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Taysha Gene Therapies (United States)

Homepage: tayshagtx.com
Alternate names: Taysha, Taysha GTx, Taysha Gene Therapies, Taysha Gene Therapies, Inc.
ROR: 0588nm138
OpenAlex ID: I4405273080
Immune Responses and Immunosuppressive Strategies for Adeno-Associated Virus-Based Gene Therapy for Treatment of Central Nervous System Disorders: Current Knowledge and Approaches
2022 · Suyash Prasad, David P. Dimmock, et al. · Human Gene Therapy · 93
Intrathecal Gene Therapy for Giant Axonal Neuropathy
2024 · Diana X. Bharucha-Goebel, Joshua J. Todd, et al. · New England Journal of Medicine · 71
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Biodistribution of Adeno-Associated Virus Gene Therapy Following Cerebrospinal Fluid-Directed Administration
2023 · Xin Chen, Daniel A. Lim, et al. · Human Gene Therapy · 70
The Efficacy of a Human-Ready miniMECP2 Gene Therapy in a Pre-Clinical Model of Rett Syndrome
2023 · Chanchal Sadhu, Christopher Lyons, et al. · Genes · 34
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SLC13A5 Deficiency Disorder: From Genetics to Gene Therapy
2022 · Kimberly Goodspeed, Judy S. Liu, et al. · Genes · 20
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CNS-dominant human FMRP isoform rescues seizures, fear, and sleep abnormalities in Fmr1-KO mice
2023 · Hayes Wong, Alexander W.M. Hooper, et al. · JCI Insight · 15
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Gene Therapy: Novel Approaches to Targeting Monogenic Epilepsies
2022 · Kimberly Goodspeed, Rachel M. Bailey, et al. · Frontiers in Neurology · 11
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Standardized Nomenclature and Reporting for PacBio HiFi Sequencing and Analysis of rAAV Gene Therapy Vectors
2024 · Eric Talevich, Elizabeth Tseng, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 3
rAAV9 vector biodistribution in nonhuman primate brain and spinal cord following lumbar intrathecal infusion
2026 · Emdadul Haque, Nino Devidze, et al. · Frontiers in Medicine · 1
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Understanding Caregivers’ Experiences of Rett Syndrome: A Multinational Study of Symptoms and Meaningful Outcomes of Potential Treatments
2026 · Bruria Ben-Zeev, Elsa Rossignol, et al. · Neurology and Therapy
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AAV downstream challenges: specialist insights
2024 · Nathalie Clement, William Kish, et al. · Cell and Gene Therapy Insights
Detect Lysosomal Storage Diseases, a No-charge Sponsored Testing Program, Enables Access to Genetic Testing, Treatment, and Clinical Trials for Individuals With Suspected Lysosomal Storage Disorders
2022 · Britt Johnson, Kathleen Crosby, et al. · Molecular Genetics and Metabolism
Detect Lysosomal Storage Diseases: A no-charge, sponsored, testing program that enables access to genetic testing, treatment, and clinical trials for individuals with suspected lysosomal disorders
2022 · Heather M. McLaughlin, Michele Clarke, et al. · Molecular Genetics and Metabolism
Connect: Designing a first-in-human gene replacement therapy clinical trial for CLN1
2022 · Fernanda Leal-Pardinas, Andy Cunningham, et al. · Molecular Genetics and Metabolism
Co-creating a gene therapy clinical trial with GM2 gangliosidosis caregivers: A virtual approach to patient engagement
2021 · Kristin LaBounty Phillips, Emily McGinnis, et al. · Molecular Genetics and Metabolism
Works count: 15
Citation count: 809
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