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Items: 1 to 20 of 24

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
AbstractArticlePDF–4.8M
2.
Cell-Type-Specific Gene Expression in Developing Mouse Neocortex: Intermediate Progenitors Implicated in Axon Development
Francesco Bedogni, Robert F. Hevner
Front Mol Neurosci. 2021; 14: 686034. Published online 2021 Jul 12. doi: 10.3389/fnmol.2021.686034
PMCID:
PMC8313239
AbstractArticlePDF–1.6M
3.
Inhibition of a transcriptional repressor rescues hearing in a splicing factor–deficient mouse
Yoko Nakano, Susan Wiechert, Bernd Fritzsch, Botond Bánfi
Life Sci Alliance. 2020 Dec; 3(12): e202000841. Published online 2020 Oct 21. doi: 10.26508/lsa.202000841
PMCID:
PMC7652395
AbstractArticlePDF–3.4M
4.
Mouse screen reveals multiple new genes underlying mouse and human hearing loss
Neil J. Ingham, Selina A. Pearson, Valerie E. Vancollie, Victoria Rook, Morag A. Lewis, Jing Chen, Annalisa Buniello, Elisa Martelletti, Lorenzo Preite, Chi Chung Lam, Felix D. Weiss, Zӧe Powis, Pim Suwannarat, Christopher J. Lelliott, Sally J. Dawson, Jacqueline K. White, Karen P. Steel
PLoS Biol. 2019 Apr; 17(4): e3000194. Published online 2019 Apr 11. doi: 10.1371/journal.pbio.3000194
PMCID:
PMC6459510
AbstractArticlePDF–5.1M
5.
Nav1.2 haplodeficiency in excitatory neurons causes absence-like seizures in mice
Ikuo Ogiwara, Hiroyuki Miyamoto, Tetsuya Tatsukawa, Tetsushi Yamagata, Tojo Nakayama, Nafiseh Atapour, Eriko Miura, Emi Mazaki, Sara J. Ernst, Dezhi Cao, Hideyuki Ohtani, Shigeyoshi Itohara, Yuchio Yanagawa, Mauricio Montal, Michisuke Yuzaki, Yushi Inoue, Takao K. Hensch, Jeffrey L. Noebels, Kazuhiro Yamakawa
Commun Biol. 2018; 1: 96. Published online 2018 Jul 19. doi: 10.1038/s42003-018-0099-2
PMCID:
PMC6115194
AbstractArticlePDF–3.5M
6.
Transcriptome analysis reveals transmembrane targets on transplantable midbrain dopamine progenitors
Chris R. Bye, Marie E. Jönsson, Anders Björklund, Clare L. Parish, Lachlan H. Thompson
Proc Natl Acad Sci U S A. 2015 Apr 14; 112(15): E1946–E1955. Published online 2015 Mar 9. doi: 10.1073/pnas.1501989112
PMCID:
PMC4403171
AbstractArticlePDF–1.9M
7.
Identification of Genes Important for Cutaneous Function Revealed by a Large Scale Reverse Genetic Screen in the Mouse
Tia DiTommaso, Lynelle K. Jones, Denny L. Cottle, The WTSI Mouse Genetics Program, Anna-Karin Gerdin, Valerie E. Vancollie, Fiona M. Watt, Ramiro Ramirez-Solis, Allan Bradley, Karen P. Steel, John P. Sundberg, Jacqueline K. White, Ian M. Smyth
PLoS Genet. 2014 Oct; 10(10): e1004705. Published online 2014 Oct 23. doi: 10.1371/journal.pgen.1004705
PMCID:
PMC4207618
AbstractArticlePDF–1.8M
8.
Scn3b knockout mice exhibit abnormal sino-atrial and cardiac conduction properties
P Hakim, N Brice, R Thresher, J Lawrence, Y Zhang, A P Jackson, A A Grace, C L-H Huang
Acta Physiol (Oxf) 2010 Jan; 198(1): 47–59. doi: 10.1111/j.1748-1716.2009.02048.x
PMCID:
PMC3763209
AbstractArticlePDF–401K
9.
Patterned expression of ion channel genes in mouse dorsal raphe nucleus determined with the Allen Mouse Brain Atlas
J. Scott Templin, Sun Jung Bang, Mariano Soiza-Reilly, Charles B. Berde, Kathryn G. Commons
Brain Res. Author manuscript; available in PMC 2013 May 31.
Published in final edited form as: Brain Res. 2012 May 31; 1457: 1–12. Published online 2012 Apr 4. doi: 10.1016/j.brainres.2012.03.066
PMCID:
PMC3606056
AbstractArticlePDF–7.6M
10.
A conditional knockout resource for the genome–wide study of mouse gene function
William C. Skarnes, Barry Rosen, Anthony P. West, Manousos Koutsourakis, Wendy Bushell, Vivek Iyer, Alejandro O. Mujica, Mark Thomas, Jennifer Harrow, Tony Cox, David Jackson, Jessica Severin, Patrick Biggs, Jun Fu, Michael Nefedov, Pieter J. de Jong, A. Francis Stewart, Allan Bradley
Nature. Author manuscript; available in PMC 2013 Feb 14.
Published in final edited form as: Nature. 2011 Jun 15; 474(7351): 337–342. Published online 2011 Jun 15. doi: 10.1038/nature10163
PMCID:
PMC3572410
AbstractArticlePDF–1.1M
11.
A Mutation in the Srrm4 Gene Causes Alternative Splicing Defects and Deafness in the Bronx Waltzer Mouse
Yoko Nakano, Israt Jahan, Gregory Bonde, Xingshen Sun, Michael S. Hildebrand, John F. Engelhardt, Richard J. H. Smith, Robert A. Cornell, Bernd Fritzsch, Botond Bánfi
PLoS Genet. 2012 Oct; 8(10): e1002966. Published online 2012 Oct 4. doi: 10.1371/journal.pgen.1002966
PMCID:
PMC3464207
AbstractArticlePDF–4.1M
12.
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
13.
A High-Resolution Anatomical Atlas of the Transcriptome in the Mouse Embryo
Graciana Diez-Roux, Sandro Banfi, Marc Sultan, Lars Geffers, Santosh Anand, David Rozado, Alon Magen, Elena Canidio, Massimiliano Pagani, Ivana Peluso, Nathalie Lin-Marq, Muriel Koch, Marchesa Bilio, Immacolata Cantiello, Roberta Verde, Cristian De Masi, Salvatore A. Bianchi, Juliette Cicchini, Elodie Perroud, Shprese Mehmeti, Emilie Dagand, Sabine Schrinner, Asja Nürnberger, Katja Schmidt, Katja Metz, Christina Zwingmann, Norbert Brieske, Cindy Springer, Ana Martinez Hernandez, Sarah Herzog, Frauke Grabbe, Cornelia Sieverding, Barbara Fischer, Kathrin Schrader, Maren Brockmeyer, Sarah Dettmer, Christin Helbig, Violaine Alunni, Marie-Annick Battaini, Carole Mura, Charlotte N. Henrichsen, Raquel Garcia-Lopez, Diego Echevarria, Eduardo Puelles, Elena Garcia-Calero, Stefan Kruse, Markus Uhr, Christine Kauck, Guangjie Feng, Nestor Milyaev, Chuang Kee Ong, Lalit Kumar, MeiSze Lam, Colin A. Semple, Attila Gyenesei, Stefan Mundlos, Uwe Radelof, Hans Lehrach, Paolo Sarmientos, Alexandre Reymond, Duncan R. Davidson, Pascal Dollé, Stylianos E. Antonarakis, Marie-Laure Yaspo, Salvador Martinez, Richard A. Baldock, Gregor Eichele, Andrea Ballabio
PLoS Biol. 2011 Jan; 9(1): e1000582. Published online 2011 Jan 18. doi: 10.1371/journal.pbio.1000582
PMCID:
PMC3022534
AbstractArticlePDF–3.8M
14.
Ezh2, the histone methyltransferase of PRC2, regulates the balance between self-renewal and differentiation in the cerebral cortex
João D. Pereira, Stephen N. Sansom, James Smith, Marc-Werner Dobenecker, Alexander Tarakhovsky, Frederick J. Livesey
Proc Natl Acad Sci U S A. 2010 Sep 7; 107(36): 15957–15962. Published online 2010 Aug 23. doi: 10.1073/pnas.1002530107
PMCID:
PMC2936600
AbstractArticlePDF–1.8M
15.
CARM1 is required for proper control of proliferation and differentiation of pulmonary epithelial cells
Karen B. O'Brien, Meritxell Alberich-Jordà, Neelu Yadav, Olivier Kocher, Annalisa DiRuscio, Alexander Ebralidze, Elena Levantini, Natasha J. L. Sng, Manoj Bhasin, Tyler Caron, Daehoon Kim, Ulrich Steidl, Gang Huang, Balázs Halmos, Scott J. Rodig, Mark T. Bedford, Daniel G. Tenen, Susumu Kobayashi
Development. 2010 Jul 1; 137(13): 2147–2156. doi: 10.1242/dev.037150
PMCID:
PMC2882134
AbstractArticle
16.
Loss-of-function mutation of the SCN3B-encoded sodium channel β3 subunit associated with a case of idiopathic ventricular fibrillation
Carmen R. Valdivia, Argelia Medeiros-Domingo, Bin Ye, Win-Kuang Shen, Timothy J. Algiers, Michael J. Ackerman, Jonathan C. Makielski
Cardiovasc Res. 2010 Jun 1; 86(3): 392–400. Published online 2009 Dec 30. doi: 10.1093/cvr/cvp417
PMCID:
PMC2868175
AbstractArticlePDF–465K
17.
Scn3b knockout mice exhibit abnormal ventricular electrophysiological properties
Parvez Hakim, Iman S. Gurung, Thomas H. Pedersen, Rosemary Thresher, Nicola Brice, Jason Lawrence, Andrew A. Grace, Christopher L.-H. Huang
Prog Biophys Mol Biol. 2008 Oct; 98(2-3): 251–266. doi: 10.1016/j.pbiomolbio.2009.01.005
PMCID:
PMC2764399
AbstractArticle
18.
The Level of the Transcription Factor Pax6 Is Essential for Controlling the Balance between Neural Stem Cell Self-Renewal and Neurogenesis
Stephen N. Sansom, Dean S. Griffiths, Andrea Faedo, Dirk-Jan Kleinjan, Youlin Ruan, James Smith, Veronica van Heyningen, John L. Rubenstein, Frederick J. Livesey
PLoS Genet. 2009 Jun; 5(6): e1000511. Published online 2009 Jun 12. doi: 10.1371/journal.pgen.1000511
PMCID:
PMC2686252
AbstractArticlePDF–4.5M
19.
Sodium channel Scn1b null mice exhibit prolonged QT and RR intervals
Luis F. Lopez-Santiago, Laurence S. Meadows, Sara J. Ernst, Chunling Chen, Jyoti Dhar Malhotra, Dyke P. McEwen, Audrey Speelman, Jeffrey L. Noebels, Sebastian K.G. Maier, Anatoli N. Lopatin, Lori L. Isom
J Mol Cell Cardiol. Author manuscript; available in PMC 2008 Nov 1.
Published in final edited form as: J Mol Cell Cardiol. 2007 Nov; 43(5): 636–647. Published online 2007 Aug 10. doi: 10.1016/j.yjmcc.2007.07.062
PMCID:
PMC2099572
AbstractArticlePDF–2.0M
20.
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

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