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Items: 1 to 20 of 31

1.
MYT1L haploinsufficiency in human neurons and mice causes autism-associated phenotypes that can be reversed by genetic and pharmacologic intervention
Bettina Weigel, Jana F. Tegethoff, Sarah D. Grieder, Bryce Lim, Bhuvaneswari Nagarajan, Yu-Chao Liu, Jule Truberg, Dimitris Papageorgiou, Juan M. Adrian-Segarra, Laura K. Schmidt, Janina Kaspar, Eric Poisel, Elisa Heinzelmann, Manu Saraswat, Marleen Christ, Christian Arnold, Ignacio L. Ibarra, Joaquin Campos, Jeroen Krijgsveld, Hannah Monyer, Judith B. Zaugg, Claudio Acuna, Moritz Mall
Mol Psychiatry. 2023; 28(5): 2122–2135. Published online 2023 Feb 14. doi: 10.1038/s41380-023-01959-7
PMCID:
PMC10575775
AbstractArticlePDF–9.5M
2.
2p25.3 microduplications involving MYT1L: further phenotypic characterization through an assessment of 16 new cases and a literature review
Malek Bouassida, Matthieu Egloff, Jonathan Levy, Nicolas Chatron, Laura Bernardini, Gwenaël Le Guyader, Anne-Claude Tabet, Caroline Schluth-Bolard, Francesco Brancati, Maria Grazia Giuffrida, Rodolphe Dard, Juliette Clorennec, Juliette Coursimault, François Vialard, Bérénice Hervé
Eur J Hum Genet. 2023 Aug; 31(8): 895–904. Published online 2023 May 15. doi: 10.1038/s41431-023-01379-9
PMCID:
PMC10400587
AbstractArticlePDF–1007K
3.
Chr21 protein–protein interactions: enrichment in proteins involved in intellectual disability, autism, and late-onset Alzheimer’s disease
Julia Viard, Yann Loe-Mie, Rachel Daudin, Malik Khelfaoui, Christine Plancon, Anne Boland, Francisco Tejedor, Richard L Huganir, Eunjoon Kim, Makoto Kinoshita, Guofa Liu, Volker Haucke, Thomas Moncion, Eugene Yu, Valérie Hindie, Henri Bléhaut, Clotilde Mircher, Yann Herault, Jean-François Deleuze, Jean-Christophe Rain, Michel Simonneau, Aude-Marie Lepagnol-Bestel
Life Sci Alliance. 2022 Dec; 5(12): e202101205. Published online 2022 Aug 1. doi: 10.26508/lsa.202101205
PMCID:
PMC9348576
AbstractArticlePDF–3.0M
4.
Co-Occurrence of Fragile X Syndrome with a Second Genetic Condition: Three Independent Cases of Double Diagnosis
Elisabetta Tabolacci, Maria Grazia Pomponi, Laura Remondini, Roberta Pietrobono, Daniela Orteschi, Veronica Nobile, Cecilia Pucci, Elisa Musto, Marika Pane, Eugenio M. Mercuri, Giovanni Neri, Maurizio Genuardi, Pietro Chiurazzi, Marcella Zollino
Genes (Basel) 2021 Dec; 12(12): 1909. Published online 2021 Nov 27. doi: 10.3390/genes12121909
PMCID:
PMC8701878
AbstractArticlePDF–1.6M
5.
The Neuronal Transcription Factor Myt1L Interacts via a Conserved Motif with the PAH1 domain of Sin3 to Recruit the Sin3L/Rpd3L Histone Deacetylase Complex
Ryan Dale Marcum, Ishwar Radhakrishnan
FEBS Lett. Author manuscript; available in PMC 2021 Jun 24.
Published in final edited form as: FEBS Lett. 2020 Jul; 594(14): 2322–2330. Published online 2020 May 23. doi: 10.1002/1873-3468.13811
PMCID:
PMC8224932
AbstractArticlePDF–1.6M
6.
A web-based survey on various symptoms of computer vision syndrome and the genetic understanding based on a multi-trait genome-wide association study
Keito Yoshimura, Yuji Morita, Kenji Konomi, Sachiko Ishida, Daisuke Fujiwara, Keisuke Kobayashi, Masami Tanaka
Sci Rep. 2021; 11: 9446. Published online 2021 May 3. doi: 10.1038/s41598-021-88827-y
PMCID:
PMC8093242
AbstractArticlePDF–1.8M
7.
MYT1L: A systematic review of genetic variation encompassing schizophrenia and autism
Patricia Mansfield, John N. Constantino, Dustin Baldridge
Am J Med Genet B Neuropsychiatr Genet. Author manuscript; available in PMC 2021 Jun 1.
Published in final edited form as: Am J Med Genet B Neuropsychiatr Genet. 2020 Jun; 183(4): 227–233. Published online 2020 Apr 8. doi: 10.1002/ajmg.b.32781
PMCID:
PMC7605444
AbstractArticlePDF–512K
8.
The crucial role of DNA-dependent protein kinase and myelin transcription factor 1-like protein in the miR-141 tumor suppressor network
Bo Wang, Dongping Li, Youli Yao, Mieke Heyns, Anna Kovalchuk, Yaroslav Ilnytskyy, Rocio Rodriguez-Juarez, Roderick T. Bronson, Gerlinde A.S. Metz, Olga Kovalchuk, Igor Kovalchuk
Cell Cycle. 2019; 18(21): 2876–2892. Published online 2019 Sep 16. doi: 10.1080/15384101.2019.1652033
PMCID:
PMC6791708
AbstractArticlePDF–2.8M
9.
Myt1l induced direct reprogramming of pericytes into cholinergic neurons
Xing‐Guang Liang, Chao Tan, Cheng‐Kun Wang, Rong‐Rong Tao, Yu‐Jie Huang, Kui‐Fen Ma, Kohji Fukunaga, Ming‐Zhu Huang, Feng Han
CNS Neurosci Ther. 2018 Sep; 24(9): 801–809. Published online 2018 Feb 17. doi: 10.1111/cns.12821
PMCID:
PMC6490008
AbstractArticlePDF–1.4M
10.
Myt1 and Myt1l transcription factors limit proliferation in GBM cells by repressing YAP1 expression.
Tiffany A. Melhuish, Izabela Kowalczyk, Arkadi Manukyan, Ying Zhang, Anant Shah, Roger Abounader, David Wotton
Biochim Biophys Acta Gene Regul Mech. Author manuscript; available in PMC 2019 Nov 1.
Published in final edited form as: Biochim Biophys Acta Gene Regul Mech. 2018 Nov; 1861(11): 983–995. Published online 2018 Oct 10. doi: 10.1016/j.bbagrm.2018.10.005
PMCID:
PMC6203443
AbstractArticlePDF–1.9M
11.
Histone Interaction Landscapes Visualized by Crosslinking Mass Spectrometry in Intact Cell Nuclei
Domenico Fasci, Hugo van Ingen, Richard A. Scheltema, Albert J. R. Heck
Mol Cell Proteomics. 2018 Oct; 17(10): 2018–2033. Published online 2018 Jul 18. doi: 10.1074/mcp.RA118.000924
PMCID:
PMC6166682
AbstractArticlePDF–3.8M
12.
MYT1L mutations cause intellectual disability and variable obesity by dysregulating gene expression and development of the neuroendocrine hypothalamus
Patricia Blanchet, Martina Bebin, Shaam Bruet, Gregory M. Cooper, Michelle L. Thompson, Benedicte Duban-Bedu, Benedicte Gerard, Amelie Piton, Sylvie Suckno, Charu Deshpande, Virginia Clowes, Julie Vogt, Peter Turnpenny, Michael P. Williamson, Yves Alembik, Clinical Sequencing Exploratory Research Study Consortium, Deciphering Developmental Disorders Consortium, Eric Glasgow, Alisdair McNeill
PLoS Genet. 2017 Aug; 13(8): e1006957. Published online 2017 Aug 31. doi: 10.1371/journal.pgen.1006957
PMCID:
PMC5597252
AbstractArticlePDF–7.6M
13.
Associations of the Intellectual Disability Gene MYT1L with Helix–Loop–Helix Gene Expression, Hippocampus Volume and Hippocampus Activation During Memory Retrieval
Agnieszka Kepa, Lourdes Martinez Medina, Susanne Erk, Deepak P Srivastava, Alinda Fernandes, Roberto Toro, Sabine Lévi, Barbara Ruggeri, Cathy Fernandes, Franziska Degenhardt, Stephanie H Witt, Andreas Meyer-Lindenberg, Jean-Christophe Poncer, Jean-Luc Martinot, Marie-Laure Paillère Martinot, Christian P Müller, Andreas Heinz, Henrik Walter, Gunter Schumann, Sylvane Desrivières
Neuropsychopharmacology. 2017 Dec; 42(13): 2516–2526. Prepublished online 2017 May 4. Published online 2017 Jun 7. doi: 10.1038/npp.2017.91
PMCID:
PMC5549840
AbstractArticlePDF–547K
14.
Aurora kinase A regulates Survivin stability through targeting FBXL7 in gastric cancer drug resistance and prognosis
M Kamran, Z-J Long, D Xu, S-S Lv, B Liu, C-L Wang, J Xu, E W-F Lam, Q Liu
Oncogenesis. 2017 Feb; 6(2): e298. Published online 2017 Feb 20. doi: 10.1038/oncsis.2016.80
PMCID:
PMC5337621
AbstractArticlePDF–2.8M
15.
De novo genic mutations among a Chinese autism spectrum disorder cohort
Tianyun Wang, Hui Guo, Bo Xiong, Holly A.F. Stessman, Huidan Wu, Bradley P. Coe, Tychele N. Turner, Yanling Liu, Wenjing Zhao, Kendra Hoekzema, Laura Vives, Lu Xia, Meina Tang, Jianjun Ou, Biyuan Chen, Yidong Shen, Guanglei Xun, Min Long, Janice Lin, Zev N. Kronenberg, Yu Peng, Ting Bai, Honghui Li, Xiaoyan Ke, Zhengmao Hu, Jingping Zhao, Xiaobing Zou, Kun Xia, Evan E. Eichler
Nat Commun. 2016; 7: 13316. Published online 2016 Nov 8. doi: 10.1038/ncomms13316
PMCID:
PMC5105161
AbstractArticlePDF–584K
16.
Mechanisms and Disease Associations of Haplotype-Dependent Allele-Specific DNA Methylation
Catherine Do, Charles F. Lang, John Lin, Huferesh Darbary, Izabela Krupska, Aulona Gaba, Lynn Petukhova, Jean-Paul Vonsattel, Mary P. Gallagher, Robin S. Goland, Raphael A. Clynes, Andrew Dwork, John G. Kral, Catherine Monk, Angela M. Christiano, Benjamin Tycko
Am J Hum Genet. 2016 May 5; 98(5): 934–955. Published online 2016 May 5. doi: 10.1016/j.ajhg.2016.03.027
PMCID:
PMC4863666
AbstractArticlePDF–2.8M
17.
Genetic Associations with Plasma B12, B6, and Folate Levels in an Ischemic Stroke Population from the Vitamin Intervention for Stroke Prevention (VISP) Trial
Keith L. Keene, Wei-Min Chen, Fang Chen, Stephen R. Williams, Stacey D. Elkhatib, Fang-Chi Hsu, Josyf C. Mychaleckyj, Kimberly F. Doheny, Elizabeth W. Pugh, Hua Ling, Cathy C. Laurie, Stephanie M. Gogarten, Ebony B. Madden, Bradford B. Worrall, Michele M. Sale
Front Public Health. 2014; 2: 112. Published online 2014 Aug 6. doi: 10.3389/fpubh.2014.00112
PMCID:
PMC4123605
AbstractArticlePDF–874K
18.
A role for hydrogen bonding in DNA recognition by the non–classical CCHHC type zinc finger, NZF–1
Angelique N. Besold, Deborah L. Amick, Sarah L. J. Michel
Mol Biosyst. Author manuscript; available in PMC 2015 Jul 3.
Published in final edited form as: Mol Biosyst. 2014 Jul 3; 10(7): 1753–1756. Published online 2014 May 13. doi: 10.1039/c4mb00246f
PMCID:
PMC4066409
AbstractArticlePDF–538K
19.
Neutralization of terminal differentiation in gliomagenesis
Jian Hu, Allen L. Ho, Liang Yuan, Baoli Hu, Sujun Hua, Soyoon Sarah Hwang, Jianhua Zhang, Tianyi Hu, Hongwu Zheng, Boyi Gan, Gongxiong Wu, Yaoqi Alan Wang, Lynda Chin, Ronald A. DePinho
Proc Natl Acad Sci U S A. 2013 Sep 3; 110(36): 14520–14527. Published online 2013 Aug 5. doi: 10.1073/pnas.1308610110
PMCID:
PMC3767545
AbstractArticlePDF–1.6M
20.
Clinical Significance of MYT1L Gene Polymorphisms in Chinese Patients with Gastric Cancer
Yangmei Zhang, Haixia Zhu, Xunlei Zhang, Dongying Gu, Xichang Zhou, Meilin Wang, Chunxiang Cao, Xiaojing Zhang, Xiaomin Wu, Weida Gong, Yongfei Tang, Jianwei Zhou, Cuiju Tang, Zhengdong Zhang, Jinfei Chen
PLoS One. 2013; 8(8): e71979. Published online 2013 Aug 28. doi: 10.1371/journal.pone.0071979
PMCID:
PMC3756043
AbstractArticlePDF–275K

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