Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Cercopithecus aethiop"'
Autor:
Cristian Rosso, Stefania Varani, Marco Lombardo, Arianna Quintavalla, Claudio Trombini, Margherita Ortalli
The treatment of human leishmaniasis is currently based on few compounds that are highly toxic, expensive and have a high rate of treatment failure. A number of recent studies on new drugs focuses on natural or semi-synthetic compounds. Among them, t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7361b626b59b6615604882263551f8e
http://hdl.handle.net/11585/691213
http://hdl.handle.net/11585/691213
Autor:
Michela Ciano, Maria Gabriella Caporaso, Maria Camilla Ciardulli, Daniela Sarnataro, Stefano Bonatti, Simona Allocca, Andrea Scaloni, Massimo D'Agostino, Chiara D'Ambrosio
Publikováno v:
International Journal of Molecular Sciences
Volume 19
Issue 7
International journal of molecular sciences (Online) 19 (2018). doi:10.3390/ijms19071892
info:cnr-pdr/source/autori:Allocca S, Ciano M, Ciardulli MC, D'Ambrosio C, Scaloni A, Sarnataro D, Caporaso MG, D'Agostino M, Bonatti S./titolo:An ?B-Crystallin Peptide Rescues Compartmentalization and Trafficking Response to Cu Overload of ATP7B-H1069Q, the Most Frequent Cause of Wilson Disease in the Caucasian Population./doi:10.3390%2Fijms19071892/rivista:International journal of molecular sciences (Online)/anno:2018/pagina_da:/pagina_a:/intervallo_pagine:/volume:19
International Journal of Molecular Sciences, Vol 19, Iss 7, p 1892 (2018)
Volume 19
Issue 7
International journal of molecular sciences (Online) 19 (2018). doi:10.3390/ijms19071892
info:cnr-pdr/source/autori:Allocca S, Ciano M, Ciardulli MC, D'Ambrosio C, Scaloni A, Sarnataro D, Caporaso MG, D'Agostino M, Bonatti S./titolo:An ?B-Crystallin Peptide Rescues Compartmentalization and Trafficking Response to Cu Overload of ATP7B-H1069Q, the Most Frequent Cause of Wilson Disease in the Caucasian Population./doi:10.3390%2Fijms19071892/rivista:International journal of molecular sciences (Online)/anno:2018/pagina_da:/pagina_a:/intervallo_pagine:/volume:19
International Journal of Molecular Sciences, Vol 19, Iss 7, p 1892 (2018)
The H1069Q substitution is the most frequent mutation of the Cu transporter ATP7B that causes Wilson disease in the Caucasian population. ATP7B localizes to the Golgi complex in hepatocytes, but, in the presence of excessive Cu, it relocates to the e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bc39f588c5ffb6a4bc6bfbfec50c53e
Autor:
Thierry Nieus, Fabio Benfenati, Annyesha Satapathy, Enrico Ferrea, Joachim Scholz-Starke, Fabrizia Cesca
Publikováno v:
Journal of biological chemistry (Online) 290 (2015): 18045–18055. doi:10.1074/jbc.M115.654699
info:cnr-pdr/source/autori:Cesca, Fabrizia; Satapathy, Annyesha; Ferrea, Enrico; Nieus, Thierry; Benfenati, Fabio; Scholz-Starke, Joachim/titolo:Functional Interaction between the Scaffold Protein Kidins220%2FARMS and Neuronal Voltage-Gated Na+ Channels./doi:10.1074%2Fjbc.M115.654699/rivista:Journal of biological chemistry (Online)/anno:2015/pagina_da:18045/pagina_a:18055/intervallo_pagine:18045–18055/volume:290
info:cnr-pdr/source/autori:Cesca, Fabrizia; Satapathy, Annyesha; Ferrea, Enrico; Nieus, Thierry; Benfenati, Fabio; Scholz-Starke, Joachim/titolo:Functional Interaction between the Scaffold Protein Kidins220%2FARMS and Neuronal Voltage-Gated Na+ Channels./doi:10.1074%2Fjbc.M115.654699/rivista:Journal of biological chemistry (Online)/anno:2015/pagina_da:18045/pagina_a:18055/intervallo_pagine:18045–18055/volume:290
Kidins220 (kinase D-interacting substrate of 220 kDa)/ankyrin repeat-rich membrane spanning (ARMS) acts as a signaling platform at the plasma membrane and is implicated in a multitude of neuronal functions, including the control of neuronal activity.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a9b85c5e2a61b9fffd583501b9867f9
https://doi.org/10.1074/jbc.m115.654699
https://doi.org/10.1074/jbc.m115.654699
Autor:
Carlotta Ronchi, Tomáš Starý, Carmen Valenzuela, Isabelle Baró, Alicia de la Cruz, Marcella Rocchetti, Sanjay Kharche, Antonio Zaza, Gildas Loussouarn, Stefano Severi, Cristina Moreno, Miriam Guizy, Antonio Felipe, Anna Oliveras, Núria Comes
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Cardiovascular Research, 105(2), 223-232. Oxford University Press
Cardiovascular Research
Cardiovascular Research, Oxford University Press (OUP), 2015, Equipe 1, 105 (2), pp.223--232. ⟨10.1093/cvr/cvu250⟩
instname
Cardiovascular Research, 105(2), 223-232. Oxford University Press
Cardiovascular Research
Cardiovascular Research, Oxford University Press (OUP), 2015, Equipe 1, 105 (2), pp.223--232. ⟨10.1093/cvr/cvu250⟩
et al.
[Aims]: Polyunsaturated fatty n-3 acids (PUFAs) have been reported to exhibit antiarrhythmic properties. However, the mechanisms of action remain unclear. We studied the electrophysiological effects of eicosapentaenoic acid (EPA) and doco
[Aims]: Polyunsaturated fatty n-3 acids (PUFAs) have been reported to exhibit antiarrhythmic properties. However, the mechanisms of action remain unclear. We studied the electrophysiological effects of eicosapentaenoic acid (EPA) and doco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b722d24a7ae2f472f8dd967c7b0fd1e6
https://cris.maastrichtuniversity.nl/en/publications/41619feb-4e04-4108-9284-e6e8dfc963a1
https://cris.maastrichtuniversity.nl/en/publications/41619feb-4e04-4108-9284-e6e8dfc963a1
Autor:
Sara Francesca Colombo, Serena F Generoso, Gianluca Martire, Stefano Bonatti, Elena V. Polishchuk, Massimo D'Agostino, Arianna Crespi
Publikováno v:
The Journal of Membrane Biology. 247:1149-1159
The newly synthesized mutant L501fsX533 Frizzled-4 form and the alpha3beta4 nicotinic acetylcholine receptor expressed in the absence of nicotine accumulate in the endoplasmic reticulum of COS-7 cells and induce the formation of large areas of smooth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8e4b0c4ab24077b4a9d38cfdc8a44e0
https://doi.org/10.1007/s00232-014-9710-8
https://doi.org/10.1007/s00232-014-9710-8
Autor:
Emanuele Giurisato, Cristina Ulivieri, Alessandra Gamberucci, Davide Randazzo, Emiliana Giacomello, S Marruganti, Elisa Rossi, Vincenzo Sorrentino
Publikováno v:
Molecular Biology of the Cell
KSR2 is required for store-operated calcium entry (SOCE). KSR2 deficiency affects STIM1/ORAI1 puncta formation and cytoskeleton organization. In addition, KSR2-associated calcineurin is crucial for SOCE. These findings identify the KSR2-calcineurin c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77ff7916909169a15c80c74c9a96effa
https://doi.org/10.1091/mbc.e13-05-0292
https://doi.org/10.1091/mbc.e13-05-0292
Autor:
Alessandra Bisi, Federica Belluti, Angela Rampa, Francesca Bressan, Giovanna Angela Gentilomi, Silvia Gobbi, Francesca Bonvicini
Publikováno v:
Molecules
Volume 24
Issue 2
Molecules, Vol 24, Iss 2, p 372 (2019)
Volume 24
Issue 2
Molecules, Vol 24, Iss 2, p 372 (2019)
The occurrence of invasive fungal infections represents a substantial threat to human health that is particularly serious in immunocompromised patients. The limited number of antifungal agents, devoid of unwanted toxic effects, has resulted in an inc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2140cade5b093161a15d6844094f6626
https://doi.org/10.3390/molecules24020372
https://doi.org/10.3390/molecules24020372
Autor:
Pia Rossi, Bruno Sterlini, Enrico Castroflorio, Antonella Marte, Franco Onofri, Flavia Valtorta, Luca Maragliano, Anna Corradi, Fabio Benfenati
Publikováno v:
The Journal of Biological Chemistry
Proline-rich transmembrane protein 2 (PRRT2) has been identified as the single causative gene for a group of paroxysmal syndromes of infancy, including epilepsy, paroxysmal movement disorders, and migraine. On the basis of topology predictions, PRRT2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb99c32254f60eccd9f574dc04fd6ab7
Autor:
Vasco Cachatra, Susana Santos, Angelo Fontana, Adele Cutignano, Helena Vieira, Laura Grauso, Marta Isabel Heitor Cerejo, Helena Gaspar, Nuno R. Neng, Joana R. Xavier
Publikováno v:
Marine Drugs, Vol 14, Iss 10, p 179 (2016)
Marine Drugs; Volume 14; Issue 10; Pages: 179
Marine Drugs
Marine drugs 14 (2016): 1–14. doi:10.3390/md14100179
info:cnr-pdr/source/autori:Helena Gaspar, Adele Cutignano, Laura Grauso, Nuno Neng, Vasco Cachatra, Angelo Fontana, Joana Xavier, Marta Cerejo, Helena Vieira and Susana Santos/titolo:Erylusamides: Novel Atypical Glycolipids from Erylus cf. deficiens/doi:10.3390%2Fmd14100179/rivista:Marine drugs/anno:2016/pagina_da:1/pagina_a:14/intervallo_pagine:1–14/volume:14
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Marine Drugs; Volume 14; Issue 10; Pages: 179
Marine Drugs
Marine drugs 14 (2016): 1–14. doi:10.3390/md14100179
info:cnr-pdr/source/autori:Helena Gaspar, Adele Cutignano, Laura Grauso, Nuno Neng, Vasco Cachatra, Angelo Fontana, Joana Xavier, Marta Cerejo, Helena Vieira and Susana Santos/titolo:Erylusamides: Novel Atypical Glycolipids from Erylus cf. deficiens/doi:10.3390%2Fmd14100179/rivista:Marine drugs/anno:2016/pagina_da:1/pagina_a:14/intervallo_pagine:1–14/volume:14
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Among marine organisms, sponges are the richest sources of pharmacologically-active compounds. Stemming from a previous lead discovery program that gathered a comprehensive library of organic extracts of marine sponges from the off-shore region of Po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11b12fe89bab8b03f76f41bfaa78ada6
http://hdl.handle.net/11588/705209
http://hdl.handle.net/11588/705209
Autor:
Michael P. Murphy, Charles Joseph O'Kane, Phoebe Heard, Angeleen Fleming, Claudia Rose, David C. Rubinsztein, Sovan Sarkar, Gauri Krishna, Marie Quick, Moisés García-Arencibia, Benjamin R. Underwood, Viktor I. Korolchuk, Maurizio Renna, Sara Imarisio
Publikováno v:
Human Molecular Genetics
Many neurodegenerative diseases exhibit protein accumulation and increased oxidative stress. Therapeutic strategies include clearing aggregate-prone proteins by enhancing autophagy or decreasing oxidative stress with antioxidants. Many autophagy-indu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0840f5420c83edef34f71184b374039
https://doi.org/10.1093/hmg/ddq253
https://doi.org/10.1093/hmg/ddq253