Giorgio Casari
Giorgio Casari
Vita-Salute San Raffaele University and San Raffaele Scientific Institute
Verified email at hsr.it
TitleCited byYear
Guidelines for the use and interpretation of assays for monitoring autophagy
DJ Klionsky, FC Abdalla, H Abeliovich, RT Abraham, A Acevedo-Arozena, ...
Autophagy 8 (4), 445-544, 2012
7494*2012
Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption
DB Simon, Y Lu, KA Choate, H Velazquez, E Al-Sabban, M Praga, ...
Science 285 (5424), 103-106, 1999
10771999
Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump α2 subunit associated with familial hemiplegic migraine type 2
M De Fusco, R Marconi, L Silvestri, L Atorino, L Rampoldi, L Morgante, ...
Nature genetics 33 (2), 192, 2003
9652003
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
S Kathiresan, BF Voight, S Purcell, K Musunuru, D Ardissino, ...
Nature genetics 41 (3), 334-341, 2009
8822009
Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease
G Casari, M De Fusco, S Ciarmatori, M Zeviani, M Mora, P Fernandez, ...
Cell 93 (6), 973-983, 1998
8021998
Polymorphisms of α-adducin and salt sensitivity in patients with essential hypertension
D Cusi, C Barlassina, T Azzani, G Casari, L Citterio, M Devoto, N Glorioso, ...
The Lancet 349 (9062), 1353-1357, 1997
6701997
The nicotinic receptor β2 subunit is mutant in nocturnal frontal lobe epilepsy
M De Fusco, A Becchetti, A Patrignani, G Annesi, A Gambardella, ...
Nature genetics 26 (3), 275, 2000
4722000
Mitochondrial import and enzymatic activity of PINK1 mutants associated to recessive parkinsonism
L Silvestri, V Caputo, E Bellacchio, L Atorino, B Dallapiccola, EM Valente, ...
Human molecular genetics 14 (22), 3477-3492, 2005
4632005
Two point mutations within the adducin genes are involved in blood pressure variation
G Bianchi, G Tripodi, G Casari, S Salardi, BR Barber, R Garcia, P Leoni, ...
Proceedings of the National Academy of Sciences 91 (9), 3999-4003, 1994
3411994
In search of antisense
G Lavorgna, D Dahary, B Lehner, R Sorek, CM Sanderson, G Casari
Trends in biochemical sciences 29 (2), 88-94, 2004
3322004
Axonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transport
F Ferreirinha, A Quattrini, M Pirozzi, V Valsecchi, G Dina, V Broccoli, ...
The Journal of clinical investigation 113 (2), 231-242, 2004
2982004
Autosomal dominant restless legs syndrome maps on chromosome 14q
MT Bonati, L Ferini‐Strambi, P Aridon, A Oldani, M Zucconi, G Casari
Brain 126 (6), 1485-1492, 2003
2972003
Mutations of mitochondrial DNA polymerase γA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia
E Lamantea, V Tiranti, A Bordoni, A Toscano, F Bono, S Servidei, ...
Annals of neurology 52 (2), 211-219, 2002
2672002
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood
EL Heinzen, KJ Swoboda, Y Hitomi, F Gurrieri, S Nicole, B de Vries, ...
Nature genetics 44 (9), 1030, 2012
2482012
Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia
L Atorino, L Silvestri, M Koppen, L Cassina, A Ballabio, R Marconi, ...
The Journal of cell biology 163 (4), 777-787, 2003
2312003
The Parkinson-associated protein PINK1 interacts with Beclin1 and promotes autophagy
S Michiorri, V Gelmetti, E Giarda, F Lombardi, F Romano, R Marongiu, ...
Cell death and differentiation 17 (6), 962, 2010
2282010
Increased sensitivity of the neuronal nicotinic receptor α2 subunit causes familial epilepsy with nocturnal wandering and ictal fear
P Aridon, C Marini, C Di Resta, E Brilli, M De Fusco, F Politi, E Parrini, ...
The American Journal of Human Genetics 79 (2), 342-350, 2006
2262006
Association of the α-adducin locus with essential hypertension
G Casari, C Barlassina, D Cusi, L Zagato, R Muirhead, M Righetti, ...
Hypertension 25 (3), 320-326, 1995
2221995
Human tenascin: primary structure, pre-mRNA splicing patterns and localization of the epitopes recognized by two monoclonal antibodies
A Siri, B Carnemolla, M Saginati, A Leprini, G Casari, F Baralle, L Zardi
Nucleic acids research 19 (3), 525-531, 1991
2091991
Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics
L Rampoldi, G Caridi, D Santon, F Boaretto, I Bernascone, G Lamorte, ...
Human molecular genetics 12 (24), 3369-3384, 2003
2042003
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