Solving the puzzle of neurological diseases: an interview with Huda Zoghbi

por Zoghbi, Huda Y.
Publicado 2017

The Atoh1-Cre Knock-In Allele Ectopically Labels a Subpopulation of Amacrine Cells and Bipolar Cells in Mouse Retina

por Wu, Sih-Rong, Zoghbi, Huda Y.
Publicado 2023

Genomic organization of Tropomodulins 2 and 4 and unusual intergenic and intraexonic splicing of YL-1 and Tropomodulin 4

por Cox, Patrick R, Siddique, Teepu, Zoghbi, Huda Y
Publicado 2001

Loss of Atoh1 from neurons regulating hypoxic and hypercapnic chemoresponses causes neonatal respiratory failure in mice

por van der Heijden, Meike E, Zoghbi, Huda Y
Publicado 2018

Rett-causing mutations reveal two domains critical for MeCP2 function and for toxicity in MECP2 duplication syndrome mice

por Heckman, Laura Dean, Chahrour, Maria H, Zoghbi, Huda Y
Publicado 2014

14-3-3 Binding to Ataxin-1(ATXN1) Regulates Its Dephosphorylation at Ser-776 and Transport to the Nucleus

por Lai, Shaojuan, O'Callaghan, Brennon, Zoghbi, Huda Y., Orr, Harry T.
Publicado 2011

Impaired spatial memory codes in a mouse model of Rett syndrome

por Kee, Sara E, Mou, Xiang, Zoghbi, Huda Y, Ji, Daoyun
Publicado 2018

Jak2-mediated phosphorylation of Atoh1 is critical for medulloblastoma growth

por Klisch, Tiemo J, Vainshtein, Anna, Patel, Akash J, Zoghbi, Huda Y
Publicado 2017

Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus

por Ben-Shachar, Shay, Chahrour, Maria, Thaller, Christina, Shaw, Chad A., Zoghbi, Huda Y.
Publicado 2009

The Chromatin Modifier MSK1/2 Suppresses Endocrine Cell Fates during Mouse Pancreatic Development

por Bhat, Neha, Park, Jeehye, Zoghbi, Huda Y., Arthur, J. Simon C., Zaret, Kenneth S.
Publicado 2016

Increased Axonal Bouton Stability during Learning in the Mouse Model of MECP2 Duplication Syndrome

por Ash, Ryan T., Fahey, Paul G., Park, Jiyoung, Zoghbi, Huda Y., Smirnakis, Stelios M.
Publicado 2018

Excessive Formation and Stabilization of Dendritic Spine Clusters in the MECP2-Duplication Syndrome Mouse Model of Autism

por Ash, Ryan Thomas, Park, Jiyoung, Suter, Bernhard, Zoghbi, Huda Yaya, Smirnakis, Stelios Manolis
Publicado 2021

Partial Loss of Ataxin-1 Function Contributes to Transcriptional Dysregulation in Spinocerebellar Ataxia Type 1 Pathogenesis

por Crespo-Barreto, Juan, Fryer, John D., Shaw, Chad A., Orr, Harry T., Zoghbi, Huda Y.
Publicado 2010

Partial loss of Tip60 slows mid-stage neurodegeneration in a spinocerebellar ataxia type 1 (SCA1) mouse model

por Gehrking, Kristin M., Andresen, J. Michael, Duvick, Lisa, Lough, John, Zoghbi, Huda Y., Orr, Harry T.
Publicado 2011

Beta-binomial modeling of CRISPR pooled screen data identifies target genes with greater sensitivity and fewer false negatives

por Jeong, Hyun-Hwan, Kim, Seon Young, Rousseaux, Maxime W.C., Zoghbi, Huda Y., Liu, Zhandong
Publicado 2019

Genetic Modifiers of MeCP2 Function in Drosophila

por Cukier, Holly N., Perez, Alma M., Collins, Ann L., Zhou, Zhaolan, Zoghbi, Huda Y., Botas, Juan
Publicado 2008

PolyA-miner: accurate assessment of differential alternative poly-adenylation from 3′Seq data using vector projections and non-negative matrix factorization

por Yalamanchili, Hari Krishna, Alcott, Callison E, Ji, Ping, Wagner, Eric J, Zoghbi, Huda Y, Liu, Zhandong
Publicado 2020

Identification and characterization of conserved noncoding cis-regulatory elements that impact Mecp2 expression and neurological functions

por Shao, Yingyao, Bajikar, Sameer S., Tirumala, Harini P., Gutierrez, Manuel Cantu, Wythe, Joshua D., Zoghbi, Huda Y.
Publicado 2021

The Transcription Factor Pou3f1 Sheds Light on the Development and Molecular Diversity of Glutamatergic Cerebellar Nuclear Neurons in the Mouse

por Wu, Joshua Po Han, Yeung, Joanna, Rahimi-Balaei, Maryam, Wu, Sih-Rong, Zoghbi, Huda, Goldowitz, Dan
Publicado 2022

Motor neuron degeneration correlates with respiratory dysfunction in SCA1

por Orengo, James P., van der Heijden, Meike E., Hao, Shuang, Tang, Jianrong, Orr, Harry T., Zoghbi, Huda Y.
Publicado 2018