For: | Toral-Lopez J, González Huerta LM, Messina-Baas O, Cuevas-Covarrubias SA. Submicroscopic 11p13 deletion including the elongator acetyltransferase complex subunit 4 gene in a girl with language failure, intellectual disability and congenital malformations: A case report . World J Clin Cases 2020; 8(21): 5296-5303 [PMID: 33269262 DOI: 10.12998/wjcc.v8.i21.5296] |
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URL: | https://www.wjgnet.com/2307-8960/full/v8/i21/5296.htm |
Number | Citing Articles |
1 |
Kaan Okay, Pelin Ünal Varış, Süha Miral, Athanasia Pavlopoulou, Yavuz Oktay, Gökhan Karakülah. Whole Genome Analysis of Dizygotic Twins With Autism Reveals Prevalent Transposon Insertion Within Neuronal Regulatory Elements: Potential Implications for Disease Etiology and Clinical Assessment. Journal of Autism and Developmental Disorders 2023; 53(3): 1091 doi: 10.1007/s10803-022-05636-6
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2 |
Marija Kojic, Nour E. H. Abbassi, Ting-Yu Lin, Alun Jones, Emma L. Wakeling, Emma Clement, Vasiliki Nakou, Matthew Singleton, Dominika Dobosz, Marios Kaliakatsos, Sebastian Glatt, Brandon J. Wainwright. A novel ELP1 mutation impairs the function of the Elongator complex and causes a severe neurodevelopmental phenotype. Journal of Human Genetics 2023; 68(7): 445 doi: 10.1038/s10038-023-01135-3
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3 |
Monika Gaik, Marija Kojic, Megan R Stegeman, Tülay Öncü‐Öner, Anna Kościelniak, Alun Jones, Ahmed Mohamed, Pak Yan Stefanie Chau, Sazia Sharmin, Andrzej Chramiec‐Głąbik, Paulina Indyka, Michał Rawski, Anna Biela, Dominika Dobosz, Amanda Millar, Vann Chau, Aycan Ünalp, Michael Piper, Mark C Bellingham, Evan E Eichler, Deborah A Nickerson, Handan Güleryüz, Nour El Hana Abbassi, Konrad Jazgar, Melissa J Davis, Saadet Mercimek‐Andrews, Sultan Cingöz, Brandon J Wainwright, Sebastian Glatt. Functional divergence of the two Elongator subcomplexes during neurodevelopment. EMBO Molecular Medicine 2022; 14(7) doi: 10.15252/emmm.202115608
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4 |
Ikram Toudji, Asmaa Toumi, Émile Chamberland, Elsa Rossignol. Interneuron odyssey: molecular mechanisms of tangential migration. Frontiers in Neural Circuits 2023; 17 doi: 10.3389/fncir.2023.1256455
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5 |
Yinwen Li, Jieqiong Chen, Ying Zheng, Zhixuan Chen, Tao Wang, Qian Sun, Xiaoling Wan, Haiyun Liu, Xiaodong Sun. A novel microdeletion of 517 kb downstream of the PAX6 gene in a Chinese family with congenital aniridia. BMC Ophthalmology 2023; 23(1) doi: 10.1186/s12886-023-03147-1
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6 |
Marija Kojic, Tomasz Gawda, Monika Gaik, Alexander Begg, Anna Salerno-Kochan, Nyoman D. Kurniawan, Alun Jones, Katarzyna Drożdżyk, Anna Kościelniak, Andrzej Chramiec-Głąbik, Soroor Hediyeh-Zadeh, Maria Kasherman, Woo Jun Shim, Enakshi Sinniah, Laura A. Genovesi, Rannvá K. Abrahamsen, Christina D. Fenger, Camilla G. Madsen, Julie S. Cohen, Ali Fatemi, Zornitza Stark, Sebastian Lunke, Joy Lee, Jonas K. Hansen, Martin F. Boxill, Boris Keren, Isabelle Marey, Margarita S. Saenz, Kathleen Brown, Suzanne A. Alexander, Sergey Mureev, Alina Batzilla, Melissa J. Davis, Michael Piper, Mikael Bodén, Thomas H. J. Burne, Nathan J. Palpant, Rikke S. Møller, Sebastian Glatt, Brandon J. Wainwright. Elp2 mutations perturb the epitranscriptome and lead to a complex neurodevelopmental phenotype. Nature Communications 2021; 12(1) doi: 10.1038/s41467-021-22888-5
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7 |
Xiao‐li Min, Sixian Lin, Jia‐yi Hu, Rui Jing, Qing Zhao, Fei‐fei Shang, Yong Zeng. The opposite effect of ELP4 and ZEB2 on TCF7L2‐mediated microglia polarization in ischemic stroke. Journal of Cell Communication and Signaling 2025; 19(1) doi: 10.1002/ccs3.12061
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