Zobrazeno 1 - 10 of 241 pro vyhledávání: '"M, Marastoni"'
1
Peptide-based cationic molecules for the production of positive charged liposomes and micelles
Autor: Elisabetta Esposito, M Marastoni, Roberto Tomatis, Rita Cortesi, Enea Menegatti, Claudio Nastruzzi
Publikováno v: Journal of Microencapsulation. 25:71-81
This paper describes the synthesis and the physico-chemical characterization of cationic peptides (CPs) for possible application as non-viral gene delivery systems. Particularly, the production of cationic liposomes and micelle solutions was consider
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74f2dfcdde1e5149cbd8d41f4df04291
https://doi.org/10.1080/02652040701711403
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2
Hybrid Zigbee–RFID Networks for Energy Saving and Lifetime Maximization
Autor: M. Marastoni, Gianluigi Ferrari, Paolo Medagliani
Publikováno v: Remote Instrumentation and Virtual Laboratories ISBN: 9781441955951
Zigbee is the standard of choice in wireless personal area networks with low power consumption, such as, sensor and control wireless networks. Since nodes may be positioned in non-easily accessible places, a high energy efficiency is required in orde
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::393a36c3893f74f5862f48bd291143b8
https://doi.org/10.1007/978-1-4419-5597-5_37
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4
Synthesis, conformation and biological activity of dermorphin and delthorphin 1 peptide-peptoid hybrids
Autor: L. Biondi, E. Giannini, F. Filira, M. Gobbo, M. Marastoni, L. Negri, B. Scolaro, R. Tomatis, R. Rocchi
Publikováno v: 18th American Peptide Symposium, Boston (MA) USA, 2003
info:cnr-pdr/source/autori:L. Biondi, E. Giannini, F. Filira, M. Gobbo, M. Marastoni, L. Negri, B. Scolaro, R. Tomatis, R. Rocchi/congresso_nome:18th American Peptide Symposium/congresso_luogo:Boston (MA) USA/congresso_data:2003/anno:2003/pagina_da:/pagina_a:/intervallo_pagine
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::6e31618c8054d7f6e65d880b2bef3bde
http://www.cnr.it/prodotto/i/104143
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5
New Insights On Mu-delta Selectivity of Opioid-peptides - Conformational-analysis of Deltorphin Analogs
Autor: T. TANCREDI, P. A. TEMUSSI, P. AMODEO, R. TOMATIS, S. SALVADORI, M. MARASTONI, V. SANTAGADA, G. BALBONI, PICONE, DELIA
The message domain of dermorphin (Tyr-D-Ala-Phe), a natural mu-opioid heptapeptide, has long been considered the main cause of the high mu-selectivity of this peptide and of its analogues. The recent discovery, in the skin of Phyllomedusa sauvagei (i
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3730::5c4490082318678ea2b43ef765ca4e00
http://hdl.handle.net/11588/475151
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6
Synthesis and biological activity of chelator-peptide T conjugates
Autor: M, Marastoni, S, Spisani, R, Tomatis
Publikováno v: Arzneimittel-Forschung. 48(10)
The solid phase procedure was used to prepare two peptide T derivatives in which the 4-[(1,4,8,11-tetraazacyclotetradec-1-yl)methyl]benzoyl unit is linked to their N-terminus. In a human monocyte chemotaxis assay, both chelator-peptide conjugates sho
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a5765a97310d62c73993b0f24b7cfec3
https://pubmed.ncbi.nlm.nih.gov/9825124
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7
Structure-activity relationships of HIV-1 protease inhibitors containing gem-diaminoserine core unit
Autor: M, Marastoni, F, Bortolotti, S, Salvadori, R, Tomatis
Publikováno v: Arzneimittel-Forschung. 48(6)
Two series of peptidomimetics containing 1,1-diamino-2-hydroxyethane (gSer) core structure were prepared, from amino acid starting materials, and evaluated as inhibitors of HIV-1 protease (HIV-1 Pr). Asymmetrical pseudodipeptides, Y-Xaa-gSer-Y (Y = Z
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::e486692d44d2c26d662ebf9f777267a5
https://pubmed.ncbi.nlm.nih.gov/9689433
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8
Rational design of dynorphin A analogues with delta-receptor selectivity and antagonism for delta- and kappa-receptors
Autor: R, Guerrini, A, Capasso, M, Marastoni, S D, Bryant, P S, Cooper, L H, Lazarus, P A, Temussi, S, Salvadori
Publikováno v: Bioorganicmedicinal chemistry. 6(1)
Substitution of 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid (Tic) in place of Gly2 in dynorphin A-(1-13)-NH2 and -(1-11)-NH2 (DYN) analogues (1 and 2) decreased the affinity to the kappa, delta, and mu receptors, and kappa selectivity. The analo
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9c207099850e7d875268e4bdc5bbc81c
https://pubmed.ncbi.nlm.nih.gov/9502105
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9
Symmetry-based HIV protease inhibitors containing (S,S) or (R,R) tartaric acid core structure
Autor: M, Marastoni, M, Bergonzoni, F, Bortolotti, R, Tomatis
Publikováno v: Arzneimittel-Forschung. 47(7)
Two series of symmetry-based HIV protease inhibitors containing (S,S) or (R,R) tartaric acid core structure were prepared and tested for inhibitory property against the enzyme. All compounds showed weak antiprotease activity.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::7ddb546b90225b59ac12eeac8994a51d
https://pubmed.ncbi.nlm.nih.gov/9272250
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10
Effects of peptide T derivatives on the proliferation of cultured human keratinocytes
Autor: M, Marastoni, V, Scaranari, F, Fantini, C, Sevignani, R, Tomatis
Publikováno v: Arzneimittel-Forschung. 45(8)
[D-Ala1]peptideT-amide, the linear hexapeptide H-Thr-Hse-Asn-Tyr-Thr-Asp-OH (LPT) and its cyclic analog, cyclo(-Thr-Hse-Asn-Tyr-Thr-Asp-) (CPT), were tested for their effects on the proliferation of cultured normal human keratinocytes (KTs) in compar
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ca43807661414746be4523fc061d22d6
https://pubmed.ncbi.nlm.nih.gov/7575755
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