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1.
Analyst ; 145(4): 1202-1206, 2020 Feb 17.
Artigo em Inglês | MEDLINE | ID: mdl-31859691

RESUMO

A new strategy for ELISA-based detection in small volumes based on porous antibody-containing protein microparticles was developed and employed for the determination of human immunoglobulin G demonstrating both increase in sensitivity and decrease in antibody consumption by ten times compared to a conventional planar ELISA.


Assuntos
Ensaio de Imunoadsorção Enzimática/métodos , Imunoglobulina G/química , Microesferas , Anticorpos Imobilizados/química , Anticorpos Imobilizados/imunologia , Imunoglobulina G/imunologia , Limite de Detecção , Modelos Moleculares , Porosidade , Conformação Proteica
2.
Cancers (Basel) ; 14(21)2022 Oct 29.
Artigo em Inglês | MEDLINE | ID: mdl-36358751

RESUMO

Gastrointestinal stromal tumors (GISTs) are malignant mesenchymal tumors arising from the intestinal pacemaker cells of Cajal. They compose a heterogenous group of tumors due to a variety of molecular alterations. The most common gain-of-function mutations in GISTs are either in the KIT (60-70%) or platelet-derived growth factor receptor alpha (PDGFRA) genes (10-15%), which are mutually exclusive. However, a smaller subset, lacking KIT and PDGFRA mutations, is considered wild-type GISTs and presents distinct molecular findings with the activation of different proliferative pathways, structural chromosomal and epigenetic changes, such as inactivation of the NF1 gene, mutations in the succinate dehydrogenase (SDH), BRAF, and RAS genes, and also NTRK fusions. Currently, a molecular evaluation of GISTs is imperative in many scenarios, aiding in treatment decisions from the (neo)adjuvant to the metastatic setting. Here, we review the most recent data on the molecular profile of GISTs and highlight therapeutic implications according to distinct GIST molecular subtypes.

3.
IDCases ; 10: 71-74, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28966914

RESUMO

Paracoccidioidomycosis (PCM) is a systemic granulomatous disease caused by Paracoccidioides brasiliensis or P. lutzii. It is a neglected tropical infectious disease that poses a major public health burden in endemic areas of Latin America. Mucosae of the upper digestive and respiratory tracts are commonly involved and many patients have disease at multiple mucosal sites, with or without lung involvement. Mucosal PCM presenting as solitary true vocal fold disease is relatively rare. We present the case of a 67-year-old Brazilian forest guard who presented with a 6-month history of hoarseness and globus pharyngeus due to a solitary left true vocal fold infiltration and vegetation diagnosed as PCM. Silent pulmonary disease was also present. A laryngoscopy video is offered as supplemental material to this report. He completely remitted after surgical removal and amphotericin B deoxycholate treatment.

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