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Titolo Data di pubblicazione Autori Tipo File
Morphological and ultrastructural changes in PC12 pheochromocytoma cells induced by a combined treatment with NGF and taxol 1982 CATTANEO, ANTONINO + 1.1 Articolo in rivista
Morphological basis for pineal secretion in domestic Ungulata 1990 CAPSONI, SIMONA + 4.1 Contributo in Atti di convegno
Morphometric live mitochondrial imaging by confocal microscopy as a new tool to detect impaired human mesenchymal stem cells 2011 DI PRIMIO, CRISTINA + 4.2 Abstract in Atti di convegno
Motilita’ cellulare. Voce del Dizionario delle Scienze Fisiche. 1988 CATTANEO, ANTONINO 2.4 Voce (in dizionario o enciclopedia)
A mouse model for creatine transporter deficiency reveals early onset cognitive impairment and neuropathology associated with brain aging 2016 PIZZORUSSO, TOMMASO + 1.1 Articolo in rivista
Mössbauer studies of frataxin role in iron-sulfur cluster assembly and dysfunction-related disease 2012 Pastore A + 1.1 Articolo in rivista
Multilevel investigation of Tau pathology: from the cytoplasm to the nucleus 2019 Siano, Giacomo Doctoral Thesis
MULTIMODAL ACTIVATION AND REGULATION OF NEURONAL MECHANOSENSITIVE CATION CHANNELS 2008 PELLEGRINI, Monica + 2.1 Contributo in volume (Capitolo o Saggio)
Multiple domains of TonEBP cooperate to stimulate transcription in response to hypertonicity 2003 Colla, Emanuela + 1.1 Articolo in rivista
Multiple sequence alignment based on structural properties 2010 Gezici, Gizem + 4.1 Contributo in Atti di convegno
Multiscale morphology of organic semiconductor thin films controls the adhesion and viability of human neural cells 2010 TONAZZINI, ILARIA + 1.1 Articolo in rivista
Muscular dystrophy in adult and aged anti-NGF transgenic mice resembles an inclusion body myopathy 2000 CAPSONI, SIMONACATTANEO, ANTONINO + 1.1 Articolo in rivista
Mutant Exon1 Huntingtin Aggregation is Regulated by T3 Phosphorylation-Induced Structural Changes and Crosstalk between T3 Phosphorylation and Acetylation at K6 2017 Pastore Annalisa + 1.1 Articolo in rivista
The mutational landscape of Burkitt-like lymphoma with 11q aberration is distinct from that of Burkitt lymphoma 2019 Raimondi F. + 1.1 Articolo in rivista
Mutations in Bcl9 and Pygo genes cause congenital heart defects by tissue-specific perturbation of Wnt/β-catenin signaling 2018 Chiavacci E.Ripoll J. + 1.1 Articolo in rivista
Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28 2010 Pastore A + 1.1 Articolo in rivista
Mutations of cytochrome c identified in patients with thrombocytopenia THC4 affect both apoptosis and cellular bioenergetics 2014 PASTORE, ANNALISA + 1.1 Articolo in rivista
MUTEINS OF HNGF, THERAPEUTIC USES AND PHARMACEUTICAL COMPOSITIONS 2006 CAPSONI, SIMONACATTANEO, ANTONINO + 6.1 Brevetto
MYH9 related disease: a novel missense Ala95Asp mutation of the MYH9 gene 2009 PASTORE, ANNALISA + 1.1 Articolo in rivista
MYH9 related disease: four novel mutations of the tail domain of myosin-9 correlating with a mild clinical phenotype 2010 Pastore A + 1.1 Articolo in rivista
Mostrati risultati da 980 a 999 di 1.721
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