Résultats de la recherche - Stefania Assereto
- Résultat(s) 1 - 5 résultats de 5
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1
Molecular analysis and characterization of nine novel CTSK mutations in twelve patients affected by pycnodysostosis par Mariarosaria Donnarumma, Stefano Regis, Barbara Tappino, Camillo Rosano, Stefania Assereto, Fabio Corsolini, Maja Di Rocco, Mirella Filocamo
Publié 2007Artigo -
2
Novel Compound Heterozygous Mutations in<i>TBC</i><i>1</i><i>D</i><i>24</i>Cause Familial Malignant Migrating Partial Seizures of Infancy par Mathieu Milh, Antonio Falace, Nathalie Villeneuve, Nicola Vanni, Pierre Cacciagli, Stefania Assereto, Rima Nabbout, Fabio Benfenati, Federico Zara, B. Chabrol, Laurent Villard, Anna Fassio
Publié 2013Artigo -
3
Therapeutic Potential of Proteasome Inhibition in Duchenne and Becker Muscular Dystrophies par Elisabetta Gazzerro, Stefania Assereto, Andrea Bonetto, Federica Sotgia, Sonia Scarfı̀, Angela Pistorio, Gloria Bonuccelli, Michele Cilli, Claudio Bruno, Federico Zara, Michael P. Lisanti, Carlo Minetti
Publié 2010Artigo -
4
Enhancement of Muscle T Regulatory Cells and Improvement of Muscular Dystrophic Process in mdx Mice by Blockade of Extracellular ATP/P2X Axis par Elisabetta Gazzerro, Sımona Baldassari, Stefania Assereto, Floriana Fruscione, Angela Pistorio, Chiara Panicucci, Stefano Volpi, Lisa Perruzza, Chiara Fiorillo, Carlo Minetti, Elisabetta Traggiai, Fabio Grassi, Claudio Bruno
Publié 2015Artigo -
5
The leukodystrophy protein FAM126A (hyccin) regulates PtdIns(4)P synthesis at the plasma membrane par Jeremy M. Baskin, Xudong Wu, Romain Christiano, Michael S. Oh, Curtis Schauder, Elisabetta Gazzerro, Mirko Messa, Sımona Baldassari, Stefania Assereto, Roberta Biancheri, Federico Zara, Carlo Minetti, Andrea Raimondi, Mikael Simons, Tobias C. Walther, Karin M. Reinisch, Pietro De Camilli
Publié 2015Artigo
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Biology
Medicine
Cell biology
Genetics
Internal medicine
Duchenne muscular dystrophy
Dystrophin
Gene
Muscular dystrophy
Mutation
Anatomy
Biochemistry
Blockade
Bortezomib
Cancer research
Cathepsin K
Cell
Central nervous system
Computer science
Disease
Dystroglycan
Endocrinology
Epilepsy
Etiology
Extracellular
In vitro
Intellectual disability
Kinase
Laminin
Leukodystrophy