Cargando…

The Role of Exosomes in Lysosomal Storage Disorders

Exosomes, small membrane-bound organelles formed from endosomal membranes, represent a heterogenous source of biological and pathological biomarkers capturing the metabolic status of a cell. Exosomal cargo, including lipids, proteins, mRNAs, and miRNAs, can either act as inter-cellular messengers or...

Descripción completa

Detalles Bibliográficos
Autores principales:	Gleason, Adenrele M., Woo, Elizabeth G., McKinney, Cindy, Sidransky, Ellen
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2021
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8071119/ https://www.ncbi.nlm.nih.gov/pubmed/33920837 http://dx.doi.org/10.3390/biom11040576

Ejemplares similares

Induced pluripotent stem cell models of lysosomal storage disorders
por: Borger, Daniel K., et al.
Publicado: (2017)

Glucocerebrosidase and its relevance to Parkinson disease
por: Do, Jenny, et al.
Publicado: (2019)

Exosomes: Origins and Therapeutic Potential for Neurodegenerative Disease
por: Sarko, Diana K., et al.
Publicado: (2017)

Lysosomal storage disorders
por: Cabrera-Salazar, Mario A, et al.
Publicado: (2007)

Lysosomal Storage Disorders and Malignancy
por: Pastores, Gregory M., et al.
Publicado: (2017)

Lysosomal storage disorders: The cellular impact of lysosomal dysfunction
por: Platt, Frances M., et al.
Publicado: (2012)

Lysosomal storage and impaired autophagy lead to inflammasome activation in Gaucher macrophages
por: Aflaki, Elma, et al.
Publicado: (2015)

Autophagy in lysosomal storage disorders
por: Lieberman, Andrew P., et al.
Publicado: (2012)

Insight into the Role of Extracellular Vesicles in Lysosomal Storage Disorders
por: Tancini, Brunella, et al.
Publicado: (2019)

Metabolism of Glycosphingolipids and Their Role in the Pathophysiology of Lysosomal Storage Disorders
por: Ryckman, Alex E., et al.
Publicado: (2020)

Mitochondrial Dysfunction in Lysosomal Storage Disorders
por: de la Mata, Mario, et al.
Publicado: (2016)

Lyso-IP: Uncovering Pathogenic Mechanisms of Lysosomal Dysfunction
por: Chen, Chase, et al.
Publicado: (2022)

Technological advances expand our knowledge of lysosomal dysfunction in neurodegeneration
por: Chen, Chase, et al.
Publicado: (2022)

Lysosomes and Lysosomal Storage Diseases
por: Noebels, Jeffrey L.
Publicado: (1981)

Lysosomal Storage Disorders Shed Light on Lysosomal Dysfunction in Parkinson’s Disease
por: Blumenreich, Shani, et al.
Publicado: (2020)

Interstitial lung disease in lysosomal storage disorders
por: Borie, Raphaël, et al.
Publicado: (2021)

Molecular study of lysosomal storage disorders in India
por: Sheth, Jayesh
Publicado: (2014)

Molecular basis of lysosomal storage disorders in India
por: Kondurkar, Shweta P, et al.
Publicado: (2014)

Sortilin inhibition treats multiple neurodegenerative lysosomal storage disorders
por: Leppert, Hannah G., et al.
Publicado: (2023)

Lysosomal storage diseases
por: Ferreira, Carlos R., et al.
Publicado: (2017)

Biomarkers in the diagnosis of lysosomal storage disorders: proteins, lipids, and inhibodies
por: Aerts, Johannes M. F. G., et al.
Publicado: (2011)

Lysosomal Storage Disorders: Molecular Basis and Therapeutic Approaches
por: Moro, Enrico
Publicado: (2021)

Enzyme replacement therapy for lysosomal storage disorders in India
por: Muranjan, Mamta
Publicado: (2014)

Lysosomal storage disorders: Molecular basis and laboratory testing
por: Filocamo, Mirella, et al.
Publicado: (2011)

Recent advances in gene therapy for lysosomal storage disorders
por: Rastall, David PW, et al.
Publicado: (2015)

Neonatal Expanded Screening toward lysosomal storage disorders
por: Burlina, Alberto, et al.
Publicado: (2015)

Lysosomal storage disorders for the pediatric rheumatologist: the example of mucopolysaccharydoses
por: Cimaz, Rolando, et al.
Publicado: (2015)

Niemann-Pick Disease: An Underdiagnosed Lysosomal Storage Disorder
por: Panigrahi, Inusha, et al.
Publicado: (2019)

Biomarkers for Lysosomal Storage Disorders with an Emphasis on Mass Spectrometry
por: Mashima, Ryuichi, et al.
Publicado: (2020)

Impaired autophagy: The collateral damage of lysosomal storage disorders
por: Myerowitz, Rachel, et al.
Publicado: (2020)

Acetyl-leucine slows disease progression in lysosomal storage disorders
por: Kaya, Ecem, et al.
Publicado: (2020)

Mechanisms of Mitochondrial Dysfunction in Lysosomal Storage Disorders: A Review
por: Stepien, Karolina M., et al.
Publicado: (2020)

Role of the Lactide:Glycolide Ratio in PLGA Nanoparticle Stability and Release under Lysosomal Conditions for Enzyme Replacement Therapy of Lysosomal Storage Disorders
por: del Moral, Maria, et al.
Publicado: (2023)

Lipid‐induced lysosomal damage after demyelination corrupts microglia protective function in lysosomal storage disorders
por: Gabandé‐Rodríguez, Enrique, et al.
Publicado: (2018)

Biomarkers in Lysosomal Storage Diseases
por: Bobillo Lobato, Joaquin, et al.
Publicado: (2016)

Prevalence of lysosomal storage disorders in Australia from 2009 to 2020
por: Chin, Sharon J, et al.
Publicado: (2021)

Pompe disease: Shared and unshared features of lysosomal storage disorders
por: Lim, Jeong-A, et al.
Publicado: (2015)

Less Is More: Substrate Reduction Therapy for Lysosomal Storage Disorders
por: Coutinho, Maria Francisca, et al.
Publicado: (2016)

Pompe Disease: New Developments in an Old Lysosomal Storage Disorder
por: Meena, Naresh K., et al.
Publicado: (2020)

Current State of the Art of Newborn Screening for Lysosomal Storage Disorders
por: Millington, David S., et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_4f9ikhhqlviotstt1tnrf9ilra