T Michael Redmond

发表

Safety and efficacy of gene transfer for Leber's congenital amaurosis.

Kathleen A. Marshall, R. Hertle, M. Maguire, 2008, The New England journal of medicine.

In vivo assessment of rodent retinal structure using spectral domain optical coherence tomography.

C. Grimm, M. Seeliger, P. Humphries, 2012, Advances in experimental medicine and biology.

Impairment of the transient pupillary light reflex in Rpe65(-/-) mice and humans with leber congenital amaurosis.

Krzysztof Palczewski, Jean Bennett, A. V. Cideciyan, 2004, Investigative ophthalmology & visual science.

Protection of Rpe65-deficient mice identifies rhodopsin as a mediator of light-induced retinal degeneration

Farhad Hafezi, Andreas Wenzel, C. Grimm, 2000, Nature Genetics.

Gene Therapy for Leber's Congenital Amaurosis is Safe and Effective Through 1.5 Years After Vector Administration

Jean Bennett, Gui-Shuang Ying, Francesco Testa, 2009, Molecular therapy : the journal of the American Society of Gene Therapy.

Spectral domain optical coherence tomography in mouse models of retinal degeneration.

Andreas Wenzel, C. Grimm, A. Wenzel, 2009, Investigative ophthalmology & visual science.

Isolation and characterization of monkey interphotoreceptor retinoid-binding protein, a unique extracellular matrix component of the retina.

G. Chader, T Michael Redmond, F. Robey, 1985, Biochemistry.

The dual roles of RPE65 S-palmitoylation in membrane association and visual cycle function

S. Uppal, T Michael Redmond, E. Poliakov, 2019, Scientific Reports.

Correlation of regenerable opsin with rod ERG signal in Rpe65-/- mice during development and aging.

Jian-xing Ma, R. Crouch, Z. Ablonczy, 2002, Investigative ophthalmology & visual science.

Expression of β-Carotene 15,15′ Monooxygenase in Retina and RPE-Choroid

S. Bernstein, A. Boulanger, R. Fariss, 2003, Investigative Opthalmology & Visual Science.

A History of the Classical Visual Cycle.

J. Nickerson, T Michael Redmond, Charles B. Wright, 2015, Progress in molecular biology and translational science.

Inhibitory effects of fenretinide metabolites N-[4-methoxyphenyl]retinamide (MPR) and 4-oxo-N-(4-hydroxyphenyl)retinamide (3-keto-HPR) on fenretinide molecular targets β-carotene oxygenase 1, stearoyl-CoA desaturase 1 and dihydroceramide Δ4-desaturase 1

Danielle B. Gutierrez, T Michael Redmond, E. Poliakov, 2017, PloS one.

The mechanism of fenretinide (4-HPR) inhibition of β-carotene monooxygenase 1. New suspect for the visual side effects of fenretinide.

A. Gubin, T Michael Redmond, E. Poliakov, 2012, Advances in experimental medicine and biology.

[46] Genetic analysis of RPE65: From human disease to mouse model

C. Hamel, T Michael Redmond, 2000 .

Organ distribution of transgene expression following intranasal mucosal delivery of recombinant replication-defective adenovirus gene transfer vector

P. Rakoczy, Xiaohuai Zhou, C. Lai, 2008, Genetic vaccines and therapy.

Expression of ABCA4 in the retinal pigment epithelium and its implications for Stargardt macular degeneration

S. Sarfare, D. Bok, M. Radeke, 2018, Proceedings of the National Academy of Sciences.

Key Role of Conserved Histidines in Recombinant Mouse β-Carotene 15,15′-Monooxygenase-1 Activity*

T Michael Redmond, N. J. Miller-Ihli, E. Poliakov, 2005, Journal of Biological Chemistry.

A developmentally regulated microsomal protein specific for the pigment epithelium of the vertebrate retina

E. Harris, C. Hamel, T Michael Redmond, 1993, Journal of neuroscience research.

Cloning of cDNAs encoding human interphotoreceptor retinoid-binding protein (IRBP) and comparison with bovine IRBP sequences.

J. Nickerson, T Michael Redmond, J. Si, 1989, Gene.

Utility of In Vitro Mutagenesis of RPE65 Protein for Verification of Mutational Pathogenicity Before Gene Therapy.

J. Bennett, M. Gorin, M. Borchert, 2019, JAMA ophthalmology.

Inflammatory cytokines regulate microRNA-155 expression in human retinal pigment epithelial cells by activating JAK/STAT pathway.

T Michael Redmond, J. Hooks, C. Vijayasarathy, 2010, Biochemical and biophysical research communications.

Uveitis induced in primates by IRBP: humoral and cellular immune responses.

G. Chader, I. Gery, T. Kuwabara, 1987, Experimental eye research.

Interspecies conservation of structure of interphotoreceptor retinoid-binding protein. Similarities and differences as adjudged by peptide mapping and N-terminal sequencing.

G. Chader, T Michael Redmond, F. Robey, 1986, The Biochemical journal.

Extracellular cGMP phosphodiesterase related to the rod outer segment phosphodiesterase isolated from bovine and monkey retinas.

G. Chader, J. Passonneau, T Michael Redmond, 1985, Biochemistry.

RPE65 Is an Iron(II)-dependent Isomerohydrolase in the Retinoid Visual Cycle*

Ying Chen, Jian-xing Ma, R. Crouch, 2006, Journal of Biological Chemistry.

A comprehensive clinical and biochemical functional study of a novel RPE65 hypomorphic mutation.

B. Lorenz, C. Friedburg, M. Preising, 2008, Investigative ophthalmology & visual science.

RPE65 takes on another role in the vertebrate retina

T Michael Redmond, 2017, Proceedings of the National Academy of Sciences.

Inhibition of thyroid hormone receptor locally in the retina is a therapeutic strategy for retinal degeneration

Hongwei Ma, T. Scanlan, Xi-Qin Ding, 2017, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Targeting iodothyronine deiodinases locally in the retina is a therapeutic strategy for retinal degeneration

W. Hauswirth, S. Boye, Hongwei Ma, 2016, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Identification of beta‐carotene 15,15′‐monooxygenase as a peroxisome proliferator‐activated receptor target gene

N. Copeland, D. Gilbert, N. Jenkins, 2003, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Localization of corneal superoxide dismutase by biochemical and histocytochemical techniques.

E. Duke, R. Crouch, J. Simson, 1984, Experimental eye research.

Localization of the gene for interphotoreceptor retinoid-binding protein to mouse chromosome 14 near Np-1.

C. Kozak, D. Farber, J. Nickerson, 1990, Genomics.

Genetic analysis of RPE65: from human disease to mouse model.

C. Hamel, T Michael Redmond, 2000, Methods in enzymology.

Endogenous fatty acids are covalently and noncovalently bound to interphotoreceptor retinoid-binding protein in the monkey retina.

G. Chader, N. Bazan, T Michael Redmond, 1985, The Journal of biological chemistry.

Identification, Expression, and Substrate Specificity of a Mammalian β-Carotene 15,15′-Dioxygenase*

S. Yu, E. Gantt, T Michael Redmond, 2001, The Journal of Biological Chemistry.

Molecular cloning and expression of RPE65, a novel retinal pigment epithelium-specific microsomal protein that is post-transcriptionally regulated in vitro.

C. Hamel, T Michael Redmond, B. Detrick, 1993, The Journal of biological chemistry.

Recognition of peptides that are immunopathogenic but cryptic. Mechanisms that allow lymphocytes sensitized against cryptic peptides to initiate pathogenic autoimmune processes.

J. Berzofsky, G. Chader, I. Gery, 1991, Journal of immunology.

Repeated determinants within the retinal interphotoreceptor retinoid-binding protein (IRBP): immunological properties of the repeats of an immunodominant determinant.

H. Margalit, J. Berzofsky, G. Chader, 1990, Cellular immunology.

Uveitis and immune responses in primates immunized with IRBP-derived synthetic peptides.

G. Chader, I. Gery, S. Kotake, 1990, Current eye research.

Rat T-cell lines specific to a nonimmunodominant determinant of a retinal protein (IRBP) produce uveoretinitis and pinealitis.

G. Chader, I. Gery, T. Kuwabara, 1989, Cellular immunology.

Identification of an immunodominant and highly immunopathogenic determinant in the retinal interphotoreceptor retinoid-binding protein (IRBP)

H. Margalit, J. Berzofsky, G. Chader, 1989, The Journal of experimental medicine.

Synthesis of an immunopathogenic fusion protein derived from a bovine interphotoreceptor retinoid-binding protein cDNA clone.

D. J. Barrett, J. Nickerson, I. Gery, 1989, Gene.

Immune responses to peptides derived from the retinal protein IRBP: immunopathogenic determinants are not necessarily immunodominant.

H. Margalit, J. Berzofsky, G. Chader, 1989, Clinical immunology and immunopathology.

Synthetic peptides derived from IRBP induce EAU and EAP in Lewis rats.

H. Margalit, J. Cornette, G. Chader, 1988, Current eye research.

An inducible amphipathic α-helix mediates subcellular targeting and membrane binding of RPE65

S. Uppal, Tishina Tittley, T Michael Redmond, 2022, Life Science Alliance.

Palmitoylation of Metazoan Carotenoid Oxygenases

I. Rogozin, S. Uppal, T Michael Redmond, 2020, Molecules.

Resveratrol attenuates CXCL11 expression induced by proinflammatory cytokines in retinal pigment epithelial cells.

T Michael Redmond, C. Vijayasarathy, W. Samuel, 2015, Cytokine.

mRNA for interphotoreceptor retinoid-binding protein (IRBP): distribution and size diversity in vertebrate species.

G. Chader, A. Albini, J. Nickerson, 1989, Experimental eye research.

RPE65 is highly uveitogenic in rats.

I. Gery, Chi-Chao Chan, D. Ham, 2002, Investigative ophthalmology & visual science.

What can we learn about AMD from other retinal diseases ?

J. Nathans, D. Zack, A. Swaroop, 1999 .

Mole quantity of RPE65 and its productivity in the generation of 11-cis-retinal from retinyl esters in the living mouse eye.

E. Pugh, A. Lyubarsky, T Michael Redmond, 2005, Biochemistry.

The Rpe65 rd12 allele exerts a semidominant negative effect on vision in mice.

J. Boatright, J. Nickerson, Wei Feng, 2014, Investigative ophthalmology & visual science.

Identification of a KRAB-Zinc Finger Protein Binding to the Rpe65 Gene Promoter

T Michael Redmond, E. Poliakov, Zhongjian Lu, 2005, Current eye research.

Spontaneous activity of opsin apoprotein is a cause of Leber congenital amaurosis

G. Fain, M. Woodruff, Zhongyan Wang, 2003, Nature Genetics.

Cone opsin mislocalization in Rpe65-/- mice: a defect that can be corrected by 11-cis retinal.

M. Seeliger, R. Crouch, P. Humphries, 2005, Investigative ophthalmology & visual science.

Uveitis induced in primates by interphotoreceptor retinoid-binding protein.

I. Gery, T. Kuwabara, R. Nussenblatt, 1986, Archives of ophthalmology.

Biochemical evidence for the tyrosine involvement in cationic intermediate stabilization in mouse β-carotene 15 , 15 '-monooxygenase

B. Grigorenko, T Michael Redmond, E. Poliakov, 2015 .

Inhibition of RPE65 Retinol Isomerase Activity by Inhibitors of Lipid Metabolism*

Abdulkerim Eroglu, T Michael Redmond, E. Poliakov, 2014, The Journal of Biological Chemistry.

In utero gene therapy rescues vision in a murine model of congenital blindness.

T. Aleman, A. Cideciyan, S. Jacobson, 2004, Molecular therapy : the journal of the American Society of Gene Therapy.

Effect of Rpe65 knockout on accumulation of lipofuscin fluorophores in the retinal pigment epithelium.

T Michael Redmond, M. Katz, 2001, Investigative ophthalmology & visual science.

A QTL on distal Chromosome 3 that influences the severity of light-induced damage to mouse photoreceptors

D. Farber, Tammy M. Rickabaugh, T. Redmond, 2000, Mammalian Genome.

RPE65, the major retinal pigment epithelium microsomal membrane protein, associates with phospholipid liposomes.

S. Yu, C. Hamel, T Michael Redmond, 1997, Archives of biochemistry and biophysics.

Decreased expression of insulin‐like growth factor binding protein‐5 during N‐(4‐hydroxyphenyl)retinamide‐induced neuronal differentiation of ARPE‐19 human retinal pigment epithelial cells: Regulation by CCAAT/enhancer‐binding protein

I. Pascual, T Michael Redmond, C. Vijayasarathy, 2010, Journal of cellular physiology.

The Upstream Region of the Rpe65 Gene Confers Retinal Pigment Epithelium-specific Expression in Vivo and in Vitro and Contains Critical Octamer and E-box Binding Sites*

S. Yu, A. Boulanger, T Michael Redmond, 2000, The Journal of Biological Chemistry.

Rpe65 is necessary for production of 11-cis-vitamin A in the retinal visual cycle

D. Bok, D. Hamasaki, Jian-xing Ma, 1998, Nature Genetics.

Mutations in RPE65 cause Leber's congenital amaurosis

E. Zrenner, M. Claustres, C. Bareil, 1997, Nature Genetics.

Interphotoreceptor retinoid-binding protein. Gene characterization, protein repeat structure, and its evolution.

M. Gonda, G. Chader, J. Nickerson, 1989, The Journal of biological chemistry.

Cyanogen bromide fragments of bovine interphotoreceptor retinoid-binding protein induce experimental autoimmune uveoretinitis in Lewis rats.

J. Nickerson, I. Gery, T. Kuwabara, 1988, Current eye research.

cDNA clones encoding bovine interphotoreceptor retinoid binding protein.

D. J. Barrett, D. Oprian, G. Chader, 1985, Biochemical and biophysical research communications.

Origin and Evolution of Retinoid Isomerization Machinery in Vertebrate Visual Cycle: Hint from Jawless Vertebrates

I. Rogozin, A. Gubin, Yan Li, 2012, PloS one.

Proposed therapy, developed in a Pcdh15-deficient mouse, for progressive loss of vision in human Usher syndrome

S. Riazuddin, Z. Ahmed, A. Griffith, 2021, eLife.

Potential therapy for progressive vision loss due to PCDH15-associated Usher Syndrome developed in an orthologous Usher mouse

S. Riazuddin, Z. Ahmed, A. Griffith, 2021, bioRxiv.

Complementation test of Rpe65 knockout and tvrm148.

J. Boatright, J. Nickerson, M. Pardue, 2013, Investigative ophthalmology & visual science.

The Functional Consequences of the Novel Ribosomal Pausing Site in SARS-CoV-2 Spike Glycoprotein RNA

I. Rogozin, S. Uppal, M. Kane, 2021, International journal of molecular sciences.

Technical Brief: Subretinal injection and electroporation into adult mouse eyes

J. Boatright, J. Nickerson, T Michael Redmond, 2008, Molecular vision.

Generation of knockout animal models.

T Michael Redmond, 2001, Methods in molecular medicine.

Aromatic Residues in the Substrate Cleft of RPE65 Protein Govern Retinol Isomerization and Modulate Its Progression*

T Michael Redmond, E. Poliakov, S. Gentleman, 2012, The Journal of Biological Chemistry.

Retinyl esters are the substrate for isomerohydrolase.

Jian-xing Ma, R. Crouch, T Michael Redmond, 2003, Biochemistry.

Appropriately differentiated ARPE-19 cells regain phenotype and gene expression profiles similar to those of native RPE cells

L. Tan, T Michael Redmond, O. Postnikova, 2017, Molecular vision.

Experimental autoimmune uveoretinitis (EAU) induced by retinal interphotoreceptor retinoid-binding protein (IRBP): differences between EAU induced by IRBP and by S-antigen.

G. Chader, I. Gery, T. Kuwabara, 1987, Clinical immunology and immunopathology.

IRBP from bovine retina is poorly uveitogenic in guinea pigs and is identical to A-antigen.

G. Chader, I. Gery, T. Kuwabara, 1987, Current eye research.

Intrachoroidal neovascularization in transgenic mice overexpressing vascular endothelial growth factor in the retinal pigment epithelium.

R. D'Amato, A. Joussen, A. Adamis, 2001, The American journal of pathology.

Proinflammatory cytokines decrease the expression of genes critical for RPE function

T Michael Redmond, W. Samuel, T. Duncan, 2016, Molecular vision.

The gene for the retinal pigment epithelium-specific protein RPE65 is localized to human 1p31 and mouse 3.

N. Copeland, D. Gilbert, N. Jenkins, 1994, Genomics.

Aberrant RNA splicing is the major pathogenic effect in a knock‐in mouse model of the dominantly inherited c.1430A>G human RPE65 mutation

I. Rogozin, L. Gieser, Lijin Dong, 2019, Human mutation.

Mutation of key residues of RPE65 abolishes its enzymatic role as isomerohydrolase in the visual cycle.

T Michael Redmond, E. Poliakov, Shirley Yu, 2005, Proceedings of the National Academy of Sciences of the United States of America.

RPE65 Palmitoylation: A Tale of Lipid Posttranslational Modification.

S. Uppal, T Michael Redmond, E. Poliakov, 2019, Advances in experimental medicine and biology.

Expression, purification, and MALDI analysis of RPE65.

J. Zhang, R. Crouch, Z. Ablonczy, 2001, Investigative ophthalmology & visual science.

Expression , Purification , and MALDI Analysis of RPE 65

Jian-xing Ma, R. Crouch, Z. Ablonczy, 2001 .

Pretreatment of human retinal pigment epithelial cells with sterculic acid forestalls fenretinide-induced apoptosis

T Michael Redmond, T. Duncan, S. William, 2022, Scientific Reports.

Phylogenetic analysis of the metazoan carotenoid oxygenase superfamily: a new ancestral gene assemblage of BCO-like (BCOL) proteins

I. Rogozin, T Michael Redmond, E. Poliakov, 2017, Scientific Reports.

Multiple A2E treatments lead to melanization of rod outer segment–challenged ARPE-19 cells

Craig J. Thomas, B. Brooks, T Michael Redmond, 2014, Molecular vision.

Multiple A 2 E treatments lead to melanization of rod outer segment – challenged ARPE-19 cells

Aparna, Craig J. Thomas, B. Brooks, 2014 .

Dissociation between lymphocyte activation for proliferation and for the capacity to adoptively transfer uveoretinitis.

G. Chader, I. Gery, T. Kuwabara, 1987, Journal of immunology.

The molecular biology of IRBP: application to problems of uveitis, protein chemistry, and evolution.

G. Chader, J. Nickerson, T Michael Redmond, 1991, Progress in clinical and biological research.

Interphotoreceptor Retinoid-Binding Protein: A Link Between Retinal Rod Photoreceptor Cells and Pineal Gland

G. Chader, I. Gery, T. Kuwabara, 1986 .

CIB2 regulates mTORC1 signaling and is essential for autophagy and visual function

S. Riazuddin, Z. Ahmed, S. Riazuddin, 2021, Nature Communications.

Uveoretinitis and pinealitis induced by immunization with interphotoreceptor retinoid-binding protein.

G. Chader, I. Gery, T. Kuwabara, 1986, Investigative ophthalmology & visual science.

Immunochemical distribution of interphotoreceptor retinoid-binding protein in selected species.

G. Chader, T Michael Redmond, H. Hess, 1986, Investigative ophthalmology & visual science.

Immunological features of synthetic peptides derived from the retinal protein IRBP: differences between immunodominant and non-dominant peptides.

G. Chader, I. Gery, M. D. de Smet, 1990, Current eye research.

Differential regulation of microRNA-146a and microRNA-146b-5p in human retinal pigment epithelial cells by interleukin-1β, tumor necrosis factor-α, and interferon-γ

E. Flemington, T Michael Redmond, J. Hooks, 2013, Molecular vision.

Mouse model of human RPE65 P25L hypomorph resembles wild type under normal light rearing but is fully resistant to acute light damage.

Lijin Dong, T Michael Redmond, Shirley Yu, 2015, Human molecular genetics.

Role of the 3'-untranslated region of RPE65 mRNA in the translational regulation of the RPE65 gene: identification of a specific translation inhibitory element.

T Michael Redmond, S. -. Liu, 1998, Archives of biochemistry and biophysics.

Lymphocyte responses to retinal-specific antigens in uveitis patients and healthy subjects.

G. Chader, A. Palestine, I. Gery, 1988, Current eye research.

Immunohistochemical analysis of experimental autoimmune uveoretinitis (EAU) induced by interphotoreceptor retinoid-binding protein (IRBP) in the rat.

G. Chader, C. Chan, I. Gery, 1987, Immunological investigations.

Serial adoptive transfer of experimental autoimmune uveoretinitis in rats.

G. Chader, C. Chan, I. Gery, 1990, Investigative ophthalmology & visual science.

MicroRNA expression in human retinal pigment epithelial (ARPE-19) cells: Increased expression of microRNA-9 by N-(4-Hydroxyphenyl)retinamide

N. Raghavachari, T Michael Redmond, W. Samuel, 2010, Molecular vision.

Protection of Rpe 65-deficient mice identifies rhodopsin as a mediator of light-induced retinal degeneration

C. Grimm, A. Wenzel, C. Remé, 2000 .

Fenretinide Induces Ubiquitin‐Dependent Proteasomal Degradation of Stearoyl‐CoA Desaturase in Human Retinal Pigment Epithelial Cells

T Michael Redmond, C. Vijayasarathy, W. Samuel, 2014, Journal of cellular physiology.

Mitogen‐activated protein kinase pathway mediates N‐(4‐hydroxyphenyl)retinamide‐induced neuronal differentiation in the ARPE‐19 human retinal pigment epithelial cell line

T Michael Redmond, C. Vijayasarathy, W. Samuel, 2008, Journal of neurochemistry.

New views on RPE65 deficiency: the rod system is the source of vision in a mouse model of Leber congenital amaurosis

C. Grimm, A. Wenzel, C. Remé, 2001, Nature Genetics.

Suppressing thyroid hormone signaling preserves cone photoreceptors in mouse models of retinal degeneration

Hongwei Ma, W. Baehr, Xi-Qin Ding, 2014, Proceedings of the National Academy of Sciences.

Evolutionary aspects and enzymology of metazoan carotenoid cleavage oxygenases.

I. Rogozin, S. Uppal, T Michael Redmond, 2020, Biochimica et biophysica acta. Molecular and cell biology of lipids.

11-cis-Retinal Reduces Constitutive Opsin Phosphorylation and Improves Quantum Catch in Retinoid-deficient Mouse Rod Photoreceptors*

Jian-xing Ma, R. Crouch, Z. Ablonczy, 2002, The Journal of Biological Chemistry.

9-cis Retinal Increased in Retina of RPE65 Knockout Mice with Decrease in Coat Pigmentation†

T. Sarna, R. Crouch, B. Rohrer, 2006, Photochemistry and photobiology.

Recombinant adeno-associated virus type 2-mediated gene delivery into the Rpe65-/- knockout mouse eye results in limited rescue

P. Rakoczy, Xiaohuai Zhou, C. Lai, 2004, Genetic vaccines and therapy.

Assessing the efficacy of gene therapy in Rpe65-/- mice using photoentrainment of circadian rhythm.

K. Narfström, N. Barnett, T Michael Redmond, 2006, Advances in experimental medicine and biology.

Genetic Vaccines and Therapy

P. Rakoczy, Xiaohuai Zhou, C. Lai, 2004 .

Functional and structural evaluation after AAV.RPE65 gene transfer in the canine model of Leber's congenital amaurosis.

K. Narfström, P. Rakoczy, T. van Veen, 2003, Advances in experimental medicine and biology.

Functional and structural recovery of the retina after gene therapy in the RPE65 null mutation dog.

M. Seeliger, K. Narfström, P. Rakoczy, 2003, Investigative ophthalmology & visual science.

Aromatic lipophilic spin traps effectively inhibit RPE65 isomerohydrolase activity.

T Michael Redmond, E. Poliakov, S. Gentleman, 2011, Biochemistry.

Expression of beta-carotene 15,15' monooxygenase in retina and RPE-choroid.

S. Bernstein, A. Boulanger, R. Fariss, 2003, Investigative ophthalmology & visual science.

Acute radiolabeling of retinoids in eye tissues of normal and rpe65-deficient mice.

T Michael Redmond, N. Qtaishat, D. R. Pepperberg, 2003, Investigative ophthalmology & visual science.

Unusual immunologic properties of the uveitogenic interphotoreceptor retinoid-binding protein-derived peptide R23.

G. Chader, I. Gery, S. Kotake, 1991, Investigative ophthalmology & visual science.

Subretinal delivery and electroporation in pigmented and nonpigmented adult mouse eyes.

J. Boatright, J. Nickerson, T Michael Redmond, 2012, Methods in molecular biology.

Identification of RPE65 in transformed kidney cells1

R. Crouch, T. Redmond, T Michael Redmond, 1999, FEBS letters.

Low-Density Lipoprotein Receptor (LDLR) Is Involved in Internalization of Lentiviral Particles Pseudotyped with SARS-CoV-2 Spike Protein in Ocular Cells

I. Rogozin, T. Eggerman, S. Uppal, 2023, International journal of molecular sciences.

Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial

Kathleen A. Marshall, G. Ying, E. Stone, 2009, The Lancet.

Focus on Molecules: RPE65, the visual cycle retinol isomerase.

T Michael Redmond, 2009, Experimental eye research.

Effect of Leu/Met variation at residue 450 on isomerase activity and protein expression of RPE65 and its modulation by variation at other residues.

T Michael Redmond, E. Poliakov, Shirley Yu, 2007, Molecular vision.

Recombinant adeno-associated virus type 2-mediated gene delivery into the Rpe65-/- knockout mouse eye results in limited rescue

E. Rakoczy, P. Rakoczy, Xiaohuai Zhou, 2004, Genetic Vaccines and Therapy.

Sequence and structure of the mouse gene for RPE65.

A. Boulanger, T Michael Redmond, S. Liu, 2001, Molecular vision.

RPE65, Visual Cycle Retinol Isomerase, Is Not Inherently 11-cis-specific

T Michael Redmond, E. Poliakov, S. Gentleman, 2009, The Journal of Biological Chemistry.

Stimulation in vitro of lymphocytes for induction of uveoretinitis without any significant proliferation.

G. Chader, I. Gery, S. Kotake, 1990, Journal of immunology.

Loss of CIB2 causes non-canonical autophagy deficits and visual impairment

S. Riazuddin, P. Scott, T Michael Redmond, 2020, bioRxiv.

The RPE65-Deficient Mouse as a Model for RPE65-Associated Leber’s Congenital Amaurosis and Related Disorders

T Michael Redmond, 1999 .

Genetic Vaccines and Therapy

P. Rakoczy, Xiaohuai Zhou, C. Lai, 2004 .