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Giorgio Casari
Giorgio Casari
Vita-Salute San Raffaele University and San Raffaele Scientific Institute
Email verificata su hsr.it
Titolo
Citata da
Citata da
Anno
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
DJ Klionsky, AK Abdel-Aziz, S Abdelfatah, M Abdellatif, A Abdoli, S Abel, ...
autophagy 17 (1), 1-382, 2021
12823*2021
Autoantibodies against type I IFNs in patients with life-threatening COVID-19
P Bastard, LB Rosen, Q Zhang, E Michailidis, HH Hoffmann, Y Zhang, ...
Science 370 (6515), eabd4585, 2020
23652020
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
13081999
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
Heart Attack Risk in Puget Sound. Schwartz Stephen M 20 26 Siscovick David S ...
Nature genetics 41 (3), 334-341, 2009
12832009
Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump α2 subunit associated with familial hemiplegic migraine type 2
MD Fusco, R Marconi, L Silvestri, L Atorino, L Rampoldi, L Morgante, ...
Nature genetics 33 (2), 192-196, 2003
11972003
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
9561998
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
7701997
The nicotinic receptor β2 subunit is mutant in nocturnal frontal lobe epilepsy
MD Fusco, A Becchetti, A Patrignani, G Annesi, A Gambardella, ...
Nature genetics 26 (3), 275-276, 2000
5642000
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
5512005
Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis
EA Stahl, D Wegmann, G Trynka, J Gutierrez-Achury, R Do, BF Voight, ...
Nature genetics 44 (5), 483-489, 2012
4652012
Autoantibodies neutralizing type I IFNs are present in~ 4% of uninfected individuals over 70 years old and account for~ 20% of COVID-19 deaths
P Bastard, A Gervais, T Le Voyer, J Rosain, Q Philippot, J Manry, ...
Science immunology 6 (62), eabl4340, 2021
4182021
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), 1030-1034, 2012
4022012
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
3732004
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
3712004
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
3701994
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
3502003
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
3282002
X-linked recessive TLR7 deficiency in~ 1% of men under 60 years old with life-threatening COVID-19
T Asano, B Boisson, F Onodi, D Matuozzo, M Moncada-Velez, ...
Science immunology 6 (62), eabl4348, 2021
3242021
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
3132003
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 & Differentiation 17 (6), 962-974, 2010
2962010
Il sistema al momento non pu eseguire l'operazione. Riprova pi tardi.
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