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Search Results - Soardi, Michela
Search Results - Soardi, Michela
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Modeling Sarcoglycanopathy in Danio rerio
by
Dalla Barba, Francesco
,
Soardi, Michela
,
Mouhib, Leila
,
Risato, Giovanni
,
Akyürek, Eylem Emek
,
Lucon-Xiccato, Tyrone
,
Scano, Martina
,
Benetollo, Alberto
,
Sacchetto, Roberta
,
Richard, Isabelle
,
Argenton, Francesco
,
Bertolucci, Cristiano
,
Carotti, Marcello
,
Sandonà, Dorianna
Published in
International journal of molecular sciences
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Combined Use of CFTR Correctors in LGMD2D Myotubes Improves Sarcoglycan Complex Recovery
by
Carotti, Marcello
,
Scano, Martina
,
Fancello, Irene
,
Richard, Isabelle
,
Risato, Giovanni
,
Bensalah, Mona
,
Soardi, Michela
,
Sandonà, Dorianna
Published in
International journal of molecular sciences
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CFTR corrector C17 is effective in muscular dystrophy, in vivo proof of concept in LGMDR3
by
Scano, Martina
,
Benetollo, Alberto
,
Nogara, Leonardo
,
Bondì, Michela
,
Dalla Barba, Francesco
,
Soardi, Michela
,
Furlan, Sandra
,
Akyurek, Eylem Emek
,
Caccin, Paola
,
Carotti, Marcello
,
Sacchetto, Roberta
,
Blaauw, Bert
,
Sandonà, Dorianna
Published in
Human molecular genetics
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Repairing folding-defective α-sarcoglycan mutants by CFTR correctors, a potential therapy for limb-girdle muscular dystrophy 2D
by
Carotti, Marcello
,
Marsolier, Justine
,
Soardi, Michela
,
Bianchini, Elisa
,
Gomiero, Chiara
,
Fecchio, Chiara
,
Henriques, Sara F
,
Betto, Romeo
,
Sacchetto, Roberta
,
Richard, Isabelle
,
Sandonà, Dorianna
Published in
Human molecular genetics
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Modeling Sarcoglycanopathy in Danio rerio
by
Dalla Barba, Francesco
,
Soardi, Michela
,
Mouhib, Leila
,
Risato, Giovanni
,
Akyürek, Eylem Emek
,
Lucon-Xiccato, Tyrone
,
Scano, Martina
,
Benetollo, Alberto
,
Sacchetto, Roberta
,
Richard, Isabelle
,
Argenton, Francesco
,
Bertolucci, Cristiano
,
Carotti, Marcello
,
Sandonà, Dorianna
Published in
International journal of molecular sciences
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Modeling Sarcoglycanopathy in IDanio rerio/I
by
Dalla Barba, Francesco
,
Soardi, Michela
,
Mouhib, Leila
,
Risato, Giovanni
,
Akyürek, Eylem Emek
,
Lucon-Xiccato, Tyrone
,
Scano, Ma
,
Benetollo, Alberto
,
Sacchetto, Roberta
,
Richard, Isabelle
,
Argenton, Francesco
,
Bertolucci, Cristiano
,
Carotti, Marcello
,
Sandonà, Dorianna
Published in
International journal of molecular sciences
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In vitro functional studies of rare CYP21A2 mutations and establishment of an activity gradient for nonclassic mutations improve phenotype predictions in congenital adrenal hyperpl...
by
Barbaro, Michela
,
Soardi, Fernanda C.
,
Östberg, Linus J.
,
Persson, Bengt
,
de Mello, Maricilda Palandi
,
Wedell, Anna
,
Lajic, Svetlana
Published in
Clinical endocrinology (Oxford)
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Functional studies of CYP21A2 mutants complement structural and clinical predictions of disease severity in CAH
by
Barbaro, Michela
,
Soardi, Fernanda C.
,
Palandi de Mello, Maricilda
,
Wedell, Anna
,
Lajic, Svetlana
Published in
Clinical endocrinology (Oxford)
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In vitro functional studies of rare CYP 21A2 mutations and establishment of an activity gradient for nonclassic mutations improve phenotype predictions in congenital adrenal hyperp...
by
Barbaro, Michela
,
Soardi, Fernanda C.
,
Östberg, Linus J.
,
Persson, Bengt
,
de Mello, Maricilda Palandi
,
Wedell, Anna
,
Lajic, Svetlana
Published in
Clinical endocrinology (Oxford)
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Functional studies of CYP21A2 mutants complement structural and clinical predictions of disease severity in CAH
by
Barbaro, Michela
,
Soardi, Fernanda C
,
de Mello, Maricilda Palandi
,
Wedell, Anna
,
Lajic, Svetlana
Published in
Clinical endocrinology
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