Ida Annunziata Department of Genetics St. Jude Children's Research Hospital Biography Publications Institution JoVE Articles Ida Annunziata has not added a biography. If you are Ida Annunziata and would like to personalize this page please email our Author Liaison for assistance. 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 Isolering och karakterisering av exosomer från skelettmuskulaturfibroblaster Diantha van de Vlekkert1, Xiaohui Qiu1, Ida Annunziata1, Alessandra d'Azzo1 1Department of Genetics, St. Jude Children's Research Hospital JoVE 61127 Biologia Mitokondrier-associerade ER Membran (MAMS) och glykosfingolipid berikat mikroområden (GEMS): Isolering från mushjärna Ida Annunziata*1, Annette Patterson*1, Alessandra d'Azzo1 1Department of Genetics, St Jude Children's Research Hospital JoVE 50215 Neuroscienze
Isolering och karakterisering av exosomer från skelettmuskulaturfibroblaster Diantha van de Vlekkert1, Xiaohui Qiu1, Ida Annunziata1, Alessandra d'Azzo1 1Department of Genetics, St. Jude Children's Research Hospital JoVE 61127 Biologia
Mitokondrier-associerade ER Membran (MAMS) och glykosfingolipid berikat mikroområden (GEMS): Isolering från mushjärna Ida Annunziata*1, Annette Patterson*1, Alessandra d'Azzo1 1Department of Genetics, St Jude Children's Research Hospital JoVE 50215 Neuroscienze