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Items: 1 to 20 of 23

1.
Genetic determinants of micronucleus formation in vivo
D. J. Adams, B. Barlas, R. E. McIntyre, I. Salguero, L. van der Weyden, A. Barros, J. R. Vicente, N. Karimpour, A. Haider, M. Ranzani, G. Turner, N. A. Thompson, V. Harle, R. Olvera-León, C. D. Robles-Espinoza, A. O. Speak, N. Geisler, W. J. Weninger, S. H. Geyer, J. Hewinson, N. A. Karp, The Sanger Mouse Genetics Project, B. Fu, F. Yang, Z. Kozik, J. Choudhary, L. Yu, M. S. van Ruiten, B. D. Rowland, C. J. Lelliott, M. del Castillo Velasco-Herrera, R. Verstraten, L. Bruckner, A. G. Henssen, M. A. Rooimans, J. de Lange, T. J. Mohun, M. J. Arends, K. A. Kentistou, P. A. Coelho, Y. Zhao, H. Zecchini, J. R. B. Perry, S. P. Jackson, G. Balmus
Nature. 2024; 627(8002): 130–136. Published online 2024 Feb 14. doi: 10.1038/s41586-023-07009-0
PMCID:
PMC10917660
ArticlePDF–4.8M
2.
Role of major and brain-specific Sgce isoforms in the pathogenesis of myoclonus-dystonia syndrome
Jianfeng Xiao, Satya R. Vemula, Yi Xue, Mohammad M. Khan, Francesca A. Carlisle, Adrian J. Waite, Derek J. Blake, Ioannis Dragatsis, Yu Zhao, Mark S. LeDoux
Neurobiol Dis. Author manuscript; available in PMC 2018 Feb 1.
Published in final edited form as: Neurobiol Dis. 2017 Feb; 98: 52–65. Published online 2016 Nov 24. doi: 10.1016/j.nbd.2016.11.003
PMCID:
PMC5283163
ArticlePDF–1.4M
3.
Abnormal nuclear envelopes in the striatum and motor deficits in DYT11 myoclonus-dystonia mouse models
Fumiaki Yokoi, Mai T. Dang, Tong Zhou, Yuqing Li
Hum Mol Genet. 2012 Feb 15; 21(4): 916–925. Published online 2011 Nov 11. doi: 10.1093/hmg/ddr528
PMCID:
PMC3263984
ArticlePDF–445K
4.
Abnormal nuclear envelope in the cerebellar Purkinje cells and impaired motor learning in DYT11 myoclonus-dystonia mouse models
Fumiaki Yokoi, Mai T. Dang, Guang Yang, JinDong Li, Atbin Doroodchi, Tong Zhou, Yuqing Li
Behav Brain Res. Author manuscript; available in PMC 2013 Feb 1.
Published in final edited form as: Behav Brain Res. 2012 Feb 1; 227(1): 12–20. Published online 2011 Oct 21. doi: 10.1016/j.bbr.2011.10.024
PMCID:
PMC3242862
ArticlePDF–3.2M
5.
Earlier onset of motor deficits in mice with double mutations in Dyt1 and Sgce
Fumiaki Yokoi, Guang Yang, JinDong Li, Mark P. DeAndrade, Tong Zhou, Yuqing Li
J Biochem. 2010 Oct; 148(4): 459–466. Published online 2010 Jul 13. doi: 10.1093/jb/mvq078
PMCID:
PMC2981491
ArticlePDF–231K
6.
Combined deficiency of alpha and epsilon sarcoglycan disrupts the cardiac dystrophin complex
Alessio Lancioni, Ida Luisa Rotundo, Yvonne Monique Kobayashi, Luca D'Orsi, Stefania Aurino, Gerardo Nigro, Giulio Piluso, Dario Acampora, Mafalda Cacciottolo, Kevin P. Campbell, Vincenzo Nigro
Hum Mol Genet. 2011 Dec 1; 20(23): 4644–4654. Published online 2011 Sep 2. doi: 10.1093/hmg/ddr398
PMCID:
PMC3209833
ArticlePDF–683K
7.
Sarcoglycan Complex: IMPLICATIONS FOR METABOLIC DEFECTS IN MUSCULAR DYSTROPHIES
Séverine Groh, Haihong Zong, Matthew M. Goddeeris, Connie S. Lebakken, David Venzke, Jeffrey E. Pessin, Kevin P. Campbell
J Biol Chem. 2009 Jul 17; 284(29): 19178–19182. Published online 2009 Jun 3. doi: 10.1074/jbc.C109.010728
PMCID:
PMC2740540
ArticlePDF–1.3M
8.
Zac1 (Lot1), a Potential Tumor Suppressor Gene, and the Gene for ɛ-Sarcoglycan Are Maternally Imprinted Genes: Identification by a Subtractive Screen of Novel Uniparental Fibroblast Lines
Graziella Piras, Aboubaker El Kharroubi, Serguei Kozlov, Diana Escalante-Alcalde, Lidia Hernandez, Neal G. Copeland, Debra J. Gilbert, Nancy A. Jenkins, Colin L. Stewart
Mol Cell Biol. 2000 May; 20(9): 3308–3315. doi: 10.1128/mcb.20.9.3308-3315.2000
PMCID:
PMC85624
ArticlePDF–1.2M
9.
Identification of a Large Novel Imprinted Gene Cluster on Mouse Proximal Chromosome 6
Ryuichi Ono, Hirosuke Shiura, Hiroyuki Aburatani, Takashi Kohda, Tomoko Kaneko-Ishino, Fumitoshi Ishino
Genome Res. 2003 Jul; 13(7): 1696–1705. doi: 10.1101/gr.906803
PMCID:
PMC403743
ArticlePDF–1.3M
10.
Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, TFPI2/Tfpi2, which requires EHMT2 and EED for allelic-silencing
David Monk, Alexandre Wagschal, Philippe Arnaud, Pari-Sima Müller, Layla Parker-Katiraee, Déborah Bourc’his, Stephen W. Scherer, Robert Feil, Philip Stanier, Gudrun E. Moore
Genome Res. 2008 Aug; 18(8): 1270–1281. doi: 10.1101/gr.077115.108
PMCID:
PMC2493428
ArticlePDF–1.2M
11.
Role of Tet1 in genomic imprinting erasure
Shinpei Yamaguchi, Li Shen, Yuting Liu, Damian Sendler, Yi Zhang
Nature. Author manuscript; available in PMC 2014 Jun 19.
Published in final edited form as: Nature. 2013 Dec 19; 504(7480): 460–464. Published online 2013 Dec 1. doi: 10.1038/nature12805
PMCID:
PMC3957231
ArticlePDF–3.3M
12.
Generalized disruption of inherited genomic imprints leads to wide-ranging placental defects and dysregulated fetal growth
K. P. Himes, E. Koppes, J. Richard Chaillet
Dev Biol. Author manuscript; available in PMC 2014 Jan 1.
Published in final edited form as: Dev Biol. 2013 Jan 1; 373(1): 72–82. Published online 2012 Oct 17. doi: 10.1016/j.ydbio.2012.10.010
PMCID:
PMC3508140
ArticlePDF–7.3M
13.
Barx2 and Fgf10 regulate ocular glands branching morphogenesis by controlling extracellular matrix remodeling
Cindy Tsau, Masataka Ito, Anastasia Gromova, Matthew P. Hoffman, Robyn Meech, Helen P. Makarenkova
Development. 2011 Aug 1; 138(15): 3307–3317. doi: 10.1242/dev.066241
PMCID:
PMC3133920
Article
14.
Expression at the Imprinted Dlk1-Gtl2 Locus Is Regulated by Proneural Genes in the Developing Telencephalon
Julie Seibt, Olivier Armant, Anne Le Digarcher, Diogo Castro, Vidya Ramesh, Laurent Journot, François Guillemot, Pierre Vanderhaeghen, Tristan Bouschet
PLoS One. 2012; 7(11): e48675. Published online 2012 Nov 6. doi: 10.1371/journal.pone.0048675
PMCID:
PMC3490856
ArticlePDF–4.1M
15.
Cell Type-specific Alternative Splicing Governs Cell Fate in the Developing Cerebral Cortex
Xiaochang Zhang, Ming Hui Chen, Xuebing Wu, Andrew Kodani, Jean Fan, Ryan Doan, Manabu Ozawa, Jacqueline Ma, Nobuaki Yoshida, Jeremy F. Reiter, Douglas L. Black, Peter V. Kharchenko, Phillip A. Sharp, Christopher A. Walsh
Cell. Author manuscript; available in PMC 2017 Jan 20.
Published in final edited form as: Cell. 2016 Aug 25; 166(5): 1147–1162.e15. doi: 10.1016/j.cell.2016.07.025
PMCID:
PMC5248659
ArticlePDF–3.7M
16.
Overlapping Activities of Two Neuronal Splicing Factors Switch the GABA Effect from Excitatory to Inhibitory by Regulating REST
Yoko Nakano, Susan Wiechert, Botond Bánfi
Cell Rep. Author manuscript; available in PMC 2019 Jun 9.
Published in final edited form as: Cell Rep. 2019 Apr 16; 27(3): 860–871.e8. doi: 10.1016/j.celrep.2019.03.072
PMCID:
PMC6556397
ArticlePDF–2.3M
17.
BGEM: An In Situ Hybridization Database of Gene Expression in the Embryonic and Adult Mouse Nervous System
Susan Magdaleno, Patricia Jensen, Craig L Brumwell, Anna Seal, Karen Lehman, Andrew Asbury, Tony Cheung, Tommie Cornelius, Diana M Batten, Christopher Eden, Shannon M Norland, Dennis S Rice, Nilesh Dosooye, Sundeep Shakya, Perdeep Mehta, Tom Curran
PLoS Biol. 2006 Apr; 4(4): e86. Published online 2006 Mar 28. doi: 10.1371/journal.pbio.0040086
PMCID:
PMC1413568
ArticlePDF–99K
18.
Genome-wide expression profiling of mid-gestation placenta and embryo using a 15,000 mouse developmental cDNA microarray
Tetsuya S. Tanaka, Saied A. Jaradat, Meng K. Lim, George J. Kargul, Xiaohong Wang, Marija J. Grahovac, Serafino Pantano, Yuri Sano, Yulan Piao, Ramaiah Nagaraja, Hirofumi Doi, William H. Wood, III, Kevin G. Becker, Minoru S. H. Ko
Proc Natl Acad Sci U S A. 2000 Aug 1; 97(16): 9127–9132. doi: 10.1073/pnas.97.16.9127
PMCID:
PMC16833
ArticlePDF–847K
19.
Wnk1 kinase deficiency lowers blood pressure in mice: A gene-trap screen to identify potential targets for therapeutic intervention
Brian P. Zambrowicz, Alejandro Abuin, Ramiro Ramirez-Solis, Lizabeth J. Richter, James Piggott, Hector BeltrandelRio, Eric C. Buxton, Joel Edwards, Rick A. Finch, Carl J. Friddle, Anupma Gupta, Gwenn Hansen, Yi Hu, Wenhu Huang, Crystal Jaing, Billie Wayne Key, Jr., Peter Kipp, Buckley Kohlhauff, Zhi-Qing Ma, Diane Markesich, Robert Payne, David G. Potter, Ny Qian, Joseph Shaw, Jeff Schrick, Zheng-Zheng Shi, Mary Jean Sparks, Isaac Van Sligtenhorst, Peter Vogel, Wade Walke, Nianhua Xu, Qichao Zhu, Christophe Person, Arthur T. Sands
Proc Natl Acad Sci U S A. 2003 Nov 25; 100(24): 14109–14114. Published online 2003 Nov 10. doi: 10.1073/pnas.2336103100
Correction in:
Proc Natl Acad Sci U S A. 2004 Mar 23; 101(12): 4332.
PMCID:
PMC283554
ArticlePDF–481K
20.
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
ArticlePDF–3.4M

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