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1.
Asian Pac J Cancer Prev ; 25(3): 747-756, 2024 Mar 01.
Artigo em Inglês | MEDLINE | ID: mdl-38546057

RESUMO

QDs are semiconductor nanocrystalline materials with distinct optical and electronic characteristics due to their microscopic size and quantum mechanical properties. They are often composed of materials such as cadmium selenide (CdSe), cadmium telluride (CdTe), or indium phosphide (InP) and are typically in the size range of 2 to 10 nanometers in diameter. These tiny particles are used in various scientific and technological applications. Some key characteristics and applications of quantum dots are size-dependent Optical Properties with tunable emission. The color of light emitted by quantum dots highly depends on their size. Smaller QDs emit blue or green light, while larger ones emit red or near-infrared light. This tunability makes them valuable in various applications, especially in molecular medicine and oncology research. Quantum dots can exhibit a high quantum yield, meaning they efficiently emit light when excited, making them excellent fluorescent probes for non-invasive imaging. This review discusses the applications of QDs and their role in biomedical research and patient care, focusing on non-invasive imaging and preventive oncology.


Assuntos
Compostos de Cádmio , Nanopartículas , Pontos Quânticos , Humanos , Pontos Quânticos/química , Compostos de Cádmio/química , Telúrio , Nanopartículas/química
2.
Twin Res Hum Genet ; 25(3): 156-164, 2022 06.
Artigo em Inglês | MEDLINE | ID: mdl-35786423

RESUMO

Nature and nurture have always been a prerogative of evolutionary biologists. The environment's role in shaping an organism's phenotype has always intrigued us. Since the inception of humankind, twinning has existed with an unsettled parley on the contribution of nature (i.e. genetics) versus nurture (i.e. environment), which can influence the phenotypes. The study of twins measures the genetic contribution and that of the environmental influence for a particular trait, acting as a catalyst, fine-tuning the phenotypic trajectories. This is further evident because a number of human diseases show a spectrum of clinical manifestations with the same underlying molecular aberration. As of now, there is no definite way to conclude just from the genomic data the severity of a disease or even to predict who will get affected. This greatly justifies initiating a twin registry for a country as diverse and populated as India. There is an unmet need to set up a nationwide database to carefully curate the information on twins, serving as a valuable biorepository to study their overall susceptibility to disease. Establishing a twin registry is of paramount importance to harness the wealth of human information related to the biomedical, anthropological, cultural, social and economic significance.


Assuntos
Doenças em Gêmeos , Gêmeos , Doenças em Gêmeos/epidemiologia , Doenças em Gêmeos/genética , Humanos , Índia/epidemiologia , Sistema de Registros , Gêmeos/genética , Recursos Humanos
3.
Sci Rep ; 7: 43711, 2017 03 02.
Artigo em Inglês | MEDLINE | ID: mdl-28252110

RESUMO

HIV maturation inhibitors are an emerging class of anti-retroviral compounds that inhibit the viral protease-mediated cleavage of the Gag, CA-SP1 (capsid-spacer peptide 1) peptide to mature CA. The first-in-class maturation inhibitor bevirimat (BVM) displayed potent activity against HIV-1 clade B but was ineffective against other HIV-1 clades including clade C. Another pyridone-based maturation inhibitor, PF-46396 displayed potent activity against HIV-1 clade B. In this study, we aimed at determining the activity of PF-46396 against HIV-1 clade C. We employed various biochemical and virological assays to demonstrate that PF-46396 is effective against HIV-1 clade C. We observed a dose dependent accumulation of CA-SP1 intermediate in presence of the compound. We carried out mutagenesis in the CA- SP1 region of HIV-1 clade C Gag and observed that the mutations conferred resistance against the compound. Many mutations inhibited Gag processing thereby reducing virus release in the absence of the compound. However, presence of PF-46396 rescued these defects and enhanced virus release, replication capacity and infectivity of HIV-1 clade C. These results put together identify PF-46396 as a broadly active maturation inhibitor against HIV-1 clade B and C and help in rational designing of novel analogs with reduced toxicity and increased efficacy for its potential use in clinics.


Assuntos
Fármacos Anti-HIV/farmacologia , Genótipo , HIV-1/efeitos dos fármacos , HIV-1/genética , Motivos de Aminoácidos , Sequência de Aminoácidos , Fármacos Anti-HIV/química , Proteínas do Capsídeo/química , Proteínas do Capsídeo/metabolismo , Relação Dose-Resposta a Droga , Resistencia a Medicamentos Antineoplásicos , Infecções por HIV/tratamento farmacológico , Infecções por HIV/virologia , Protease de HIV/metabolismo , HIV-1/fisiologia , Humanos , Testes de Sensibilidade Microbiana , Estrutura Molecular , Mutação , Ligação Proteica , Domínios e Motivos de Interação entre Proteínas , Proteólise/efeitos dos fármacos , Replicação Viral/efeitos dos fármacos , Produtos do Gene gag do Vírus da Imunodeficiência Humana/metabolismo
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