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Items: 11

1.
ATP2C2 and DYX1C1 are putative modulators of dyslexia‐related MMR
Bent Müller, Gesa Schaadt, Johannes Boltze, Frank Emmrich, LEGASCREEN Consortium, Michael A. Skeide, Nicole E. Neef, Indra Kraft, Jens Brauer, Angela D. Friederici, Holger Kirsten, Arndt Wilcke
Brain Behav. 2017 Nov; 7(11): e00851. Published online 2017 Oct 18. doi: 10.1002/brb3.851
PMCID:
PMC5698869
AbstractArticlePDF–630K
2.
Oestrogen receptor β regulates epigenetic patterns at specific genomic loci through interaction with thymine DNA glycosylase
Yun Liu, William Duong, Claudia Krawczyk, Nancy Bretschneider, Gábor Borbély, Mukesh Varshney, Christian Zinser, Primo Schär, Joëlle Rüegg
Epigenetics Chromatin. 2016; 9: 7. Published online 2016 Feb 16. doi: 10.1186/s13072-016-0055-7
PMCID:
PMC4756533
AbstractArticlePDF–2.1M
3.
Deficits in learning and memory in mice with a mutation of the candidate dyslexia susceptibility gene Dyx1c1
Amanda R. Rendall, Aarti Tarkar, Hector M. Contreras-Mora, Joseph J. LoTurco, R. Holly Fitch
Brain Lang. Author manuscript; available in PMC 2018 Sep 1.
Published in final edited form as: Brain Lang. 2017 Sep; 172: 30–38. Published online 2015 May 16. doi: 10.1016/j.bandl.2015.04.008
PMCID:
PMC4646737
AbstractArticlePDF–1.3M
4.
Global genetic analysis in mice unveils central role for cilia in congenital heart disease
You Li, Nikolai T. Klena, George C Gabriel, Xiaoqin Liu, Andrew J. Kim, Kristi Lemke, Yu Chen, Bishwanath Chatterjee, William Devine, Rama Rao Damerla, Chien-fu Chang, Hisato Yagi, Jovenal T. San Agustin, Mohamed Thahir, Shane Anderton, Caroline Lawhead, Anita Vescovi, Herbert Pratt, Judy Morgan, Leslie Haynes, Cynthia L. Smith, Janan T. Eppig, Laura Reinholdt, Richard Francis, Linda Leatherbury, Madhavi K. Ganapathiraju, Kimimasa Tobita, Gregory J. Pazour, Cecilia W. Lo
Nature. Author manuscript; available in PMC 2015 Nov 28.
Published in final edited form as: Nature. 2015 May 28; 521(7553): 520–524. Published online 2015 Mar 25. doi: 10.1038/nature14269
PMCID:
PMC4617540
AbstractArticlePDF–518K
5.
Acute-phase protein serum amyloid A3 is a novel paracrine coupling factor that controls bone homeostasis
Roman Thaler, Ines Sturmlechner, Silvia Spitzer, Scott M. Riester, Monika Rumpler, Jochen Zwerina, Klaus Klaushofer, Andre J. van Wijnen, Franz Varga
FASEB J. 2015 Apr; 29(4): 1344–1359. Published online 2014 Dec 9. doi: 10.1096/fj.14-265512
PMCID:
PMC4396610
AbstractArticle
6.
DYX1C1 is required for axonemal dynein assembly and ciliary motility
Aarti Tarkar, Niki T. Loges, Christopher E. Slagle, Richard Francis, Gerard W. Dougherty, Joel V. Tamayo, Brett Shook, Marie Cantino, Daniel Schwartz, Charlotte Jahnke, Heike Olbrich, Claudius Werner, Johanna Raidt, Petra Pennekamp, Marouan Abouhamed, Rim Hjeij, Gabriele Köhler, Matthias Griese, You Li, Kristi Lemke, Nikolas Klena, Xiaoqin Liu, George Gabriel, Kimimasa Tobita, Martine Jaspers, Lucy C. Morgan, Adam J. Shapiro, Stef J.F. Letteboer, Dorus A. Mans, Johnny L. Carson, Margaret W. Leigh, Whitney E. Wolf, Serafine Chen, Jane S. Lucas, Alexandros Onoufriadis, Vincent Plagnol, Miriam Schmidts, Karsten Boldt, UK10K, Ronald Roepman, Maimoona Zariwala, Cecilia W. Lo, Hannah M. Mitchison, Michael R. Knowles, Rebecca D. Burdine, Joseph J. LoTurco, Heymut Omran
Nat Genet. Author manuscript; available in PMC 2014 Apr 26.
Published in final edited form as: Nat Genet. 2013 Sep; 45(9): 995–1003. Published online 2013 Jul 21. doi: 10.1038/ng.2707
PMCID:
PMC4000444
AbstractArticlePDF–2.1M
7.
Nuclear Orphan Receptor TAK1/TR4-Deficient Mice Are Protected Against Obesity-Linked Inflammation, Hepatic Steatosis, and Insulin Resistance
Hong Soon Kang, Kyoko Okamoto, Yong-Sik Kim, Yukimasa Takeda, Carl D. Bortner, Huaixin Dang, Taira Wada, Wen Xie, Xiao-Ping Yang, Grace Liao, Anton M. Jetten
Diabetes. 2011 Jan; 60(1): 177–188. Published online 2010 Sep 23. doi: 10.2337/db10-0628
PMCID:
PMC3012170
AbstractArticlePDF–728K
8.
RIKEN Integrated Sequence Analysis (RISA) System—384-Format Sequencing Pipeline with 384 Multicapillary Sequencer
Kazuhiro Shibata, Masayoshi Itoh, Katsunori Aizawa, Sumiharu Nagaoka, Nobuya Sasaki, Piero Carninci, Hideaki Konno, Junichi Akiyama, Katsuo Nishi, Tokuji Kitsunai, Hideo Tashiro, Mari Itoh, Noriko Sumi, Yoshiyuki Ishii, Shin Nakamura, Makoto Hazama, Tsutomu Nishine, Akira Harada, Rintaro Yamamoto, Hiroyuki Matsumoto, Sumito Sakaguchi, Takashi Ikegami, Katsuya Kashiwagi, Syuji Fujiwake, Kouji Inoue, Yoshiyuki Togawa, Masaki Izawa, Eiji Ohara, Masanori Watahiki, Yuko Yoneda, Tomokazu Ishikawa, Kaori Ozawa, Takumi Tanaka, Shuji Matsuura, Jun Kawai, Yasushi Okazaki, Masami Muramatsu, Yorinao Inoue, Akira Kira, Yoshihide Hayashizaki
Genome Res. 2000 Nov; 10(11): 1757–1771. doi: 10.1101/gr.152600
PMCID:
PMC310992
AbstractArticlePDF–3.4M
9.
Normalization and Subtraction of Cap-Trapper-Selected cDNAs to Prepare Full-Length cDNA Libraries for Rapid Discovery of New Genes
Piero Carninci, Yuko Shibata, Norihito Hayatsu, Yuichi Sugahara, Kazuhiro Shibata, Masayoshi Itoh, Hideaki Konno, Yasushi Okazaki, Masami Muramatsu, Yoshihide Hayashizaki
Genome Res. 2000 Oct; 10(10): 1617–1630. doi: 10.1101/gr.145100
PMCID:
PMC310980
AbstractArticlePDF–1.4M
10.
A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain
Mikko Taipale, Nina Kaminen, Jaana Nopola-Hemmi, Tuomas Haltia, Birgitta Myllyluoma, Heikki Lyytinen, Kurt Muller, Minna Kaaranen, Perttu J. Lindsberg, Katariina Hannula-Jouppi, Juha Kere
Proc Natl Acad Sci U S A. 2003 Sep 30; 100(20): 11553–11558. Published online 2003 Sep 3. doi: 10.1073/pnas.1833911100
PMCID:
PMC208796
AbstractArticlePDF–439K
11.
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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