Kevin D. Foust

Publications

• Intravenous AAV9 Efficiently Transduces Myenteric Neurons in Neonate and Juvenile Mice
  Frontiers in Molecular Neuroscience. 2014  |   Pubmed ID: 25360081
• Improving Single Injection CSF Delivery of AAV9-mediated Gene Therapy for SMA - a Dose Response Study in Mice and Nonhuman Primates
  Molecular Therapy : the Journal of the American Society of Gene Therapy. Oct, 2014  |   Pubmed ID: 25358252
• Microglia Induce Motor Neuron Death Via the Classical NF-κB Pathway in Amyotrophic Lateral Sclerosis
  Neuron. Mar, 2014  |   Pubmed ID: 24607225
• Therapeutic AAV9-mediated Suppression of Mutant SOD1 Slows Disease Progression and Extends Survival in Models of Inherited ALS
  Molecular Therapy : the Journal of the American Society of Gene Therapy. Dec, 2013  |   Pubmed ID: 24008656
• Systemic Delivery of MeCP2 Rescues Behavioral and Cellular Deficits in Female Mouse Models of Rett Syndrome
  The Journal of Neuroscience : the Official Journal of the Society for Neuroscience. Aug, 2013  |   Pubmed ID: 23966684
• Targeted Delivery of Self-complementary Adeno-associated Virus Serotype 9 to the Brain, Using Magnetic Resonance Imaging-guided Focused Ultrasound
  Human Gene Therapy. Nov, 2012  |   Pubmed ID: 22838844
• Adeno-associated Virus Serotype 9 Transduction in the Central Nervous System of Nonhuman Primates
  Human Gene Therapy. Apr, 2012  |   Pubmed ID: 22201473
• A Single Administration of Morpholino Antisense Oligomer Rescues Spinal Muscular Atrophy in Mouse
  Human Molecular Genetics. Apr, 2012  |   Pubmed ID: 22186025
• Recombinant AAV Delivery to the Central Nervous System
  Methods in Molecular Biology (Clifton, N.J.). 2011  |   Pubmed ID: 22034030
• Astrocytes from Familial and Sporadic ALS Patients Are Toxic to Motor Neurons
  Nature Biotechnology. Sep, 2011  |   Pubmed ID: 21832997
• Systemic Gene Delivery in Large Species for Targeting Spinal Cord, Brain, and Peripheral Tissues for Pediatric Disorders
  Molecular Therapy : the Journal of the American Society of Gene Therapy. Nov, 2011  |   Pubmed ID: 21811247
• A Role for Glia in the Progression of Rett's Syndrome
  Nature. Jul, 2011  |   Pubmed ID: 21716289
• Early Heart Failure in the SMNDelta7 Model of Spinal Muscular Atrophy and Correction by Postnatal ScAAV9-SMN Delivery
  Human Molecular Genetics. Oct, 2010  |   Pubmed ID: 20639395
• Rescue of the Spinal Muscular Atrophy Phenotype in a Mouse Model by Early Postnatal Delivery of SMN
  Nature Biotechnology. Mar, 2010  |   Pubmed ID: 20190738
• Over the Barrier and Through the Blood: to CNS Delivery We Go
  Cell Cycle (Georgetown, Tex.). Dec, 2009  |   Pubmed ID: 19949299
• AAV As a Gene Transfer Vector for the Treatment of Neurological Disorders: Novel Treatment Thoughts for ALS
  Current Gene Therapy. Oct, 2009  |   Pubmed ID: 19860657
• Nigrostriatal RAAV-mediated GDNF Overexpression Induces Robust Weight Loss in a Rat Model of Age-related Obesity
  Molecular Therapy : the Journal of the American Society of Gene Therapy. Jun, 2009  |   Pubmed ID: 19277011
• Intravascular AAV9 Preferentially Targets Neonatal Neurons and Adult Astrocytes
  Nature Biotechnology. Jan, 2009  |   Pubmed ID: 19098898
• Recombinant Adeno-associated Virus-mediated Global Anterograde Delivery of Glial Cell Line-derived Neurotrophic Factor to the Spinal Cord: Comparison of Rubrospinal and Corticospinal Tracts in the Rat
  Human Gene Therapy. Jan, 2008  |   Pubmed ID: 18072858
• Neonatal Intraperitoneal or Intravenous Injections of Recombinant Adeno-associated Virus Type 8 Transduce Dorsal Root Ganglia and Lower Motor Neurons
  Human Gene Therapy. Jan, 2008  |   Pubmed ID: 18052722
• Recombinant Adeno-associated Viral Vectors As Therapeutic Agents to Treat Neurological Disorders
  Molecular Therapy : the Journal of the American Society of Gene Therapy. Mar, 2006  |   Pubmed ID: 16412695