Search Results - "Spratt, Kaye"
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Gene Editing of CCR5 in Autologous CD4 T Cells of Persons Infected with HIV
Published in The New England journal of medicine (06-03-2014)“…In this small study, investigators genetically disrupted the HIV receptor CCR5 in CD4 T cells of aviremic persons who were infected with HIV. After reinfusion…”
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Delayed administration of a bio-engineered zinc-finger VEGF-A gene therapy is neuroprotective and attenuates allodynia following traumatic spinal cord injury
Published in PloS one (20-05-2014)“…Following spinal cord injury (SCI) there are drastic changes that occur in the spinal microvasculature, including ischemia, hemorrhage, endothelial cell death…”
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3
An engineered transcription factor which activates VEGF-A enhances recovery after spinal cord injury
Published in Neurobiology of disease (01-02-2010)“…Abstract Spinal cord injury (SCI) leads to local vascular disruption and progressive ischemia, which contribute to secondary degeneration. Enhancing…”
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Treatment of traumatic brain injury using zinc-finger protein gene therapy targeting VEGF-A
Published in Journal of neurotrauma (20-11-2012)“…Vascular endothelial growth factor (VEGF) plays a role in angiogenesis and has been shown to be neuroprotective following central nervous system trauma. In the…”
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Induction of angiogenesis in a mouse model using engineered transcription factors
Published in Nature medicine (01-12-2002)“…The relationship between the structure of zinc-finger protein (ZFP) transcription factors and DNA sequence binding specificity has been extensively studied…”
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A Designed Zinc-finger Transcriptional Repressor of Phospholamban Improves Function of the Failing Heart
Published in Molecular therapy (01-08-2012)“…Selective inhibition of disease-related proteins underpins the majority of successful drug–target interactions. However, development of effective antagonists…”
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Gene Transfer of an Engineered Transcription Factor Promoting Expression of VEGF-A Protects Against Experimental Diabetic Neuropathy
Published in Diabetes (New York, N.Y.) (01-06-2006)“…Gene Transfer of an Engineered Transcription Factor Promoting Expression of VEGF-A Protects Against Experimental Diabetic Neuropathy Sally A. Price 1 , Carolyn…”
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Zinc-Finger Protein-Targeted Gene Regulation: Genomewide Single-Gene Specificity
Published in Proceedings of the National Academy of Sciences - PNAS (14-10-2003)“…Zinc-finger protein transcription factors (ZFP TFs) can be designed to control the expression of any desired target gene, and thus provide potential…”
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Engineered Zinc Finger Protein–Mediated VEGF-A Activation Restores Deficient VEGF-A in Sensory Neurons in Experimental Diabetes
Published in Diabetes (New York, N.Y.) (01-02-2010)“…Engineered Zinc Finger Protein–Mediated VEGF-A Activation Restores Deficient VEGF-A in Sensory Neurons in Experimental Diabetes Elizabeth J. Pawson 1 , Beatriz…”
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ZFN-Mediated Gene Targeting at the Albumin Locus in Liver Results in Therapeutic Levels of Human FIX in Mice and Non-Human Primates
Published in Blood (03-12-2015)“…Hemophilia is an attractive target for gene therapy, since activity levels as low as 1% to 2% of normal are beneficial and levels of ~5% prevent spontaneous…”
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Efficient clinical scale gene modification via zinc finger nuclease-targeted disruption of the HIV co-receptor CCR5
Published in Human gene therapy (01-03-2013)“…Since HIV requires CD4 and a co-receptor, most commonly C-C chemokine receptor 5 (CCR5), for cellular entry, targeting CCR5 expression is an attractive…”
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Persistent and therapeutic concentrations of human factor IX in mice after hepatic gene transfer of recombinant AAV vectors
Published in Nature genetics (01-07-1997)“…Haemophilia B, or factor IX deficiency, is a X-linked recessive disorder that occurs in about one in 25,000 males, and severely affected people are at risk for…”
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Prolonged Production of NADPH Oxidase-Corrected Granulocytes after Gene Therapy of Chronic Granulomatous Disease
Published in Proceedings of the National Academy of Sciences - PNAS (28-10-1997)“…Little is known about the potential for engraftment of autologous hematopoietic stem cells in human adults not subjected to myeloablative conditioning…”
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Efficient and stable adeno-associated virus-mediated transduction in the skeletal muscle of adult immunocompetent mice
Published in Human gene therapy (01-11-1997)“…Recombinant adeno-associated virus (rAAV) vectors were evaluated for gene transfer into the skeletal muscle of adult immunocompetent mice. A study using a…”
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Ocular Gene Transfer with Self-Complementary AAV Vectors
Published in Investigative ophthalmology & visual science (01-07-2007)“…Self-complementary AAV (scAAV) vectors have been developed to circumvent rate-limiting second-strand synthesis in single-stranded AAV vector genomes and to…”
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Gene therapy for traumatic central nervous system injury and stroke using an engineered zinc finger protein that upregulates VEGF-A
Published in Journal of neurotrauma (01-09-2011)“…Recent studies have identified anti-apoptotic functions for vascular endothelial growth factor (VEGF) in the central nervous system (CNS). However, VEGF…”
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Selective uptake and sustained expression of AAV vectors following subcutaneous delivery
Published in The journal of gene medicine (01-01-1999)“…Background Recombinant adeno‐associated viral (rAAV) vectors are capable of long‐term expression of secreted and intracellular proteins following delivery to…”
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Isolation and characterization of the human pulmonary surfactant apoprotein gene
Published in Nature (London) (01-09-1985)“…Pulmonary surfactant is a phospholipid-protein complex which serves to lower the surface tension at the air-liquid interface in the alveoli of the mammalian…”
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Combination dosing of CLN1 gene therapy extends lifespan in a mouse model of infantile neuronal ceroid lipofuscinosis
Published in Molecular genetics and metabolism (01-02-2018)Get full text
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Intravenous administration of CLN3 gene therapy for juvenile neuronal ceroid lipofuscinosis
Published in Molecular genetics and metabolism (01-02-2018)Get full text
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