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Policlinico S.Orsola-Malpighi Bologna
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Cited by
Year
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy
B Pandit, A Sarkozy, LA Pennacchio, C Carta, K Oishi, S Martinelli, ...
Nature genetics 39 (8), 1007-1012, 2007
7722007
Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair
V Cordeddu, E Di Schiavi, LA Pennacchio, A Ma'ayan, A Sarkozy, ...
Nature genetics 41 (9), 1022-1026, 2009
4532009
Molecular and Biological Characterization of Deformed Wing Virus of Honeybees (Apis mellifera L.)
G Lanzi, JR De Miranda, MB Boniotti, CE Cameron, A Lavazza, L Capucci, ...
Journal of virology 80 (10), 4998-5009, 2006
4072006
A restricted spectrum of NRAS mutations causes Noonan syndrome
IC Cirstea, K Kutsche, R Dvorsky, L Gremer, C Carta, D Horn, AE Roberts, ...
Nature genetics 42 (1), 27-29, 2010
3532010
Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: Molecular diversity and associated phenotypic spectrum
A Sarkozy, C Carta, S Moretti, G Zampino, MC Digilio, F Pantaleoni, ...
Human mutation 30 (4), 695-702, 2009
3452009
Heterozygous germline mutations in the CBL tumor-suppressor gene cause a Noonan syndrome-like phenotype
S Martinelli, A De Luca, E Stellacci, C Rossi, S Checquolo, F Lepri, ...
The American Journal of Human Genetics 87 (2), 250-257, 2010
2762010
Detection and preliminary characterization of a new rabbit calicivirus related to rabbit hemorrhagic disease virus but nonpathogenic
L Capucci, P Fusi, A Lavazza, ML Pacciarini, C Rossi
Journal of Virology 70 (12), 8614-8623, 1996
2721996
Use of the diabetes risk score for opportunistic screening of undiagnosed diabetes and impaired glucose tolerance: the IGLOO (Impaired Glucose Tolerance and Long-Term Outcomes …
M Franciosi, G De Berardis, MCE Rossi, M Sacco, M Belfiglio, F Pellegrini, ...
Diabetes care 28 (5), 1187-1194, 2005
2472005
Transmission of HIV drug resistance and the predicted effect on current first-line regimens in Europe
LM Hofstra, N Sauvageot, J Albert, I Alexiev, F Garcia, D Struck, ...
Clinical infectious diseases 62 (5), 655-663, 2016
1892016
Functional dysregulation of CDC42 causes diverse developmental phenotypes
S Martinelli, OHF Krumbach, F Pantaleoni, S Coppola, E Amin, ...
The American Journal of Human Genetics 102 (2), 309-320, 2018
1582018
Activating mutations in RRAS underlie a phenotype within the RASopathy spectrum and contribute to leukaemogenesis
E Flex, M Jaiswal, F Pantaleoni, S Martinelli, M Strullu, EK Fansa, A Caye, ...
Human molecular genetics 23 (16), 4315-4327, 2014
1582014
SOS1 mutations in Noonan syndrome: molecular spectrum, structural insights on pathogenic effects, and genotype–phenotype correlations
F Lepri, A De Luca, L Stella, C Rossi, G Baldassarre, F Pantaleoni, ...
Human mutation 32 (7), 760-772, 2011
1382011
Antigenicity of the rabbit hemorrhagic disease virus studied by its reactivity with monoclonal antibodies
L Capucci, G Frigoli, L Rønshold, A Lavazza, E Brocchi, C Rossi
Virus Research 37 (3), 221-238, 1995
1181995
Identification and characterization of a 3C-like protease from rabbit hemorrhagic disease virus, a calicivirus
B Boniotti, C Wirblich, M Sibilia, G Meyers, HJ Thiel, C Rossi
Journal of virology 68 (10), 6487-6495, 1994
1151994
Mutations of the Igβ gene cause agammaglobulinemia in man
S Ferrari, V Lougaris, S Caraffi, R Zuntini, J Yang, A Soresina, A Meini, ...
The Journal of experimental medicine 204 (9), 2047-2051, 2007
1072007
Markedly different ATP requirements for rRNA synthesis and mtDNA light strand transcription versus mRNA synthesis in isolated human mitochondria.
G Gaines, C Rossi, G Attardi
Journal of Biological Chemistry 262 (4), 1907-1915, 1987
951987
3C-like protease of rabbit hemorrhagic disease virus: identification of cleavage sites in the ORF1 polyprotein and analysis of cleavage specificity
C Wirblich, M Sibilia, MB Boniotti, C Rossi, HJ Thiel, G Meyers
Journal of Virology 69 (11), 7159-7168, 1995
921995
Activating mutations affecting the Dbl homology domain of SOS2 cause Noonan syndrome
V Cordeddu, JC Yin, C Gunnarsson, C Virtanen, S Drunat, F Lepri, ...
Human mutation 36 (11), 1080-1087, 2015
892015
Detection and identification of Leptospira interrogans serovars by PCR coupled with restriction endonuclease analysis of amplified DNA
ML Savio, C Rossi, P Fusi, S Tagliabue, ML Pacciarini
Journal of Clinical Microbiology 32 (4), 935-941, 1994
731994
Enhanced MAPK1 function causes a neurodevelopmental disorder within the RASopathy clinical spectrum
M Motta, L Pannone, F Pantaleoni, G Bocchinfuso, FC Radio, S Cecchetti, ...
The American Journal of Human Genetics 107 (3), 499-513, 2020
722020
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