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Human Molecular Genetics|January 26, 2006
Polyglutamine expansion causes neurodegeneration by altering the neuronal differentiation programGretta Abou-Sleymane, Frédéric Chalmel, Dominique Helmlinger, et al.
Plos Biology|February 24, 2006
Glutamine-expanded ataxin-7 alters TFTC/STAGA recruitment and chromatin structure leading to photoreceptor dysfunctionDominique Helmlinger, Sara Hardy, Gretta Abou-Sleymane, et al.
EMBO Reports|July 17, 2010
The structural plasticity of SCA7 domains defines their differential nucleosome-binding propertiesJacques Bonnet, Ying-Hui Wang, Gianpiero Spedale, et al.
Human Molecular Genetics|April 30, 2004
Ataxin-7 is a subunit of GCN5 histone acetyltransferase-containing complexesDominique Helmlinger, Sara Hardy, Souphatta Sasorith, et al.
Pediatric Radiology|June 22, 2018
Morphological features in juvenile Huntington disease associated with cerebellar atrophy - magnetic resonance imaging morphometric analysisAbderrahmane Hedjoudje, Gaël Nicolas, Alice Goldenberg, et al.
Cell|February 5, 2013
LBR and lamin A/C sequentially tether peripheral heterochromatin and inversely regulate differentiationIrina Solovei, Audrey S Wang, Katharina Thanisch, et al.
Human Molecular Genetics|April 13, 2018
Homozygous TAF8 mutation in a patient with intellectual disability results in undetectable TAF8 protein, but preserved RNA polymerase II transcriptionFarrah El-Saafin, Cynthia Curry, Tao Ye, et al.
Molecular Cell|January 22, 2008
A TFTC/STAGA module mediates histone H2A and H2B deubiquitination, coactivates nuclear receptors, and counteracts heterochromatin silencingYue Zhao, Guillaume Lang, Saya Ito, et al.
Plos Genetics|October 3, 2014
H2B mono-ubiquitylation facilitates fork stalling and recovery during replication stress by coordinating Rad53 activation and chromatin assemblyChia-Yeh Lin, Meng-Ying Wu, Sophie Gay, et al.
American Journal of Medical Genetics. Part A|January 5, 2011
ARX polyalanine expansions are highly implicated in familial cases of mental retardation with infantile epilepsy and/or hand dystoniaMireille Cossée, Laurence Faivre, Christophe Philippe, et al.
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