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The Journal of Biological Chemistry|April 2, 2011
Structure and histone binding properties of the Vps75-Rtt109 chaperone-lysine acetyltransferase complexDan Su, Qi Hu, Hui Zhou, et al.
Molecular Pharmacology|July 19, 2006
Solution NMR of acetylcholine binding protein reveals agonist-mediated conformational change of the C-loopFan Gao, Georges Mer, Marco Tonelli, et al.
Nature Genetics|May 3, 2011
Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing lossChristopher J Klein, Maria-Victoria Botuyan, Yanhong Wu, et al.
Neurology. Genetics|December 22, 2025
Expanding the Molecular and Pathologic Spectrum of HSPB8 Myopathy and Distal Motor NeuropathyBrendan Nicholas Putko, Eric J Sorenson, Gaofeng Cui, et al.
The EMBO Journal|March 1, 2012
RNF8- and RNF168-dependent degradation of KDM4A/JMJD2A triggers 53BP1 recruitment to DNA damage sitesFrédérick A Mallette, Francesca Mattiroli, Gaofeng Cui, et al.
Brain : a Journal of Neurology|February 14, 2015
Defects of mutant DNMT1 are linked to a spectrum of neurological disordersJonathan Baets, Xiaohui Duan, Yanhong Wu, et al.
The Journal of Biological Chemistry|September 29, 2012
The potassium channel interacting protein 3 (DREAM/KChIP3) heterodimerizes with and regulates calmodulin functionPradeep L Ramachandran, Theodore A Craig, Elena A Atanasova, et al.
Annals of Neurology|December 27, 2016
Genomic analysis reveals frequent TRAF7 mutations in intraneural perineuriomasChristopher J Klein, Yanhong Wu, Mark E Jentoft, et al.
Acta Neuropathologica Communications|April 30, 2021
Filamentous tangles with nemaline rods in MYH2 myopathy: a novel phenotypeNicolas N Madigan, Michael J Polzin, Gaofeng Cui, et al.
Neurology|February 1, 2013
DNMT1 mutation hot spot causes varied phenotypes of HSAN1 with dementia and hearing lossChristopher J Klein, Tom Bird, Nilufer Ertekin-Taner, et al.
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