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SOTGIA F

Last name: SOTGIA F

    Recent uploads

  • 2004 (v1)
    Publication
    Metadata-only
    Caveolinopathies: mutations in caveolin-3 cause four distinct autosomal dominant muscle diseases
    Woodman S Sotgia F Galbiati F

    No description

    Uploaded on: April 14, 2023
  • 2006 (v1)
    Publication
    Metadata-only
    Caveolin-1 Deficiency (-/-)Conveys Cell Autonomous Defects in Mammary Epithelia, with Abnormal 3D Lumen Formation, EGF-independent Growth, and Increased Branching Capacity
    Sotgia F Williams TM Schubert W

    No description

    Uploaded on: April 14, 2023
  • 1993 (v1)
    Publication
    Metadata-only
    Caveolinopathies
    Bruno C Sotgia F Gazzerro E

    No description

    Uploaded on: October 11, 2023
  • 2003 (v1)
    Publication
    Metadata-only
    Phosphofructokinase muscle-specific isoform requires caveolin-3 expression for plasma membrane recruitment and caveolar targeting: implications for the pathogenesis of caveolin-related muscle diseases
    Sotgia F Bonuccelli G Minetti C

    No description

    Uploaded on: April 14, 2023
  • 2005 (v1)
    Publication
    Metadata-only
    Caveolin-1-Deficient Mice Have An Increased Mammary Stem Cell Population, with Upregulation of Wnt / ?-Catenin Signaling
    Sotgia F Williams TM Cohen AW

    No description

    Uploaded on: March 25, 2023
  • 2007 (v1)
    Publication
    Metadata-only
    Caveolin-1(-/-)- and caveolin-2(-/-)-deficient mice both display numerous skeletal muscle abnormalities, with tubular aggregate formation.
    Schubert W Sotgia F Cohen AW

    No description

    Uploaded on: April 14, 2023
  • 2010 (v1)
    Publication
    Metadata-only
    Therapeutic potential of proteasome inhibition in Duchenne and Becker muscular dystrophies.
    Gazzerro E Assereto S Bonetto A

    No description

    Uploaded on: April 14, 2023
  • 2012 (v1)
    Publication
    Metadata-only
    Hyccin, the Molecule Mutated in the Leukodystrophy Hypomyelination and Congenital Cataract (HCC), Is a Neuronal Protein.
    Gazzerro E BALDASSARI, SIMONA Giacomini C

    "Hypomyelination and Congenital Cataract", HCC (MIM #610532), is an autosomal recessive disorder characterized by congenital cataract and diffuse cerebral and peripheral hypomyelination. HCC is caused by deficiency of Hyccin, a protein whose biological role has not been clarified yet. Since the identification of the cell types expressing a...

    Uploaded on: March 27, 2023

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