In the description of the production properties of gauge bosons (W±, Z0, γ*) at colliders, the lowest-order graph normally is not sufficient. The contributions of higher orders can be introduced either by an explicit order-by-order matrix-element calculation, by a resummation procedure or by a parton-shower algorithm. Each approach has its advantages and disadvantages. We here introduce a method t

Cross-talk between the W+ and W- sources of hadron production at LEP2 offers a hope to learn about basic properties of QCD, but at the same time threatens high-precision measurements of the W boson mass. Directly visible effects are not expected to be large, however. It is, therefore, important to develop methods to measure the level of interconnection in the data - 'connectometers'. In this artic

Over the years, many jet clustering algorithms have been proposed for the analysis of hadronic final states in e+e- annihilations. These have somewhat different emphasis and are therefore more or less suited for various applications. We here review some of the most used and compare them from a theoretical and experimental point of view.

In the hadroproduction of charm in the context of string fragmentation, the pull of a beam remnant at the other end of a string may give a charm hadron more energy than the perturbatively produced charm quark. The collapse of a low-mass string to a single hadron is the extreme case in this direction, and gives rise to asymmetries between charm and anticharm hadron spectra. We study these phenomena

We present new algorithms for simulating Bose–Einstein correlations among final-state bosons in an event generator. The algorithms are all based on introducing Bose–Einstein correlations as a shift of final-state momenta among identical bosons, and differ only in the way energy and momentum conservation is ensured. The benefits and shortcomings of this approach, that may be viewed as a local rewei

A real photon has a complicated nature, whereby it may remain unresolved or fluctuate into a vector meson or a perturbative qq̄ pair. In γγ events, this gives three by three combinations of the nature of the two incoming photons, and thus six distinct event classes. The properties of these classes are partly constrained by the choices already made in our related γp model. It is therefore possible

We propose a generic ansatz for the extension of parton distributions of the real photon to those of the virtual photon. Alternatives and approximations are studied that allow closed-form parametrizations.

The structure of the general solution of the inhomogeneous evolution equations allows the separation of a photon structure function into perturbative ("anomalous") and non-perturbative contributions. The former part is fully calculable, and can be identified with the high-mass contributions to the dispersion integral in the photon mass. Properly normalized "state" distributions can be defined, whe

It is becoming increasingly clear that many proteins start to fold cotranslationally before the entire polypeptide chain has been synthesized on the ribosome. One class of proteins that a priori would seem particularly prone to cotranslational folding is repeat proteins, that is, proteins that are built from an array of nearly identical sequence repeats. However, while the folding of repeat protei

Nucleotides in the free pool are more susceptible to nonenzymatic methylation than those protected in the DNA double helix. Methylated nucleotides like O6-methyl-dGTP can be mutagenic and toxic if incorporated into DNA. Removal of methylated nucleotides from the nucleotide pool may therefore be important to maintain genome integrity. We show that MutT homologue 1 (MTH1) efficiently catalyzes the h

The causal association of NUDT1 (=MTH1) and OGG1 with hereditary colorectal cancer (CRC) remains unclear. Here, we sought to provide additional evidence for or against the causal contribution of NUDT1 and OGG1 mutations to hereditary CRC and/or polyposis. Mutational screening was performed using pooled DNA amplification and targeted next-generation sequencing in 529 families (441 uncharacterized M

Botulinum neurotoxins (BoNTs) are a family of highly dangerous bacterial toxins, with seven major serotypes (BoNT/A-G). Members of BoNTs, BoNT/A1 and BoNT/B1, have been utilized to treat an increasing number of medical conditions. The clinical trials are ongoing for BoNT/A2, another subtype of BoNT/A, which showed promising therapeutic properties. Both BoNT/A1 and BoNT/A2 utilize three isoforms of

Botulinum neurotoxins (BoNTs) are among the most potent toxins known and are also used to treat an increasing number of medical disorders. There are seven well-established serotypes (BoNT/A-G), which all act as zinc-dependent endopeptidases targeting specific members of the SNARE proteins required for synaptic vesicle exocytosis in neurons. A new toxin serotype, BoNT/X, was recently identified. It

Human NUDT22 belongs to the diverse NUDIX family of proteins, but has, until now, remained uncharacterized. Here we show that human NUDT22 is a Mg2+-dependent UDP-glucose and UDP-galactose hydrolase, producing UMP and glucose 1-phosphate or galactose 1-phosphate. We present the structure of human NUDT22 alone and in a complex with the substrate UDP-glucose. These structures reveal a partially cons

Botulinum neurotoxins (BoNTs), produced by various Clostridium strains, are a family of potent bacterial toxins and potential bioterrorism agents. Here we report that an Enterococcus faecium strain isolated from cow feces carries a BoNT-like toxin, designated BoNT/En. It cleaves both VAMP2 and SNAP-25, proteins that mediate synaptic vesicle exocytosis in neurons, at sites distinct from known BoNT

This paper presents a time-interleaved pipelined-SAR converter targeting a multi-band mobile communication receiver. The input buffer is based on a super-source follower and linearized by selecting a specific bias current and drain bias resistor. Time interleaved sampling time mismatch is resolved by using a common sample and hold circuit, and gain mismatch is corrected by fine tuning respective s

With a diverse network of substrates, NUDIX hydrolases have emerged as a key family of nucleotide-metabolizing enzymes. NUDT5 (also called NUDIX5) has been implicated in ADP-ribose and 8-oxo-guanine metabolism and was recently identified as a rheostat of hormone-dependent gene regulation and proliferation in breast cancer cells. Here, we further elucidate the physiological relevance of known NUDT5

MTH1 hydrolyzes oxidized nucleoside triphosphates, thereby sanitizing the nucleotide pool from oxidative damage. This prevents incorporation of damaged nucleotides into DNA, which otherwise would lead to mutations and cell death. The high level of reactive oxygen species in cancer cells leads to a higher level of oxidized nucleotides in cancer cells compared to that in nonmalignant cells, making c

Proteolysis plays an important role in mitochondrial biogenesis, from the processing of newly imported precursor proteins to the degradation of mitochondrial targeting peptides. Disruption of peptide degradation activity in yeast, plant and mammalian mitochondria is known to have deleterious consequences for organism physiology, highlighting the important role of mitochondrial peptidases. In the p