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Select item 105757751.

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

Abstract Article PDF–9.5M

Select item 104005872.

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

Abstract Article PDF–1007K

Select item 93485763.

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

Abstract Article PDF–3.0M

Select item 87018784.

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

Abstract Article PDF–1.6M

Select item 82249325.

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

Abstract Article PDF–1.6M

Select item 80932426.

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

Abstract Article PDF–1.8M

Select item 76054447.

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

Abstract Article PDF–512K

Select item 67917088.

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

Abstract Article PDF–2.8M

Select item 64900089.

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

Abstract Article PDF–1.4M

Select item 620344310.

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

Abstract Article PDF–1.9M

Select item 616668211.

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

Abstract Article PDF–3.8M

Select item 559725212.

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

Abstract Article PDF–7.6M

Select item 554984013.

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

Abstract Article PDF–547K

Select item 533762114.

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

Abstract Article PDF–2.8M

Select item 510516115.

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

Abstract Article PDF–584K

Select item 486366616.

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

Abstract Article PDF–2.8M

Select item 412360517.

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

Abstract Article PDF–874K

Select item 406640918.

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

Abstract Article PDF–538K

Select item 376754519.

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

Abstract Article PDF–1.6M

Select item 375604320.

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

Abstract Article PDF–275K

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