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1.
Phys Rev Lett ; 131(15): 152501, 2023 Oct 13.
Artículo en Inglés | MEDLINE | ID: mdl-37897780

RESUMEN

^{180m}Ta is a rare nuclear isomer whose decay has never been observed. Its remarkably long lifetime surpasses the half-lives of all other known ß and electron capture decays due to the large K-spin differences and small energy differences between the isomeric and lower-energy states. Detecting its decay presents a significant experimental challenge but could shed light on neutrino-induced nucleosynthesis mechanisms, the nature of dark matter, and K-spin violation. For this study, we repurposed the Majorana Demonstrator, an experimental search for the neutrinoless double-beta decay of ^{76}Ge using an array of high-purity germanium detectors, to search for the decay of ^{180m}Ta. More than 17 kg, the largest amount of tantalum metal ever used for such a search, was installed within the ultralow-background detector array. In this Letter, we present results from the first year of Ta data taking and provide an updated limit for the ^{180m}Ta half-life on the different decay channels. With new limits up to 1.5×10^{19} yr, we improved existing limits by 1-2 orders of magnitude which are the most sensitive searches for a single ß and electron capture decay ever achieved. Over all channels, the decay can be excluded for T_{1/2}<0.29×10^{18} yr.

2.
Phys Rev Lett ; 129(8): 081803, 2022 Aug 19.
Artículo en Inglés | MEDLINE | ID: mdl-36053699

RESUMEN

Axions were originally proposed to explain the strong-CP problem in QCD. Through axion-photon coupling, the Sun could be a major source of axions, which could be measured in solid state detection experiments with enhancements due to coherent Primakoff-Bragg scattering. The Majorana Demonstrator experiment has searched for solar axions with a set of ^{76}Ge-enriched high purity germanium detectors using a 33 kg-yr exposure collected between January, 2017 and November, 2019. A temporal-energy analysis gives a new limit on the axion-photon coupling as g_{aγ}<1.45×10^{-9} GeV^{-1} (95% confidence level) for axions with mass up to 100 eV/c^{2}. This improves laboratory-based limits between about 1 eV/c^{2} and 100 eV/c^{2}.

3.
Science ; 216(4549): 1018-20, 1982 May 28.
Artículo en Inglés | MEDLINE | ID: mdl-6177041

RESUMEN

The epidermis of live human skin has a permanent electric dipole moment perpendicular to its surface. Voltage responses to a rapid change of temperature are pyroeletric, while voltage responses to pressure pulses are piezoelectric in nature. The time course of the responses depends on dX/dt (X, temperature or pressure). The epidermal surface can react to all physical environmental influences to which nonbiological pyroelectric materials are known to respond. Epidermal voltage signals can be perceived through the intraepidermal and the superficial dermal nervous network. The pyroelectric and piezoelectric properties are also measurable on dead, dry skin samples.


Asunto(s)
Epidermis/fisiología , Fenómenos Biomecánicos , Electrofisiología , Humanos , Queratinas/fisiología , Temperatura
4.
Hypertension ; 25(4 Pt 1): 511-6, 1995 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-7536711

RESUMEN

We tested the hypothesis that low-density lipoprotein (LDL) and its acetylated form influence surface expression of vascular adhesion molecules on human endothelial cells. Vascular adhesion molecule surface expression was assessed with flow cytometry on cultured endothelial cells with a modified enzyme-linked immunosorbent assay. LDL acetylation was determined by chromatography. Monocyte adhesion to endothelial cells was assessed with U937 cells by direct counting. Tumor necrosis factor-alpha (10 ng/mL), a positive control, induced a time-dependent expression of vascular adhesion molecules (P < .05), which peaked at 5 hours. Incubation of endothelial cells with LDL (1.3 to 26.0 mmol/L) led to an increase in expression at 2 and 5 hours (P < .05). Prolonged (24-hour) exposure to LDL resulted in a second peak. The effect of acetylated LDL on expression was not different from that of native LDL. Incubation with the protein kinase C inhibitor staurosporine (5 x 10(-8) mol/L) blocked the effects of both native and acetylated LDL completely (P < .05). The calcium channel blocker nitrendipine (10(-7) mol/L) did not influence the expression of vascular adhesion molecule at 2 and 5 hours but did reduce the effect of LDL on expression at 24 hours. LDL (2.6 mmol/L) also induced a significant increase in the surface expression of intercellular adhesion molecule-1 but did not affect the expression of endothelial adhesion molecules. LDL (2.6 mmol/L) induced a significant increase in monocyte binding. We conclude that LDL can induce the expression of vascular adhesion molecules on endothelial cells.(ABSTRACT TRUNCATED AT 250 WORDS)


Asunto(s)
Moléculas de Adhesión Celular/biosíntesis , Endotelio Vascular/efectos de los fármacos , Lipoproteínas LDL/farmacología , Bloqueadores de los Canales de Calcio/farmacología , Células Cultivadas , Interacciones Farmacológicas , Endotelio Vascular/metabolismo , Ensayo de Inmunoadsorción Enzimática , Citometría de Flujo , Humanos , Proteína Quinasa C/farmacología , Factor de Necrosis Tumoral alfa/farmacología , Molécula 1 de Adhesión Celular Vascular
5.
Plant Cell Rep ; 15(12): 958-62, 1996 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-24178283

RESUMEN

Particle bombardment and Agrobacterium-mediated DNA delivery into immature embryos and microbulbs were used to investigate the expression of the uidA gene in in vitro onion cultures. Both methods were successful in delivering DNA and subsequent uidA expression was observed. Optimal transient ß-glucuronidase activity was observed in immature embryos that had been pre-cultured for three days and bombarded at a distance of 3 cm from the stopping plate, under 25 in Hg vacuum, using 900-1300 psi rupture discs. The CaMV35S-uidA gene construct gave five fold higher transient ß-glucuronidase activity than the uidA gene construct regulated by any of four other promoters initially chosen for high experession in monocotyledonous tissues.

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