5 research outputs found
Identification and estimation of a large factor model with structural instability
This paper tackles the identification and estimation of a high dimensional factor model with unknown number of latent factors and a single break in the number of factors and/or factor loadings occurring at unknown common date. First, we propose a least squares estimator of the change point based on the second moments of estimated pseudo factors and show that the estimation error of the proposed estimator is Op(1). We also show that the proposed estimator has some degree of robustness to misspecification of the number of pseudo factors. With the estimated change point plugged in, consistency of the estimated number of pre and post-break factors and convergence rate of the estimated pre and post-break factor space are then established under fairly general assumptions. The finite sample performance of our estimators is investigated using Monte Carlo experiments
Asymptotic power of the sphericity test under weak and strong factors in a fixed effects panel data model
This paper studies the asymptotic power for the sphericity test in a fixed effect panel data model proposed by Baltagi et al. (2011 Baltagi, B. H., Feng, Q., Kao, C. (2011). Testing for sphericity in a fixed effects panel data model. Econometrics Journal 14:25–47.), (JBFK). This is done under the alternative hypotheses of weak and strong factors. By weak factors, we mean that the Euclidean norm of the vector of the factor loadings is O(1). By strong factors, we mean that the Euclidean norm of the vector of factor loadings is , where n is the number of individuals in the panel. To derive the limiting distribution of JBFK under the alternative, we first derive the limiting distribution of its raw data counterpart. Our results show that, when the factor is strong, the test statistic diverges in probability to infinity as fast as Op(nT). However, when the factor is weak, its limiting distribution is a rightward mean shift of the limit distribution under the null. Second, we derive the asymptotic behavior of the difference between JBFK and its raw data counterpart. Our results show that when the factor is strong, this difference is as large as Op(n). In contrast, when the factor is weak, this difference converges in probability to a constant. Taken together, these results imply that when the factor is strong, JBFK is consistent, but when the factor is weak, JBFK is inconsistent even though its asymptotic power is nontrivial
Single-Spin Dirac Fermion and Chern Insulator Based on Simple Oxides
It is highly desirable to combine
recent advances in the topological
quantum phases with technologically relevant materials. Chromium dioxide
(CrO<sub>2</sub>) is a half-metallic material, widely used in high-end
data storage applications. Using first-principles calculations, we
show that a novel class of half semimetallic Dirac electronic phase
emerges at the interface CrO<sub>2</sub> with TiO<sub>2</sub> in both
thin film and superlattice configurations, with four spin-polarized
Dirac points in momentum-space (<b><i>k</i></b>-space)
band structure. When the spin and orbital degrees of freedom are allowed
to couple, the CrO<sub>2</sub>/TiO<sub>2</sub> superlattice becomes
a Chern insulator without external fields or additional doping. With
topological gaps equivalent to 43 K and a Chern number ±2, the
ensuing quantization of Hall conductance to ±2<i>e</i><sup>2</sup>/<i>h</i> will enable potential development
of these highly industrialized oxides for applications in topologically
high fidelity data storage and energy-efficient electronic and spintronic
devices
Table_1_Contrast-enhanced ultrasonography for differential diagnosis of adnexal masses.xlsx
BackgroundQuantitative contrast-enhanced ultrasonography parameters are affected by various factors. We evaluated corrected quantitative contrast enhanced ultrasonography in differentiating benign adnexal tumors from malignant tumors.MethodsPatients with adnexal masses who underwent conventional and contrast-enhanced ultrasonography were included. Contrast-enhanced ultrasonography parameters such as base intensity, arrival time, peak intensity, time to peak intensity, ascending slope, and descending slope were measured. Corrected (time to peak intensity − arrival time) mass/(time to peak intensity − arrival time) uterus and (peak intensity − base intensity) mass/(peak intensity − base intensity) uterus were calculated. Lesions were confirmed by pathologic examination of surgical specimens.ResultsThis study included 31 patients with 35 adnexal lesions including 20 (57.10%) benign and 15 (42.90%) malignant lesions. The corrected contrast-enhanced ultrasonography quantitative parameters in lesions were statistically different between malignant and benign groups (Pmass/(time to peak intensity − arrival time) uterus, ascending slope, and (peak intensity − base intensity) mass/(peak intensity − base intensity) uterus, and descending slope for differentiating malignant adnexal masses from benign tumors were 1.05 (area under curve: 0.93, PConclusionsCorrected contrast-enhanced ultrasonography parameters provide practical differential diagnosis value of adnexal lesions with high reliability for sonologists.</p
Multiplexed Targeting of Barrett’s Neoplasia with a Heterobivalent Ligand: Imaging Study on Mouse Xenograft in Vivo and Human Specimens ex Vivo
Esophageal adenocarcinoma (EAC) is
a molecularly heterogeneous
disease that is rising rapidly in incidence and has poor prognosis.
We developed a heterobivalent peptide to target detection of early
Barrett’s neoplasia by combining monomer heptapeptides specific
for either EGFR or ErbB2 in a heterodimer configuration. The structure
of a triethylene glycol linker was optimized to maximize binding interactions
to the surface receptors on cells. The Cy5.5-labeled heterodimer QRH*–KSP*–E3–Cy5.5
demonstrated specific binding to each target and showed 3-fold greater
fluorescence intensity and 2-fold higher affinity compared with those
of either monomer alone. Peak uptake in xenograft tumors was observed
at 2 h postinjection with systemic clearance by ∼24 h in vivo.
Furthermore, ligand binding was evaluated on human esophageal specimens
ex vivo, and 88% sensitivity and 87% specificity were found for the
detection of either high-grade dysplasia (HGD) or EAC. This peptide
heterodimer shows promise for targeted detection of early Barrett’s
neoplasia in clinical study
