCD. In contrast, we exhibit new and fastly converging low--energy theorems in the P--waves which should be used to constrain the data analysis. We also discuss the importance of polarization observables to accurately pin down certain multipoles and give predictions for the reaction $\gamma n \to \pi^0 n$.

Neutral pion photoproduction off nucleons revisited

We derive novel low--energy theorems for single pion production off nucleons through the isovector axial current. We find that the $k^2$-dependence of the multipole $L_{0+}^{(+)}$ at threshold is given by the nucleon scalar form factor, namely $\sigma(k^2-M_\pi^2 ) /(3 \pi M_\pi F_\pi )$. The relation to PCAC results for soft pions including electroweak form factors is also clarified.

Low--Energy Theorems for Weak Pion Production

Several lattice collaborations performing simulations with 2+1 light dynamical quarks have experienced difficulties in fitting their data with standard Nf=3 chiral expansions at next-to-leading order, yielding low values of the quark condensate and/or the decay constant in the Nf=3 chiral limit. A reordering of these expansions seems required to analyse these data in a consistent way. We discuss such a reordering, known as Resummed Chiral Perturbation Theory, in the case of pseudoscalar masses and decay constants, pion and kaon electromagnetic form factors and Kl3} form factors. We show that it provides a good fit of the recent results of two lattice collaborations (PACS-CS and RBC/UKQCD). We describe the emerging picture for the pattern of chiral symmetry breaking, marked by a strong dependence of the observables on the strange quark mass and thus a significant difference between chiral symmetry breaking in the Nf=2 and Nf=3 chiral limits. We discuss the consequences for the ratio of decay constants F_K/F_pi and the Kl3 form factor at vanishing momentum transfer.

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Véronique Bernard

Papers

Regulation of Intraneuronal Trafficking of G-Protein-Coupled Receptors by Neurotransmitters In Vivo

Neutral pion photoproduction off nucleons revisited

Low--Energy Theorems for Weak Pion Production

Chiral dynamics with strange quarks in the light of recent lattice simulations

Nucleon structure uncertainties in parity-violating quasi-elastic electron scattering