32 research outputs found
(0,2) Deformations of Linear Sigma Models
We study (0,2) deformations of a (2,2) supersymmetric gauged linear sigma
model for a Calabi-Yau hypersurface in a Fano toric variety. In the non-linear
sigma model these correspond to some of the holomorphic deformations of the
tangent bundle on the hypersurface. Combinatorial formulas are given for the
number of these deformations, and we show that these numbers are exchanged by
mirror symmetry in a subclass of the models.Comment: 35 pages; uses xy-fig; typos fixed, acknowledgments adde
Factors associated with disease progression in early-diagnosed pulmonary arterial hypertension associated with systemic sclerosis: longitudinal data from the DETECT cohort
OBJECTIVE: Pulmonary arterial hypertension (PAH) is a severe complication of systemic sclerosis (SSc). In this longitudinal study, we aimed to identify factors associated with an unfavourable outcome in patients with SSc with early PAH (SSc-PAH) from the DETECT cohort. METHODS: Patients with SSc-PAH enrolled in DETECT were observed for up to 3 years. Associations between cross-sectional variables and disease progression (defined as the occurrence of any of the following events: WHO Functional Class worsening, combination therapy for PAH, hospitalisation or death) were analysed by univariable logistic regression. RESULTS: Of 57 patients with PAH (median observation time 12.6 months), 25 (43.9%) had disease progression. The following factors (OR (95% CI)) were associated with disease progression: male gender (4.1 (1.2 to 14.1)), high forced vital capacity % predicted/carbon monoxide lung diffusion capacity (DLCO)% predicted ratio (3.6 (1.2 to 10.7)), high Borg Dyspnoea Index (1.7 (1.1 to 2.6)) and low DLCO% predicted (non-linear relationship). CONCLUSION: More than 40% of early-diagnosed patients with SSc-PAH had disease progression during a short follow-up time, with male gender, functional capacity and pulmonary function tests at PAH diagnosis being associated with progression. This suggests that even mild PAH should be considered a high-risk complication of SSc
Heterotic Models from Vector Bundles on Toric Calabi-Yau Manifolds
We systematically approach the construction of heterotic E_8 X E_8 Calabi-Yau
models, based on compact Calabi-Yau three-folds arising from toric geometry and
vector bundles on these manifolds. We focus on a simple class of 101 such
three-folds with smooth ambient spaces, on which we perform an exhaustive scan
and find all positive monad bundles with SU(N), N=3,4,5 structure groups,
subject to the heterotic anomaly cancellation constraint. We find that
anomaly-free positive monads exist on only 11 of these toric three-folds with a
total number of bundles of about 2000. Only 21 of these models, all of them on
three-folds realizable as hypersurfaces in products of projective spaces, allow
for three families of quarks and leptons. We also perform a preliminary scan
over the much larger class of semi-positive monads which leads to about 44000
bundles with 280 of them satisfying the three-family constraint. These 280
models provide a starting point for heterotic model building based on toric
three-folds.Comment: 41 pages, 5 figures. A table modified and a table adde
Explicit de Sitter Flux Vacua for Global String Models with Chiral Matter
We address the open question of performing an explicit stabilisation of all
closed string moduli (including dilaton, complex structure and Kaehler moduli)
in fluxed type IIB Calabi-Yau compactifications with chiral matter. Using toric
geometry we construct Calabi-Yau manifolds with del Pezzo singularities.
D-branes located at such singularities can support the Standard Model gauge
group and matter content. In order to control complex structure moduli
stabilisation we consider Calabi-Yau manifolds which exhibit a discrete
symmetry that reduces the effective number of complex structure moduli. We
calculate the corresponding periods in the symplectic basis of invariant
three-cycles and find explicit flux vacua for concrete examples. We compute the
values of the flux superpotential and the string coupling at these vacua.
Starting from these explicit complex structure solutions, we obtain AdS and dS
minima where the Kaehler moduli are stabilised by a mixture of D-terms,
non-perturbative and perturbative alpha'-corrections as in the LARGE Volume
Scenario. In the considered example the visible sector lives at a dP_6
singularity which can be higgsed to the phenomenologically interesting class of
models at the dP_3 singularity.Comment: 49 pages, 5 figures; v2: references adde
Topological invariants and fibration structure of complete intersection Calabi-Yau four-folds
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1.
In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for bona fide autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field