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T. Li

Replacement Gene Therapy with a Human RPGRIP1 Sequence Slows Photoreceptor Degeneration in a Murine Model of Leber Congenital Amaurosis
2010 · Basil S. Pawlyk, Oleg V. Bulgakov, et al. · Human Gene Therapy · 79
Deficiency of PLA2G6 Induces Ferroptosis in Dopaminergic Neurons and Contributes to Parkinson’s Disease Pathogenesis via Disruption of PRDX6/FTH1/GPX4 Axis
2025 · Taole Li, Jiabin Liu, et al. · Molecular Neurobiology · 12
Investigating sex-specific associations of Parkinson's disease with sex hormones and sex hormones-related phenotypes using Mendelian randomization
2025 · Shulin Liu, Yuxuan Hu, et al. · Parkinsonism & Related Disorders · 4
Functional and Structural Deficits of Cone Photoreceptors in Mice Lacking PCDH15, a Protein Encoded by the Ush1F Gene
2006 · Xun Sun, Basil S. Pawlyk, et al. · Investigative Ophthalmology & Visual Science · 3
Phenotypic Characterization of the LOXL1 Null Mouse
2009 · Janey L. Wiggs, Basil S. Pawlyk, et al. · Investigative Ophthalmology & Visual Science · 2
Subcellular Localization of Whirlin and Its Interaction With Ush2a in the Photoreceptors
2006 · J. Yang, X. Liu, et al. · Investigative Ophthalmology & Visual Science · 2
The Ciliary Rootlet Provides Structural Support for Photoreceptor Outer Segments
2005 · J. Yang, Jiangang Gao, et al. · Investigative Ophthalmology & Visual Science · 2
Identifying the NEAT1/miR-26b-5p/S100A2 axis as a regulator in Parkinson’s disease based on the ferroptosis-related genes
2024 · Taole Li, Jifeng Guo · PLoS ONE · 1
Genetic and Biochemical Analyses of the Ush2A Protein (Usherin)
2005 · X. Liu, Oleg V. Bulgakov, et al. · Investigative Ophthalmology & Visual Science · 1
Mutations in PLA2G6 impair ER–mitochondria contacts and ceramide homeostasis via GRP75 in Parkinson’s disease
2025 · Jiabin Liu, Qiao Yin, et al. · Research Square
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Retraction Note: Gene therapy with a promoter targeting both rods and cones rescues retinal degeneration caused by AIPL1 mutations
2024 · X. Sun, B. Pawlyk, et al. · Gene Therapy
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Evaluation of QSAR models for predicting mutagenicity: outcome of the Second Ames/QSAR international challenge project
2023 · Furuhama, A., Kitazawa, A., et al. · Figshare
Replacement Gene Therapy in Mouse Models of LCA Lacking AIPL1
2009 · Xun Sun, Basil S. Pawlyk, et al. · Investigative Ophthalmology & Visual Science
Retinal and Inner Ear Defects in Mice Lacking Nherf-1, a Potential New Model for Usher Syndrome
2008 · Xun Sun, Michael Adamian, et al. · Investigative Ophthalmology & Visual Science
Replacement Gene Therapy Preserves Photoreceptor Function And Survival in a Mouse Model of Retinal Degeneration Lacking Tulp1
2008 · Oleg V. Bulgakov, X. Liu, et al. · Investigative Ophthalmology & Visual Science
N-Terminal Mutation of Whirlin Disrupts the Usher Syndrome II (USH2) Protein Complex and Causes Retinal and Inner Ear Defects in Mice
2008 · Jun Yang, X. Liu, et al. · Investigative Ophthalmology & Visual Science
Mpp4 at the Photoreceptor Synaptic Terminals: Anchoring Plasma Membrane Calcium ATPases and Modulating Calcium Homeostasis
2007 · J. Yang, Basil S. Pawlyk, et al. · Investigative Ophthalmology & Visual Science
A single abbreviated ORF15 variant appears sufficient to reconstitute RPGR function in vivo
2004 · Donghyun Hong, Basil S. Pawlyk, et al. · Investigative Ophthalmology & Visual Science
Works count: 18
Citation count: 106
H-index: 3
I10-index: 2
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