Stem cell‐derived retinal pigment epithelium from patients with age‐related macular degeneration exhibit reduced metabolism and matrix interactions
Published 2019 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Stem cell‐derived retinal pigment epithelium from patients with age‐related macular degeneration exhibit reduced metabolism and matrix interactions
Authors
Keywords
-
Journal
Stem Cells Translational Medicine
Volume 9, Issue 3, Pages 364-376
Publisher
Wiley
Online
2019-12-16
DOI
10.1002/sctm.19-0321
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Whole-genome methylation profiling of the retinal pigment epithelium of individuals with age-related macular degeneration reveals differential methylation of the SKI, GTF2H4, and TNXB genes
- (2019) Louise F. Porter et al. Clinical Epigenetics
- Age-related macular degeneration (AMD) mitochondria modulate epigenetic mechanisms in retinal pigment epithelial cells
- (2019) Sonali Nashine et al. EXPERIMENTAL EYE RESEARCH
- Age-related macular degeneration
- (2018) Paul Mitchell et al. LANCET
- Nitrite ion modifies tyrosine and lysine residues of extracellular matrix proteins
- (2018) Mai T. Thao et al. NITRIC OXIDE-BIOLOGY AND CHEMISTRY
- Changes in extracellular matrix cause RPE cells to make basal deposits and activate the alternative complement pathway
- (2017) Rosario Fernandez-Godino et al. HUMAN MOLECULAR GENETICS
- WikiPathways: a multifaceted pathway database bridging metabolomics to other omics research
- (2017) Denise N Slenter et al. NUCLEIC ACIDS RESEARCH
- Drusen in patient-derived hiPSC-RPE models of macular dystrophies
- (2017) Chad A. Galloway et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Concerted regulation of retinal pigment epithelium basement membrane and barrier function by angiocrine factors
- (2017) Ignacio Benedicto et al. Nature Communications
- Differentiation of RPE cells from integration-free iPS cells and their cell biological characterization
- (2017) Roni A. Hazim et al. Stem Cell Research & Therapy
- Altered bioenergetics and enhanced resistance to oxidative stress in human retinal pigment epithelial cells from donors with age-related macular degeneration
- (2017) Deborah A. Ferrington et al. Redox Biology
- Extracellular matrix nitration alters growth factor release and activates bioactive complement in human retinal pigment epithelial cells
- (2017) Mark A. Fields et al. PLoS One
- Alpha crystallins in the retinal pigment epithelium and implications for the pathogenesis and treatment of age-related macular degeneration
- (2016) Ram Kannan et al. BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS
- Looking into the future: Using induced pluripotent stem cells to build two and three dimensional ocular tissue for cell therapy and disease modeling
- (2016) Min Jae Song et al. BRAIN RESEARCH
- Nanofiber Scaffold-Based Tissue-Engineered Retinal Pigment Epithelium to Treat Degenerative Eye Diseases
- (2016) Nathan A. Hotaling et al. JOURNAL OF OCULAR PHARMACOLOGY AND THERAPEUTICS
- Repressed SIRT1/PGC-1α pathway and mitochondrial disintegration in iPSC-derived RPE disease model of age-related macular degeneration
- (2016) Nady Golestaneh et al. Journal of Translational Medicine
- mTOR pathway activation in age-related retinal disease
- (2016) Chen Zhao et al. Aging-US
- Differential DNA methylation identified in the blood and retina of AMD patients
- (2015) Verity F Oliver et al. Epigenetics
- Patient-Specific Induced Pluripotent Stem Cells for Disease Modeling and Phenotypic Drug Discovery
- (2015) Shibing Tang et al. JOURNAL OF MEDICINAL CHEMISTRY
- Automated, high-throughput derivation, characterization and differentiation of induced pluripotent stem cells
- (2015) Daniel Paull et al. NATURE METHODS
- Reengineering Human Bruch's Membrane Increases Rod Outer Segment Phagocytosis by Human Retinal Pigment Epithelium
- (2015) Ernesto F. Moreira et al. Translational Vision Science & Technology
- Patient-Specific iPSC-Derived RPE for Modeling of Retinal Diseases
- (2015) Huy Nguyen et al. Journal of Clinical Medicine
- Differentiation of Human Protein-Induced Pluripotent Stem Cells toward a Retinal Pigment Epithelial Cell Fate
- (2015) Jie Gong et al. PLoS One
- Smoke Exposure Causes Endoplasmic Reticulum Stress and Lipid Accumulation in Retinal Pigment Epithelium through Oxidative Stress and Complement Activation
- (2014) Kannan Kunchithapautham et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Clinical Classification of Age-related Macular Degeneration
- (2013) Frederick L. Ferris et al. OPHTHALMOLOGY
- Engineering a Blood-Retinal Barrier With Human Embryonic Stem Cell-Derived Retinal Pigment Epithelium: Transcriptome and Functional Analysis
- (2013) Shaomin Peng et al. Stem Cells Translational Medicine
- Systems-level analysis of age-related macular degeneration reveals global biomarkers and phenotype-specific functional networks
- (2012) Aaron M Newman et al. Genome Medicine
- Cell culture model that mimics drusen formation and triggers complement activation associated with age-related macular degeneration
- (2011) L. V. Johnson et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Age-related accumulation of 3-nitrotyrosine and nitro-A2E in human Bruch's membrane
- (2010) L.S. Murdaugh et al. EXPERIMENTAL EYE RESEARCH
- Complement: a key system for immune surveillance and homeostasis
- (2010) Daniel Ricklin et al. NATURE IMMUNOLOGY
- REVIEW PAPER: Animals as Models of Age-Related Macular Degeneration
- (2010) C. J. Zeiss VETERINARY PATHOLOGY
- B-crystallin regulation of angiogenesis by modulation of VEGF
- (2009) S. Kase et al. BLOOD
- The dynamic nature of Bruch's membrane
- (2009) J.C. Booij et al. PROGRESS IN RETINAL AND EYE RESEARCH
Become a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get StartedAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started