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1.
MAbs ; 15(1): 2211692, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-37184206

RESUMEN

The annual "Antibody Industrial Symposium", co-organized by LabEx MAbImprove and MabDesign, held its 10th anniversary edition in Montpellier, France, on June 28-29, 2022. The meeting focused on new results and concepts in antibody engineering (naked, mono- or multi-specific, conjugated to drugs or radioelements) and also on new cell-based therapies, such as chimeric antigenic receptor (CAR)-T cells. The symposium, which brought together scientists from academia and industry, also addressed issues concerning the production of these molecules and cells, and the necessary steps to ensure a strong intellectual property protection of these new molecules and approaches. These two days of exchanges allowed a rich discussion among the various actors in the field of therapeutic antibodies.


Asunto(s)
Anticuerpos Monoclonales , Inmunoterapia Adoptiva , Anticuerpos Monoclonales/uso terapéutico , Francia
2.
Chem Commun (Camb) ; (17): 1974-6, 2008 May 07.
Artículo en Inglés | MEDLINE | ID: mdl-18536792

RESUMEN

Pyrene excimer fluorescence is effectively quenched by non-nucleosidic perylene diimides upon DNA duplex formation.


Asunto(s)
ADN/química , Imidas/química , Perileno/análogos & derivados , Dicroismo Circular , Fluorescencia , Estructura Molecular , Perileno/química , Espectrofotometría , Temperatura
3.
Biochim Biophys Acta ; 1697(1-2): 211-23, 2004 Mar 11.
Artículo en Inglés | MEDLINE | ID: mdl-15023362

RESUMEN

There is today a blatant need for new antifungal agents, because of the recent increase in life-threatening infections involving an ever-greater number of fungal strains. Fungi make extensive use of kinases in the regulation of essential processes, in particular the cell cycle. Most fungal kinases, however, are shared with higher eukaryotes. Only the kinases which have no human homologs, such as the histidine kinases, can be used as targets for antifungal drugs design. This review describes efforts directed towards the discovery of drugs active against a novel target, the atypical cell cycle kinase, Civ1.


Asunto(s)
Antifúngicos/química , Antifúngicos/farmacología , Quinasas Ciclina-Dependientes , Proteínas Serina-Treonina Quinasas/antagonistas & inhibidores , Purinas/química , Purinas/farmacología , Secuencia de Aminoácidos , Proteínas de Ciclo Celular/antagonistas & inhibidores , Inhibidores Enzimáticos/química , Inhibidores Enzimáticos/farmacología , Proteínas Fúngicas/antagonistas & inhibidores , Hongos/efectos de los fármacos , Hongos/enzimología , Hongos/fisiología , Modelos Moleculares , Datos de Secuencia Molecular , Relación Estructura-Actividad , Quinasa Activadora de Quinasas Ciclina-Dependientes
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