MeCP2 binds to non-CG methylated DNA as neurons mature, influencing transcription and the timing of onset for Rett syndrome
Chen, Lin, Chen, Kaifu, Lavery, Laura A., Baker, Steven Andrew, Shaw, Chad A., Li, Wei, Zoghbi, Huda Y.
Published in Proceedings of the National Academy of Sciences - PNAS (28.04.2015)
Published in Proceedings of the National Academy of Sciences - PNAS (28.04.2015)
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Reversal of phenotypes in MECP2 duplication mice using genetic rescue or antisense oligonucleotides
Sztainberg, Yehezkel, Chen, Hong-mei, Swann, John W., Hao, Shuang, Tang, Bin, Wu, Zhenyu, Tang, Jianrong, Wan, Ying-Wooi, Liu, Zhandong, Rigo, Frank, Zoghbi, Huda Y.
Published in Nature (London) (03.12.2015)
Published in Nature (London) (03.12.2015)
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Postnatal Neurodevelopmental Disorders: Meeting at the Synapse?
Zoghbi, Huda Y.
Published in Science (American Association for the Advancement of Science) (31.10.2003)
Published in Science (American Association for the Advancement of Science) (31.10.2003)
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MeCP2 Controls Excitatory Synaptic Strength by Regulating Glutamatergic Synapse Number
Chao, Hsiao-Tuan, Zoghbi, Huda Y., Rosenmund, Christian
Published in Neuron (Cambridge, Mass.) (04.10.2007)
Published in Neuron (Cambridge, Mass.) (04.10.2007)
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Reduction of Nuak1 Decreases Tau and Reverses Phenotypes in a Tauopathy Mouse Model
Lasagna-Reeves, Cristian A., de Haro, Maria, Hao, Shuang, Park, Jeehye, Rousseaux, Maxime W.C., Al-Ramahi, Ismael, Jafar-Nejad, Paymaan, Vilanova-Velez, Luis, See, Lauren, De Maio, Antonia, Nitschke, Larissa, Wu, Zhenyu, Troncoso, Juan C., Westbrook, Thomas F., Tang, Jianrong, Botas, Juan, Zoghbi, Huda Y.
Published in Neuron (Cambridge, Mass.) (19.10.2016)
Published in Neuron (Cambridge, Mass.) (19.10.2016)
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MeCP2, a Key Contributor to Neurological Disease, Activates and Represses Transcription
Chahrour, Maria, Jung, Sung Yun, Shaw, Chad, Zhou, Xiaobo, Wong, Stephen T.C, Qin, Jun, Zoghbi, Huda Y
Published in Science (American Association for the Advancement of Science) (30.05.2008)
Published in Science (American Association for the Advancement of Science) (30.05.2008)
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Cerebellar Transcriptome Profiles of ATXN1 Transgenic Mice Reveal SCA1 Disease Progression and Protection Pathways
Ingram, Melissa, Wozniak, Emily A.L., Duvick, Lisa, Yang, Rendong, Bergmann, Paul, Carson, Robert, O’Callaghan, Brennon, Zoghbi, Huda Y., Henzler, Christine, Orr, Harry T.
Published in Neuron (Cambridge, Mass.) (16.03.2016)
Published in Neuron (Cambridge, Mass.) (16.03.2016)
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Molecular profiling predicts meningioma recurrence and reveals loss of DREAM complex repression in aggressive tumors
Patel, Akash J., Wan, Ying-Wooi, Al-Ouran, Rami, Revelli, Jean-Pierre, Cardenas, Maria F., Oneissi, Mazen, Xi, Liu, Jalali, Ali, Magnotti, John F., Muzny, Donna M., Doddapaneni, HarshaVardhan, Sebastian, Sherly, Heck, Kent A., Goodman, J. Clay, Gopinath, Shankar P., Liu, Zhandong, Rao, Ganesh, Plon, Sharon E., Yoshor, Daniel, Wheeler, David A., Zoghbi, Huda Y., Klisch, Tiemo J.
Published in Proceedings of the National Academy of Sciences - PNAS (22.10.2019)
Published in Proceedings of the National Academy of Sciences - PNAS (22.10.2019)
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Pumilio1 Haploinsufficiency Leads to SCA1-like Neurodegeneration by Increasing Wild-Type Ataxin1 Levels
Gennarino, Vincenzo A., Singh, Ravi K., White, Joshua J., De Maio, Antonia, Han, Kihoon, Kim, Ji-Yoen, Jafar-Nejad, Paymaan, di Ronza, Alberto, Kang, Hyojin, Sayegh, Layal S., Cooper, Thomas A., Orr, Harry T., Sillitoe, Roy V., Zoghbi, Huda Y.
Published in Cell (12.03.2015)
Published in Cell (12.03.2015)
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