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Items: 1 to 20 of 55

1.
DCDC2 inhibits hepatic stellate cell activation and ameliorates CCl4-induced liver fibrosis by suppressing Wnt/β-catenin signaling
Qing-Qing Liu, Jing Chen, Tao Ma, Wei Huang, Cui-Hua Lu
Sci Rep. 2024; 14: 9425. Published online 2024 Apr 24. doi: 10.1038/s41598-024-59698-w
PMCID:
PMC11043443
AbstractArticlePDF–4.8M
2.
Developmental dyslexia susceptibility genes DNAAF4, DCDC2, and NRSN1 are associated with brain function in fluently reading adolescents and young adults
Nea Rinne, Patrik Wikman, Elisa Sahari, Juha Salmi, Elisabet Einarsdóttir, Juha Kere, Kimmo Alho
Cereb Cortex. 2024 Apr; 34(4): bhae144. Published online 2024 Apr 12. doi: 10.1093/cercor/bhae144
PMCID:
PMC11014888
AbstractArticlePDF–1.2M
3.
Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample
Kerstin U. Ludwig, Johannes Schumacher, Gerd Schulte-Körne, Inke R. König, Andreas Warnke, Ellen Plume, Heidi Anthoni, Myriam Peyrard-Janvid, Haiying Meng, Andreas Ziegler, Helmut Remschmidt, Juha Kere, Jeffrey R. Gruen, Bertram Müller-Myhsok, Markus M. Nöthen, Per Hoffmann
Psychiatr Genet. Author manuscript; available in PMC 2022 Dec 14.
Published in final edited form as: Psychiatr Genet. 2008 Dec; 18(6): 310–312. doi: 10.1097/YPG.0b013e3283063a78
PMCID:
PMC9748830
AbstractArticlePDF–55K
4.
Scalable multiplex co-fractionation/mass spectrometry platform for accelerated protein interactome discovery
Pierre C. Havugimana, Raghuveera Kumar Goel, Sadhna Phanse, Ahmed Youssef, Dzmitry Padhorny, Sergei Kotelnikov, Dima Kozakov, Andrew Emili
Nat Commun. 2022; 13: 4043. Published online 2022 Jul 13. doi: 10.1038/s41467-022-31809-z
PMCID:
PMC9279285
AbstractArticlePDF–2.5M
5.
Integration of GWAS and brain transcriptomic analyses in a multi-ethnic sample of 35,245 older adults identifies DCDC2 gene as predictor of episodic memory maintenance
Yizhe Gao, Daniel Felsky, Dolly Reyes-Dumeyer, Sanjeev Sariya, Miguel Arce Rentería, Yiyi Ma, Hans-Ulrich Klein, Stephanie Cosentino, Philip L. De Jager, David A. Bennett, Adam M. Brickman, Gerard D. Schellenberg, Richard Mayeux, Sandra Barral
Alzheimers Dement. Author manuscript; available in PMC 2022 Oct 24.
Published in final edited form as: Alzheimers Dement. 2022 Oct; 18(10): 1797–1811. Published online 2021 Dec 7. doi: 10.1002/alz.12524
PMCID:
PMC9170841
ArticlePDF–810K
6.
White matter deficits correlate with visual motion perception impairments in dyslexic carriers of the DCDC2 genetic risk variant
Daniela Perani, Paola Scifo, Guido M. Cicchini, Pasquale Della Rosa, Chiara Banfi, Sara Mascheretti, Andrea Falini, Cecilia Marino, Maria Concetta Morrone
Exp Brain Res. 2021; 239(9): 2725–2740. Published online 2021 Jul 6. doi: 10.1007/s00221-021-06137-1
PMCID:
PMC8448712
AbstractArticlePDF–1.3M
7.
Identifying dyslexia: Link between maze learning and dyslexia susceptibility gene, DCDC2, in young children
Lisa A. Gabel, Kelsey Voss, Evelyn Johnson, Esther R. Lindström, Dongnhu T. Truong, Erin M. Murray, Karla Carino, Christiana M. Nielsen, Steven Paniagua, Jeffrey R. Gruen
Dev Neurosci. Author manuscript; available in PMC 2022 Jun 29.
Published in final edited form as: Dev Neurosci. 2021; 43(2): 116–133. Published online 2021 Jun 29. doi: 10.1159/000516667
PMCID:
PMC8292181
AbstractArticlePDF–1.8M
8.
Dual Proteome-scale Networks Reveal Cell-specific Remodeling of the Human Interactome
Edward L. Huttlin, Raphael J. Bruckner, Jose Navarrete-Perea, Joe R. Cannon, Kurt Baltier, Fana Gebreab, Melanie P. Gygi, Alexandra Thornock, Gabriela Zarraga, Stanley Tam, John Szpyt, Brandon M. Gassaway, Alexandra Panov, Hannah Parzen, Sipei Fu, Arvene Golbazi, Eila Maenpaa, Keegan Stricker, Sanjukta Guha Thakurta, Tian Zhang, Ramin Rad, Joshua Pan, David P. Nusinow, Joao A. Paulo, Devin K. Schweppe, Laura Pontano Vaites, J. Wade Harper, Steven P. Gygi
Cell. Author manuscript; available in PMC 2022 May 27.
Published in final edited form as: Cell. 2021 May 27; 184(11): 3022–3040.e28. Published online 2021 May 6. doi: 10.1016/j.cell.2021.04.011
PMCID:
PMC8165030
AbstractArticlePDF–2.2M
9.
Effect of READ1 on latent profiles of reading disorder and comorbid attention and language impairment subtypes
Miao Li, Dongnhu T. Truong, Mellissa DeMille, Jeffrey G. Malins, Maureen W. Lovett, Joan Bosson-Heenan, Jeffrey R Gruen, Jan C. Frijters
Child Neuropsychol. Author manuscript; available in PMC 2021 May 28.
Published in final edited form as: Child Neuropsychol. 2020 Feb; 26(2): 145–169. Published online 2019 Aug 14. doi: 10.1080/09297049.2019.1648642
PMCID:
PMC8163097
AbstractArticlePDF–269K
10.
Do Genes Associated with Dyslexia of Chinese Characters Evolve Neutrally?
Kumiko V. Nishiyama, Yoko Satta, Jun Gojobori
Genes (Basel) 2020 Jun; 11(6): 658. Published online 2020 Jun 17. doi: 10.3390/genes11060658
PMCID:
PMC7349701
AbstractArticlePDF–1.6M
11.
DCDC2 READ1 regulatory element: how temporal processing differences may shape language
Kevin Tang, Mellissa M. C. DeMille, Jan C. Frijters, Jeffrey R. Gruen
Proc Biol Sci. 2020 Jun 10; 287(1928): 20192712. Published online 2020 Jun 3. doi: 10.1098/rspb.2019.2712
PMCID:
PMC7341942
AbstractArticlePDF–627K
12.
A reference map of the human binary protein interactome
Katja Luck, Dae-Kyum Kim, Luke Lambourne, Kerstin Spirohn, Bridget E. Begg, Wenting Bian, Ruth Brignall, Tiziana Cafarelli, Francisco J. Campos-Laborie, Benoit Charloteaux, Dongsic Choi, Atina G. Coté, Meaghan Daley, Steven Deimling, Alice Desbuleux, Amélie Dricot, Marinella Gebbia, Madeleine F. Hardy, Nishka Kishore, Jennifer J. Knapp, István A. Kovács, Irma Lemmens, Miles W. Mee, Joseph C. Mellor, Carl Pollis, Carles Pons, Aaron D. Richardson, Sadie Schlabach, Bridget Teeking, Anupama Yadav, Mariana Babor, Dawit Balcha, Omer Basha, Christian Bowman-Colin, Suet-Feung Chin, Soon Gang Choi, Claudia Colabella, Georges Coppin, Cassandra D’Amata, David De Ridder, Steffi De Rouck, Miquel Duran-Frigola, Hanane Ennajdaoui, Florian Goebels, Liana Goehring, Anjali Gopal, Ghazal Haddad, Elodie Hatchi, Mohamed Helmy, Yves Jacob, Yoseph Kassa, Serena Landini, Roujia Li, Natascha van Lieshout, Andrew MacWilliams, Dylan Markey, Joseph N. Paulson, Sudharshan Rangarajan, John Rasla, Ashyad Rayhan, Thomas Rolland, Adriana San-Miguel, Yun Shen, Dayag Sheykhkarimli, Gloria M. Sheynkman, Eyal Simonovsky, Murat Taşan, Alexander Tejeda, Vincent Tropepe, Jean-Claude Twizere, Yang Wang, Robert J. Weatheritt, Jochen Weile, Yu Xia, Xinping Yang, Esti Yeger-Lotem, Quan Zhong, Patrick Aloy, Gary D. Bader, Javier De Las Rivas, Suzanne Gaudet, Tong Hao, Janusz Rak, Jan Tavernier, David E. Hill, Marc Vidal, Frederick P. Roth, Michael A. Calderwood
Nature. Author manuscript; available in PMC 2020 Oct 8.
Published in final edited form as: Nature. 2020 Apr; 580(7803): 402–408. Published online 2020 Apr 8. doi: 10.1038/s41586-020-2188-x
PMCID:
PMC7169983
AbstractArticlePDF–5.4M
13.
DCDC2 Polymorphism Is Associated with Left Temporoparietal Gray and White Matter Structures during Development
Fahimeh Darki, Myriam Peyrard-Janvid, Hans Matsson, Juha Kere, Torkel Klingberg
J Neurosci. 2014 Oct 22; 34(43): 14455–14462. doi: 10.1523/JNEUROSCI.1216-14.2014
PMCID:
PMC6608392
AbstractArticlePDF–911K
14.
The DCDC2/intron 2 deletion and white matter disorganization: Focus on developmental dyslexia
Cecilia Marino, Paola Scifo, Pasquale A. Della Rosa, Sara Mascheretti, Andrea Facoetti, Maria L. Lorusso, Roberto Giorda, Monica Consonni, Andrea Falini, Massimo Molteni, Jeffrey R. Gruen, Daniela Perani
Cortex. Author manuscript; available in PMC 2018 May 30.
Published in final edited form as: Cortex. 2014 Aug; 57: 227–243. Published online 2014 May 9. doi: 10.1016/j.cortex.2014.04.016
PMCID:
PMC5975637
AbstractArticlePDF–502K
15.
Worldwide distribution of the DCDC2 READ1 regulatory element and its relationship with phoneme variation across languages
Mellissa M. C. DeMille, Kevin Tang, Chintan M. Mehta, Christopher Geissler, Jeffrey G. Malins, Natalie R. Powers, Beatrice M. Bowen, Andrew K. Adams, Dongnhu T. Truong, Jan C. Frijters, Jeffrey R. Gruen
Proc Natl Acad Sci U S A. 2018 May 8; 115(19): 4951–4956. Published online 2018 Apr 16. doi: 10.1073/pnas.1710472115
Correction in:
Proc Natl Acad Sci U S A. 2018 May 29; 115(22): E5251.
PMCID:
PMC5948951
AbstractArticlePDF–1.0M
16.
Association of Attention-Deficit/Hyperactivity Disorder with a Candidate Region for Reading Disabilities on Chromosome 6p
Jillian M. Couto, Lissette Gomez, Karen Wigg, Abel Ickowicz, Tejaswee Pathare, Molly Malone, James L. Kennedy, Russell Schachar, Cathy L. Barr
Biol Psychiatry. Author manuscript; available in PMC 2018 Jan 2.
Published in final edited form as: Biol Psychiatry. 2009 Aug 15; 66(4): 368–375. Published online 2009 Apr 11. doi: 10.1016/j.biopsych.2009.02.016
PMCID:
PMC5750043
AbstractArticlePDF–450K
17.
The DCDC2 deletion is not a risk factor for dyslexia
T S Scerri, E Macpherson, A Martinelli, W C Wa, A P Monaco, J Stein, M Zheng, C Suk-Han Ho, C McBride, M Snowling, C Hulme, M E Hayiou-Thomas, M M Y Waye, J B Talcott, S Paracchini
Transl Psychiatry. 2017 Jul; 7(7): e1182. Published online 2017 Jul 25. doi: 10.1038/tp.2017.151
PMCID:
PMC5538127
AbstractArticlePDF–200K
18.
Association of Reading Disabilities With Regions Marked by Acetylated H3 Histones in KIAA0319
Jillian M. Couto, Izzy Livne-Bar, Katherine Huang, Zhaodong Xu, Tasha Cate-Carter, Yu Feng, Karen Wigg, Tom Humphries, Rosemary Tannock, Elizabeth N. Kerr, Maureen W. Lovett, Rod Bremner, Cathy L. Barr
Am J Med Genet B Neuropsychiatr Genet. Author manuscript; available in PMC 2017 Apr 5.
Published in final edited form as: Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5; 153B(2): 447–462. doi: 10.1002/ajmg.b.30999
PMCID:
PMC5381965
AbstractArticlePDF–1.2M
19.
Mutations in DCDC2 (doublecortin domain-containing protein 2) in neonatal sclerosing cholangitis
Tassos Grammatikopoulos, Melissa Sambrotta, Sandra Strautnieks, Pierre Foskett, A S Knisely, Bart Wagner, Maesha Deheragoda, Chris Starling, Giorgina Mieli-Vergani, Joshua Smith, University of Washington Center for Mendelian Genomics, Laura Bull, Richard J Thompson
J Hepatol. Author manuscript; available in PMC 2017 Dec 1.
Published in final edited form as: J Hepatol. 2016 Dec; 65(6): 1179–1187. Published online 2016 Jul 25. doi: 10.1016/j.jhep.2016.07.017
PMCID:
PMC5116266
AbstractArticlePDF–3.0M
20.
A dynamic protein interaction landscape of the human centrosome-cilium interface
Gagan D. Gupta, Étienne Coyaud, João Gonçalves, Bahareh A. Mojarad, Yi Liu, Qianzhu Wu, Ladan Gheiratmand, David Comartin, Johnny M. Tkach, Sally W.T. Cheung, Mikhail Bashkurov, Monica Hasegan, James D. Knight, Zhen-Yuan Lin, Markus Schueler, Friedhelm Hildebrandt, Jason Moffat, Anne-Claude Gingras, Brian Raught, Laurence Pelletier
Cell. Author manuscript; available in PMC 2016 Dec 3.
Published in final edited form as: Cell. 2015 Dec 3; 163(6): 1484–1499. doi: 10.1016/j.cell.2015.10.065
PMCID:
PMC5089374
AbstractArticlePDF–1.5M

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