Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Giorgia Busolin"'
Autor:
Daniela Zizioli, Natascia Tiso, Adele Guglielmi, Claudia Saraceno, Giorgia Busolin, Roberta Giuliani, Deepak Khatri, Eugenio Monti, Giuseppe Borsani, Francesco Argenton, Dario Finazzi
Publikováno v:
Neurobiology of Disease, Vol 85, Iss , Pp 35-48 (2016)
ABSTRACT: Pantothenate Kinase Associated Neurodegeneration (PKAN) is an autosomal recessive disorder with mutations in the pantothenate kinase 2 gene (PANK2), encoding an essential enzyme for Coenzyme A (CoA) biosynthesis. The molecular connection be
Externí odkaz:
https://doaj.org/article/fbb3bc3650774261af792211cf7b098c
Autor:
Lavanya Adusumilli, Nicola Facchinello, Cathleen Teh, Giorgia Busolin, Minh TN Le, Henry Yang, Giorgia Beffagna, Stefano Campanaro, Wai Leong Tam, Francesco Argenton, Bing Lim, Vladimir Korzh, Natascia Tiso
Publikováno v:
Cells, Vol 9, Iss 3, p 711 (2020)
During the development of the central nervous system, the proliferation of neural progenitors and differentiation of neurons and glia are tightly regulated by different transcription factors and signaling cascades, such as the Wnt and Shh pathways. T
Externí odkaz:
https://doaj.org/article/ab56c64bcad743c1bd56ad6e5c4d4762
Autor:
Mariana Delfino-Machín, Romain Madelaine, Giorgia Busolin, Masataka Nikaido, Sarah Colanesi, Karen Camargo-Sosa, Edward W P Law, Stefano Toppo, Patrick Blader, Natascia Tiso, Robert N Kelsh
Publikováno v:
PLoS ONE, Vol 12, Iss 3, p e0172947 (2017)
The development of functional peripheral ganglia requires a balance of specification of both neuronal and glial components. In the developing dorsal root ganglia (DRGs), these components form from partially-restricted bipotent neuroglial precursors d
Externí odkaz:
https://doaj.org/article/9b15253e64a3408f9f3daf3a9fa5bc6a
Autor:
Emanuela Leonardi, Simonetta Andreazza, Stefano Vanin, Giorgia Busolin, Carlo Nobile, Silvio C E Tosatto
Publikováno v:
PLoS ONE, Vol 6, Iss 3, p e18142 (2011)
Mutations of human leucine-rich glioma inactivated (LGI1) gene encoding the epitempin protein cause autosomal dominant temporal lateral epilepsy (ADTLE), a rare familial partial epileptic syndrome. The LGI1 gene seems to have a role on the transmissi
Externí odkaz:
https://doaj.org/article/c8b9b3cd58cc4a8ba3dd125b1188fd6f
Autor:
Francesco Argenton, Vladimir Korzh, Bing Lim, Cathleen Teh, Henry Yang, Minh T.N. Le, Wai Leong Tam, Giorgia Beffagna, Giorgia Busolin, Natascia Tiso, Lavanya Adusumilli, Nicola Facchinello, Stefano Campanaro
Publikováno v:
Cells
Volume 9
Issue 3
Cells, Vol 9, Iss 3, p 711 (2020)
Volume 9
Issue 3
Cells, Vol 9, Iss 3, p 711 (2020)
During the development of the central nervous system, the proliferation of neural progenitors and differentiation of neurons and glia are tightly regulated by different transcription factors and signaling cascades, such as the Wnt and Shh pathways. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5854377fd1a8e00af9fd1b12403f86d9
http://hdl.handle.net/11577/3331583
http://hdl.handle.net/11577/3331583
Autor:
Fabrizio A. de Falco, Carlo Nobile, Simona Binelli, Laura Rigon, Lia Santulli, Carlo Di Bonaventura, Gabriella Egeo, Antonio Gambardella, Andrea Vettori, Patrizia Pulitano, Valeria Vianello Dri, Giorgia Busolin, Paola Banfi, Oriano Mecarelli, Clementina Boniver, Anna Teresa Giallonardo, Angela La Neve, Salvatore Striano, Pasquale Striano, Elena Pasini, Roberto Michelucci
Publikováno v:
Epilepsy Research and Treatment
Autosomal dominant lateral temporal epilepsy (ADTLE) is an inherited epileptic syndrome characterized by ictal auditory symptoms or aphasia, negative MRI findings, and relatively benign evolution. Mutations responsible for ADLTE have been found in th
Autor:
Libero Vitello, Carlo Di Bonaventura, Gessica Smaniotto, Giangennaro Coppola, Francesca Felicia Operto, Carlo Nobile, Sandra Furlan, Giorgia Busolin, Erica Diani, Roberto Michelucci, Alfredo D'Aniello, Gabriella Egeo, Anna Teresa Giallonardo
Publikováno v:
Epilepsia. 52:1258-1264
Summary Purpose: To describe the clinical and genetic findings of four families with autosomal dominant lateral temporal epilepsy. Methods: A personal and family history was obtained from each affected and unaffected subject along with a physical and
Autor:
Roy Hofi, Natascia Tiso, Giorgia Busolin, Lihee Asaf, Nathan D. Lawson, Julian Nicenboim, Gabriella Almog, Gideon Hen, Masahiro Shin, Karina Yaniv, Oded Mayseless
Publikováno v:
Development.
Formation and remodeling of vascular beds are complex processes orchestrated by multiple signaling pathways. While it is well accepted that vessels of a particular organ display specific features that enable them to fulfill distinct functions, the em
Publikováno v:
Neurological Sciences. 34:761-763
Essential tremor (ET) is a common progressive movement disorder characterized by a clear genetic predisposition. In the last years, many efforts have been done to map susceptibility loci for ET. Here, we report a clinical and genetic study of a famil
Autor:
Matteo Astone, Francesco Argenton, Patrizia Porazzi, Natascia Tiso, Martina Milanetto, Enrico Moro, Andrea Vettori, Federica Marelli, Nicola Facchinello, Marina Campione, Giorgia Busolin, Marco Schiavone, Olivier Ek, A. Casari, Luca Persani
Publikováno v:
Endocrine Abstracts.