Sanford L. Boye
University of Florida
H-index: 56
North America-United States
Top articles of Sanford L. Boye
Title | Journal | Author(s) | Publication Date |
---|---|---|---|
Correction: Site-specific modifications to AAV8 capsid yields enhanced brain transduction in the neonatal MPS IIIB mouse | Gene Therapy | Janine A Gilkes Benjamin L Judkins Brontie N Herrera Ronald J Mandel Sanford L Boye | 2023 |
Modification of rAAV capsid to improve retinal vascular endothelial tropism | Investigative Ophthalmology & Visual Science | Ramesh Periasamy Dwani Patel Sanford L Boye Shannon E Boye Daniel M Lipinski | 2023/6/1 |
Modified AAV capsid proteins and uses thereof | 2023/9/26 | ||
Six-month safety and efficacy of ATSN-101 in patients with Leber congenital amaurosis caused by biallelic mutations in GUCY2D (LCA1) | Investigative Ophthalmology & Visual Science | Christine Nichols Kay Paul Yang Artur V Cideciyan Allen Ho Andreas K Lauer | 2023/6/1 |
Enhancing AAV-mediated transduction of ocular tissues with hyaluronic acid | 2023/9/5 | ||
β-secretase 1 overexpression by AAV-mediated gene delivery prevents retina degeneration in a mouse model of age-related macular degeneration | Molecular Therapy | Xiaoping Qi Carolina Francelin Sayak Mitter Sanford L Boye Hongmei Gu | 2023/7/5 |
Preclinical studies in support of phase I/II clinical trials to treat GUCY2D-associated Leber congenital amaurosis | Molecular Therapy Methods & Clinical Development | Sanford L Boye Catherine O’Riordan James Morris Michael Lukason David Compton | 2023/3/9 |
Rhesus macaque model of Bardet-Biedl syndrome: Progression and response to gene therapy | Investigative Ophthalmology & Visual Science | Martha Neuringer Junghyun Ryu Jon D Hennebold Carol Hanna Fernanda Burch | 2023/6/1 |
Intravitreal Administration of AAV2-SIRT1 Reverses Diabetic Retinopathy in a Mouse Model of Type 2 Diabetes | Translational Vision Science & Technology | Yvonne Adu-Agyeiwaah Cristiano P Vieira Bright Asare-Bediako Sergio Li Calzi Mariana DuPont | 2023/4/3 |
Dual-AAV vector-mediated expression of MYO7A improves vestibular function in a mouse model of Usher syndrome 1B | Molecular Therapy-Methods & Clinical Development | Samantha C Lau Mhamed Grati Kevin Isgrig Moaz Sinan Kaitlyn R Calabro | 2023/9/14 |
Dual aav-myo7a vectors with improved safety for the treatment of ush1b | 2023/5/18 | ||
Improved aav-mediated x-linked retinoschisis therapies | 2023/8/24 | ||
Disease correction by delivery of aav8 vectors expressing codon optimized naglu | 2023/6/15 | ||
Methods and compositions for treating cone-rod retinal dystrophy | 2023/11/7 | ||
Nonhuman primate model of Usher Syndrome Type 1B: course of retinal degeneration and initial gene therapy results | Investigative Ophthalmology & Visual Science | Lauren Renner Junghyun Ryu Jon D Hennebold Sanford L Boye Carol Hanna | 2023/6/1 |
Development of an AAV-CRISPR-Cas9-based treatment for dominant cone-rod dystrophy 6 | Molecular Therapy-Methods & Clinical Development | Russell W Mellen Kaitlyn R Calabro K Tyler McCullough Sean M Crosson Alejandro de la Cova | 2023/9/14 |
Overexpression of β-secretase 1 (BACE1) by AAV-mediated gene delivery prevents retinal degeneration in a mouse model of age-related macular degeneration. | Molecular Therapy: the Journal of the American Society of Gene Therapy | X Qi C Francelin S Mitter SL Boye H Gu | 2023/4/3 |
Improving retinal vascular endothelial cell tropism through rational rAAV capsid design | Plos one | Ramesh Periasamy Dwani D Patel Sanford L Boye Shannon E Boye Daniel M Lipinski | 2023/5/11 |
Intravitreal injection of a rationally designed AAV capsid library in non-human primate identifies variants with enhanced retinal transduction and neutralizing antibody evasion | Molecular Therapy | Patrick C Kellish Damien Marsic Sean M Crosson Shreyasi Choudhury Miranda L Scalabrino | 2023/12/6 |
Optimization of Capillary-Based Western Blotting for MYO7A | Kaitlyn R Calabro Sanford L Boye Shannon E Boye | 2023/7/14 |