Cargando…

Glomerular endothelial cell heterogeneity in Alport syndrome

Glomerular endothelial cells (GEC) are a crucial component of the glomerular physiology and their damage contributes to the progression of chronic kidney diseases. How GEC affect the pathology of Alport syndrome (AS) however, is unclear. We characterized GEC from wild type (WT) and col4α5 knockout A...

Descripción completa

Detalles Bibliográficos
Autores principales:	Soloyan, Hasmik, Thornton, Matthew, Villani, Valentina, Khatchadourian, Patrick, Cravedi, Paolo, Angeletti, Andrea, Grubbs, Brendan, De Filippo, Roger, Perin, Laura, Sedrakyan, Sargis
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group UK 2020
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7351764/ https://www.ncbi.nlm.nih.gov/pubmed/32651395 http://dx.doi.org/10.1038/s41598-020-67588-0

Ejemplares similares

Intravital imaging reveals glomerular capillary distension and endothelial and immune cell activation early in Alport syndrome
por: Gyarmati, Georgina, et al.
Publicado: (2022)

A glomerulus-on-a-chip to recapitulate the human glomerular filtration barrier
por: Petrosyan, Astgik, et al.
Publicado: (2019)

Identification and Characterization of the Wilms Tumor Cancer Stem Cell
por: Petrosyan, Astgik, et al.
Publicado: (2023)

Author Correction: A glomerulus-on-a-chip to recapitulate the human glomerular filtration barrier
por: Petrosyan, Astgik, et al.
Publicado: (2019)

Emerging Technologies to Study the Glomerular Filtration Barrier
por: Gong, Emma, et al.
Publicado: (2021)

Direct Isolation and Characterization of Human Nephron Progenitors
por: Da Sacco, Stefano, et al.
Publicado: (2016)

Amniotic fluid stem cell-derived vesicles protect from VEGF-induced endothelial damage
por: Sedrakyan, S., et al.
Publicado: (2017)

The Variability of Estimated Glomerular Filtration Rate Decline in Alport Syndrome
por: Langsford, David, et al.
Publicado: (2016)

SOX9+/PTF1A+ Cells Define the Tip Progenitor Cells of the Human Fetal Pancreas of the Second Trimester
por: Villani, Valentina, et al.
Publicado: (2019)

Molecular and Cellular Mechanisms Underlying the Initiation and Progression of Alport Glomerular Pathology
por: Cosgrove, Dominic, et al.
Publicado: (2022)

Phenotypic heterogeneity in females with X-linked Alport syndrome
por: Allred, Samuel C., et al.
Publicado: (2015)

Glomerular Basement Membrane Protein Expression and the Diagnosis and Prognosis of Autosomal Dominant Alport Syndrome
por: Akihisa, Taro, et al.
Publicado: (2019)

Laminin α2-Mediated Focal Adhesion Kinase Activation Triggers Alport Glomerular Pathogenesis
por: Delimont, Duane, et al.
Publicado: (2014)

The Accumulation of VEGFA in the Glomerular Basement Membrane and Its Relationship with Podocyte Injury and Proteinuria in Alport Syndrome
por: Wang, Haiyan, et al.
Publicado: (2015)

A Novel Source of Cultured Podocytes
por: Da Sacco, Stefano, et al.
Publicado: (2013)

Alport Syndrome With Kidney Cysts Is Still Alport Syndrome
por: Savige, Judy, et al.
Publicado: (2021)

Complement and Complement Targeting Therapies in Glomerular Diseases
por: Andrighetto, Sofia, et al.
Publicado: (2019)

Refractory Minimal Change Disease and Focal Segmental Glomerular Sclerosis Treated With Anakinra
por: Angeletti, Andrea, et al.
Publicado: (2021)

X-Linked Alport Dogs Demonstrate Mesangial Filopodial Invasion of the Capillary Tuft as an Early Event in Glomerular Damage
por: Clark, Sabrina D., et al.
Publicado: (2016)

Women and Alport syndrome
por: Rheault, Michelle N.
Publicado: (2011)

Alport's Syndrome in Pregnancy
por: Mehta, Suchita, et al.
Publicado: (2013)

The 2019 and 2021 International Workshops on Alport Syndrome
por: Daga, Sergio, et al.
Publicado: (2022)

Protective Effect of Human Amniotic Fluid Stem Cells in an Immunodeficient Mouse Model of Acute Tubular Necrosis
por: Perin, Laura, et al.
Publicado: (2010)

Podocyte Depletion in Thin GBM and Alport Syndrome
por: Wickman, Larysa, et al.
Publicado: (2016)

Glomerular Endothelial Cells as Instigators of Glomerular Sclerotic Diseases
por: Sol, Marloes, et al.
Publicado: (2020)

Sindrome de Alport : revisión bibliográfica
por: Velasco Bello, Fernando Mario
Publicado: (1994)

Advances and unmet needs in genetic, basic and clinical science in Alport syndrome: report from the 2015 International Workshop on Alport Syndrome
por: Gross, Oliver, et al.
Publicado: (2017)

Immune responses to SARS-CoV-2 in dialysis and kidney transplantation
por: Cantarelli, Chiara, et al.
Publicado: (2022)

Alport syndrome: facts and opinions
por: Kashtan, Clifford
Publicado: (2017)

Genetic diagnosis of Alport syndrome
por: Cheong, Hae Il
Publicado: (2019)

Alport Syndrome Classification and Management
por: Warady, Bradley A., et al.
Publicado: (2020)

Novel Therapies for Alport Syndrome
por: Chavez, Efren, et al.
Publicado: (2022)

Auditory Perception in Alport’s Syndrome
por: Viveiros, Carla Mherlyn, et al.
Publicado: (2015)

Clinical practice recommendations for the treatment of Alport syndrome: a statement of the Alport Syndrome Research Collaborative
por: Kashtan, Clifford E., et al.
Publicado: (2012)

Amniotic Fluid Stem Cells Inhibit the Progression of Bleomycin-Induced Pulmonary Fibrosis via CCL2 Modulation in Bronchoalveolar Lavage
por: Garcia, Orquidea, et al.
Publicado: (2013)

The severity of glomerular endothelial cell injury is associated with infiltrating macrophage heterogeneity in endocapillary proliferative glomerulonephritis
por: Arai, Momoko, et al.
Publicado: (2021)

HCV-Associated Nephropathies in the Era of Direct Acting Antiviral Agents
por: Angeletti, Andrea, et al.
Publicado: (2019)

EPO in Patients With COVID-19: More Than an Erythropoietic Hormone
por: Leventhal, Jeremy, et al.
Publicado: (2020)

Outcomes of kidney transplantation in Alport syndrome compared with other forms of renal disease
por: Kelly, Yvelynne P., et al.
Publicado: (2016)

The 2014 International Workshop on Alport Syndrome
por: Miner, Jeffrey H, et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_vgakgdmc25ugqje46jp0j69r94