Huda Y. Zoghbi
Affiliations: | Baylor College of Medicine, Houston, TX |
Area:
SCA1, SCA7, Rett's syndrome, and Math1Google:
"Huda Zoghbi"Mean distance: 14.28 (cluster 11) | S | N | B | C | P |
Cross-listing: BCM Tree
Parents
Sign in to add mentorMarvin A. Fishman | post-doc | 1982-1985 | Baylor College of Medicine |
Arthur L. Beaudet | post-doc | 1985-1988 | Baylor College of Medicine |
Children
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Publications
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Duvick L, Southern WM, Benzow K, et al. (2023) Regional vulnerability in a neurodegenerative disease: Delineating SCA1 CNS and muscle therapeutic targets using a conditional mutant ATXN1 mouse. Biorxiv : the Preprint Server For Biology |
Handler HP, Duvick L, Mitchell JS, et al. (2022) Decreasing mutant ATXN1 nuclear localization improves a spectrum of SCA1-like phenotypes and brain region transcriptomic profiles. Neuron |
Coffin SL, Durham MA, Nitschke L, et al. (2022) Disruption of the ATXN1-CIC complex reveals the role of additional nuclear ATXN1 interactors in spinocerebellar ataxia type 1. Neuron |
Lee WS, Al-Ramahi I, Jeong HH, et al. (2022) Cross-species genetic screens identify transglutaminase 5 as a regulator of polyglutamine-expanded ataxin-1. The Journal of Clinical Investigation. 132 |
He L, Caudill MS, Jing J, et al. (2022) A weakened recurrent circuit in the hippocampus of Rett syndrome mice disrupts long-term memory representations. Neuron |
Orengo JP, Nitschke L, van der Heijden ME, et al. (2022) Reduction of mutant ATXN1 rescues premature death in a conditional SCA1 mouse model. Jci Insight. 7 |
Zhou J, Hamdan H, Yalamanchili HK, et al. (2022) Disruption of MeCP2-TCF20 complex underlies distinct neurodevelopmental disorders. Proceedings of the National Academy of Sciences of the United States of America. 119 |
McKnight D, Bean L, Karbassi I, et al. (2021) Recommendations by the ClinGen Rett/Angelman-like expert panel for gene-specific variant interpretation methods. Human Mutation |
Vázquez-Vélez GE, Zoghbi HY. (2021) Parkinson's Disease Genetics and Pathophysiology. Annual Review of Neuroscience. 44: 87-108 |
Shao Y, Sztainberg Y, Wang Q, et al. (2021) Antisense oligonucleotide therapy in a humanized mouse model of duplication syndrome. Science Translational Medicine. 13 |