| Year |
Citation |
Score |
| 2024 |
Chang YT, Lee YJ, Haque M, Chang HC, Javed S, Lin YC, Cho Y, Abramovitz J, Chin G, Khamis A, Raja R, Murai KK, Huang WH. Comparative analyses of the Smith-Magenis syndrome protein RAI1 in mice and common marmoset monkeys. The Journal of Comparative Neurology. 532: e25589. PMID 38289192 DOI: 10.1002/cne.25589 |
0.819 |
|
| 2023 |
Javed S, Chang YT, Cho Y, Lee YJ, Chang HC, Haque M, Lin YC, Huang WH. Smith-Magenis syndrome protein RAI1 regulates body weight homeostasis through hypothalamic BDNF-producing neurons and neurotrophin downstream signalling. Elife. 12. PMID 37956053 DOI: 10.7554/eLife.90333 |
0.512 |
|
| 2022 |
Chang HC, Lee YJ, Javed S, Haque M, Chang YT, Lin YC, Oram C, Huang WH. rAAV-CRISPRa therapy corrects Rai1 haploinsufficiency and rescues selective disease features in Smith-Magenis syndrome mice. The Journal of Biological Chemistry. 102728. PMID 36410433 DOI: 10.1016/j.jbc.2022.102728 |
0.657 |
|
| 2022 |
Chang YT, Kowalczyk M, Fogerson PM, Lee YJ, Haque M, Adams EL, Wang DC, DeNardo LA, Tessier-Lavigne M, Huguenard JR, Luo L, Huang WH. Loss of enhances hippocampal excitability and epileptogenesis in mouse models of Smith-Magenis syndrome. Proceedings of the National Academy of Sciences of the United States of America. 119: e2210122119. PMID 36256819 DOI: 10.1073/pnas.2210122119 |
0.679 |
|
| 2021 |
Javed S, Lee YJ, Xu J, Huang WH. Temporal dissection of Rai1 function reveals brain-derived neurotrophic factor as a potential therapeutic target for Smith-Magenis syndrome. Human Molecular Genetics. PMID 34463714 DOI: 10.1093/hmg/ddab245 |
0.847 |
|
| 2020 |
Javed S, Selliah T, Lee YJ, Huang WH. Dosage-sensitive genes in autism spectrum disorders: From neurobiology to therapy. Neuroscience and Biobehavioral Reviews. PMID 32858083 DOI: 10.1016/J.Neubiorev.2020.08.009 |
0.778 |
|
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