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Risultati 40291 - 40375 di 67812 (tempo di esecuzione: 0.129 secondi).
Titolo Data di pubblicazione Autori File
Mutamento del giudice dibattimentale e sopravvenuta irripetibilità della prova 1-gen-1994 MARANDOLA, ANTONIA ANTONELLA
Mutamento dell'attività esercitata e deducibilità degli interessi passivi. 1-gen-2006 STEVANATO, DARIO
Mutant p53 as a guardian of the cancer cell 1-gen-2019 Mantovani, FiammaCollavin, LicioDel Sal, Giannino
Mutant p53 as an antigen in cancer immunotherapy 1-gen-2020 Sobhani N.Generali D.Li Y. +
Mutant p53 Gains Its Function via c-Myc Activation upon CDK4 Phosphorylation at Serine 249 and Consequent PIN1 Binding 1-gen-2017 Del Sal, Giannino +
Mutant p53 improves cancer cells’ resistance to endoplasmic reticulum stress by sustaining activation of the UPR regulator ATF6 1-gen-2019 Sicari D.Bellazzo A.Valentino E.Apollonio M.Pontisso I.Di Cristino F.Dal Ferro M.Bicciato S.Del Sal G.Collavin L. +
Mutant p53 induces Golgi tubulo-vesiculation driving a prometastatic secretome 1-gen-2020 Capaci V.Campaner E.Ulloa Severino L.Scaini D.Bossi F.Collavin L.Mantovani F.Del Sal G. +
Mutant p53 potentiates the oncogenic effects of insulin by inhibiting the tumor suppressor DAB2IP 1-gen-2017 VALENTINO, ELENASICARI, DARIADEL SAL, GIANNINOCOLLAVIN, LICIO +
Mutant p53 Reprograms TNF Signaling in Cancer Cells through Interaction with the Tumor Suppressor DAB2IP 1-gen-2014 BELLAZZO, ARIANNARAMI, DAMIANOBULLA, ROBERTADEL SAL, GIANNINOCOLLAVIN, LICIO +
Mutant p53 sustains serine-glycine synthesis and essential amino acids intake promoting breast cancer growth 1-gen-2023 Tombari, CamillaZannini, AlessandroBertolio, RebeccaTriboli, LucaCaputo, ManuelRustighi, AlessandraMantovani, FiammaBaldassarre, GustavoBicciato, SilvioDel Sal, Giannino +
Mutant p53 tunes the NRF2-dependent antioxidant response to support survival of cancer cells 1-gen-2018 Lisek, KamilCampaner, ElenaCiani, YariDel Sal, Giannino +
Mutant prion protein expression causes motor and memory deficits and abnormal sleep patterns in a transgenic mouse model 1-gen-2008 MARCON, Gabriella +
Mutation rates in main tumour driver genes predict prognosis in patients with superficial spreading or nodular primary melanoma: results from the CARAMEL study by the Italian Melanoma Intergroup (IMI) 1-gen-2026 Pizzichetta, Maria AntoniettaCanzonieri, Vincenzo +
Mutational landscape of Zika virus strains worldwide and its structural impact on proteins 1-gen-2019 Crovella S. +
Mutational status of IGHV is the most reliable prognostic marker in trisomy 12 chronic lymphocytic leukemia 1-gen-2017 Zaja, FrancescoPozzato, Gabriele +
Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 3. 1-gen-2001 GASPARINI, PAOLO +
Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families 1-gen-2011 GNAN, CHIARADE ROCCO, DANIELASAVOIA, ANNA +
Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction. 1-gen-2003 SINAGRA, GIANFRANCO +
Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus 1-gen-1999 GASPARINI, PAOLO +
Mutations in L-type amino acid transporter-2 support SLC7A8 as a novel gene involved in age-related hearing loss 1-gen-2018 Girotto, GiorgiaVuckovic, DraganaMezzavilla, MassimoGasparini, Paolo +
Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes 1-gen-2000 SAVOIA, ANNA +
Mutations in PLS1, encoding fimbrin, cause autosomal dominant nonsyndromic hearing loss 1-gen-2019 Mezzavilla M.Faletra F.Gasparini P.Girotto G. +
Mutations in proline 82 of p53 impair its activation by Pin1 and Chk2 in response to DNA damage 1-gen-2005 DEL SAL, GIANNINO +
Mutations in the 3' untranslated region (3' UTR) of NOTCH1 are associated with low CD20 expression levels in chronic lymphocytic leukemia 1-gen-2017 BITTOLO, TAMARABOMBEN, RICCARDOD'AGARO, TIZIANAZUCCHETTO, ANTONELLAMACOR, PAOLOZaja, FrancescoPOZZATO, GABRIELE +
Mutations in the 5′ UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2 1-gen-2011 SAVOIA, ANNAGNAN, CHIARADE ROCCO, DANIELADI STAZIO, MARIATERESA +
Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human Neurodevelopment 1-gen-2019 De Zorzi R.Fortuna S. +
Mutations in the TMPRSS3 gene are a rare cause of childhood nonsyndromic deafness in Caucasian patients. 1-gen-2002 GASPARINI, PAOLO +
Mutations in TTC19 cause mitochondrial complex III deficiency and neurological impairment in humans and flies. 1-gen-2011 D'ADAMO, ADAMO PIO +
Mutations of cytochrome c identified in patients with thrombocytopenia THC4 affect both apoptosis and cellular bioenergetics. 1-gen-2014 DE ROCCO, DANIELANICCHIA, ELENASAVOIA, ANNA +
Mutations of RUNX1 in families with inherited thrombocytopenia 1-gen-2017 DE ROCCO, DANIELABOTTEGA, ROBERTAGNAN, CHIARASAVOIA, ANNA +
Mutations of the Fanconi anemia group A gene (FAA) in Italian patients 1-gen-1997 SAVOIA, ANNA +
Mutations that impair interaction properties of TRIM32 associated with limb-girdle muscular dystrophy 2H 1-gen-2008 MERONI, GERMANA +
Mutual evaluation of global gravity models (EGM2008 and GOCE) and terrestrial data in Amazon Basin, Brazil 1-gen-2013 BRAITENBERG, CARLA +
Mutual friction and vortex Hall angle in a strongly interacting Fermi superfluid 1-gen-2025 Scazza F. +
Mutual influence between eosinophil-peroxidase (EPO) and neutrophils: neutrophils reversibly inhibit EPO enzymatic activity and EPO increases neutrophil adhesiveness. 1-gen-1990 ZABUCCHI, GIULIANOMENEGAZZI, RENZO +
MVK mutations and associated clinical features in Italian patients affected with autoinflammatory disorders and recurrent fever. 1-gen-2005 A. Tommasini +
MVRDV four projects 1-gen-2015 BRADASCHIA, MAURIZIO
MwoI and SmaI RFLPs polymorphisms of porcine obese gene and their association with carcass and meat characteristics of heavy pigs 1-gen-2004 FLORIS, RominaPALLAVICINI, AlbertoGRAZIOSI, GIORGIO +
My brother has severe sepsis. Should he receive selective decontamination of the digestive tract (SDD)? 1-gen-2008 Berlot G.Gullo A. +
Myastenia gravis relapse associated with sarcoidosis 1-gen-2000 MELATO, MAURO +
Myasthenia gravis after allogeneic bone marrow transplantation. A case report and a review of the literature 1-gen-1997 ZAJA, FrancescoFANIN, Renato +
Myasthenia gravis after allogeneic bone marrow transplantation: a case report 1-gen-1995 ZAJA, FrancescoFANIN, Renato +
MYC protein expression scoring and its impact on the prognosis of aggressive B-cell lymphoma patients 1-gen-2019 Zaja, Francesco +
MYC Rearranged Aggressive B-Cell Lymphomas: A Report on 100 Patients of the Fondazione Italiana Linfomi (FIL) 1-gen-2019 Romano, AlessandraGreco, AntonioZaja, Francesco +
Mycobacterial phagosomes associate less annexins I, VI, VII and XI, but not II, concomitantly with a diminished phagolysosomal fusion 1-gen-2003 GIULIANINI, PIERO GIULIO +
Mycobacterium chimaera infections: An update 1-gen-2020 Luzzati, RobertoDi Bella, Stefano +
Mycobacterium fortuitum infection in silver arowana (Osteoglossum bicirrhosum) 1-gen-2019 P. Pastorino +
Mycobacterium tuberculosis isolates belonging to katG gyrA group 2 are associated with clustered cases of tuberculosis in Italian patients 1-gen-2004 DOLZANI, LUCILLABANFI, ELENALAGATOLLA, CRISTINATONIN, ENRICO ANGELO +
Mycochemicals in wild and cultivated mushrooms: nutrition and health 1-gen-2021 Francesca CateniGiuseppe Procida +
Mycophenolate Mofetil for Immune Thrombocytopenia. Reply 1-gen-2021 Francesco Zaja +
Mycosis fungoides is not associated with HCV virus infection 1-gen-2004 BONIN, SerenaTREVISAN, GIUSTOSTANTA, GIORGIO +
Mycosis fungoides: is it a Borrelia burgdorferi-associated disease? 1-gen-2006 BONIN, SerenaTREVISAN, GIUSTOSTANTA, GIORGIO +
Myelography iodinated contrast media. 2. Conformational versatility of iopamidol in the solid state 1-gen-2017 BELLICH, BARBARATAVAGNACCO, LETIZIAGIANNINI, GIOVANNADE ZORZI, RITAGEREMIA, SILVANOCESARO, ATTILIO +
Myelography iodinated contrast media. I. unraveling the atropisomerism properties in solution 1-gen-2015 FONTANIVE, LUCACESARO, ATTILIOGAMINI, AMELIATAVAGNACCO, LETIZIA +
Myeloid and T-Cell Microenvironment Immune Features Identify Two Prognostic Sub-Groups in High-Grade Gastroenteropancreatic Neuroendocrine Neoplasms 1-gen-2021 Mangogna, Alessandro +
Myeloperoxidase exerts microbicidal activity against Mycobacterium tuberculosis 1-gen-1999 BORELLI, VIOLETTABANFI, ELENAZABUCCHI, GIULIANO +
MYELOstudy: lymph node stage of aggressiveness in medullary thyroid cancer-a retrospective multi-center study analysis 1-gen-2026 Dobrinja, ChiaraMastronardi, Manuela +
MYH9 -Related Thrombocytopenia: Four Novel Variants Affecting the Tail Domain of the Non-Muscle Myosin Heavy Chain IIA Associated with a Mild Clinical Evolution of the Disorder 1-gen-2019 de Rocco, DanielaGiangregorio, TaniaSavoia, Anna +
MYH9 gene mutations associated with bleeding 1-gen-2017 SAVOIA, ANNADE ROCCO, DANIELA +
MYH9 related disease: a novel missense Ala95Asp mutation of the MYH9 gene. 1-gen-2009 DE ROCCO, DANIELAGIROTTO, GIORGIASAVOIA, ANNA +
MYH9 related disease: four novel mutations of the tail domain of myosin-9 correlating with a mild clinical phenotype 1-gen-2010 DE ROCCO, DANIELAGIROTTO, GIORGIASAVOIA, ANNA +
MYH9-related disease - Report on 5 German families and description of a novel mutation. Ann Hematol 89:1057-1059, 2010 1-gen-2010 SAVOIA, ANNADE ROCCO, DANIELA +
MYH9-Related Disease: A Novel Prognostic Model to Predict the Clinical Evolution of the Disease Based on Genotype-Phenotype Correlations. 1-gen-2014 DE ROCCO, DANIELANICCHIA, ELENASAVOIA, ANNA +
MYH9-related disease: five novel mutations expanding the spectrum of causative mutations and confirming genotype/phenotype correlations 1-gen-2013 DE ROCCO, DANIELABOTTEGA, ROBERTASAVOIA, ANNA +
MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness 1-gen-2003 SAVOIA, ANNA +
MYH9-related Disorders: Report on a Patient of Greek Origin Presenting With Macroscopic Hematuria and Presenile Cataract, Caused by an R1165C Mutation 1-gen-2012 SAVOIA, ANNA +
MYH9: Structure, functions and role of non-muscle myosin IIA in human disease 1-gen-2018 Savoia, Anna +
Mylène Bédard, Virginie Fournier, Arianne Gibeau et Adrien Rannaud (dir.), “Contemporanéités d’Angéline de Montbrun et de Laure Conan”, Voix et Images, vol. 44, n. 1 (130), automne 2018 1-gen-2020 Amandine Bonesso
MYO5B Gene Mutations: A Not Negligible Cause of Intrahepatic Cholestasis of Infancy with Normal Gamma-glutamyl Transferase Phenotype 1-gen-2022 Matarazzo, LorenzaBianco, Anna MonicaAthanasakis, EmmanouilMaggiore, GiuseppeD'Adamo, Adamo Pio +
MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss. 1-gen-2001 GASPARINI, PAOLO +
Myoblast adhesion, proliferation and differentiation on human elastin-like polypeptide (HELP) hydrogels 1-gen-2017 D'ANDREA, PAOLACOK, MICHELAULLOA SEVERINO, LUISAVITA, FRANCESCASCAINI, DENISCASALIS, LOREDANALORENZON, PaolaDONATI, IVANBANDIERA, Antonella +
Myocardial disease caused by adriamycin. Experimental animal models and possible pharmacologic prevention. 1-gen-1982 DECORTI, GIULIANA +
Myocardial effects of fetal endoscopic tracheal occlusion in lambs with CDH 1-gen-2016 BUSSANI, ROSSANAZANDONÀ, LORENZOSILVESTRI, FURIO +
Myocardial iron overload by cardiovascular magnetic resonance native segmental T1 mapping: a sensitive approach that correlates with cardiac complications 1-gen-2021 De Luca A.Sinagra G. +
Myocardial ischaemia in Vaquez's disease. 1-gen-1984 MELATO, MAURO +
Myocardial oxygen supply and demand imbalance predicts mortality in older nursing home residents: The PARTAGE study 1-gen-2024 Salvi, PaoloGrillo, AndreaBaldi, CorradoRovina, MatteoSimon, GiuliaFabris, BrunoCarretta, Renzo +
Myocardial perfusion in cardiac amyloidosis 1-gen-2024 Porcari, Aldostefano +
Myocardial Perfusion with Multislice Computed Tomography in Stable Angina Pectoris 1-gen-2014 ROSSI, ALEXIA +
Myocardial Recovery in Recent Onset Dilated Cardiomyopathy: Role of CDCP1 and Cardiac Fibrosis 1-gen-2023 Mestroni, LuisaMerlo, MarcoSinagra, Gianfranco +
MYOCARDIAL REGENERATION BY ACTIVATION OF MULTIPOTENT CARDIAC STEM CELLS IN ISCHEMIC HEART FAILURE. 1-gen-2005 SILVESTRI, FURIOBUSSANI, ROSSANA +
Myocardial Stretch in Early Systole is a Key Determinant of the Synchrony of Left Ventricular Mechanical Activity in vivo 1-gen-2013 PEDRIZZETTI, Gianni +
Myocarditis and pericarditis during COVID-19 pandemic: a study of the Italian Society of Cardiology 1-gen-2025 Fabris, EnricoMerlo, MarcoD'Agata Mottolese, BiancamariaPerrone Filardi, PasqualeSinagra, Gianfranco +
Myocarditis and Pericarditis in Focus: A Brief Report Comparing the 2025 ESC Guidelines and Latest ACC Position Papers 1-gen-2026 Collini, ValentinoSinagra, Gianfranco +
Myocarditis and pericarditis in focus: A critical appraisal of the 2025 ESC vs ACC position statements from the Italian society of cardiology working group on cardiomyopathies and pericardial diseases 1-gen-2026 Collini, ValentinoMerlo, MarcoPerrone-Filardi, PasqualeSinagra, Gianfranco +
Myocarditis evolving in cardiomyopathy: When genetics and offending causes work together 1-gen-2019 Artico J.Gentile P.Merlo M.Sinagra G. +
Risultati 40291 - 40375 di 67812 (tempo di esecuzione: 0.129 secondi).
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