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Scientific Reports|February 18, 2018
Functional analysis of SLC39A8 mutations and their implications for manganese deficiency and mitochondrial disordersEun-Kyung Choi, Trang-Tiffany Nguyen, Neil Gupta, et al.Cells|February 25, 2023
Sexually Dimorphic Alterations in the Transcriptome and Behavior with Loss of Histone Demethylase KDM5CKatherine M Bonefas, Christina N Vallianatos, Brynne Raines, et al.Cell Reports|October 6, 2017
Loss of Kdm5c Causes Spurious Transcription and Prevents the Fine-Tuning of Activity-Regulated Enhancers in NeuronsMarilyn Scandaglia, Jose P Lopez-Atalaya, Alejandro Medrano-Fernandez, et al.Biochemical and Biophysical Research Communications|August 25, 2004
Characterization of BHC80 in BRAF-HDAC complex, involved in neuron-specific gene repressionShigeki Iwase, Aya Januma, Kiyoko Miyamoto, et al.Frontiers in Molecular Neuroscience|April 20, 2018
Altered Gene-Regulatory Function of KDM5C by a Novel Mutation Associated With Autism and Intellectual DisabilityChristina N Vallianatos, Clara Farrehi, Michael J Friez, et al.FEBS Letters|May 11, 2006
A component of BRAF-HDAC complex, BHC80, is required for neonatal survival in miceShigeki Iwase, Naomi Shono, Arata Honda, et al.European Journal of Human Genetics : EJHG|October 15, 2009
Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype-phenotype correlationSinitdhorn Rujirabanjerd, John Nelson, Patrick S Tarpey, et al.Nature|September 14, 2007
A histone H3 lysine 27 demethylase regulates animal posterior developmentFei Lan, Peter E Bayliss, John L Rinn, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 10, 2017
Epigenetic Etiology of Intellectual DisabilityShigeki Iwase, Nathalie G Bérubé, Zhaolan Zhou, et al.Journal of Neurochemistry|November 27, 2021
A neurodegeneration gene, WDR45, links impaired ferritinophagy to iron accumulationLuisa Aring, Eun-Kyung Choi, Huira Kopera, et al.Pageof 143