Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Vanessa Capone"'
Autor:
Emanuela Clemente, Konstantinos Efthymakis, Erminia Carletti, Vanessa Capone, Samantha Sperduti, Giuseppina Bologna, Marco Marchisio, Marta Di Nicola, Matteo Neri, Michele Sallese
Publikováno v:
PLoS ONE, Vol 14, Iss 12, p e0226478 (2019)
Non-celiac wheat sensitivity (NCWS), also referred to as non-celiac gluten sensitivity, is a recently described disorder triggered by wheat/gluten ingestion. NCWS elicits a wide range of symptoms including diarrhoea, intestinal discomfort, and fatigu
Externí odkaz:
https://doaj.org/article/69b2dac1962a4824b193c54cafe509a6
Autor:
Roberto Chiesa, Laura Pietrangelo, Francesca Ornaghi, Emanuela Clemente, Feliciano Protasi, Samantha Sperduti, Vanessa Capone, Michele Sallese, Antonella Di Campli, Elena Restelli
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1864:3164-3180
Loss-of-function mutations in the SIL1 gene are linked to Marinesco-Sjogren syndrome (MSS), a rare multisystem disease of infancy characterized by cerebellar and skeletal muscle degeneration. SIL1 is a ubiquitous adenine nucleotide exchange factor fo
Autor:
Liliana Comerio, Vanessa Capone, Valentina Grande, Michele Sallese, Francesca Ornaghi, Jeffrey M. Axten, Fabio Fiordaliso, Roberto Chiesa, Nicholas J. Laping, Daniele Tolomeo, Alessandro Corbelli, Antonio Masone, Elena Restelli
Publikováno v:
Human Molecular Genetics. 27:2477-2489
Marinesco-Sjögren syndrome (MSS) is a rare, early onset, autosomal recessive multisystem disorder characterized by cerebellar ataxia, cataracts and myopathy. Most MSS cases are caused by loss-of-function mutations in the gene encoding SIL1, a nucleo
Autor:
Michele Sallese, Marta Di Nicola, Marco Marchisio, Matteo Neri, Giuseppina Bologna, Vanessa Capone, Konstantinos Efthymakis, Samantha Sperduti, Erminia Carletti, Emanuela Clemente
Publikováno v:
PLoS ONE, Vol 14, Iss 12, p e0226478 (2019)
PLoS ONE
PLoS ONE
Non-celiac wheat sensitivity (NCWS), also referred to as non-celiac gluten sensitivity, is a recently described disorder triggered by wheat/gluten ingestion. NCWS elicits a wide range of symptoms including diarrhoea, intestinal discomfort, and fatigu
Autor:
Elena Quaglio, Vanessa Capone, Vladimiro Artuso, Fabio Fiordaliso, Ignazio Roiter, Davide Ortolan, Michele Sallese, Alessandro Corbelli, Galina V. Beznoussenko, Elena Restelli, Manuela Pozzoli, Roberto Chiesa
Publikováno v:
The Journal of Biological Chemistry
Fatal familial insomnia (FFI), genetic Creutzfeldt–Jakob disease (gCJD), and Gerstmann–Sträussler–Scheinker (GSS) syndrome are neurodegenerative disorders linked to prion protein (PrP) mutations. The pathogenic mechanisms are not known, but in
Akademický článek
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Autor:
Clemente, Emanuela1,2 (AUTHOR), Efthymakis, Konstantinos2,3 (AUTHOR), Carletti, Erminia1,2 (AUTHOR), Capone, Vanessa1,2 (AUTHOR), Sperduti, Samantha1,2 (AUTHOR), Bologna, Giuseppina2,3 (AUTHOR), Marchisio, Marco2,3 (AUTHOR), Di Nicola, Marta1 (AUTHOR), Neri, Matteo2,3 (AUTHOR) Michele.sallese@unich.it, Sallese, Michele1,2 (AUTHOR) Michele.sallese@unich.it
Publikováno v:
PLoS ONE. 12/13/2019, Vol. 14 Issue 12, p1-18. 18p.
Autor:
Michele Sallese, Alberto Luini, Capone Vanessa, Monica Giannotta, Antonio Tamburro, Giorgia Fragassi
Publikováno v:
BioMed Research International, Vol 2015 (2015)
BioMed Research International (Online) 2015 (2015): 319454. doi:10.1155/2015/319454
info:cnr-pdr/source/autori:Giannotta, Monica; Fragassi, Giorgia; Tamburro, Antonio; Vanessa, Capone; Luini, Alberto; Sallese, Michele/titolo:Prohibitin: A Novel Molecular Player in KDEL Receptor Signalling./doi:10.1155%2F2015%2F319454/rivista:BioMed Research International (Online)/anno:2015/pagina_da:319454/pagina_a:/intervallo_pagine:319454/volume:2015
BioMed Research International
BioMed Research International (Online) 2015 (2015): 319454. doi:10.1155/2015/319454
info:cnr-pdr/source/autori:Giannotta, Monica; Fragassi, Giorgia; Tamburro, Antonio; Vanessa, Capone; Luini, Alberto; Sallese, Michele/titolo:Prohibitin: A Novel Molecular Player in KDEL Receptor Signalling./doi:10.1155%2F2015%2F319454/rivista:BioMed Research International (Online)/anno:2015/pagina_da:319454/pagina_a:/intervallo_pagine:319454/volume:2015
BioMed Research International
The KDEL receptor (KDELR) is a seven-transmembrane-domain protein involved in retrograde transport of protein chaperones from the Golgi complex to the endoplasmic reticulum. Our recent findings have shown that the Golgi-localised KDELR acts as a func