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2.
Phys Rev Lett ; 93(10): 101801, 2004 Sep 03.
Artículo en Inglés | MEDLINE | ID: mdl-15447395

RESUMEN

Muon neutrino disappearance probability as a function of neutrino flight length L over neutrino energy E was studied. A dip in the L/E distribution was observed in the data, as predicted from the sinusoidal flavor transition probability of neutrino oscillation. The observed L/E distribution constrained nu(micro)<-->nu(tau) neutrino oscillation parameters; 1.9x10(-3)0.90 at 90% confidence level.

3.
Phys Rev Lett ; 93(2): 021802, 2004 Jul 09.
Artículo en Inglés | MEDLINE | ID: mdl-15323899

RESUMEN

A search for a nonzero neutrino magnetic moment has been conducted using 1496 live days of solar neutrino data from Super-Kamiokande-I. Specifically, we searched for distortions to the energy spectrum of recoil electrons arising from magnetic scattering due to a nonzero neutrino magnetic moment. In the absence of a clear signal, we found micro(nu)

4.
Gene Ther ; 11(10): 865-73, 2004 May.
Artículo en Inglés | MEDLINE | ID: mdl-15042118

RESUMEN

Several retinal and choroidal diseases are potentially treatable by intraocular delivery of genes whose products may counter or neutralize abnormal gene expression that occurs as part of the diseases. However, prior to considering a transgene, it is necessary to thoroughly investigate the effects of its expression in normal and diseased eyes. An efficient way to do this is to combine tissue-specific promoters with inducible promoter systems in transgenic mice. In this study, we used this approach to evaluate the effects of ectopic expression of angiopoietin-1 (Ang1) in normal eyes and those with ocular neovascularization. Adult mice with induced expression of Ang1 ubiquitously, or specifically in the retina, appeared normal and had no identifiable changes in retinal or choroidal blood vessels or in retinal function as assessed by electroretinography. Increased expression of Ang1 in eyes with severe retinal ischemia or in eyes with rupture of Bruch's membrane significantly suppressed the development of retinal or choroidal neovascularization, respectively. This inhibition of ocular neovascularization is particularly interesting and noteworthy, because overexpression of Ang1 in skin stimulates neovascularization. Ang1 also significantly reduced VEGF-induced retinal vascular permeability. These data suggest that intraocular delivery of ang1 has potential for treatment of ocular neovascularization and macular edema.


Asunto(s)
Angiopoyetina 1/fisiología , Barrera Hematorretinal/fisiología , Neovascularización Coroidal/fisiopatología , Neovascularización Retiniana/fisiopatología , Angiopoyetina 1/genética , Angiopoyetina 1/metabolismo , Animales , Neovascularización Coroidal/etiología , Neovascularización Coroidal/metabolismo , Isquemia/complicaciones , Isquemia/metabolismo , Ratones , Ratones Transgénicos , Regiones Promotoras Genéticas , Retina/metabolismo , Neovascularización Retiniana/etiología , Neovascularización Retiniana/metabolismo , Vasos Retinianos/fisiopatología
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