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Mostrati risultati da 191.867 a 191.886 di 304.334
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
A novel multi-view image coding scheme based on view-warping and 3D-DCT 2010 ZAMARIN, MARCOMILANI, SIMONEZANUTTIGH, PIETROCORTELAZZO, GUIDO MARIA JOURNAL OF VISUAL COMMUNICATION AND IMAGE REPRESENTATION - -
Novel multicharged silver(I)–NHC complexes derived from zwitterionic 1,3-symmetrically and 1,3-unsymmetrically substituted imidazoles and benzimidazoles: Synthesis and cytotoxic properties 2016 MARZANO, CRISTINATISATO, FRANCESCOPORCHIA, MARINAGANDIN, VALENTINA + JOURNAL OF ORGANOMETALLIC CHEMISTRY - -
Novel Multifunctional Magnetic Inorganic Composites: Synthesis and Characterization 2019 Paolo SgarbossaMARANGONI, GIOVANNIRoberta BertaniLucia Del BiancoDaniele Pavarin + - - BOOK OF ABSTRACTS
Novel Multifunctional Magnetic Inorganic Composites: Synthesis and Characterization 2019 Giovanni MarangoniRoberta BertaniLucia Del BiancoDaniele PavarinPaolo Sgarbossa + - - Poster
Novel multifunctional nanocomposites from titanate nanosheets and semiconductor quantum dots 2011 ANTONELLO, ALESSANDROBRUSATIN, GIOVANNAGUGLIELMI, MASSIMOBELLO, VALENTINAPEROTTO, GIOVANNIMATTEI, GIOVANNIMARTUCCI, ALESSANDRO + OPTICAL MATERIALS - -
A novel Multiplicative Polynomial Kernel for Volterra series identification 2020 Dalla LiberaR. CarliPillonetto - - Proceedings of the 21st IFAC World Congress, Berlin, Germany, 12-17 July 2020
A novel murine model for arrhythmogenic cardiomyopathy points to a pathogenic role of Wnt signaling and miRNA dysregulation. 2019 Calore MartinaLorenzon AlessandraVitiello LiberoPoloni GiuliaBeffagna GiorgiaDazzo EmanuelaSACCHETTO, CLAUDIABonaldo PaoloBraghetta PaolaRampazzo Alessandra + CARDIOVASCULAR RESEARCH - -
A novel mutation (8342G → A) in the mitochondrial tRNA(Lys) gene associated with progressive external ophthalmoplegia and myoclonus 1999 Mora M.Zeviani M. + NEUROMUSCULAR DISORDERS - -
A novel mutation in ABCD1 unveils different clinical phenotypes in a family with adrenoleukodystrophy 2017 Margoni, M + JOURNAL OF CLINICAL NEUROSCIENCE - -
A novel mutation in isoform 3 of the plasma membrane Ca2+ pump impairs cellular Ca2+ homeostasis in a patient with cerebellar ataxia and laminin subunit 1α mutations. 2015 CALI', TITOLOPREIATO, RAFFAELEFRIZZARIN, MARTINAZANOTTI, GIUSEPPEBRINI, MARISACARAFOLI, ERNESTO + THE JOURNAL OF BIOLOGICAL CHEMISTRY - -
A novel mutation in MECOM affects MPL regulation in vitro and results in thrombocytopenia and bone marrow failure 2023 Marzollo, AntonioGabelli, MariaTretti-Parenzan, CaterinaBiffi, AlessandraBresolin, Silvia + BRITISH JOURNAL OF HAEMATOLOGY - -
Novel mutation in mitochondrial Elongation Factor EF-Tu associated to dysplastic leukoencephalopathy and defective mitochondrial DNA translation 2017 Zeviani M.Francisci S.Bertini E. + BIOCHIMICA ET BIOPHYSICA ACTA. MOLECULAR BASIS OF DISEASE - -
Novel mutation in mitochondrial Elongation Factor EF-Tu associated to dysplastic leukoencephalopathy and defective mitochondrial DNA translation 2017 Fernandez-Vizarra, ErikaZeviani, Massimo + BIOCHIMICA ET BIOPHYSICA ACTA. MOLECULAR BASIS OF DISEASE - -
A novel mutation in OCTN2 transporter in italian patients with primary carnitine deficiency 2002 MOGNATO, MADDALENAANGELINI C. + - - Neurological sciences
A novel mutation in the mitochondrial tRNA(Val) gene associated with a complex neurological presentation 1998 Mora M.Zeviani M. + ANNALS OF NEUROLOGY - -
A novel mutation in the mitochondrial tRNAPro gene associated with late-onset ataxia, retinitis pigmentosa, deafness, leukoencephalopathy and complex I deficiency 2009 Zeviani M. + EUROPEAN JOURNAL OF HUMAN GENETICS - -
A novel mutation in the Surf1 gene in a child with leigh disease, peripheral neuropathy, and cytochrome-c oxidase deficiency 2002 Bado M.Zeviani M. + JOURNAL OF CHILD NEUROLOGY - -
A novel mutation in the upstream open reading frame of the CDKN1B gene causes a MEN4 phenotype 2013 OCCHI, GIANLUCAREGAZZO, DANIELABOARETTO, FRANCESCACIATO, DENISFERASIN, SERGIOOPOCHER, GIUSEPPEMANTERO, FRANCOSCARONI, CARLA + PLOS GENETICS - -
A novel mutation of the EYA4 gene associated with post-lingual hearing loss in a proband is co-segregating with a novel PAX3 mutation in two congenitally deaf family members 2018 CESCA, FEDERICABETTELLA, ELISAPOLLI, ROBERTACAMA, ELONASCIMEMI, PIETROSANTARELLI, ROSAMARIAMURGIA, ALESSANDRA INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY - -
Novel mutation of the mitofusin 2 gene in a family with Charcot-Marie-Tooth disease type 2 (CMT2A). 2014 LUCCHETTA, MARTABOARETTO, FRANCESCACampagnolo MBRIANI, CHIARA + MUSCLE & NERVE - -
Mostrati risultati da 191.867 a 191.886 di 304.334
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