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1.
Acad Emerg Med ; 16(2): 168-77, 2009 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-19076107

RESUMEN

Early diagnosis of persons infected with human immunodeficiency virus (HIV) through diagnostic testing and screening is a critical priority for individual and public health. Emergency departments (EDs) have an important role in this effort. As EDs gain experience in HIV testing, it is increasingly apparent that implementing testing is conceptually and operationally complex. A wide variety of HIV testing practice and research models have emerged, each reflecting adaptations to site-specific factors and the needs of local populations. The diversity and complexity inherent in nascent ED HIV testing practice and research are associated with the risk that findings will not be described according to a common lexicon. This article presents a comprehensive set of terms and definitions that can be used to describe ED-based HIV testing programs, developed by consensus opinion from the inaugural meeting of the National ED HIV Testing Consortium. These definitions are designed to facilitate discussion, increase comparability of future reports, and potentially accelerate wider implementation of ED HIV testing.


Asunto(s)
Infecciones por VIH/diagnóstico , Terminología como Asunto , Comunicación , Servicio de Urgencia en Hospital/economía , Servicio de Urgencia en Hospital/organización & administración , Guías como Asunto , Infecciones por VIH/economía , Humanos , Notificación Obligatoria
2.
Dev Cell ; 8(5): 717-26, 2005 May.
Artículo en Inglés | MEDLINE | ID: mdl-15866162

RESUMEN

Zebrafish meltdown (mlt) mutants develop cystic expansion of the posterior intestine as a result of stromal invasion of nontransformed epithelial cells. Positional cloning identified zebrafish smooth muscle myosin heavy chain (myh11) as the responsible gene. The mlt mutation constitutively activates the Myh11 ATPase, which disrupts smooth muscle cells surrounding the posterior intestine. Adjacent epithelial cells ectopically express metalloproteinases, integrins, and other genes implicated in human cancer cell invasion. Knockdown and pharmacological inhibition of these genes restores intestinal structure in mlt mutants despite persistent smooth muscle defects. These data identify an essential role for smooth muscle signaling in the maintenance of epithelial architecture and support gene expression analyses and other studies that identify a role for stromal genes in cancer cell invasion. Furthermore, they suggest that high-throughput screens to identify regulators of cancer cell invasion may be feasible in zebrafish.


Asunto(s)
Intestinos/crecimiento & desarrollo , Cadenas Pesadas de Miosina/genética , Cadenas Pesadas de Miosina/metabolismo , Proteínas de Pez Cebra/genética , Proteínas de Pez Cebra/metabolismo , Secuencia de Aminoácidos , Animales , Secuencia de Bases , ADN/genética , Epitelio/crecimiento & desarrollo , Humanos , Hibridación in Situ , Datos de Secuencia Molecular , Músculo Liso/crecimiento & desarrollo , Músculo Liso/metabolismo , Mutación , Fenotipo , Homología de Secuencia de Aminoácido , Transducción de Señal , Pez Cebra/genética , Pez Cebra/crecimiento & desarrollo , Pez Cebra/metabolismo
3.
Hum Pathol ; 33(3): 372-5, 2002 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-11979380

RESUMEN

Colonic adenocarcinomas are among the most common type of tumors. In this report, we present the morphologic, immunohistochemical, and microsatellite findings of 2 cases with a distinct invasive papillary component. Both tumors arose from polyps in middle-aged patients, followed an aggressive course, and showed a superficial adenomatous component. The immunohistochemical stains showed that the tumor cells were negative for p27 and p53; both tumors were microsatellite stable, that is, with no microsatellite instability in the 6 markers studied, and there was no loss of the mismatch repair proteins hMSH2 or hMLH1. These findings suggest that these tumors follow the tumor-suppressor pathway and represent an aggressive subtype of colonic adenocarcinoma.


Asunto(s)
Adenocarcinoma Papilar/secundario , Adenoma Velloso/patología , Neoplasias del Colon/patología , Proteínas de Unión al ADN , Proteínas Adaptadoras Transductoras de Señales , Adenocarcinoma Papilar/química , Adenocarcinoma Papilar/cirugía , Adenoma Velloso/química , Adenoma Velloso/cirugía , Adulto , Biomarcadores de Tumor/análisis , Proteínas Portadoras , Neoplasias del Colon/química , Neoplasias del Colon/cirugía , Neoplasias Colorrectales Hereditarias sin Poliposis/patología , ADN de Neoplasias/análisis , Diagnóstico Diferencial , Femenino , Humanos , Inmunohistoquímica , Masculino , Persona de Mediana Edad , Homólogo 1 de la Proteína MutL , Proteína 2 Homóloga a MutS , Proteínas de Neoplasias/análisis , Neoplasias Primarias Secundarias , Proteínas Nucleares , Proteínas Proto-Oncogénicas/análisis
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