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SOTGIA F

Last name: SOTGIA F

    Recent uploads

  • 2009 (v1)
    Publication
    Metadata-only
    Caveolinopathies: from the biology of caveolin-3 to human diseases.
    GAZZERRO E SOTGIA F BRUNO C

    No description

    Uploaded on: October 11, 2023
  • 1998 (v1)
    Publication
    Metadata-only
    Molecular genetics of the caveolin gene family: Implications for human cancers, Diabetes, Alzheimer disease, and muscular dystrophy
    ENGELMAN JA ZHANG X GALBIATI F

    No description

    Uploaded on: December 5, 2022
  • 2000 (v1)
    Publication
    Metadata-only
    Mutation in the CAV3 gene causes partial caveolin-3 deficiency and hyperCKemia
    CARBONE I BRUNO C SOTGIA F

    No description

    Uploaded on: December 5, 2022
  • 2006 (v1)
    Publication
    Metadata-only
    Pharmacological rescue of the dystrophin-glycoprotein complex in Duchenne and Becker skeletal muscle explants by proteasome inhibitor treatment
    ASSERETO S STRINGARA S SOTGIA F

    No description

    Uploaded on: April 14, 2023
  • 2002 (v1)
    Publication
    Metadata-only
    Impairment of caveolae formation and T-system disorganization in human muscular dystrophy with caveolin-3 deficiency
    MINETTI, CARLO BADO M BRODA P

    No description

    Uploaded on: March 25, 2023
  • 2002 (v1)
    Publication
    Metadata-only
    Familial isolated hyperCKemia associated with a new mutation in the caveolin-3 (CAV-3) gene
    MERLINI L CARBONE I CAPANNI C

    No description

    Uploaded on: October 11, 2023
  • 1998 (v1)
    Publication
    Metadata-only
    Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy.
    MINETTI, CARLO SOTGIA F BRUNO C

    No description

    Uploaded on: April 14, 2023
  • 2008 (v1)
    Publication
    Metadata-only
    Truncation of Caveolin-3 causes autosomal-recessive Rippling Muscle Disease
    TRAVERSO M BRUNO C BROCCOLINI A

    No description

    Uploaded on: April 14, 2023
  • 1999 (v1)
    Publication
    Metadata-only
    Increased number of caveolae and caveolin-3 over-expression in Duchenne muscular dystrophy
    REPETTO S BADO M BRODA P

    No description

    Uploaded on: December 5, 2022
  • 2008 (v1)
    Publication
    Metadata-only
    Caveolin-3 T78M and T78K missense mutations lead to different phenotypes in vivo and in vitro.
    TRAVERSO M GAZZERRO E ASSERETO S

    No description

    Uploaded on: April 14, 2023
  • 2007 (v1)
    Publication
    Metadata-only
    Phenotypic characterization of hypomyelination and congenital cataract
    BIANCHERI R ZARA F BRUNO C

    Phenotypic Characterization of Hypomyelination and Congenital Cataract Roberta Biancheri, MD, PhD,1 Federico Zara, PhD,1 Claudio Bruno, MD,1 Andrea Rossi, MD,2 Laura Bordo, BSc,1 Elisabetta Gazzerro, MD,1 Federica Sotgia, PhD,1,3 Marina Pedemonte, MD,1 Sara Scapolan, MD,1 Massimo Bado, MD,1 Graziella Uziel, MD,4 Marianna Bugiani, MD,4 Laura...

    Uploaded on: March 31, 2023

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