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A Novel Embedded OTP NVM Using Standard Foundry CMOS Logic Technology

2006 21st IEEE Non-Volatile Semiconductor Memory Workshop, 2006, p.24-26

2006

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Impaired production of both normal and mutant C1 inhibitor proteins in type I hereditary angioedema with a duplication in exon 8

The Journal of immunology (1950), 1996-07, Vol.157 (1), p.405-410

1996

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A 15ns 4Mb NVSRAM in 0.13u SONOS Technology

2008 Joint Non-Volatile Semiconductor Memory Workshop and International Conference on Memory Technology and Design, 2008, p.83-86

2008

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Long-term and age-dependent restoration of visual function in a mouse model of CNGB3-associated achromatopsia following gene therapy

Human molecular genetics, 2011-08, Vol.20 (16), p.3161-3175

2011

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Onecut1 is essential for horizontal cell genesis and retinal integrity

The Journal of neuroscience, 2013-08, Vol.33 (32), p.13053-13065

2013

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Compromised phagosome maturation underlies RPE pathology in cell culture and whole animal models of Smith-Lemli-Opitz Syndrome

Autophagy, 2018-10, Vol.14 (10), p.1796-1817

2018

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A partial structural and functional rescue of a retinitis pigmentosa model with compacted DNA nanoparticles

PloS one, 2009-04, Vol.4 (4), p.e5290-e5290

2009

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Inherited Retinal Degeneration Caused by Dehydrodolichyl Diphosphate Synthase Mutation-Effect of an ALG6 Modifier Variant

International journal of molecular sciences, 2024-01, Vol.25 (2), p.1004

2024

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Gerard (“Jerry”) Anthony Lutty, PhD— In Memoriam (1947–2021)

Experimental eye research, 2022-03, Vol.216, p.108949, Article 108949

2022

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Prevention of Retinal Degeneration in a Rat Model of Smith-Lemli-Opitz Syndrome

Scientific reports, 2018-01, Vol.8 (1), p.1286-13, Article 1286

2018

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Insights into the mechanisms of macular degeneration associated with the R172W mutation in RDS

Human molecular genetics, 2014-06, Vol.23 (12), p.3102-3114

2014

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A Dpagt1 Missense Variant Causes Degenerative Retinopathy without Myasthenic Syndrome in Mice

International journal of molecular sciences, 2022-10, Vol.23 (19), p.12005

2022

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A high-density dual-polysilicon 5 volt-only EEPROM cell

International Electron Devices Meeting 1991 [Technical Digest], 1991, p.299-302

1991

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A Dhdds K42E knock-in RP59 mouse model shows inner retina pathology and defective synaptic transmission

Cell death & disease, 2023-07, Vol.14 (7), p.420-420, Article 420

2023

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Gene delivery to mitotic and postmitotic photoreceptors via compacted DNA nanoparticles results in improved phenotype in a mouse model of retinitis pigmentosa

The FASEB journal, 2010-04, Vol.24 (4), p.1178-1191

2010

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Long-term and age-dependent restoration of visual function in a mouse model of CNGB3-associated achromatopsia following gene therapy

Human molecular genetics, 2011-08, Vol.20 (16), p.3161-3175

2011

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Early-onset, slow progression of cone photoreceptor dysfunction and degeneration in CNG channel subunit CNGB3 deficiency

Investigative ophthalmology & visual science, 2011-05, Vol.52 (6), p.3557-3566

2011

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Retinal degeneration in a rat model of Smith-Lemli-Opitz Syndrome: thinking beyond cholesterol deficiency

Advances in experimental medicine and biology, 2010, Vol.664, p.481

Fliesler, Steven J

2010

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Dependence of visual and cognitive outcomes on animal holder configuration in a rodent model of blast overpressure exposure

Vision research (Oxford), 2021-11, Vol.188, p.162-173

2021

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Loss of Caveolin-1 Impairs Retinal Function Due to Disturbance of Subretinal Microenvironment

The Journal of biological chemistry, 2012-05, Vol.287 (20), p.16424-16434

2012

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Differential developmental deficits in retinal function in the absence of either protein tyrosine sulfotransferase-1 or -2

PloS one, 2012-06, Vol.7 (6), p.e39702-e39702

2012

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Peroxisome deficiency-induced ER stress and SREBP-2 pathway activation in the liver of newborn PEX2 knock-out mice

Biochimica et biophysica acta, 2012-06, Vol.1821 (6), p.895-907

2012

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Peroxisome Deficiency Causes a Complex Phenotype because of Hepatic SREBP/Insig Dysregulation Associated with Endoplasmic Reticulum Stress

The Journal of biological chemistry, 2009-03, Vol.284 (11), p.7232-7245

2009

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The Relationship between Opsin Overexpression and Photoreceptor Degeneration

Investigative ophthalmology & visual science, 2001-03, Vol.42 (3), p.589-600

2001

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Author Correction: Prevention of Retinal Degeneration in a Rat Model of Smith-Lemli-Opitz Syndrome

Scientific reports, 2018-03, Vol.8 (1), p.4289-3, Article 4289

2018

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A Novel Embedded OTP NVM Using Standard Foundry CMOS Logic Technology

Impaired production of both normal and mutant C1 inhibitor proteins in type I hereditary angioedema with a duplication in exon 8

A 15ns 4Mb NVSRAM in 0.13u SONOS Technology

Long-term and age-dependent restoration of visual function in a mouse model of CNGB3-associated achromatopsia following gene therapy

Onecut1 is essential for horizontal cell genesis and retinal integrity

Compromised phagosome maturation underlies RPE pathology in cell culture and whole animal models of Smith-Lemli-Opitz Syndrome

A partial structural and functional rescue of a retinitis pigmentosa model with compacted DNA nanoparticles

Inherited Retinal Degeneration Caused by Dehydrodolichyl Diphosphate Synthase Mutation-Effect of an ALG6 Modifier Variant

Gerard (“Jerry”) Anthony Lutty, PhD— In Memoriam (1947–2021)

Prevention of Retinal Degeneration in a Rat Model of Smith-Lemli-Opitz Syndrome

Insights into the mechanisms of macular degeneration associated with the R172W mutation in RDS

A Dpagt1 Missense Variant Causes Degenerative Retinopathy without Myasthenic Syndrome in Mice

A high-density dual-polysilicon 5 volt-only EEPROM cell

A Dhdds K42E knock-in RP59 mouse model shows inner retina pathology and defective synaptic transmission

Gene delivery to mitotic and postmitotic photoreceptors via compacted DNA nanoparticles results in improved phenotype in a mouse model of retinitis pigmentosa

Long-term and age-dependent restoration of visual function in a mouse model of CNGB3-associated achromatopsia following gene therapy

Early-onset, slow progression of cone photoreceptor dysfunction and degeneration in CNG channel subunit CNGB3 deficiency

Retinal degeneration in a rat model of Smith-Lemli-Opitz Syndrome: thinking beyond cholesterol deficiency

Dependence of visual and cognitive outcomes on animal holder configuration in a rodent model of blast overpressure exposure

Loss of Caveolin-1 Impairs Retinal Function Due to Disturbance of Subretinal Microenvironment

Differential developmental deficits in retinal function in the absence of either protein tyrosine sulfotransferase-1 or -2

Peroxisome deficiency-induced ER stress and SREBP-2 pathway activation in the liver of newborn PEX2 knock-out mice

Peroxisome Deficiency Causes a Complex Phenotype because of Hepatic SREBP/Insig Dysregulation Associated with Endoplasmic Reticulum Stress

The Relationship between Opsin Overexpression and Photoreceptor Degeneration

Author Correction: Prevention of Retinal Degeneration in a Rat Model of Smith-Lemli-Opitz Syndrome

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