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MANCINELLI, ENZO

MANCINELLI, ENZO  

DIPARTIMENTO DI SCIENZE BIOMOLECOLARI E BIOTECNOLOGIE (attivo dal 01/06/2003 al 27/04/2012)  

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Titolo Data di pubblicazione Autori Tipo File Abstract
A putative role of ribonuclear inclusions and MBNL1 in the impairment of gallbladder smooth muscle contractility with cholelithiasis in myotonic dystrophy type 1 1-gen-2008 R. CardaniE. MancinelliL. BonavinaG. Meola + Article (author) -
Acetazolamide prevents vacuolar myopathy in skeletal muascle of K+ -depleted rats 1-gen-2008 MANCINELLI, ENZOG. Meola + Article (author) -
Apoptosis induced by proteasome inhibition in human myoblast cultures 1-gen-2006 J. SassoneG. MeolaE. MancinelliV. Silani + Article (author) -
Biomolecular identification of (CCTG)n mutation in myotonic dystrophy type 2 (DM2) by FISH on muscle biopsy 1-gen-2004 R. CardaniE. MancinelliV. SansoneG. Meola + Article (author) -
Clinical, muscle pathology and FISH biomolecular findings correlation in 42 Italian patients with myotonic dystrophy type 2 10-set-2009 E. MancinelliV. SansoneG. Meola + Conference Object -
Colocalization of ribonuclear inclusions and MBNL1 foci with no impairment of muscle differentiation in DM2 1-gen-2005 G. MeolaR. CardaniE. Mancinelli + Book Part (author) -
Colocalization of ribonuclear inclusions with muscle blind like-proteins in a family with myotonic dystrophy type 2 associated with a short CCTG expansion 15-dic-2008 S. LucchiariS. PagliaraniS.P. CortiE. MancinelliM. ServidaM.E. FrugugliettiV. SansoneN. BresolinG.P. ComiG. Meola + Article (author) -
Diagnostic role of ribonuclear inclusions and MBNL1 foci in muscle biopsy in a large italian cohort of myotonic dystrophy type 2 (DM2) patients 1-gen-2011 G. MeolaL.V. RennaV. SansoneE. Mancinelli + Article (author) -
Double genetic trouble (DM2/FSHD) in a Sardinian DM2/PROMM family 11-set-2009 G. MeolaG.P. ComiE. Mancinelli + Conference Object -
Gene expression analysis in Myotonic Dystrophy : indications for a common molecular pathogenic pathway in DM1 and DM2 1-gen-2007 E. MancinelliG. Meola + Article (author) -
Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2 1-giu-2003 G. MeolaE. Mancinelli + Article (author) -
Increased apoptosis, huntingtin inclusions and altered differentiation in muscle cell cultures from Huntington's disease subjects 1-dic-2006 J. SassoneG. MeolaE. MancinelliV. Silani + Article (author) -
Involvement of cdc25mm/ras-grf1-dependent signaling in the control of neuronal excitability 1-gen-2001 D. ParolaroM. SalaE. MancinelliE. SturaniR. Zippel + Article (author) -
Meccanismi di base nella fisiologia cellulare : Come sopravvivere alla biofisica delle cellule 1-gen-2019 M. MAZZANTIE. MANCINELLI Book (author) -
Muscle biopsy and cell cultures: potential diagnostic tools in hereditary skeletal muscle channelopathies 1-gen-2003 G. MeolaV. SansoneE. Mancinelli + Article (author) -
Muscleblind-like protein 1 nuclear sequestration and splicing pattern in myotonic dystrophy type 2 1-gen-2006 R. CARDANIE. MANCINELLIG. MEOLA + Article (author) -
Muscleblind-like protein 1 nuclear sequestration is a molecular pathology marker of DM1 and DM2 1-gen-2006 R CardaniE MancinelliV SansoneG Meola + Article (author) -
Muscular cell cultures show features of dysfunction and apoptosis in Huntington's disease 1-gen-2005 V. SilaniG. MeolaE. Mancinelli + Article (author) -
Pathogenic role of ribonuclear inclusions in myotonic dystrophy type 2: myth or reality? 1-giu-2008 P. TremoladaE. MancinelliG. Meola + Article (author) -
Proteome profile in Myotonic Dystrophy type 2 myotubes reveals dysfunction in protein processing and mitochondrial pathways 4-feb-2010 F. RusconiE. MancinelliG. ColomboR. CardaniG. MeolaR. Zippel + Article (author) -