Xiang-Jiao Yang
Affiliations: | McGill University, Montreal, QC, Canada |
Area:
Molecular BiologyGoogle:
"Xiang-Jiao Yang"
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Publications
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| Yan K, Mousavi N, Yang XJ. (2023) Analysis of Lysine Acetylation and Acetylation-like Acylation In Vitro and In Vivo. Current Protocols. 3: e738 |
| Latypova X, Vincent M, Mollé A, et al. (2021) Haploinsufficiency of the Sin3/HDAC corepressor complex member SIN3B causes a syndromic intellectual disability/autism spectrum disorder. American Journal of Human Genetics |
| Wakeling E, McEntagart M, Bruccoleri M, et al. (2021) Missense substitutions at a conserved 14-3-3 binding site in HDAC4 cause a novel intellectual disability syndrome. Hgg Advances. 2: 100015 |
| Humbert J, Salian S, Makrythanasis P, et al. (2020) De Novo KAT5 Variants Cause a Syndrome with Recognizable Facial Dysmorphisms, Cerebellar Atrophy, Sleep Disturbance, and Epilepsy. American Journal of Human Genetics |
| Yan K, Rousseau J, Machol K, et al. (2020) Deficient histone H3 propionylation by BRPF1-KAT6 complexes in neurodevelopmental disorders and cancer. Science Advances. 6: eaax0021 |
| Li L, Ghorbani M, Weisz-Hubshman M, et al. (2019) Lysine acetyltransferase 8 is involved in cerebral development and syndromic intellectual disability. The Journal of Clinical Investigation |
| Li L, Jin J, Yang XJ. (2019) Histone Deacetylase 3 Governs Perinatal Cerebral Development via Neural Stem and Progenitor Cells. Iscience. 20: 148-167 |
| Li L, Jayabal S, Ghorbani M, et al. (2019) ATAT1 regulates forebrain development and stress-induced tubulin hyperacetylation. Cellular and Molecular Life Sciences : Cmls |
| Cogné B, Ehresmann S, Beauregard-Lacroix E, et al. (2019) Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability. American Journal of Human Genetics |
| Han Z, Wu H, Kim S, et al. (2018) Revealing the Protein Propionylation Activity of the Histone Acetyltransferase Males absent on the first (MOF). The Journal of Biological Chemistry |