MrsShannon Boye
PROF
MD-PEDIATRICS
GRANTS
- GRANTCharacterization of ocular phenotype of the YG8-800 mouse model of FA and retinal-targeted treatment by AAV based CRISPR-Cas9 gene editingFriedreichs Ataxia Research Alliance5 Mar 2025 - 28 Feb 2027
- GRANTDevelopment of a New Gene Therapy for Autosomal Dominant Retinitis PigmentosaFoundation for Fighting Blindness1 Jan 2025 - 31 Dec 2026
- GRANTMouse model of KIZFoundation for Fighting Blindness25 Sep 2024 - 14 Sep 2025
- GRANTEngineering AAV for safe and efficient gene delivery to the human retinaNational Institute of Health Nei5 Sep 2024 - 30 Jun 2029
- GRANTPDE6A Gene Therapy AgreementStiftung Für Medizininnovationen20 Aug 2024 - 19 Aug 2027
- GRANTNatural history and AAV-mediated interventions for dominant negative and haploinsufficient mouse models of PRPH2-associated diseaseFoundation for Fighting Blindness1 Apr 2024 - 31 Mar 2027
- GRANTNonhuman Primate Model of Inherited Photoreceptor DegenerationNational Institute of Health Nei5 Feb 2024 - 31 Mar 2026
- GRANTCreation of a Translational Nonhuman Primate Model of Usher Syndrome 1BFoundation for Fighting Blindness6 Nov 2023 - 31 Mar 2026
- GRANTAAV-Mediated Therapy for Visual Impairment associated with Friedreich’s AtaxiaFriedreichs Ataxia Research Alliance30 Aug 2023 - 31 Aug 2025
- GRANTTask Order 17: Evaluation of multiple lots of AAV-hRS1 in Rs1-/- KO miceAtsena Therapeutics17 Jul 2023 - 31 Mar 2024
- GRANTMaintenance of RS1 Mouse Model#Atsena Therapeutics13 Feb 2023 - 30 Jun 2027
- GRANTCharacterization and mitigation of AAV-induced ocular inflamationFoundation for Fighting Blindness10 Feb 2023 - 31 Mar 2026
- GRANTTask Order #15- Assessment of AAV-GUCY2D vectors in Gucy2e KO miceAtsena Therapeutics5 Oct 2022 - 31 Mar 2023
- GRANTMaintenance of CNGB3 Mouse ModelsAtsena Therapeutics27 Sep 2022 - 10 Jul 2023
- GRANTTask Order #13- ‘Development of AAV Candidates for the Treatment of Ocular Friedrich’s Ataxia’Atsena Therapeutics27 Sep 2022 - 10 Jul 2023
- GRANTATSN-AVT-ROD-004: Axon Targeting Motif IdentificationAtsena Therapeutics19 Apr 2022 - 14 Apr 2023
- GRANTAssessment of Candidate Vectors for AAV-mediated Delivery of ABCA4Atsena Therapeutics15 Apr 2022 - 28 Feb 2027
- GRANTAchroma Check_BoyeAchroma Corporation30 Jan 2022 - 30 Apr 2025
- GRANTTask Order 10 - ATSN-CAP-RD-02 Lead Capsid Vector EvaluationAtsena Therapeutics19 Jan 2022 - 15 Jun 2022
- GRANTPropagation of a Nonhuman Primate Model of Usher SyndromeFoundation for Fighting Blindness22 Nov 2021 - 31 Aug 2023
- GRANTATSN-CAP-RD-01, P2 Peptide Library SelectionAtsena Therapeutics17 Nov 2021 - 30 Jun 2023
- GRANTTask Order #8 ATSN-201 Vector Bridging StudyAtsena Therapeutics7 Sep 2021 - 30 Sep 2022
- GRANTTask 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 micAtsena Therapeutics12 May 2021 - 31 Dec 2022
- GRANTVascular Gene Delivery and Early Disease Biomarkers in Diabetic Retinopathy Yr. 3National Institute of Health Nei19 Oct 2020 - 31 Aug 2023
- GRANTAAV-MEDIATED THERAPY FOR VISUAL IMPAIRMENT ASSOCIATED WITH FRIEDREICH'S ATAXIAFriedreichs Ataxia Research Alliance17 Sep 2020 - 30 Sep 2022