Yvan Campos

发表

The Arg482His mutation in the beta-galactosidase gene is responsible for a high frequency of GM1 gangliosidosis carriers in a Cypriot village.

A. Drousiotou, E. Zammarchi, A. Morrone, 2005, Genetic testing.

Palmitoylation is a post-translational modification of Alix regulating the membrane organization of exosome-like small extracellular vesicles.

V. Martorana, S. Caruso, A. Cupane, 2018, Biochimica et biophysica acta. General subjects.

Ozz-E3 Ubiquitin Ligase Targets Sarcomeric Embryonic Myosin Heavy Chain during Muscle Development

A. J. Harris, E. Zanoteli, N. Vergani, 2010, PloS one.

Magnetic Resonance Imaging Findings and Novel Mutations in GM1 Gangliosidosis

A. Drousiotou, L. Sztriha, T. Georgiou, 2005, Journal of child neurology.

Biophysical and functional study of CRL5Ozz, a muscle specific ubiquitin ligase complex

A. Nourse, R. Kalathur, Yvan Campos, 2022, Scientific Reports.

Emphysema in an adult with galactosialidosis linked to a defect in primary elastic fiber assembly.

P. Paré, D. Sin, A. Lehman, 2012, Molecular genetics and metabolism.

Alix-mediated assembly of the actomyosin–tight junction polarity complex preserves epithelial polarity and epithelial barrier

S. Frase, Young-Goo Han, D. Solecki, 2016, Nature Communications.

Alix Protein Is Substrate of Ozz-E3 Ligase and Modulates Actin Remodeling in Skeletal Muscle*

D. Ustek, N. Vergani, Yvan Campos, 2012, The Journal of Biological Chemistry.

Mitochondrial alterations in dynamin 2-related centronuclear myopathy.

E. Zanoteli, A. Oliveira, M. Vainzof, 2009, Arquivos de neuro-psiquiatria.

Distinct functions of dimeric and monomeric scaffold protein Alix in regulating F-actin assembly and loading of exosomal cargo

Jeroen A. A. Demmers, R. Kalathur, Yvan Campos, 2022, The Journal of biological chemistry.

Regulated lysosomal exocytosis mediates cancer progression

D. Finkelstein, C. Morton, Ida Annunziata, 2015, Science Advances.

AAV-mediated gene therapy for galactosialidosis: A long-term safety and efficacy study

Ida Annunziata, Yvan Campos, A. d’Azzo, 2021, Molecular therapy. Methods & clinical development.

Identification and characterization of the nano‐sized vesicles released by muscle cells

Yvan Campos, A. d’Azzo, A. De Luca, 2013, FEBS letters.

Conventional and Unconventional Therapeutic Strategies for Sialidosis Type I

C. Toro, C. Tifft, C. Gellera, 2020, Journal of clinical medicine.

Ozz-E3, a muscle-specific ubiquitin ligase, regulates beta-catenin degradation during myogenesis.

R. Rottier, J. Conaway, Yvan Campos, 2004, Developmental cell.

MYC competes with MiT/TFE in regulating lysosomal biogenesis and autophagy through an epigenetic rheostat

M. Roussel, D. Finkelstein, G. Neale, 2019, Nature Communications.

Heterodimerization of the Sialidase NEU1 with the Chaperone Protective Protein/Cathepsin A Prevents Its Premature Oligomerization*

Erik J. Bonten, G. Taylor, B. Waddell, 2009, The Journal of Biological Chemistry.

Excessive exosome release is the pathogenic pathway linking a lysosomal deficiency to generalized fibrosis

C. Feghali-Bostwick, Ida Annunziata, J. Demmers, 2019, Science Advances.

Sialidosis Presenting as Severe Nonimmune Fetal Hydrops is Associated with Two Novel Mutations in Lysosomal α-Neuraminidase

David J. Loren, E. Gilbert-Barness, A. Hamvas, 2005, Journal of Perinatology.

Altered GM1 catabolism affects NMDAR-mediated Ca2+ signaling at ER-PM junctions and increases synaptic spine formation

Ida Annunziata, Yvan Campos, A. d’Azzo, 2023, bioRxiv.

Four novel mutations in patients from the Middle East with the infantile form of GM1‐gangliosidosis

A. Drousiotou, E. Zammarchi, A. Morrone, 2004, Human mutation.

Mitochondrial proteostasis mediated by CRL5Ozz and Alix maintains skeletal muscle function

J. Opferman, G. Grosveld, G. Palacios, 2023, bioRxiv.

Altered GM1 catabolism affects NMDAR-mediated Ca2+ signaling at ER-PM junctions and increases synaptic spine formation in a GM1-gangliosidosis model

Ida Annunziata, Yvan Campos, Elida Gomero, 2024, Cell reports.