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Non-ATG-initiated translation directed by microsatellite expansions

Proceedings of the National Academy of Sciences - PNAS, 2011-01, Vol.108 (1), p.260-265

2011

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Prevention of Neurocognitive Deficiency in Mucopolysaccharidosis Type II Mice by Central Nervous System-Directed, AAV9-Mediated Iduronate Sulfatase Gene Transfer

Human gene therapy, 2017-08, Vol.28 (8), p.626-638

2017

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Amelioration of Ischemic Brain Injury in Rats with Human Umbilical Cord Blood Stem Cells: Mechanisms of Action

Cell transplantation, 2016-01, Vol.25 (8), p.1473-1488

2016

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Comparative Effectiveness of Intracerebroventricular, Intrathecal, and Intranasal Routes of AAV9 Vector Administration for Genetic Therapy of Neurologic Disease in Murine Mucopolysaccharidosis Type I

Frontiers in molecular neuroscience, 2021-05, Vol.14, p.618360-618360

2021

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SDF-1 overexpression by mesenchymal stem cells enhances GAP-43-positive axonal growth following spinal cord injury

Restorative neurology and neuroscience, 2017-01, Vol.35 (4), p.395-411

2017

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Direct gene transfer to the CNS prevents emergence of neurologic disease in a murine model of mucopolysaccharidosis type I

Neurobiology of disease, 2011-07, Vol.43 (1), p.123-133

2011

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Comparison of Endovascular and Intraventricular Gene Therapy With Adeno-Associated Virus–α-L-Iduronidase for Hurler Disease

Neurosurgery, 2014-01, Vol.74 (1), p.99-111

2014

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Effects of Bone-Marrow–Derived MSC Transplantation on Functional Recovery in a Rat Model of Spinal Cord Injury

Cell transplantation, 2017-08, Vol.26 (8), p.1472-1482

2017

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Tauroursodeoxycholic Acid Reduces Apoptosis and Protects against Neurological Injury after Acute Hemorrhagic Stroke in Rats

Proceedings of the National Academy of Sciences - PNAS, 2003-05, Vol.100 (10), p.6087-6092

2003

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Intracerebroventricular Transplantation of Human Bone Marrow-Derived Multipotent Progenitor Cells in an Immunodeficient Mouse Model of Mucopolysaccharidosis Type I (MPS-I)

Cell transplantation, 2012-01, Vol.21 (7), p.1577-1593

2012

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Characterization of an immunodeficient mouse model of mucopolysaccharidosis type I suitable for preclinical testing of human stem cell and gene therapy

Brain research bulletin, 2007-11, Vol.74 (6), p.429-438

2007

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Effects of Bone-Marrow–Derived MSC Transplantation on Functional Recovery in a Rat Model of Spinal Cord Injury: Comparisons of Transplant Locations and Cell Concentrations

Cell transplantation, 2017-08, Vol.26 (8), p.1472-1482

2017

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Transplantation of a Novel Cell Line Population of Umbilical Cord Blood Stem Cells Ameliorates Neurological Deficits Associated with Ischemic Brain Injury

Stem cells and development, 2005-12, Vol.14 (6), p.722-733

2005

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Effects of bone-marrow-derived MSC transplantation on functional recovery in a rat model of spinal cord injury: comparisons of transplant locations and cell concentrations

Cell transplantation, 2017

2017

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Lysosomal enzyme can bypass the blood–brain barrier and reach the CNS following intranasal administration

Molecular genetics and metabolism, 2012-05, Vol.106 (1), p.131-134

2012

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Infusion of Human Umbilical Cord Blood Ameliorates Neurologic Deficits in Rats with Hemorrhagic Brain Injury

Annals of the New York Academy of Sciences, 2005-05, Vol.1049 (1), p.84-96

2005

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Poster 158 Developmental Myosin Expression in Skeletal Muscle Post-Stroke

Archives of physical medicine and rehabilitation, 2011, Vol.92 (10), p.1737-1737

2011

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Poster 85: Influence of Spontaneous Physical Activity on Muscle Plasticity Poststroke

Archives of physical medicine and rehabilitation, 2010, Vol.91 (10), p.e30-e30

2010

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Spatial Navigation and Working Memory Tests Demonstrate Neurological Deficits in a Murine Model of Mucopolysaccharidosis Type II (Hunter Syndrome)

Molecular genetics and metabolism, 2012-02, Vol.105 (2), p.S48-S48

2012

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Intrathecal and intranasal infusion of adeno-associated virus vector: non-invasive routes of administration achieving corrective levels of iduronidase expression throughout the brain for gene therapy of mucopolysaccharidosis type I

Molecular genetics and metabolism, 2014-02, Vol.111 (2), p.S75-S76

2014

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Gene therapy for Hunter syndrome: Prevention of neurocognitive deficit in MPS II mice by engraftment with lentiviral vector-transduced hematopoietic stem cells (HSC) but not with wild type HSC

Molecular genetics and metabolism, 2013-02, Vol.108 (2), p.S64-S64

2013

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Increased Longevity and Metabolic Correction Following Syngeneic Bone Marrow Transplantation in a Murine Model of Mucopolysaccharidosis Type I

Bone marrow transplantation (Basingstoke), 2011-12, Vol.47 (9), p.1235-1240

2011

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152. Long-term biochemical and neurobehavioral correction in a murine model of mucopolysaccharidosis type I following neonatal intracerebroventricular administration of a therapeutic adeno-associated virus vector

Molecular genetics and metabolism, 2010-02, Vol.99 (2), p.S40

2010

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153. Syngeneic Bone marrow transplantation in a murine model of mucopolysaccharidosis type I

Molecular genetics and metabolism, 2009-02, Vol.96 (2), p.S46-S46

2009

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86. Ex vivo lentiviral gene transfer targeting hematopoietic stem cells for therapy of mucopolysaccharidosis type, Hunter syndrome

Molecular genetics and metabolism, 2009-02, Vol.96 (2), p.S30-S31

2009

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Non-ATG-initiated translation directed by microsatellite expansions

Prevention of Neurocognitive Deficiency in Mucopolysaccharidosis Type II Mice by Central Nervous System-Directed, AAV9-Mediated Iduronate Sulfatase Gene Transfer

Amelioration of Ischemic Brain Injury in Rats with Human Umbilical Cord Blood Stem Cells: Mechanisms of Action

Comparative Effectiveness of Intracerebroventricular, Intrathecal, and Intranasal Routes of AAV9 Vector Administration for Genetic Therapy of Neurologic Disease in Murine Mucopolysaccharidosis Type I

SDF-1 overexpression by mesenchymal stem cells enhances GAP-43-positive axonal growth following spinal cord injury

Direct gene transfer to the CNS prevents emergence of neurologic disease in a murine model of mucopolysaccharidosis type I

Comparison of Endovascular and Intraventricular Gene Therapy With Adeno-Associated Virus–α-L-Iduronidase for Hurler Disease

Effects of Bone-Marrow–Derived MSC Transplantation on Functional Recovery in a Rat Model of Spinal Cord Injury

Tauroursodeoxycholic Acid Reduces Apoptosis and Protects against Neurological Injury after Acute Hemorrhagic Stroke in Rats

Intracerebroventricular Transplantation of Human Bone Marrow-Derived Multipotent Progenitor Cells in an Immunodeficient Mouse Model of Mucopolysaccharidosis Type I (MPS-I)

Characterization of an immunodeficient mouse model of mucopolysaccharidosis type I suitable for preclinical testing of human stem cell and gene therapy

Effects of Bone-Marrow–Derived MSC Transplantation on Functional Recovery in a Rat Model of Spinal Cord Injury: Comparisons of Transplant Locations and Cell Concentrations

Transplantation of a Novel Cell Line Population of Umbilical Cord Blood Stem Cells Ameliorates Neurological Deficits Associated with Ischemic Brain Injury

Effects of bone-marrow-derived MSC transplantation on functional recovery in a rat model of spinal cord injury: comparisons of transplant locations and cell concentrations

Lysosomal enzyme can bypass the blood–brain barrier and reach the CNS following intranasal administration

Infusion of Human Umbilical Cord Blood Ameliorates Neurologic Deficits in Rats with Hemorrhagic Brain Injury

Poster 158 Developmental Myosin Expression in Skeletal Muscle Post-Stroke

Poster 85: Influence of Spontaneous Physical Activity on Muscle Plasticity Poststroke

Spatial Navigation and Working Memory Tests Demonstrate Neurological Deficits in a Murine Model of Mucopolysaccharidosis Type II (Hunter Syndrome)

Intrathecal and intranasal infusion of adeno-associated virus vector: non-invasive routes of administration achieving corrective levels of iduronidase expression throughout the brain for gene therapy of mucopolysaccharidosis type I

Gene therapy for Hunter syndrome: Prevention of neurocognitive deficit in MPS II mice by engraftment with lentiviral vector-transduced hematopoietic stem cells (HSC) but not with wild type HSC

Increased Longevity and Metabolic Correction Following Syngeneic Bone Marrow Transplantation in a Murine Model of Mucopolysaccharidosis Type I

152. Long-term biochemical and neurobehavioral correction in a murine model of mucopolysaccharidosis type I following neonatal intracerebroventricular administration of a therapeutic adeno-associated virus vector

153. Syngeneic Bone marrow transplantation in a murine model of mucopolysaccharidosis type I

86. Ex vivo lentiviral gene transfer targeting hematopoietic stem cells for therapy of mucopolysaccharidosis type, Hunter syndrome

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