Limited astrocyte-to-neuron conversion in the mouse brain using NeuroD1 overexpression
Published 2022 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Limited astrocyte-to-neuron conversion in the mouse brain using NeuroD1 overexpression
Authors
Keywords
astrocytes, neurons, conversion, transdifferentiation, neurodegeneration, gene therapy, adeno-associated virus
Journal
MOLECULAR THERAPY
Volume -, Issue -, Pages -
Publisher
Elsevier BV
Online
2022-02-05
DOI
10.1016/j.ymthe.2022.01.028
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Regeneration of Functional Neurons After Spinal Cord Injury via in situ NeuroD1-Mediated Astrocyte-to-Neuron Conversion
- (2021) Brendan Puls et al. Frontiers in Cell and Developmental Biology
- Therapeutically viable generation of neurons with antisense oligonucleotide suppression of PTB
- (2021) Roy Maimon et al. NATURE NEUROSCIENCE
- Restoration of Visual Function and Cortical Connectivity After Ischemic Injury Through NeuroD1-Mediated Gene Therapy
- (2021) Yu Tang et al. Frontiers in Cell and Developmental Biology
- Revisiting astrocyte to neuron conversion with lineage tracing in vivo
- (2021) Lei-Lei Wang et al. CELL
- In vivo confusion over in vivo conversion
- (2021) Gong Chen MOLECULAR THERAPY
- Gene therapy conversion of striatal astrocytes into GABAergic neurons in mouse models of Huntington’s disease
- (2020) Zheng Wu et al. Nature Communications
- Glia-to-Neuron Conversion by CRISPR-CasRx Alleviates Symptoms of Neurological Disease in Mice
- (2020) Haibo Zhou et al. CELL
- Reversing a model of Parkinson’s disease with in situ converted nigral neurons
- (2020) Hao Qian et al. NATURE
- Non-engineered and Engineered Adult Neurogenesis in Mammalian Brains
- (2019) Wenliang Lei et al. Frontiers in Neuroscience
- A NeuroD1 AAV-Based Gene Therapy for Functional Brain Repair after Ischemic Injury through In Vivo Astrocyte-to-Neuron Conversion
- (2019) Yu-Chen Chen et al. MOLECULAR THERAPY
- Engineered AAVs for efficient noninvasive gene delivery to the central and peripheral nervous systems
- (2017) Ken Y Chan et al. NATURE NEUROSCIENCE
- A MicroRNA124 Target Sequence Restores Astrocyte Specificity of gfaABC 1 D-Driven Transgene Expression in AAV-Mediated Gene Transfer
- (2017) Grit Taschenberger et al. Molecular Therapy-Nucleic Acids
- NEUROD1 Instructs Neuronal Conversion in Non-Reactive Astrocytes
- (2017) Rebecca Brulet et al. Stem Cell Reports
- New Transgenic Mouse Lines for Selectively Targeting Astrocytes and Studying Calcium Signals in Astrocyte Processes In Situ and In Vivo
- (2016) Rahul Srinivasan et al. NEURON
- Engineering of Adult Neurogenesis and Gliogenesis
- (2016) Benedikt Berninger et al. Cold Spring Harbor Perspectives in Biology
- Ascl1 Converts Dorsal Midbrain Astrocytes into Functional Neurons In Vivo
- (2015) Y. Liu et al. JOURNAL OF NEUROSCIENCE
- CEND1 and NEUROGENIN2 Reprogram Mouse Astrocytes and Embryonic Fibroblasts to Induced Neural Precursors and Differentiated Neurons
- (2015) Katerina Aravantinou-Fatorou et al. Stem Cell Reports
- In Vivo Direct Reprogramming of Reactive Glial Cells into Functional Neurons after Brain Injury and in an Alzheimer’s Disease Model
- (2013) Ziyuan Guo et al. Cell Stem Cell
- In vivo reprogramming of astrocytes to neuroblasts in the adult brain
- (2013) Wenze Niu et al. NATURE CELL BIOLOGY
- Generation of induced neurons via direct conversion in vivo
- (2013) O. Torper et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Environmental impact on direct neuronal reprogramming in vivo in the adult brain
- (2013) Andrew Grande et al. Nature Communications
- Rational Design of Therapeutic siRNAs: Minimizing Off-targeting Potential to Improve the Safety of RNAi Therapy for Huntington's Disease
- (2011) Ryan L Boudreau et al. MOLECULAR THERAPY
- Directing Astroglia from the Cerebral Cortex into Subtype Specific Functional Neurons
- (2010) Christophe Heinrich et al. PLOS BIOLOGY
- GFAPpromoter elements required for region-specific and astrocyte-specific expression
- (2008) Youngjin Lee et al. GLIA
- Intraventricular Enzyme Replacement Improves Disease Phenotypes in a Mouse Model of Late Infantile Neuronal Ceroid Lipofuscinosis
- (2008) Michael Chang et al. MOLECULAR THERAPY
- Artificial miRNAs mitigate shRNA-mediated toxicity in the brain: Implications for the therapeutic development of RNAi
- (2008) J. L. McBride et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Add your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload NowBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started