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1.
PLoS One ; 16(6): e0252949, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-34170927

RESUMEN

To address the need for simple, safe, sensitive, and scalable SARS-CoV-2 tests, we validated and implemented a PCR test that uses a saliva collection kit use at home. Individuals self-collected 300 µl saliva in vials containing Darnell Rockefeller University Laboratory (DRUL) buffer and extracted RNA was assayed by RT-PCR (the DRUL saliva assay). The limit of detection was confirmed to be 1 viral copy/µl in 20 of 20 replicate extractions. Viral RNA was stable in DRUL buffer at room temperature up to seven days after sample collection, and safety studies demonstrated that DRUL buffer immediately inactivated virus at concentrations up to 2.75x106 PFU/ml. Results from SARS-CoV-2 positive nasopharyngeal (NP) swab samples collected in viral transport media and assayed with a standard FDA Emergency Use Authorization (EUA) test were highly correlated with samples placed in DRUL buffer. Direct comparison of results from 162 individuals tested by FDA EUA oropharyngeal (OP) or NP swabs with co-collected saliva samples identified four otherwise unidentified positive cases in DRUL buffer. Over six months, we collected 3,724 samples from individuals ranging from 3 months to 92 years of age. This included collecting weekly samples over 10 weeks from teachers, children, and parents from a pre-school program, which allowed its safe reopening while at-risk pods were quarantined. In sum, we validated a simple, sensitive, stable, and safe PCR-based test using a self-collected saliva sample as a valuable tool for clinical diagnosis and screening at workplaces and schools.


Asunto(s)
Prueba de Ácido Nucleico para COVID-19 , COVID-19 , SARS-CoV-2 , Saliva/virología , Instituciones Académicas , Manejo de Especímenes , COVID-19/diagnóstico , COVID-19/genética , Niño , Femenino , Humanos , Masculino
2.
Nature ; 425(6961): 917-25, 2003 Oct 30.
Artículo en Inglés | MEDLINE | ID: mdl-14586460

RESUMEN

The mammalian central nervous system (CNS) contains a remarkable array of neural cells, each with a complex pattern of connections that together generate perceptions and higher brain functions. Here we describe a large-scale screen to create an atlas of CNS gene expression at the cellular level, and to provide a library of verified bacterial artificial chromosome (BAC) vectors and transgenic mouse lines that offer experimental access to CNS regions, cell classes and pathways. We illustrate the use of this atlas to derive novel insights into gene function in neural cells, and into principal steps of CNS development. The atlas, library of BAC vectors and BAC transgenic mice generated in this screen provide a rich resource that allows a broad array of investigations not previously available to the neuroscience community.


Asunto(s)
Sistema Nervioso Central/metabolismo , Cromosomas Artificiales Bacterianos/genética , Perfilación de la Expresión Génica , Biblioteca de Genes , Genes Reporteros/genética , Transgenes/genética , Animales , Axones/metabolismo , Diferenciación Celular , Linaje de la Célula , Movimiento Celular , Sistema Nervioso Central/citología , Fosfodiesterasas de Nucleótidos Cíclicos Tipo 1 , Perfilación de la Expresión Génica/métodos , Regulación del Desarrollo de la Expresión Génica , Vectores Genéticos/genética , Proteínas Fluorescentes Verdes , Proteínas de Homeodominio/genética , Proteínas de Homeodominio/metabolismo , Proteínas con Homeodominio LIM , Proteínas Luminiscentes/análisis , Proteínas Luminiscentes/genética , Glicoproteínas de Membrana/genética , Glicoproteínas de Membrana/metabolismo , Ratones , Ratones Transgénicos , Proteínas del Tejido Nervioso/genética , Proteínas del Tejido Nervioso/metabolismo , Neurociencias/métodos , Hidrolasas Diéster Fosfóricas/genética , Hidrolasas Diéster Fosfóricas/metabolismo , Sinapsis/metabolismo , Factores de Transcripción
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