RAFFAELLO, ANNA

RAFFAELLO, ANNA  

Dipartimento di Scienze Biomediche - DSB  

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Risultati 1 - 20 di 38 (tempo di esecuzione: 0.031 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
Human MYO18B, a novel unconventional myosin heavy chain expressed in striated muscles moves into the myonuclei upon differentiation 2003 RAFFAELLO, ANNAMONGILLO, MARCONEGRISOLO, ENRICO MASSIMILIANOVALLE, GIORGIOSCHIAFFINO, STEFANOLANFRANCHI, GEROLAMO + JOURNAL OF MOLECULAR BIOLOGY - -
Physiological changes and temporal expression profiling in mouse fast skeletal muscles following denervation 2004 RAFFAELLO, ANNALAVEDER, PAOLOROMUALDI, CHIARATONIOLO, LUANAGERMINARIO, ELENADANIELI, DANIELAMEGIGHIAN, ARAMREGGIANI, CARLOLANFRANCHI, GEROLAMO JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY - JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY
The Ankrd2, Cdkn1c and calcyclin genes are under the control of MyoD during myogenic differentiation 2005 BEAN, CAMILLASALAMON, MICHELARAFFAELLO, ANNACAMPANARO, STEFANOLANFRANCHI, GEROLAMO + JOURNAL OF MOLECULAR BIOLOGY - -
Denervation in murine fast-twitch muscle: short-term physiological changes and temporal expression profiling 2006 RAFFAELLO, ANNALAVEDER, PAOLOROMUALDI, CHIARATONIOLO, LUANAGERMINARIO, ELENAMEGIGHIAN, ARAMDANIELI, DANIELAREGGIANI, CARLOLANFRANCHI, GEROLAMO + PHYSIOLOGICAL GENOMICS - -
Rapid disuse and denervation atrophy involve similar transcriptional changes as muscle wasting during systemic deseases. 2007 RAFFAELLO, ANNA + THE FASEB JOURNAL - -
Meta-analysis of expression signatures of muscle atrophy: gene interactionnetworks in early and late stages. 2008 CALURA ECAGNIN, STEFANORAFFAELLO, ANNALAVEDER, PAOLOLANFRANCHI, GEROLAMOROMUALDI, CHIARA BMC GENOMICS - -
JunB transcription factor maintains skeletal muscle mass and promotes hypertrophy 2010 RAFFAELLO, ANNALANFRANCHI, GEROLAMOSANDRI, MARCO + THE JOURNAL OF CELL BIOLOGY - -
Mitochondrial longevity pathways 2011 RAFFAELLO, ANNARIZZUTO, ROSARIO BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH - -
A forty-kilodalton protein of the inner membrane is the mitochondrial calcium uniporter. 2011 DE STEFANI, DIEGORAFFAELLO, ANNATEARDO, ENRICOSZABO', ILDIKO'RIZZUTO, ROSARIO NATURE - -
Molecular Definition of the Mitochondrial Ca(2+) Signalling Machinery 2011 DE STEFANI, DIEGORAFFAELLO, ANNATEARDO, ENRICOSZABO', ILDIKO'RIZZUTO, ROSARIO JOURNAL OF GENERAL PHYSIOLOGY - -
Mitochondria as sensors and regulators of calcium signalling. 2012 RIZZUTO, ROSARIODE STEFANI, DIEGORAFFAELLO, ANNAMAMMUCARI, CRISTINA NATURE REVIEWS. MOLECULAR CELL BIOLOGY - -
The mitochondrial Ca(2+) uniporter. 2012 RAFFAELLO, ANNADE STEFANI, DIEGORIZZUTO, ROSARIO CELL CALCIUM - -
The Mitochondrial Calcium Uniporter (MCU): Molecular Identity and Physiological Roles. 2013 PATRON, MARIARAFFAELLO, ANNAGRANATIERO, VERONICATOSATTO, ANNAMERLI, GIULIADE STEFANI, DIEGOMAMMUCARI, CRISTINARIZZUTO, ROSARIO + THE JOURNAL OF BIOLOGICAL CHEMISTRY - -
The mitochondrial calcium uniporter is a multimer that can include a dominant-negative pore-forming subunit. 2013 RAFFAELLO, ANNADE STEFANI, DIEGOSABBADIN, DAVIDETEARDO, ENRICOMERLI, GIULIAPICARD, ANNE ALEIDACHECCHETTO, VANESSAMORO, STEFANOSZABO', ILDIKO'RIZZUTO, ROSARIO EMBO JOURNAL - -
Adrenergic Stimulation Enhances Mitochondrial Ca2+ Uptake and Cell Death Signaling Through Pyk2-Dependent Tyrosine Phosphorylation of the Mitochondrial Ca2+ Uniporter 2013 Raffaello AnnaRizzuto Rosario + CIRCULATION - -
Adrenergic signaling regulates mitochondrial Ca2+ uptake through Pyk2-dependent tyrosine phosphorylation of the mitochondrial Ca2+ uniporter. 2014 RAFFAELLO, ANNARIZZUTO, ROSARIO + ANTIOXIDANTS & REDOX SIGNALING - -
MICU1 and MICU2 finely tune the mitochondrial Ca2+ uniporter by exerting opposite effects on MCU activity. 2014 PATRON, MARIACHECCHETTO, VANESSARAFFAELLO, ANNATEARDO, ENRICOVECELLIO REANE, DENISGRANATIERO, VERONICASZABO', ILDIKO'DE STEFANI, DIEGORIZZUTO, ROSARIO + MOLECULAR CELL - -
Electrophysiological Characterization of the Activity and Regulation of the Mitochondrial Calcium Uniporter 2014 Checchetto VanessaTeardo EnricoDe Stefani DiegoPatron MariaRaffaello AnnaSzabo IldikoRizzuto Rosario BIOPHYSICAL JOURNAL - -
Genetic defects in mitochondrial calcium handling cause neuromuscular disease 2014 De Stefani DiegoRaffaello AnnaRizzuto RosarioSzabadkai Gyorgy + EUROPEAN JOURNAL OF CLINICAL INVESTIGATION - -
Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling. 2014 SZABADKAI, GYORGYRAFFAELLO, ANNADE STEFANI, DIEGORIZZUTO, ROSARIO + NATURE GENETICS - -