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Items: 1 to 20 of 23

1.
CP49 and filensin intermediate filaments are essential for formation of cold cataract
Yuxing Li, Xi Liu, Chun-hong Xia, Paul G. FitzGerald, Rachel Li, Jessica Wang, Xiaohua Gong
Mol Vis. 2020; 26: 603–612. Published online 2020 Aug 23.
PMCID:
PMC7479064
AbstractArticlePDF–12M
2.
Resisting the Effects of Aging: A Function for the Fiber Cell Beaded Filament
Kyoung-hye Yoon, Tom Blankenship, Bradley Shibata, Paul G. FitzGerald
Invest Ophthalmol Vis Sci. Author manuscript; available in PMC 2019 Sep 16.
Published in final edited form as: Invest Ophthalmol Vis Sci. 2008 Mar; 49(3): 1030–1036. doi: 10.1167/iovs.07-1149
PMCID:
PMC6746185
AbstractArticlePDF–2.5M
3.
Expression of the type VI intermediate filament proteins CP49 and filensin in the mouse lens epithelium
Paul FitzGerald, Ning Sun, Brad Shibata, John F. Hess
Mol Vis. 2016; 22: 970–989. Published online 2016 Aug 6.
PMCID:
PMC4975932
AbstractArticlePDF–6.2M
4.
Aquaporin 0 Modulates Lens Gap Junctions in the Presence of Lens-Specific Beaded Filament Proteins
Sindhu Kumari, Junyuan Gao, Richard T. Mathias, Xiurong Sun, Amizhdini Eswaramoorthy, Nicholas Browne, Nigel Zhang, Kulandaiappan Varadaraj
Invest Ophthalmol Vis Sci. 2017 Dec; 58(14): 6006–6019. doi: 10.1167/iovs.17-22153
PMCID:
PMC5710632
AbstractArticlePDF–1.9M
5.
Removal of Hsf4 leads to cataract development in mice through down-regulation of γS-crystallin and Bfsp expression
Xiaohe Shi, Bin Cui, Zhugang Wang, Lin Weng, Zhongping Xu, Jinjin Ma, Guotong Xu, Xiangyin Kong, Landian Hu
BMC Mol Biol. 2009; 10: 10. Published online 2009 Feb 19. doi: 10.1186/1471-2199-10-10
PMCID:
PMC2653017
AbstractArticlePDF–2.7M
6.
Periplakin Interactions with Lens Intermediate and Beaded Filaments
Kyoung-hye Yoon, Paul G. FitzGerald
Invest Ophthalmol Vis Sci. Author manuscript; available in PMC 2010 Jul 26.
Published in final edited form as: Invest Ophthalmol Vis Sci. 2009 Mar; 50(3): 1283–1289. Published online 2008 Nov 21. doi: 10.1167/iovs.08-2894
PMCID:
PMC2909747
AbstractArticlePDF–1.6M
7.
A Role for Lengsin, a Recruited Enzyme, in Terminal Differentiation in the Vertebrate Lens
Keith Wyatt, Chun Gao, Jen-Yue Tsai, Robert N. Fariss, Sugata Ray, Graeme Wistow
J Biol Chem. Author manuscript; available in PMC 2010 Jul 29.
Published in final edited form as: J Biol Chem. 2008 Mar 7; 283(10): 6607–6615. Published online 2008 Jan 3. doi: 10.1074/jbc.M709144200
PMCID:
PMC2911820
AbstractArticlePDF–1.0M
8.
Wnt signaling is required for organization of the lens fiber cell cytoskeleton and development of lens three-dimensional architecture
Yongjuan Chen, Richard J.W. Stump, Frank J. Lovicu, Akihiko Shimono, John W. McAvoy
Dev Biol. Author manuscript; available in PMC 2009 Dec 1.
Published in final edited form as: Dev Biol. 2008 Dec 1; 324(1): 161–176. Published online 2008 Sep 18. doi: 10.1016/j.ydbio.2008.09.002
PMCID:
PMC2651430
AbstractArticlePDF–7.3M
9.
α6 Integrin Transactivates Insulin-like Growth Factor Receptor-1 (IGF-1R) to Regulate Caspase-3-mediated Lens Epithelial Cell Differentiation Initiation
Subhasree Basu, Suren Rajakaruna, Adèle De Arcangelis, Liping Zhang, Elisabeth Georges-Labouesse, A. Sue Menko
J Biol Chem. 2014 Feb 14; 289(7): 3842–3855. Published online 2013 Dec 31. doi: 10.1074/jbc.M113.515254
PMCID:
PMC3924254
AbstractArticlePDF–6.7M
10.
Altered aggregation properties of mutant γ-crystallins cause inherited cataract
Aileen Sandilands, Aileen M. Hutcheson, Heather A. Long, Alan R. Prescott, Gijs Vrensen, Jana Löster, Norman Klopp, Raimund B. Lutz, Jochen Graw, Shigeo Masaki, Christopher M. Dobson, Cait E. MacPhee, Roy A. Quinlan
EMBO J. 2002 Nov 15; 21(22): 6005–6014. doi: 10.1093/emboj/cdf609
PMCID:
PMC137201
AbstractArticlePDF–432K
11.
Periaxin is required for hexagonal geometry and membrane organization of mature lens fibers
Rupalatha Maddala, Nikolai P. Skiba, Robert Lalane, III, Diane L. Sherman, Peter J. Brophy, Ponugoti V. Rao
Dev Biol. Author manuscript; available in PMC 2012 Sep 1.
Published in final edited form as: Dev Biol. 2011 Sep 1; 357(1): 179–190. Published online 2011 Jul 2. doi: 10.1016/j.ydbio.2011.06.036
PMCID:
PMC3164832
AbstractArticlePDF–7.3M
12.
Cell Autonomous Roles for AP-2α in Lens Vesicle Separation and Maintenance of the Lens Epithelial Cell Phenotype
Giuseppe F. Pontoriero, Paula Deschamps, Ruth Ashery-Padan, Ryan Wong, Ying Yang, Jiri Zavadil, Ales Cvekl, Shelley Sullivan, Trevor Williams, Judith A. West-Mays
Dev Dyn. Author manuscript; available in PMC 2008 Aug 18.
Published in final edited form as: Dev Dyn. 2008 Mar; 237(3): 602–617. doi: 10.1002/dvdy.21445
PMCID:
PMC2517426
AbstractArticlePDF–2.2M
13.
Chromatin remodeling enzyme Brg1 is required for mouse lens fiber cell terminal differentiation and its denucleation
Shuying He, Melinda K Pirity, Wei-Lin Wang, Louise Wolf, Bharesh K Chauhan, Kveta Cveklova, Ernst R Tamm, Ruth Ashery-Padan, Daniel Metzger, Akira Nakai, Pierre Chambon, Jiri Zavadil, Ales Cvekl
Epigenetics Chromatin. 2010; 3: 21. Published online 2010 Nov 30. doi: 10.1186/1756-8935-3-21
PMCID:
PMC3003251
AbstractArticlePDF–2.4M
14.
Mutually regulated expression of Pax6 and Six3 and its implications for the Pax6 haploinsufficient lens phenotype
Guy Goudreau, Petros Petrou, Lixing W. Reneker, Jochen Graw, Jana Löster, Peter Gruss
Proc Natl Acad Sci U S A. 2002 Jun 25; 99(13): 8719–8724. Published online 2002 Jun 18. doi: 10.1073/pnas.132195699
PMCID:
PMC124365
AbstractArticlePDF–762K
15.
The International Mouse Phenotyping Consortium Web Portal, a unified point of access for knockout mice and related phenotyping data
Gautier Koscielny, Gagarine Yaikhom, Vivek Iyer, Terrence F. Meehan, Hugh Morgan, Julian Atienza-Herrero, Andrew Blake, Chao-Kung Chen, Richard Easty, Armida Di Fenza, Tanja Fiegel, Mark Grifiths, Alan Horne, Natasha A. Karp, Natalja Kurbatova, Jeremy C. Mason, Peter Matthews, Darren J. Oakley, Asfand Qazi, Jack Regnart, Ahmad Retha, Luis A. Santos, Duncan J. Sneddon, Jonathan Warren, Henrik Westerberg, Robert J. Wilson, David G. Melvin, Damian Smedley, Steve D. M. Brown, Paul Flicek, William C. Skarnes, Ann-Marie Mallon, Helen Parkinson
Nucleic Acids Res. 2014 Jan 1; 42(Database issue): D802–D809. Published online 2013 Nov 3. doi: 10.1093/nar/gkt977
PMCID:
PMC3964955
AbstractArticlePDF–5.7M
16.
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
17.
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
18.
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
AbstractArticlePDF–481K
19.
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
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
AbstractArticlePDF–3.4M

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