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The Journal of Clinical Investigation|October 15, 2021
Temporal manipulation of Cdkl5 reveals essential postdevelopmental functions and reversible CDKL5 deficiency disorder-related deficitsBarbara Terzic, M Felicia Davatolhagh, Yugong Ho, et al.
Nucleic Acids Research|July 17, 2008
Human DDX3 functions in translation and interacts with the translation initiation factor eIF3Chung-Sheng Lee, Anusha P Dias, Mark Jedrychowski, et al.
Human Mutation|September 12, 2006
Weak definition of IKBKAP exon 20 leads to aberrant splicing in familial dysautonomiaEl Chérif Ibrahim, Matthew M Hims, Noam Shomron, et al.
Molecular Cell|June 26, 2007
SR proteins function in coupling RNAP II transcription to pre-mRNA splicingRita Das, Jiong Yu, Zuo Zhang, et al.
Nature Communications|June 16, 2019
Altered NMDAR signaling underlies autistic-like features in mouse models of CDKL5 deficiency disorderSheng Tang, Barbara Terzic, I-Ting Judy Wang, et al.
Experimental Neurology|June 26, 2020
Aged heterozygous Cdkl5 mutant mice exhibit spontaneous epileptic spasmsPatrick J Mulcahey, Sheng Tang, Hajime Takano, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 5, 2017
Loss of CDKL5 in Glutamatergic Neurons Disrupts Hippocampal Microcircuitry and Leads to Memory Impairment in MiceSheng Tang, I-Ting Judy Wang, Cuiyong Yue, et al.
Nature Biotechnology|August 28, 2023
Joint single-cell profiling resolves 5mC and 5hmC and reveals their distinct gene regulatory effectsEmily B Fabyanic, Peng Hu, Qi Qiu, et al.
Blood|May 4, 2007
The human Shwachman-Diamond syndrome protein, SBDS, associates with ribosomal RNAKarthik A Ganapathi, Karyn M Austin, Chung-Sheng Lee, et al.
Plos Genetics|February 27, 2023
Allelic contribution of Nrxn1α to autism-relevant behavioral phenotypes in miceBing Xu, Yugong Ho, Maria Fasolino, et al.
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