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Suppression of Retinal Neovascularization in vivo by Inhibition of Vascular Endothelial Growth Factor (VEGF) Using Soluble VEGF-Receptor Chimeric Proteins

Proceedings of the National Academy of Sciences - PNAS, 1995-11, Vol.92 (23), p.10457-10461

1995

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Vascular Endothelial Growth Factor/Vascular Permeability Factor Expression in a Mouse Model of Retinal Neovascularization

Proceedings of the National Academy of Sciences - PNAS, 1995-01, Vol.92 (3), p.905-909

1995

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We need collaboration and co-creation to address challenges facing coastal communities

Nature human behaviour, 2024-05, Vol.8 (5), p.814-822

2024

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Site-specific gene modification by oligodeoxynucleotides in mouse bone marrow-derived mesenchymal stem cells

Gene therapy, 2008-07, Vol.15 (14), p.1035-1048

2008

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Oligodeoxynucleotides Inhibit Retinal Neovascularization in a Murine Model of Proliferative Retinopathy

Proceedings of the National Academy of Sciences - PNAS, 1996-05, Vol.93 (10), p.4851-4856

1996

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Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosa

Nature genetics, 1999-07, Vol.22 (3), p.248-254

1999

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Oligonucleotide-directed single-base DNA alterations in mouse embryonic stem cells

Gene therapy, 2003-01, Vol.10 (1), p.24-33

2003

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Disease Expression of RP1 Mutations Causing Autosomal Dominant Retinitis Pigmentosa

Investigative ophthalmology & visual science, 2000-06, Vol.41 (7), p.1898-1908

2000

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Delivery and mechanistic considerations for the production of knock-in mice by single-stranded oligonucleotide gene targeting

Gene therapy, 2007-02, Vol.14 (4), p.304-315

2007

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Clinical Features and Mutations in Patients with Dominant Retinitis Pigmentosa-1 (RP1)

Investigative ophthalmology & visual science, 2001-09, Vol.42 (10), p.2217-2224

2001

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Human neutrophil cytochrome b light chain (p22-phox) : gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease

The Journal of clinical investigation, 1990-11, Vol.86 (5), p.1729-1737

1990

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Cyclone Harold and the role of traditional knowledge in fostering resilience in Vanuatu

Australasian journal of disaster and trauma studies, 2022-08, Vol.26 (1), p.41-60

2022

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Pathways to photoreceptor cell death in inherited retinal degenerations

BioEssays, 2001-07, Vol.23 (7), p.605-618

Pierce, Eric A.

2001

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Necrotizing pancreatitis: contemporary analysis of 99 consecutive cases

Annals of surgery, 2001-10, Vol.234 (4), p.572-580

2001

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Point Mutation in the Cytoplasmic Domain of the Neutrophil p22-phox Cytochrome b Subunit is Associated with a Nonfunctional NADPH Oxidase and Chronic Granulomatous Disease

Proceedings of the National Academy of Sciences - PNAS, 1991-12, Vol.88 (24), p.11231-11235

1991

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Regulation of vascular endothelial growth factor by oxygen in a model of retinopathy of prematurity

Archives of ophthalmology (1960), 1996-10, Vol.114 (10), p.1219

1996

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Identification and Subcellular Localization of the RP1 Protein in Human and Mouse Photoreceptors

Investigative ophthalmology & visual science, 2002-01, Vol.43 (1), p.22-32

2002

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Human Neuropilin-1 and Neuropilin-2 Map to 10p12 and 2q34, Respectively

Genomics (San Diego, Calif.), 1999-05, Vol.57 (3), p.459-460

1999

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Progressive Photoreceptor Degeneration, Outer Segment Dysplasia, and Rhodopsin Mislocalization in Mice with Targeted Disruption of the Retinitis Pigmentosa-1 (Rp1) Gene

Proceedings of the National Academy of Sciences - PNAS, 2002-04, Vol.99 (8), p.5698-5703

2002

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AAV2 gene therapy readministration in three adults with congenital blindness

Science translational medicine, 2012-02, Vol.4 (120), p.120ra15

2012

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Identification of the porcine intestinal 1,25-dihydroxyvitamin D3 receptor on sodium dodecyl sulfate/polyacrylamide gels by renaturation and immunoblotting

Proceedings of the National Academy of Sciences - PNAS, 1985-12, Vol.82 (23), p.7825-7829

1985

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Retinal expression, regulation, and functional bioactivity of prostacyclin-stimulating factor

The Journal of clinical investigation, 2000-08, Vol.106 (4), p.541-550

2000

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Retinal degeneration and failure of photoreceptor outer segment formation in mice with targeted deletion of the Joubert syndrome gene, Ahi1

The Journal of neuroscience, 2010-06, Vol.30 (26), p.8759-8768

2010

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Acquisition errors in the absence of experience

The Behavioral and brain sciences, 1991-12, Vol.14 (4), p.628-629

Pierce, A. E.

1991

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Suppression of Retinal Neovascularization in vivo by Inhibition of Vascular Endothelial Growth Factor (VEGF) Using Soluble VEGF-Receptor Chimeric Proteins

Vascular Endothelial Growth Factor/Vascular Permeability Factor Expression in a Mouse Model of Retinal Neovascularization

We need collaboration and co-creation to address challenges facing coastal communities

Site-specific gene modification by oligodeoxynucleotides in mouse bone marrow-derived mesenchymal stem cells

Oligodeoxynucleotides Inhibit Retinal Neovascularization in a Murine Model of Proliferative Retinopathy

Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosa

Oligonucleotide-directed single-base DNA alterations in mouse embryonic stem cells

Disease Expression of RP1 Mutations Causing Autosomal Dominant Retinitis Pigmentosa

Delivery and mechanistic considerations for the production of knock-in mice by single-stranded oligonucleotide gene targeting

Clinical Features and Mutations in Patients with Dominant Retinitis Pigmentosa-1 (RP1)

Human neutrophil cytochrome b light chain (p22-phox) : gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease

Cyclone Harold and the role of traditional knowledge in fostering resilience in Vanuatu

Pathways to photoreceptor cell death in inherited retinal degenerations

Necrotizing pancreatitis: contemporary analysis of 99 consecutive cases

Point Mutation in the Cytoplasmic Domain of the Neutrophil p22-phox Cytochrome b Subunit is Associated with a Nonfunctional NADPH Oxidase and Chronic Granulomatous Disease

Regulation of vascular endothelial growth factor by oxygen in a model of retinopathy of prematurity

Identification and Subcellular Localization of the RP1 Protein in Human and Mouse Photoreceptors

Human Neuropilin-1 and Neuropilin-2 Map to 10p12 and 2q34, Respectively

Progressive Photoreceptor Degeneration, Outer Segment Dysplasia, and Rhodopsin Mislocalization in Mice with Targeted Disruption of the Retinitis Pigmentosa-1 (Rp1) Gene

AAV2 gene therapy readministration in three adults with congenital blindness

Safety and durability of effect of contralateral-eye administration of AAV2 gene therapy in patients with childhood-onset blindness caused by RPE65 mutations: a follow-on phase 1 trial

Identification of the porcine intestinal 1,25-dihydroxyvitamin D3 receptor on sodium dodecyl sulfate/polyacrylamide gels by renaturation and immunoblotting

Retinal expression, regulation, and functional bioactivity of prostacyclin-stimulating factor

Retinal degeneration and failure of photoreceptor outer segment formation in mice with targeted deletion of the Joubert syndrome gene, Ahi1

Acquisition errors in the absence of experience

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