Ida Annunziata

Publications

• Transcription Factor Competition Regulates Lysosomal Biogenesis and Autophagy
  Molecular & Cellular Oncology. 2020  |   Pubmed ID: 32158913
• Conventional and Unconventional Therapeutic Strategies for Sialidosis Type I
  Journal of Clinical Medicine. 03, 2020  |   Pubmed ID: 32143456
• MYC Competes with MiT/TFE in Regulating Lysosomal Biogenesis and Autophagy Through an Epigenetic Rheostat
  Nature Communications. 08, 2019  |   Pubmed ID: 31399583
• Excessive Exosome Release is the Pathogenic Pathway Linking a Lysosomal Deficiency to Generalized Fibrosis
  Science Advances. 07, 2019  |   Pubmed ID: 31328155
• Mitochondria-associated ER Membranes (MAMs) and Lysosomal Storage Diseases
  Cell Death & Disease. 02, 2018  |   Pubmed ID: 29491402
• Galactosialidosis: Historic Aspects and Overview of Investigated and Emerging Treatment Options
  Expert Opinion on Orphan Drugs. 2017  |   Pubmed ID: 28603679
• Pathogenesis, Emerging Therapeutic Targets and Treatment in Sialidosis
  Expert Opinion on Orphan Drugs. 2015  |   Pubmed ID: 26949572
• Regulated Lysosomal Exocytosis Mediates Cancer Progression
  Science Advances. Dec, 2015  |   Pubmed ID: 26824057
• Loss of Cellular Sialidases Does Not Affect the Sialylation Status of the Prion Protein but Increases the Amounts of Its Proteolytic Fragment C1
  PloS One. 2015  |   Pubmed ID: 26569607
• Lysosomal Multienzyme Complex: Pros and Cons of Working Together
  Cellular and Molecular Life Sciences : CMLS. Jun, 2014  |   Pubmed ID: 24337808
• Interorganellar Membrane Microdomains: Dynamic Platforms in the Control of Calcium Signaling and Apoptosis
  Cells. Aug, 2013  |   Pubmed ID: 24709798
• Lysosomal NEU1 Deficiency Affects Amyloid Precursor Protein Levels and Amyloid-β Secretion Via Deregulated Lysosomal Exocytosis
  Nature Communications. 2013  |   Pubmed ID: 24225533
• Non-erythropoietic Erythropoietin Derivatives Protect from Light-induced and Genetic Photoreceptor Degeneration
  Human Molecular Genetics. Jun, 2011  |   Pubmed ID: 21421996
• GM1-ganglioside Accumulation at the Mitochondria-associated ER Membranes Links ER Stress to Ca(2+)-dependent Mitochondrial Apoptosis
  Molecular Cell. Nov, 2009  |   Pubmed ID: 19917257
• Multiple Sulfatase Deficiency is Due to Hypomorphic Mutations of the SUMF1 Gene
  Human Mutation. Sep, 2007  |   Pubmed ID: 17657823
• Contiguous Gene Syndrome Due to an Interstitial Deletion in Xp22.3 in a Boy with Ichthyosis, Chondrodysplasia Punctata, Mental Retardation and ADHD
  European Journal of Medical Genetics. Jul-Aug, 2007  |   Pubmed ID: 17591464
• Sulfatase Modifying Factor 1 Trafficking Through the Cells: from Endoplasmic Reticulum to the Endoplasmic Reticulum
  The EMBO Journal. May, 2007  |   Pubmed ID: 17446859
• Systemic Inflammation and Neurodegeneration in a Mouse Model of Multiple Sulfatase Deficiency
  Proceedings of the National Academy of Sciences of the United States of America. Mar, 2007  |   Pubmed ID: 17360554
• Pharmacological Enhancement of Mutated Alpha-glucosidase Activity in Fibroblasts from Patients with Pompe Disease
  Molecular Therapy : the Journal of the American Society of Gene Therapy. Mar, 2007  |   Pubmed ID: 17213836
• Sulphatase Activities Are Regulated by the Interaction of Sulphatase-modifying Factor 1 with SUMF2
  EMBO Reports. Jul, 2005  |   Pubmed ID: 15962010
• Molecular and Functional Analysis of SUMF1 Mutations in Multiple Sulfatase Deficiency
  Human Mutation. Jun, 2004  |   Pubmed ID: 15146462
• The Multiple Sulfatase Deficiency Gene Encodes an Essential and Limiting Factor for the Activity of Sulfatases
  Cell. May, 2003  |   Pubmed ID: 12757706
• Mapping of MRX81 in Xp11.2-Xq12 Suggests the Presence of a New Gene Involved in Nonspecific X-linked Mental Retardation
  American Journal of Medical Genetics. Part A. Apr, 2003  |   Pubmed ID: 12673650
• Lathosterolosis, a Novel Multiple-malformation/mental Retardation Syndrome Due to Deficiency of 3beta-hydroxysteroid-delta5-desaturase
  American Journal of Human Genetics. Oct, 2002  |   Pubmed ID: 12189593