Zobrazeno 1 - 10
of 88
pro vyhledávání: '"Eduard Bardají"'
Autor:
Arash Shams, Mohammadreza Mehdizadeh, HamidReza Teimoury, Mehrsa Emami, Seyed Amin Mirmohammadi, Samahe Sadjadi, Eduard Bardají, Albert Poater, Naeimeh Bahri-Laleh
Publikováno v:
Journal of Industrial and Engineering Chemistry. 116:359-370
Autor:
Erik Strandberg, Parvesh Wadhwani, Jochen Bürck, Patrick Anders, Christian Mink, Jonas van den Berg, Raffaele A. M. Ciriello, Manuel N. Melo, Miguel A. R. B. Castanho, Eduard Bardají, Jakob P. Ulmschneider, Anne S. Ulrich
Publikováno v:
ChemBioChem
© 2022 The Authors. ChemBioChem published by Wiley-VCH GmbH. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is pr
Autor:
Imma Güell, Rafael Ferre, Kasper K. Sørensen, Esther Badosa, Iteng Ng-Choi, Emilio Montesinos, Eduard Bardají, Lidia Feliu, Knud J. Jensen, Marta Planas
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 8, Iss 1, Pp 2106-2117 (2012)
Carbohydrates are considered as promising templates for the display of multiple copies of antimicrobial peptides. Herein, we describe the design and synthesis of chimeric structures containing two or four copies of the antimicrobial peptides KKLFKKIL
Externí odkaz:
https://doaj.org/article/8a5826f686ba4afa9dedad331d47bdab
Autor:
Cristina Camó, Maria Torné, Emili Besalú, Cristina Rosés, Anna D. Cirac, Gemma Moiset, Esther Badosa, Eduard Bardají, Emilio Montesinos, Marta Planas, Lidia Feliu
Publikováno v:
Molecules, Vol 22, Iss 11, p 1817 (2017)
A library of 66 cyclic decapeptides incorporating a Trp residue was synthesized on solid phase and screened against the phytopathogenic bacteria Pseudomonas syringae pv. syringae, Xanthomonas axonopodis pv. vesicatoria, and Erwinia amylovora. The hem
Externí odkaz:
https://doaj.org/article/77ec0e8023fe45b8a31e844817f0b161
Autor:
Esther Badosa, Gemma Moiset, Laura Montesinos, Montserrat Talleda, Eduard Bardají, Lidia Feliu, Marta Planas, Emilio Montesinos
Publikováno v:
PLoS ONE, Vol 8, Iss 12, p e85515 (2013)
Production of antimicrobial peptides in plants constitutes an approach for obtaining them in high amounts. However, their heterologous expression in a practical and efficient manner demands some structural requirements such as a minimum size, the inc
Externí odkaz:
https://doaj.org/article/7074ea3b9c9b467195fb462d51b895bd
Autor:
Manuel N Melo, Rafael Ferre, Lídia Feliu, Eduard Bardají, Marta Planas, Miguel A R B Castanho
Publikováno v:
PLoS ONE, Vol 6, Iss 12, p e28549 (2011)
Consensus is gathering that antimicrobial peptides that exert their antibacterial action at the membrane level must reach a local concentration threshold to become active. Studies of peptide interaction with model membranes do identify such disruptiv
Externí odkaz:
https://doaj.org/article/0f8e4ca8a8844d4fb81a53878382ccfe
Autor:
Vasanthakumar G. Ramu, Montserrat Heras, Eduard Bardají, Jéssica Diane dos Santos, Miguel A. R. B. Castanho, Katia Conceição, Juliana Campos Junqueira, Vitor Martins de Andrade
Publikováno v:
Web of Science
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
© 2019 British Mycological Society. Published by Elsevier Ltd. All rights reserved.
Kyotorphin (KTP, l-tyrosyl-l-arginine) is an endogenous analgesic neuropeptide first isolated from bovine brain in 1979. Previous studies have shown that kyotor
Kyotorphin (KTP, l-tyrosyl-l-arginine) is an endogenous analgesic neuropeptide first isolated from bovine brain in 1979. Previous studies have shown that kyotor
Autor:
Lidia Feliu, Emilio Montesinos, Gemma Moiset, Cristina Rosés, Eduard Bardají, Cristina Camó, Emili Besalú, Anna D. Cirac, Marta Planas, Esther Badosa, Maria Torné
Publikováno v:
Molecules, Vol 22, Iss 11, p 1817 (2017)
Molecules, 2017, vol. 22, núm. 11, p.1817-1830
Articles publicats (D-Q)
DUGiDocs – Universitat de Girona
instname
Molecules; Volume 22; Issue 11; Pages: 1817
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Recercat. Dipósit de la Recerca de Catalunya
Molecules, 2017, vol. 22, núm. 11, p.1817-1830
Articles publicats (D-Q)
DUGiDocs – Universitat de Girona
instname
Molecules; Volume 22; Issue 11; Pages: 1817
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Recercat. Dipósit de la Recerca de Catalunya
A library of 66 cyclic decapeptides incorporating a Trp residue was synthesized on solid phase and screened against the phytopathogenic bacteria Pseudomonas syringae pv. syringae, Xanthomonas axonopodis pv. vesicatoria, and Erwinia amylovora. The hem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9df97caa331aec119f698795aa6b48a5
https://hdl.handle.net/2072/319836
https://hdl.handle.net/2072/319836
Autor:
Isaura Tavares, João M. Freire, Montserrat Heras, Vasanthakumar G. Ramu, Miguel A. R. B. Castanho, Antónia R. T. Pinto, Isa Serrano, Eduard Bardají
Publikováno v:
Biopolymers. 104:1-10
Amidated kyotorphin (l-Tyr-l-Arg-NH2; KTP-NH2) causes analgesia when systemically administered. The lipophilic ibuprofen-conjugated derivative of KTP-NH2 has improved analgesic efficacy. However, fast degradation by peptidases impacts negatively in t
Autor:
Miguel A. R. B. Castanho, Juliana Perazzo, Montserrat Heras, Mônica Lopes-Ferreira, Carla Lima, Eduard Bardají
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
ACS Chemical Neuroscience
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
ACS Chemical Neuroscience
© 2017 American Chemical Society
Neuropeptide kyotorphin (KTP) is a potent analgesic if administered directly into the brain. In contrast, KTP-amide (KTP-NH2) is analgesic, neuroprotective, and anti-inflammatory following systemic administratio
Neuropeptide kyotorphin (KTP) is a potent analgesic if administered directly into the brain. In contrast, KTP-amide (KTP-NH2) is analgesic, neuroprotective, and anti-inflammatory following systemic administratio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a0bf0b6c8442d9b48e00b40440f91e7
https://hdl.handle.net/10451/32603
https://hdl.handle.net/10451/32603