Zobrazeno 1 - 10
of 108
pro vyhledávání: '"Piero Angeli"'
Autor:
Francisco Prosdocimi, Piero Angeli Ruschi, Ana Cecilia Gomes Silva-Malanski, Gustavo Andrés Ferraro, Carla Christie Quijada, W. Bryan Jennings, Paulo A. Buckup
Publikováno v:
Genome. 62:77-83
Designing primers for DNA barcoding is a significant challenge for the rich Neotropical fish fauna, which is comprised of ∼6000 species. Previously, researchers required multiple pairs of PCR primers or primer cocktails to obtain standard COI (i.e.
Autor:
Catia Lambertucci, Diego Dal Ben, Michela Buccioni, Claudia Santinelli, Piero Angeli, Gabriella Marucci, Ajiroghene Thomas, Rosaria Volpini
Publikováno v:
Mini-Reviews in Medicinal Chemistry. 17:3-14
G-protein coupled receptors (GPCRs) represent important targets for drug discovery because they participate in a wide range of cellular signalling pathways that play a role in a variety of pathological conditions. The characterization of the patho-ph
Autor:
Daniel Honorato Firme, Marco Aurélio Crozariol, Gabriela Guimarães Araújo, Piero Angeli Ruschi, Marcos A. Raposo, Guilherme R. R. Brito, Renata Neves Biancalana, Nelson Buainain Neto, Ricardo Parrini, Daniel Monteiro Figueira, Claydson Pinto de Assis, Gabriella Frickes
Publikováno v:
Revista Brasileira de Ornitologia. 23:398-404
The White-chinned Swift Cypseloides cryptus is perhaps one of the rarest swift species in the New World, and many aspects of its life history are poorly known. Here we report some new information on diet and reproductive behavior of a breeding popula
Publikováno v:
Future Medicinal Chemistry. 2:1247-1252
The series of Camerino Symposia present the most recent knowledge and discoveries in the growing field of drug–receptor interactions and the design and mechanisms of drug action. Lead discovery, G protein-coupled receptors (GPCRs) and polypharmacol
Autor:
Massimo Ricciutelli, Gabriella Marucci, Gloria Cristalli, Sara Finaurini, Jan N. M. Commandeur, Carmen Lammi, Michela Buccioni, Rosaria Volpini, Piero Angeli, Meenakshisundaram Kandhavelu
Publikováno v:
Drug Metabolism Letters. 2:301-307
Evidence, obtained in rodent and primate models of Parkinsons disease (PD) and in preliminary clinical trials, indicates that adenosine A receptor antagonists might represent a promising non-dopaminergic therapeutic tool for the treatment of PD. Rece
Publikováno v:
Revista Científica Faesa. 4:47-62
The fauna composition of many ecosystems in the state of Espirito Santo is still insuffi ciently known, what makes hard to take decisions on the regional biodiversity conservation. The present paper presents the preliminary results on the ornithologi
Autor:
Francisco Prosdocimi, W. Bryan Jennings, Carolina Furtado, Piero Angeli Ruschi, Helena Magarinos Souto
Publikováno v:
Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis. 27(5)
The genome of the versicoloured emerald hummingbird (Amazilia versicolor) was partially sequenced in one—sixth of an Illumina HiSeq lane. The mitochondrial genome was assembled using MIRA and MITObim software, yielding a circular molecule of 16,861
Autor:
Piero Angeli, Anna Maria Baraldi, Claudia Sorbi, Federica Pellati, Antonio Cilia, Umberto Maria Battisti, Livio Brasili, Elena Cichero, Silvia Franchini
In this paper, the enantiomers of (±)-1, previously studied as α1 and 5-HT1A ligands, were prepared both by resolution of the racemate and asymmetric synthesis. The enantiomeric purity and absolute configuration were determined by means of HPLC and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72b96f70267e9e29239aaa77d5ae7b29
http://hdl.handle.net/11567/810290
http://hdl.handle.net/11567/810290
Autor:
Kenneth P. Minneman, Giuseppe Romeo, Gabriella Marucci, Valeria Pittalà, Maria Angela Siracusa, Maria N. Modica, Piero Angeli, Luisa Materia, Loredana Salerno, Michela Buccioni
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 16:6200-6203
A number of new pyrimido[5,4-b]indole and [1]benzothieno[3,2-d]pyrimidine derivatives were synthesized and evaluated for their binding and functional properties at alpha(1)-adrenergic receptor (alpha(1)-AR) subtypes. They behaved as potent alpha(1)-A
Autor:
Gianni Sagratini, Dario Giardinà, Ugo Gulini, Piero Angeli, Michela Buccioni, Carlo Melchiorre, Gabriella Marucci, Rodolfo Testa
Publikováno v:
European Journal of Pharmacology. 522:100-107
To shed light on the discrepancy between reported binding and functional affinity and selectivity at alpha(1b/B)-adrenoceptors, the antagonist (+)-cyclazosin was reinvestigated in rat and rabbit tissues. It displayed a competitive antagonism at alpha