619 research outputs found
Semileptonic B decays into even parity charmed mesons
By using a constituent quark model we compute the form factors relevant to
semileptonic transitions of B mesons into low-lying p-wave charmed mesons. We
evaluate the q^2 dependence of these form factors and compare them with other
model calculations. The Isgur-Wise functions tau(1/2) and tau(3/2) are also
obtained in the heavy quark limit of our results.Comment: 11 pages, 2 figure
A novel framework for the local extraction of extra-axial cerebrospinal fluid from MR brain images
The quantification of cerebrospinal fluid (CSF) in the human brain has shown to play an important role in early postnatal brain developmental. Extr a-axial fluid (EA-CSF), which is characterized by the CSF in the subarachnoid space, is promising in the early detection of children at risk for neurodevelopmental disorders. Currently, though, there is no tool to extract local EA-CSF measurements in a way that is suitable for localized analysis. In this paper, we propose a novel framework for the localized, cortical surface based analysis of EA-CSF. In our proposed processing, we combine probabilistic brain tissue segmentation, cortical surface reconstruction as well as streamline based local EA-CSF quantification. For streamline computation, we employ the vector field generated by solving a Laplacian partial differential equation (PDE) between the cortical surface and the outer CSF hull. To achieve sub-voxel accuracy while minimizing numerical errors, fourth-order Runge-Kutta (RK4) integration was used to generate the streamlines. Finally, the local EA-CSF is computed by integrating the CSF probability along the generated streamlines. The proposed local EA-CSF extraction tool was used to study the early postnatal brain development in typically developing infants. The results show that the proposed localized EA-CSF extraction pipeline can produce statistically significant regions that are not observed in previous global approach
Partial Identification of the Average Treatment Effect Using Instrumental Variables: Review of Methods for Binary Instruments, Treatments, and Outcomes
Several methods have been proposed for partially or point identifying the average treatment effect (ATE) using instrumental variable (IV) type assumptions. The descriptions of these methods are widespread across the statistical, economic, epidemiologic, and computer science literature, and the connections between the methods have not been readily apparent. In the setting of a binary instrument, treatment, and outcome, we review proposed methods for partial and point identification of the ATE under IV assumptions, express the identification results in a common notation and terminology, and propose a taxonomy that is based on sets of identifying assumptions. We further demonstrate and provide software for the application of these methods to estimate bounds. Supplementary materials for this article are available online
WISP genes are members of the connective tissue growth factor family that are up-regulated in Wnt-1-transformed cells and aberrantly expressed in human colon tumors
Wnt family members are critical to many developmental processes, and components of the Wnt signaling pathway have been linked to tumorigenesis in familial and sporadic colon carcinomas. Here we report the identification of two genes, WISP-1 and WISP-2, that are up-regulated in the mouse mammary epithelial cell line C57MG transformed by Wnt-1, but not by Wnt-4. Together with a third related gene, WISP-3, these proteins define a subfamily of the connective tissue growth factor family. Two distinct systems demonstrated WISP induction to be associated with the expression of Wnt-1. These included (i) C57MG cells infected with a Wnt-1 retroviral vector or expressing Wnt-1 under the control of a tetracyline repressible promoter, and (ii) Wnt-1 transgenic mice. The WISP-1 gene was localized to human chromosome 8q24.1-8q24.3. WISP-1 genomic DNA was amplified in colon cancer cell lines and in human colon tumors and its RNA overexpressed (2- to >30-fold) in 84% of the tumors examined compared with patient-matched normal mucosa. WISP-3 mapped to chromosome 6q22-6q23 and also was overexpressed (4- to >40-fold) in 63% of the colon tumors analyzed. In contrast, WISP-2 mapped to human chromosome 20q12-20q13 and its DNA was amplified, but RNA expression was reduced (2- to >30-fold) in 79% of the tumors. These results suggest that the WISP genes may be downstream of Wnt-1 signaling and that aberrant levels of WISP expression in colon cancer may play a role in colon tumorigenesis
Chiral shifts in heavy-light mesons
The mass shifts of the -wave and mesons due to coupling to
and channels are calculated in the coupling channel model without
fitting parameters. The strong mass shifts down for and states
have been obtained, while and states remain almost in situ. The
masses of and states of mesons have been predicted.Comment: to be published in the Proceedings of the 14th International QCD
Conference, 7th-12th July 2008, Montpellier, Franc
Causal null hypotheses of sustained treatment strategies: What can be tested with an instrumental variable?
Sometimes instrumental variable methods are used to test whether a causal effect is null rather than to estimate the magnitude of a causal effect. However, when instrumental variable methods are applied to time-varying exposures, as in many Mendelian randomization studies, it is unclear what causal null hypothesis is tested. Here, we consider different ver
Pressure-induced phase transitions of halogen-bridged binuclear metal complexes R_4[Pt_2(P_2O_5H_2)_4X]nH_2O
Recent contrasting observations for halogen (X)-bridged binuclear platinum
complexes R_4[Pt_2(P_2O_5H_2)_4X]nH_2O, that is, pressure-induced Peierls and
reverse Peierls instabilities, are explained by finite-temperature Hartree-Fock
calculations. It is demonstrated that increasing pressure transforms the
initial charge-polarization state into a charge-density-wave state at high
temperatures, whereas the charge-density-wave state oppositely declines with
increasing pressure at low temperatures. We further predict that
higher-pressure experiments should reveal successive phase transitions around
room temperature.Comment: 5 pages, 4 figures embedded, to be published in Phys. Rev. B 64,
September 1 (2001) Rapid Commu
Semileptonic Bs ->DsJ(2460)l nu decay in QCD
Using three point QCD sum rules method, the form factors relevant to the
semileptonic Bs ->DsJ (2460)l nu decay are calculated. The q2 dependence of
these form factors is evaluated and compared with the heavy quark effective
theory predictions. The dependence of the asymmetry parameter alpha,
characterizing the polarization of DsJ meson, on q2 is studied .The branching
ratio of this decay is also estimated and is shown that it can be easily
detected at LHC.Comment: 21 pages, 5 figures and 1 Tabl
Sleep onset problems and subcortical development in infants later diagnosed with autism spectrum disorder
Objective: Sleep patterns in children with autism spectrum disorder (ASD) appear to diverge from typical development in the second or third year of life. Little is known, however, about the occurrence of sleep problems in infants who later develop ASD and possible effects on early brain development. In a longitudinal neuroimaging study of infants at familial high or low risk for ASD, parent-reported sleep onset problems were examined in relation to subcortical brain volumes in the first 2 years of life. Methods: A total of 432 infants were included across three study groups: infants at high risk who developed ASD (N=71), infants at high risk who did not develop ASD (N=234), and infants at low risk (N=127). Sleep onset problem scores (derived from an infant temperament measure) were evaluated in relation to longitudinal high-resolution T1 and T2 structural imaging data acquired at 6, 12, and 24 months of age. Results: Sleep onset problems were more common at 6–12 months among infants who later developed ASD. Infant sleep onset problems were related to hippocampal volume trajectories from 6 to 24 months only for infants at high risk who developed ASD. Brain-sleep relationships were specific to the hippocampus; no significant relationships were found with volume trajectories of other subcortical structures examined (the amygdala, caudate, globus pallidus, putamen, and thalamus). Conclusions: These findings provide initial evidence that sleep onset problems in the first year of life precede ASD diagnosis and are associated with altered neurodevelopmental trajectories in infants at high familial risk who go on to develop ASD. If replicated, these findings could provide new insights into a potential role of sleep difficulties in the development of ASD
Light meson mass dependence of the positive parity heavy-strange mesons
We calculate the masses of the resonances D_{s0}^*(2317) and D_{s1}(2460) as
well as their bottom partners as bound states of a kaon and a D^*- and
B^*-meson, respectively, in unitarized chiral perturbation theory at
next-to-leading order. After fixing the parameters in the D_{s0}^*(2317)
channel, the calculated mass for the D_{s1}(2460) is found in excellent
agreement with experiment. The masses for the analogous states with a bottom
quark are predicted to be M_{B^*_{s0}}=(5696\pm 40) MeV and M_{B_{s1}}=(5742\pm
40) MeV in reasonable agreement with previous analyses. In particular, we
predict M_{B_{s1}}-M_{B_{s0}^*}=46\pm 1 MeV. We also explore the dependence of
the states on the pion and kaon masses. We argue that the kaon mass dependence
of a kaonic bound state should be almost linear with slope about unity. Such a
dependence is specific to the assumed molecular nature of the states. We
suggest to extract the kaon mass dependence of these states from lattice QCD
calculations.Comment: 10 page
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