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Blood|May 28, 2017
T cells lacking HDAC11 have increased effector functions and mediate enhanced alloreactivity in a murine modelDavid M Woods, Karrune V Woan, Fengdong Cheng, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 3, 2016
Control of embryonic stem cell self-renewal and differentiation via coordinated alternative splicing and translation of YY2Soroush Tahmasebi, Seyed Mehdi Jafarnejad, Ingrid S Tam, et al.
American Journal of Human Genetics|January 24, 2012
Mutations in KAT6B, encoding a histone acetyltransferase, cause Genitopatellar syndromePhilippe M Campeau, Jaeseung C Kim, James T Lu, et al.
American Journal of Human Genetics|September 13, 2016
De Novo Mutations in CHD4, an ATP-Dependent Chromatin Remodeler Gene, Cause an Intellectual Disability Syndrome with Distinctive DysmorphismsKarin Weiss, Paulien A Terhal, Lior Cohen, et al.
Reviews in Medical Virology|November 5, 2011
Chromosomally integrated human herpesvirus 6: questions and answersPhilip E Pellett, Dharam V Ablashi, Peter F Ambros, et al.
Molecular Cell|June 3, 2014
HDAC6 deacetylates and ubiquitinates MSH2 to maintain proper levels of MutSαMu Zhang, Shengyan Xiang, Heui-Yun Joo, et al.
Science Advances|February 4, 2020
Deficient histone H3 propionylation by BRPF1-KAT6 complexes in neurodevelopmental disorders and cancerKezhi Yan, Justine Rousseau, Keren Machol, et al.
The Journal of Clinical Investigation|December 4, 2019
Lysine acetyltransferase 8 is involved in cerebral development and syndromic intellectual disabilityLin Li, Mohammad Ghorbani, Monika Weisz-Hubshman, et al.
American Journal of Human Genetics|December 13, 2016
Mutations in the Chromatin Regulator Gene BRPF1 Cause Syndromic Intellectual Disability and Deficient Histone AcetylationKezhi Yan, Justine Rousseau, Rebecca Okashah Littlejohn, et al.
American Journal of Human Genetics|April 3, 2021
Haploinsufficiency of the Sin3/HDAC corepressor complex member SIN3B causes a syndromic intellectual disability/autism spectrum disorderXenia Latypova, Marie Vincent, Alice Mollé, et al.
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