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 mentor| Marvin A. Fishman | post-doc | 1982-1985 | Baylor |
| Arthur L. Beaudet | post-doc | 1985-1988 | Baylor |
Children
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Publications
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| Nitschke L, Coffin SL, Xhako E, et al. (2021) Modulation of ATXN1 S776 phosphorylation reveals the importance of allele-specific targeting in SCA1. Jci Insight. 6 |
| Achilly NP, He LJ, Kim OA, et al. (2021) Deleting from the cerebellum rather than its neuronal subtypes causes a delay in motor learning in mice. Elife. 10 |
| Ward CS, Huang TW, Herrera JA, et al. (2020) Loss of MeCP2 Function Across Several Neuronal Populations Impairs Breathing Response to Acute Hypoxia. Frontiers in Neurology. 11: 593554 |
| Ito-Ishida A, Baker SA, Sillitoe RV, et al. (2020) MeCP2 Levels Regulate the 3D Structure of Heterochromatic Foci in Mouse Neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience |
| Nitschke L, Tewari A, Coffin SL, et al. (2020) miR760 regulates ATXN1 levels via interaction with its 5' untranslated region. Genes & Development |
| Pang K, Wang L, Wang W, et al. (2020) Coexpression enrichment analysis at the single-cell level reveals convergent defects in neural progenitor cells and their cell-type transitions in neurodevelopmental disorders. Genome Research |
| Yalamanchili HK, Alcott CE, Ji P, et al. (2020) PolyA-miner: accurate assessment of differential alternative poly-adenylation from 3'Seq data using vector projections and non-negative matrix factorization. Nucleic Acids Research |
| Fagiolini M, Patrizi A, LeBlanc J, et al. (2020) Intellectual and Developmental Disabilities Research Centers: a multidisciplinary approach to understand the pathogenesis of MECP2-related disorders. Neuroscience |
| Alcott CE, Yalamanchili HK, Ji P, et al. (2020) Partial loss of CFIm25 causes learning deficits and aberrant neuronal alternative polyadenylation. Elife. 9 |
| Lavery LA, Ure K, Wan YW, et al. (2020) Losing Dnmt3a dependent methylation in inhibitory neurons impairs neural function by a mechanism impacting Rett syndrome. Elife. 9 |