Pages that link to "Q42850479"

The following pages link to Mimoun Azzouz (Q42850479):

Displaying 46 items.

• The AIRE -230Y Polymorphism Affects AIRE Transcriptional Activity: Potential Influence on AIRE Function in the Thymus (Q28547264) (← links)
• Viral delivery of antioxidant genes as a therapeutic strategy in experimental models of amyotrophic lateral sclerosis (Q30542282) (← links)
• PTEN depletion decreases disease severity and modestly prolongs survival in a mouse model of spinal muscular atrophy (Q30651854) (← links)
• C9ORF72 hexanucleotide repeat exerts toxicity in a stable, inducible motor neuronal cell model, which is rescued by partial depletion of Pten (Q33614811) (← links)
• Phosphatase and tensin homologue/protein kinase B pathway linked to motor neuron survival in human superoxide dismutase 1-related amyotrophic lateral sclerosis (Q33791649) (← links)
• SRSF1-dependent nuclear export inhibition of C9ORF72 repeat transcripts prevents neurodegeneration and associated motor deficits (Q33891056) (← links)
• Optimised and rapid pre-clinical screening in the SOD1(G93A) transgenic mouse model of amyotrophic lateral sclerosis (ALS). (Q34005426) (← links)
• Early detection of motor dysfunction in the SOD1G93A mouse model of Amyotrophic Lateral Sclerosis (ALS) using home cage running wheels (Q34276554) (← links)
• Development and applications of non-HIV-based lentiviral vectors in neurological disorders (Q34902118) (← links)
• Development of Nonviral Vectors Targeting the Brain as a Therapeutic Approach For Parkinson's Disease and Other Brain Disorders. (Q35877637) (← links)
• Lentiviral vectors for treating and modeling human CNS disorders (Q35880080) (← links)
• Comparison of stimulus-evoked cerebral hemodynamics in the awake mouse and under a novel anesthetic regime (Q35896262) (← links)
• Therapeutic gene silencing in neurological disorders, using interfering RNA. (Q36067060) (← links)
• Gene therapy for neurodegenerative and ocular diseases using lentiviral vectors (Q36334985) (← links)
• Gene Therapy for ALS: progress and prospects (Q36522324) (← links)
• AAV9-mediated central nervous system-targeted gene delivery via cisterna magna route in mice (Q36588788) (← links)
• PTEN regulates AMPA receptor-mediated cell viability in iPS-derived motor neurons. (Q37620711) (← links)
• Gene therapy: a promising approach to treating spinal muscular atrophy. (Q38213245) (← links)
• Current developments in gene therapy for amyotrophic lateral sclerosis (Q38470242) (← links)
• Viral delivery of C9orf72 hexanucleotide repeat expansions in mice leads to repeat-length-dependent neuropathology and behavioural deficits (Q38760731) (← links)
• Gene Therapy in the Nervous System: Failures and Successes. (Q40070708) (← links)
• C9orf72 expansion disrupts ATM-mediated chromosomal break repair. (Q40120242) (← links)
• Lentivector-mediated delivery of GDNF protects complex motor functions relevant to human Parkinsonism in a rat lesion model. (Q40347828) (← links)
• Local GDNF expression mediated by lentiviral vector protects facial nerve motoneurons but not spinal motoneurons in SOD1(G93A) transgenic mice (Q40543494) (← links)
• LRP-1-mediated intracellular antibody delivery to the Central Nervous System (Q41571914) (← links)
• PTEN depletion rescues axonal growth defect and improves survival in SMN-deficient motor neurons (Q43043778) (← links)
• Dopamine gene therapy for Parkinson's disease in a nonhuman primate without associated dyskinesia. (Q43109280) (← links)
• Corrigendum: Comparison of stimulus-evoked cerebral hemodynamics in the awake mouse and under a novel anesthetic regime. (Q43230118) (← links)
• Silencing mutant SOD1 using RNAi protects against neurodegeneration and extends survival in an ALS model (Q43628011) (← links)
• Systemic delivery of scAAV9 expressing SMN prolongs survival in a model of spinal muscular atrophy (Q44329621) (← links)
• Site Specific Modification of Adeno-Associated Virus Enables Both Fluorescent Imaging of Viral Particles and Characterization of the Capsid Interactome. (Q45325135) (← links)
• Retinoic acid receptor beta2 promotes functional regeneration of sensory axons in the spinal cord (Q46875564) (← links)
• Deficiency in the mRNA export mediator Gle1 impairs Schwann cell development in the zebrafish embryo (Q47074129) (← links)
• VEGF delivery with retrogradely transported lentivector prolongs survival in a mouse ALS model (Q47427098) (← links)
• Encapsulation of biomacromolecules within polymersomes by electroporation. (Q54195756) (← links)
• Plastin 3 Promotes Motor Neuron Axonal Growth and Extends Survival in a Mouse Model of Spinal Muscular Atrophy. (Q54253770) (← links)
• Translating SOD1 Gene Silencing toward the Clinic: A Highly Efficacious, Off-Target-free, and Biomarker-Supported Strategy for fALS. (Q55399094) (← links)
• Trophic activity of Rabies G protein-pseudotyped equine infectious anemia viral vector mediated IGF-I motor neuron gene transfer in vitro (Q61970599) (← links)
• Transduction Patterns of Pseudotyped Lentiviral Vectors in the Nervous System (Q61970603) (← links)
• Prevention of mutant SOD1 motoneuron degeneration by copper chelatorsin vitro (Q61970604) (← links)
• Progressive motor neuron impairment in an animal model of familial amyotrophic lateral sclerosis (Q61970605) (← links)
• Electromyographical and Motor Performance Studies in thepmnMouse Model of Neurodegenerative Disease (Q61970606) (← links)
• Enhancement of Mouse Sciatic Nerve Regeneration by the Long Chain Fatty Alcohol,N-Hexacosanol (Q61970607) (← links)
• Meta-Analysis of Autoimmune Regulator-Regulated Genes in Human and Murine Models: A Novel Human Model Provides Insights on the Role of Autoimmune Regulator in Regulating STAT1 and STAT1-Regulated Genes. (Q64924555) (← links)
• <i>C9ORF72</i>-derived poly-GA DPRs undergo endocytic uptake in iAstrocytes and spread to motor neurons (Q112700582) (← links)
• SMN-deficient cells exhibit increased ribosomal DNA damage (Q112702392) (← links)