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1.
J Carcinog ; 15: 1, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-27013929

RESUMEN

Breast cancer is known to metastasize in its latter stages of existence. The different angiogenic mechanisms and factors that allow for its progression are reviewed in this article. Understanding these mechanisms and factors will allow researchers to design drugs to inhibit angiogenic behaviors and control the rate of tumor growth.

2.
J Microbiol Methods ; 89(1): 12-7, 2012 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-22342195

RESUMEN

Epidemiological studies of Pierce's disease (PD) can be confounded by a lack of taxonomic detail on the bacterial causative agent, Xylella fastidiosa (Xf). PD in grape is caused by strains of Xylella fastidiosa subsp. fastidiosa, but is not caused by other subspecies of Xf that typically colonize plants other than grape. Detection assays using ELISA and qPCR are effective at detecting and quantifying Xf presence or absence, but offer no information on Xf subspecies or strain identity. Surveying insects or host plants for Xf by current ELISA or qPCR methods provides only presence/absence and quantity information for any and all Xf subspecies, potentially leading to false assessments of disease threat. This study uses a series of adjacent-hybridizing DNA melt analysis probes that are capable of efficiently discriminating Xf subspecies and strain relationships in rapid real-time PCR reactions.


Asunto(s)
Tipificación Molecular/métodos , Sondas de Oligonucleótidos/genética , Reacción en Cadena en Tiempo Real de la Polimerasa/métodos , Xylella/clasificación , Xylella/genética , Animales , ADN Bacteriano/química , ADN Bacteriano/genética , Insectos/microbiología , Datos de Secuencia Molecular , Plantas/microbiología , Análisis de Secuencia de ADN , Temperatura de Transición , Xylella/aislamiento & purificación
3.
J Microbiol Methods ; 86(3): 310-2, 2011 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-21703312

RESUMEN

We report an inexpensive, high-throughput method for isolating DNA from insect and plant samples for the purpose of detecting Xylella fastidiosa infection. Existing methods often copurify inhibitors of DNA polymerases, limiting their usefulness for PCR-based detection assays. When compared to commercially available kits, the method provides enhanced pathogen detection at a fraction of the cost.


Asunto(s)
ADN Bacteriano/aislamiento & purificación , Ensayos Analíticos de Alto Rendimiento/métodos , Insectos/microbiología , Plantas/microbiología , Xylella/genética , Xylella/aislamiento & purificación , Animales , ADN Bacteriano/genética , Enfermedades de las Plantas/microbiología
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