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1.
Phys Rev Lett ; 131(3): 031801, 2023 Jul 21.
Artículo en Inglés | MEDLINE | ID: mdl-37540863

RESUMEN

We report the first direct observation of neutrino interactions at a particle collider experiment. Neutrino candidate events are identified in a 13.6 TeV center-of-mass energy pp collision dataset of 35.4 fb^{-1} using the active electronic components of the FASER detector at the Large Hadron Collider. The candidates are required to have a track propagating through the entire length of the FASER detector and be consistent with a muon neutrino charged-current interaction. We infer 153_{-13}^{+12} neutrino interactions with a significance of 16 standard deviations above the background-only hypothesis. These events are consistent with the characteristics expected from neutrino interactions in terms of secondary particle production and spatial distribution, and they imply the observation of both neutrinos and anti-neutrinos with an incident neutrino energy of significantly above 200 GeV.

2.
Cancer Res ; 62(12): 3503-6, 2002 Jun 15.
Artículo en Inglés | MEDLINE | ID: mdl-12067995

RESUMEN

Studies of Wnt activation in gastric cancer have yielded conflicting results. The goals of this study were to determine the frequency of Wnt pathway activation and beta-catenin mutation in these tumors. Three hundred eleven gastric cancers were examined for beta-catenin expression by immunostaining and dissected using laser capture microscopy to obtain DNA from those tumors with nuclear beta-catenin. Exon 3 of beta-catenin was amplified using PCR and sequenced. Ninety gastric cancers (29%) displayed nuclear beta-catenin. DNAs from 73 tumors were amplified and sequenced; 19 (26%) contained mutations in exon 3 of beta-catenin, whereas no mutations were detected in 19 tumors negative for beta-catenin nuclear staining (P < 0.05). Most mutations were adjacent to or abolished known regulatory phosphorylation sites. Mutations in exon 3 of beta-catenin are common in gastric cancer that display nuclear beta-catenin. These results suggest that Wnt pathway activation contributes to carcinogenesis in a subset of gastric adenocarcinomas.


Asunto(s)
Adenocarcinoma/genética , Proteínas del Citoesqueleto/genética , Mutación , Proteínas Proto-Oncogénicas/fisiología , Neoplasias Gástricas/genética , Transactivadores , Proteínas de Pez Cebra , Adenocarcinoma/metabolismo , Adenocarcinoma/patología , Núcleo Celular/metabolismo , Proteínas del Citoesqueleto/metabolismo , Análisis Mutacional de ADN , Humanos , Reacción en Cadena de la Polimerasa , Transducción de Señal/genética , Transducción de Señal/fisiología , Neoplasias Gástricas/metabolismo , Neoplasias Gástricas/patología , Fracciones Subcelulares/metabolismo , Proteínas Wnt , beta Catenina
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