Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Teresa Grandi"'
Autor:
Anne Caroline Benski, G. Stancanelli, Serena Leotta, Lucia Barcellini, Teresa Grandi, Lucia Borsari, Laura Guarenti, Paola Borella
Publikováno v:
Journal of Immigrant and Minority Health. 20:1128-1136
Innovative migrant-friendly tools are needed to assist health personnel manage the high number of pregnancies within reception centers. This study tests functionality and acceptability of a new mHealth system in providing antenatal care amongst migra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ad90bb797d48f542b1d5fac6f12bb51
https://doi.org/10.1007/s10903-017-0669-2
https://doi.org/10.1007/s10903-017-0669-2
Autor:
Giulia Caron, Pierre-Alain Carrupt, Giuseppe Ermondi, Georgette Plemper van Balen, Alessandra Pagliara, Géraldine Bouchard, Teresa Grandi, Roberta Fruttero, Bernard Testa
Publikováno v:
Helvetica Chimica Acta, Vol. 84, No 2 (2001) pp. 360-374
The zwitterionic antihistamine cetirizine and its parent drug hydroxyzine as reference compound were examined for their 3D structures and dynamics. After attributing, by NMR spectroscopy, the two basic pK(a) values. the most common conformations for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efcbff58d09cd373d8cc35031d2df940
https://doi.org/10.1002/1522-2675(20010228)84:2<360::aid-hlca360>3.0.co
https://doi.org/10.1002/1522-2675(20010228)84:2<360::aid-hlca360>3.0.co
Autor:
Georgette Plemper van Balen, Pierre-Alain Carrupt, Giulia Caron, Teresa Grandi, Roberta Fruttero, Alessandra Pagliara, Géraldine Bouchard, Giuseppe Ermondi, Bernard Testa
Publikováno v:
Pharmaceutical Research. 18:694-701
Purpose. The partitioning of cetirizine in a phosphatidylcholine liposomes/water system was compared with that of hydroxyzine and acrivastine to gain insight into the mechanisms of interaction of its various electrical species with membranes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7d2d8177d55b9e7c81551a2a0cf9d86b
https://doi.org/10.1023/a:1011049830615
https://doi.org/10.1023/a:1011049830615
Autor:
Patrizia Crivori, Bernard Testa, Pierre-Alain Carrupt, Teresa Grandi, Carmela Gnerre, Fabio Sparatore
Publikováno v:
AAPS PharmSci, Vol. 1, No 4 (1999) P. E16
Benzazoles containing two or three nitrogen atoms were screened for their inhibitory activity toward monoamine oxidases MAO-A and MAO-B. In order to clarify the mechanism of interaction of these compounds with the enzyme, their electronic structure w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8faa37a3149cff7f28685b12566063d9
https://doi.org/10.1208/ps010416
https://doi.org/10.1208/ps010416
Publikováno v:
Scopus-Elsevier
The antiproliferative effects mediated by a 14-mer homopyrimidine oligonucleotide (5' CTTTCT-CTTTTCTC3'), designed to form DNA triplex with a purine region of the DNA polymerase alpha promoter, were evaluated on the human breast cancer cell line MDA-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50f2110b232d886fdaf0181d1fd6b917
https://doi.org/10.1089/oli.1.1996.6.95
https://doi.org/10.1089/oli.1.1996.6.95
Publikováno v:
Farmaco (Societa chimica italiana : 1989). 54(7)
The title ketone, a supposed metabolite of 9-methyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3- a ]quinolizine (MIQ), was prepared and found different on chromatographic comparison from the isolated metabolite M 4 . However, the pharmacological screening
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::259b16f5f165b6402dc83167ee378bd7
https://pubmed.ncbi.nlm.nih.gov/10486916
https://pubmed.ncbi.nlm.nih.gov/10486916
Autor:
Teresa Grandi, Umberto Benatti, Luigi Silvestro, Glanluca Damonte, Michela Tonetti, Anna Gasparini, Marco Glovine, Alessandro Balbi, Mauro Mazzei, Antonio De Flora
Publikováno v:
Biochemical pharmacology. 48(6)
A new dimeric fluoropyrimidine molecule (5-fluoro-2'-deoxyuridilyl-(5'→'3')-5-fluoro-2'-deoxy-5'-uridylic acid, Compound 1) was chemically synthesized from two separately deblocked 5-nuoro-2'-deoxyuridine mononucleotide moieties. Other structurally
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0dc374f66b45085f7fef19c58e5d6494
https://pubmed.ncbi.nlm.nih.gov/7945405
https://pubmed.ncbi.nlm.nih.gov/7945405
Publikováno v:
Tetrahedron Letters. 36:1331-1332
The title compounds were advantageously synthesized from 2-(dialkylamino)chromones and 1,3-diaminopropane (or 1-amino-3-bromopropane) by amine exchange. The 3-cyano derivatives 5 were directly prepared from 2-(dimethylamino)chromones 1 and KCN by nit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1197382199a35dead5816aa4aa7abd7
https://doi.org/10.1016/0040-4039(94)02469-r
https://doi.org/10.1016/0040-4039(94)02469-r