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1.
MAbs ; 15(1): 2211692, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-37184206

RESUMO

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.


Assuntos
Anticorpos Monoclonais , Imunoterapia Adotiva , Anticorpos Monoclonais/uso terapêutico , França
2.
Chem Commun (Camb) ; (17): 1974-6, 2008 May 07.
Artigo em Inglês | MEDLINE | ID: mdl-18536792

RESUMO

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


Assuntos
DNA/química , Imidas/química , Perileno/análogos & derivados , Dicroísmo Circular , Fluorescência , Estrutura Molecular , Perileno/química , Espectrofotometria , Temperatura
3.
Biochim Biophys Acta ; 1697(1-2): 211-23, 2004 Mar 11.
Artigo em Inglês | MEDLINE | ID: mdl-15023362

RESUMO

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.


Assuntos
Antifúngicos/química , Antifúngicos/farmacologia , Quinases Ciclina-Dependentes , Proteínas Serina-Treonina Quinases/antagonistas & inibidores , Purinas/química , Purinas/farmacologia , Sequência de Aminoácidos , Proteínas de Ciclo Celular/antagonistas & inibidores , Inibidores Enzimáticos/química , Inibidores Enzimáticos/farmacologia , Proteínas Fúngicas/antagonistas & inibidores , Fungos/efeitos dos fármacos , Fungos/enzimologia , Fungos/fisiologia , Modelos Moleculares , Dados de Sequência Molecular , Relação Estrutura-Atividade , Quinase Ativadora de Quinase Dependente de Ciclina
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