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Items: 13

1.
NEUROD2 function is dispensable for human pancreatic β cell specification
Perla Cota, Lama Saber, Damla Taskin, Changying Jing, Aimée Bastidas-Ponce, Matthew Vanheusden, Alireza Shahryari, Michael Sterr, Ingo Burtscher, Mostafa Bakhti, Heiko Lickert
Front Endocrinol (Lausanne) 2023; 14: 1286590. Published online 2023 Oct 25. doi: 10.3389/fendo.2023.1286590
PMCID:
PMC10634430
AbstractArticlePDF–3.7M
2.
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
3.
Disruption of NEUROD2 causes a neurodevelopmental syndrome with autistic features via cell-autonomous defects in forebrain glutamatergic neurons
Karen Runge, Rémi Mathieu, Stéphane Bugeon, Sahra Lafi, Corinne Beurrier, Surajit Sahu, Fabienne Schaller, Arthur Loubat, Leonard Herault, Stéphane Gaillard, Emilie Pallesi-Pocachard, Aurélie Montheil, Andreas Bosio, Jill A. Rosenfeld, Eva Hudson, Kristin Lindstrom, Saadet Mercimek-Andrews, Lauren Jeffries, Arie van Haeringen, Olivier Vanakker, Audrey Van Hecke, Dina Amrom, Sebastien Küry, Chana Ratner, Reena Jethva, Candace Gamble, Bernard Jacq, Laurent Fasano, Gabriel Santpere, Belen Lorente-Galdos, Nenad Sestan, Antoinette Gelot, Sylvie Giacuzz, Sandra Goebbels, Alfonso Represa, Carlos Cardoso, Harold Cremer, Antoine de Chevigny
Mol Psychiatry. 2021; 26(11): 6125–6148. Published online 2021 Jun 29. doi: 10.1038/s41380-021-01179-x
Correction in:
Mol Psychiatry. 2021; 26(12): 7852.
PMCID:
PMC8760061
AbstractArticlePDF–5.3M
4.
An expansion of NEUROD2 phenotypes to include developmental delay without seizures
Emily K. Mis, Annalisa G. Sega, Rebecca H. Signer, Tracy Cartwright, Weizhen Ji, Julian A. Martinez-Agosto, Stanley F. Nelson, Christina G. S. Palmer, Hane Lee, Thomas Mitzelfelt, Monica Konstantino, Undiagnosed Diseases Network, Lauren Jeffries, Mustafa K. Khokha, Elysa Marco, Martin G. Martin, Saquib A. Lakhani
Am J Med Genet A. Author manuscript; available in PMC 2022 Apr 1.
Published in final edited form as: Am J Med Genet A. 2021 Apr; 185(4): 1076–1080. Published online 2021 Jan 13. doi: 10.1002/ajmg.a.62064
PMCID:
PMC8212414
AbstractArticlePDF–519K
5.
Impact of cytosine methylation on DNA binding specificities of human transcription factors
Yimeng Yin, Ekaterina Morgunova, Arttu Jolma, Eevi Kaasinen, Biswajyoti Sahu, Syed Khund-Sayeed, Pratyush K. Das, Teemu Kivioja, Kashyap Dave, Fan Zhong, Kazuhiro R. Nitta, Minna Taipale, Alexander Popov, Paul A. Ginno, Silvia Domcke, Jian Yan, Dirk Schübeler, Charles Vinson, Jussi Taipale
Science. Author manuscript; available in PMC 2021 Mar 30.
Published in final edited form as: Science. 2017 May 5; 356(6337): eaaj2239. doi: 10.1126/science.aaj2239
PMCID:
PMC8009048
AbstractArticlePDF–2.6M
6.
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
7.
Novel neurodevelopmental information revealed in amniotic fluid supernatant transcripts from fetuses with trisomies 18 and 21
Lisa Hui, Donna K. Slonim, Heather C. Wick, Kirby L. Johnson, Keiko Koide, Diana W. Bianchi
Hum Genet. Author manuscript; available in PMC 2013 Nov 1.
Published in final edited form as: Hum Genet. 2012 Nov; 131(11): 1751–1759. Published online 2012 Jul 3. doi: 10.1007/s00439-012-1195-x
PMCID:
PMC3472090
AbstractArticlePDF–754K
8.
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium
Pascale Gaudet, Michael S. Livstone, Suzanna E. Lewis, Paul D. Thomas
Brief Bioinform. 2011 Sep; 12(5): 449–462. Published online 2011 Aug 27. doi: 10.1093/bib/bbr042
PMCID:
PMC3178059
AbstractArticlePDF–1.0M
9.
Common Genetic Variation in Candidate Genes and Susceptibility to Sub-types of Breast Cancer
Nasim Mavaddat, Alison M Dunning, Bruce AJ Ponder, Douglas F Easton, Paul D Pharoah
Cancer Epidemiol Biomarkers Prev. Author manuscript; available in PMC 2009 Jul 1.
Published in final edited form as: Cancer Epidemiol Biomarkers Prev. 2009 Jan; 18(1): 255–259. doi: 10.1158/1055-9965.EPI-08-0704
PMCID:
PMC2655077
AbstractArticlePDF–791K
10.
HapMap-based study of the 17q21 ERBB2 amplicon in susceptibility to breast cancer
P R Benusiglio, P D Pharoah, P L Smith, F Lesueur, D Conroy, R N Luben, G Dew, C Jordan, A Dunning, D F Easton, B A J Ponder
Br J Cancer. 2006 Dec 18; 95(12): 1689–1695. Published online 2006 Nov 21. doi: 10.1038/sj.bjc.6603473
PMCID:
PMC2360759
AbstractArticlePDF–114K
11.
The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)
Genome Res. 2004 Oct; 14(10b): 2121–2127. doi: 10.1101/gr.2596504
Correction in:
Genome Res. 2006 Jun; 16(6): 804.
PMCID:
PMC528928
AbstractArticlePDF–140K
12.
NeuroD2 and neuroD3: distinct expression patterns and transcriptional activation potentials within the neuroD gene family.
M B McCormick, R M Tamimi, L Snider, A Asakura, D Bergstrom, S J Tapscott
Mol Cell Biol. 1996 Oct; 16(10): 5792–5800. doi: 10.1128/mcb.16.10.5792
PMCID:
PMC231580
SummaryPDF–613K
13.
Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences
Mammalian Gene Collection (MGC) Program Team
Proc Natl Acad Sci U S A. 2002 Dec 24; 99(26): 16899–16903. Published online 2002 Dec 11. doi: 10.1073/pnas.242603899
PMCID:
PMC139241
AbstractArticlePDF–118K

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