Zobrazeno 1 - 10
of 238
pro vyhledávání: '"Anna Bernardi"'
Autor:
Xinyu Ning, Darshita Budhadev, Sara Pollastri, Inga Nehlmeier, Amy Kempf, Iain Manfield, W. Bruce Turnbull, Stefan Pöhlmann, Anna Bernardi, Xin Li, Yuan Guo, Dejian Zhou
Publikováno v:
JACS Au, Vol 4, Iss 8, Pp 3295-3309 (2024)
Externí odkaz:
https://doaj.org/article/757f82838ccf4e62a5f84306bc3cb42c
Autor:
Giulia Antonini, Monica Civera, Kanhaya Lal, Sarah Mazzotta, Annabelle Varrot, Anna Bernardi, Laura Belvisi
Publikováno v:
Frontiers in Molecular Biosciences, Vol 10 (2023)
Opportunistic infections from multidrug-resistant pathogens such as Burkholderia cenocepacia are a threatening risk for hospital-bound patients suffering from immunocompromised conditions or cystic fibrosis. B. cenocepacia BC2L-C lectin has been link
Externí odkaz:
https://doaj.org/article/917164ba495b4ced8dff663f7292d552
Autor:
Sarah Mazzotta, Giulia Antonini, Francesca Vasile, Emilie Gillon, Jon Lundstrøm, Annabelle Varrot, Laura Belvisi, Anna Bernardi
Publikováno v:
Molecules, Vol 28, Iss 3, p 1494 (2023)
The inhibition of carbohydrate-lectin interactions is being explored as an efficient approach to anti adhesion therapy and biofilm destabilization, two alternative antimicrobial strategies that are being explored against resistant pathogens. BC2L-C i
Externí odkaz:
https://doaj.org/article/33502112a0574c8ebfc6ee2082f51893
Publikováno v:
Beilstein Journal of Nanotechnology, Vol 10, Iss 1, Pp 2192-2206 (2019)
A class of linear and four-arm mannosylated brush copolymers based on poly(ethylene glycol) and poly(ε-caprolactone) is presented here. The synthesis through ring-opening and atom transfer radical polymerizations provided high control over molecular
Externí odkaz:
https://doaj.org/article/162c99d37c104ebca1a0adf5700252f5
Autor:
Michel Thépaut, Joanna Luczkowiak, Corinne Vivès, Nuria Labiod, Isabelle Bally, Fátima Lasala, Yasmina Grimoire, Daphna Fenel, Sara Sattin, Nicole Thielens, Guy Schoehn, Anna Bernardi, Rafael Delgado, Franck Fieschi
Publikováno v:
PLoS Pathogens, Vol 17, Iss 5, p e1009576 (2021)
The efficient spread of SARS-CoV-2 resulted in a unique pandemic in modern history. Despite early identification of ACE2 as the receptor for viral spike protein, much remains to be understood about the molecular events behind viral dissemination. We
Externí odkaz:
https://doaj.org/article/2dab28ce226f4cd4ba786236d8f23229
Autor:
Julie Elisabeth Heggelund, Alasdair Mackenzie, Tobias Martinsen, Joel Benjamin Heim, Pavel Cheshev, Anna Bernardi, Ute Krengel
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-11 (2017)
Abstract Cholera is a life-threatening disease in many countries, and new drugs are clearly needed. C-glycosidic antagonists may serve such a purpose. Here we report atomic-resolution crystal structures of three such compounds in complexes with the c
Externí odkaz:
https://doaj.org/article/d8b34731a07e4f5099ce552d4d1ee6e9
Autor:
Rafael Bermeo, Kanhaya Lal, Davide Ruggeri, Daniele Lanaro, Sarah Mazzotta, Francesca Vasile, Anne Imberty, Laura Belvisi, Annabelle Varrot, Anna Bernardi
Publikováno v:
ACS Chemical Biology. 17:2899-2910
Autor:
Vanessa Porkolab, Martin Lepšík, Stefania Ordanini, Alexander St John, Aline Le Roy, Michel Thépaut, Emanuele Paci, Christine Ebel, Anna Bernardi, Franck Fieschi
Publikováno v:
ACS Central Science
ACS Central Science, 2023, ⟨10.1021/acscentsci.2c01136⟩
ACS Central Science, 2023, ⟨10.1021/acscentsci.2c01136⟩
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5867d1310f500643c3f7c97f81d7fc6
https://hal.science/hal-04055889
https://hal.science/hal-04055889
Publikováno v:
Chemical Communications
Chemical Communications, 2022, 58 (33), pp.5136-5139. ⟨10.1039/d2cc00121g⟩
Chemical Communications, 2022, 58 (33), pp.5136-5139. ⟨10.1039/d2cc00121g⟩
International audience; The C-type lectin receptors DC-SIGN and L-SIGN bind to glycans on the SARS-CoV-2 spike glycoprotein and promote trans-infection of ACE2-expressing cells. We tested C2 triazole-modified mono- and pseudo-di-mannosides as inhibit
Autor:
Cinzia Colombo, Črtomir Podlipnik, Leonardo Lo Presti, Masahiro Niikura, Andrew J Bennet, Anna Bernardi
Publikováno v:
PLoS ONE, Vol 13, Iss 2, p e0193623 (2018)
The rise of drug-resistant influenza A virus strains motivates the development of new antiviral drugs, with different structural motifs and substitution. Recently, we explored the use of a bicyclic (bicyclo[3.1.0]hexane) analogue of sialic acid that
Externí odkaz:
https://doaj.org/article/ca6d7f24772a440ebe3b6a7ae70400bf