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Shannon Boye
Professor And Associate Division Chief - Cellular And Molecular Therapy, Department Of Pediatrics
MD-PEDS-CELL / MOLEC THERP DIV | COLLEGE-MEDICINE
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Ophthalmology
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Title
05-2024
Engineering AAV for safe and efficient gene delivery to
Engineering AAV for safe and efficient gene delivery to
11-2023
Optimizing AAV Vectors for Central Nervous System transduction
Optimizing AAV Vectors for Central Nervous System transduction
10-2023
Task Order 17: Evaluation of multiple lots of AAV-hRS1 in Rs1-/- KO mice
Task Order 17: Evaluation of multiple lots of AAV-hRS1 in Rs1-/- KO mice
08-2023
Propagation of a Nonhuman Primate Model of Usher Syndrome
Propagation of a Nonhuman Primate Model of Usher Syndrome
08-2023
Vascular Gene Delivery and Early Disease Biomarkers in Diabetic Retinopathy Yr. 3
Vascular Gene Delivery and Early Disease Biomarkers in Diabetic Retinopathy Yr. 3
07-2023
Task Order #13- #Development of AAV Candidates for the Treatment of Ocular Friedrich#s Ataxia#
Task Order #13- #Development of AAV Candidates for the Treatment of Ocular Friedrich#s Ataxia#
07-2023
Maintenance of CNGB3 Mouse Models
Maintenance of CNGB3 Mouse Models
06-2023
Therapeutic Efficacy of Novel Laterally-Spreading AAV capsids
Therapeutic Efficacy of Novel Laterally-Spreading AAV capsids
06-2023
ATSN-CAP-RD-01, P2 Peptide Library Selection
ATSN-CAP-RD-01, P2 Peptide Library Selection
05-2023
DEVELOPMENT OF AAV-CRISPR/CAS9-BASED THERAPIES FOR CONE
DEVELOPMENT OF AAV-CRISPR/CAS9-BASED THERAPIES FOR CONE
04-2023
ATSN-AVT-ROD-004: Axon Targeting Motif Identification
ATSN-AVT-ROD-004: Axon Targeting Motif Identification
03-2023
Task Order #15- Assessment of AAV-GUCY2D vectors in Gucy2e KO mice
Task Order #15- Assessment of AAV-GUCY2D vectors in Gucy2e KO mice
12-2022
Task Order #7 - Hybrid Toxicology, Efficacy and Biodistribution (BD) Study in support of an AAV gene therapy for the treatment of XLRS (ATSN-201) following subretinal administration in RS1-/- knockout mic
Task Order #7 - Hybrid Toxicology, Efficacy and Biodistribution (BD) Study in support of an AAV gene therapy for the treatment of XLRS (ATSN-201) following subretinal administration in RS1-/- knockout mic
11-2022
Enhancing Metabolism in Photoreceptors with a Modified Arrestin to Treat Retinal Degeneration
Enhancing Metabolism in Photoreceptors with a Modified Arrestin to Treat Retinal Degeneration
09-2022
Task Order #8 ATSN-201 Vector Bridging Study
Task Order #8 ATSN-201 Vector Bridging Study
09-2022
AAV-MEDIATED THERAPY FOR VISUAL IMPAIRMENT ASSOCIATED WITH FRIEDREICH'S ATAXIA
AAV-MEDIATED THERAPY FOR VISUAL IMPAIRMENT ASSOCIATED WITH FRIEDREICH'S ATAXIA
08-2022
Task Order #1 - AAV-hRS1 Pharmacology
Task Order #1 - AAV-hRS1 Pharmacology
06-2022
Task Order #3 - Maintenance of mouse models of LCA1
Task Order #3 - Maintenance of mouse models of LCA1
06-2022
Task Order 10 - ATSN-CAP-RD-02 Lead Capsid Vector Evaluation
Task Order 10 - ATSN-CAP-RD-02 Lead Capsid Vector Evaluation
04-2022
Therapy development for open-angle glaucoma
Therapy development for open-angle glaucoma
03-2022
Task Order #2 - Dual AAV-MYO7A Candidate evaluation in M
Task Order #2 - Dual AAV-MYO7A Candidate evaluation in M
05-2021
Nonhuman Primate Model of Usher Syndrome.
Nonhuman Primate Model of Usher Syndrome.
12-2020
Dual AAV vector-mediated therapy for MyosinVIIa Usher syndrome (USH1B)
Dual AAV vector-mediated therapy for MyosinVIIa Usher syndrome (USH1B)
12-2020
miscellaneous donors
miscellaneous donors
09-2020
A Ribozyme Rescue Strategy for Autosomal Dominant Retinitis Pigmentosa
A Ribozyme Rescue Strategy for Autosomal Dominant Retinitis Pigmentosa
08-2020
Vascular gene delivery and early disease biomarkers in diabetic retinopathy
Vascular gene delivery and early disease biomarkers in diabetic retinopathy
12-2019
Exploring MYO7A function in novel mouse models and improving AAV-Dual Vector Gene Therapy for Usher Syndrome 1B
Exploring MYO7A function in novel mouse models and improving AAV-Dual Vector Gene Therapy for Usher Syndrome 1B
12-2019
Cas9 mediated gene editing therapy for CORD6 cone rod dystrophy/Extension of Sponsored Research Agreement btw Editas Medicine and the University of Florida
Cas9 mediated gene editing therapy for CORD6 cone rod dystrophy/Extension of Sponsored Research Agreement btw Editas Medicine and the University of Florida
08-2019
Vascular gene delivery and early disease biomarkers in diabetic retinopathy
Vascular gene delivery and early disease biomarkers in diabetic retinopathy
05-2019
Developing efficient AAV vectors for photoreceptor targeting via the vitreous
Developing efficient AAV vectors for photoreceptor targeting via the vitreous
03-2019
Developing a dual AAV vector gene therapy for the treatment of Usher syndrome
Developing a dual AAV vector gene therapy for the treatment of Usher syndrome
12-2018
Gene Therapy for LCA1
Gene Therapy for LCA1
08-2018
AAV Capsid Library Screening
AAV Capsid Library Screening
06-2018
Cas9 mediated in vivo gene editing of photoreceptors in the nonhuman primate and in a mouse model of cone rod dystrophy
Cas9 mediated in vivo gene editing of photoreceptors in the nonhuman primate and in a mouse model of cone rod dystrophy
11-2017
AAV-mediated optogenetic gene therapy in bipolar cells
AAV-mediated optogenetic gene therapy in bipolar cells
02-2017
Dual AAV vector-mediated therapy for Myosin7a Usher syndrome (USH1B)
Dual AAV vector-mediated therapy for Myosin7a Usher syndrome (USH1B)
08-2015
XLRP NHP Research Agreement
XLRP NHP Research Agreement
06-2015
Targeting Foveal Cones Using Novel Delivery Methods and
Targeting Foveal Cones Using Novel Delivery Methods and
Publications
Search Google Scholar for Shannon Boye
Co-Investigator Network
Mavis Agbandje-Mckenna
PROFESSOR
University of Florida
MD-BIOCHEM / MOLECULAR BIOL, College-Medicine
mckenna@ufl.edu
Sanford Boye
Associate Scientist, Director of Vector Core
University of Florida
MD-POWELL GENE THERAPY CENTER, College-Medicine
sboye@ufl.edu
Barry Byrne
PROF & ASO CHR
University of Florida
MD-COGNITAL HRT CTR EXCELLENCE, College-Medicine
byrne@gtc.ufl.edu
Kaitlyn Calabro
Postdoctoral Associate
University of Florida
MD-PEDS-CELL / MOLEC THERP DIV, College-Medicine
k.calabro@ufl.edu
Jason Coleman
Assistant Professor
University of Florida
Pediatrics, Medicine
jcoleman@ufl.edu
Somnath Datta
Professor
University of Florida
PHHP-COM BIOSTATISTICS, Phhp-Com Integrated Programs
somnath.datta@ufl.edu
Carolyn Dirain
Research Scientist
University of Florida
MD-ENDOCRINOLOGY, College-Medicine
carolyn.ojano-dirain@ent.ufl.edu
Karyn Esser
Professor and Chair
University of Florida
MD-PHYSIOLOGY AND AGING, College-Medicine
kaesser@ufl.edu
William Hauswirth
Eminent Scholar
University of Florida
MD-MOLECULAR GENTCS / MICROBIO, College-Medicine
hauswrth@eye.ufl.edu
Coy Heldermon
Associate Professor
University of Florida
MD-HEMATOLOGY/ONCOLOGY, College-Medicine
coy.heldermon@medicine.ufl.edu
Brad Hoffman
Assistant Professor
University of Florida
MD-PEDS-CELL / MOLEC THERP DIV, College-Medicine
bhoffman@ufl.edu
Ronald Mandel
PROFESSOR
University of Florida
MD-NEUROSCIENCE, College-Medicine
rmandel@ufl.edu
Wesley Smith
Professor
University of Florida
MD-OPHTHALMOLOGY, College-Medicine
wcsmith@ufl.edu
Shinichi Someya
Associate Professor
University of Florida
MD-PHYSIOLOGY AND AGING, College-Medicine
someya@ufl.edu
Serge Zolotukhin
Professor
University of Florida
MD-PEDS-CELL / MOLEC THERP DIV, College-Medicine
szlt@ufl.edu
Websites
0000-0002-7312-3197
Search Google Scholar for Shannon Boye
Contact Information
shaire@ufl.edu
3522739342
PO Box 100284 GAINESVILLE, FL 32610-0284
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