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Items: 1 to 20 of 25

1.
Screening of potential target genes for cataract by analyzing mRNA expression profile of mouse Hsf4-null lens
Wenjuan Zhao, Wenqing Zhao, Jun Zhao, Dong Wang, Jinghai Li
BMC Ophthalmol. 2015; 15: 76. Published online 2015 Jul 18. doi: 10.1186/s12886-015-0066-3
PMCID:
PMC4506420
ArticlePDF–961K
2.
Functional analysis of the Hsf4lop11 allele responsible for cataracts in lop11 mice
Lina Liang, Ryan Liegel, Brad Endres, Adam Ronchetti, Bo Chang, D.J. Sidjanin
Mol Vis. 2011; 17: 3062–3071. Published online 2011 Nov 23.
PMCID:
PMC3233385
ArticlePDF–776K
3.
HSF4 Transcriptionally Activates Autophagy by Regulating ATG9a During Lens Terminal Differentiation
Jing Zhang, Ning Jiang, Chunxiao Du, Hongzan Guo, Ranqi Meng, Xinyu Hou, Mugen Liu, Yanzhong Hu, Xiukun Cui
Invest Ophthalmol Vis Sci. 2023 Jun; 64(7): 5. Published online 2023 Jun 2. doi: 10.1167/iovs.64.7.5
PMCID:
PMC10243497
ArticlePDF–4.9M
4.
Expression of the HSF4 DNA Binding Domain-EGFP Hybrid Gene Recreates Early Childhood Lamellar Cataract in Transgenic Mice
Rajendra K. Gangalum, Zhe Jing, Ankur M. Bhat, Josh Lee, Yoshiko Nagaoka, Sophie X. Deng, Meisheng Jiang, Suraj P. Bhat
Invest Ophthalmol Vis Sci. 2014 Nov; 55(11): 7227–7240. Published online 2014 Nov 13. doi: 10.1167/iovs.14-14594
PMCID:
PMC4231995
ArticlePDF–1.4M
5.
Early transposable element insertion in intron 9 of the Hsf4 gene results in autosomal recessive cataracts in lop11 and ldis1 mice
Elijah Talamas, Lavinia Jackson, Matthew Koeberl, Todd Jackson, John L. McElwee, Norman L. Hawes, Bo Chang, Monica M. Jablonski, D.J. Sidjanin
Genomics. Author manuscript; available in PMC 2006 Jul 16.
Published in final edited form as: Genomics. 2006 Jul; 88(1): 44–51. Published online 2006 Apr 3. doi: 10.1016/j.ygeno.2006.02.012
PMCID:
PMC1509100
ArticlePDF–547K
6.
The aging mouse lens transcriptome
Adam P. Faranda, Mahbubul H. Shihan, Yan Wang, Melinda K. Duncan
Exp Eye Res. Author manuscript; available in PMC 2022 Aug 1.
Published in final edited form as: Exp Eye Res. 2021 Aug; 209: 108663. Published online 2021 Jun 11. doi: 10.1016/j.exer.2021.108663
PMCID:
PMC8720273
ArticlePDF–1.8M
7.
Demyelination, Astrogliosis, and Accumulation of Ubiquitinated Proteins, Hallmarks of CNS Disease in hsf1-Deficient Mice
Sachiko Homma, Xiongjie Jin, Guanghu Wang, Naxin Tu, Jinna Min, Nathan Yanasak, Nahid F. Mivechi
J Neurosci. 2007 Jul 25; 27(30): 7974–7986. doi: 10.1523/JNEUROSCI.0006-07.2007
PMCID:
PMC6672719
ArticlePDF–829K
8.
SKAP2, a novel target of HSF4b, associates with NCK2/F-actin at membrane ruffles and regulates actin reorganization in lens cell
Li Zhou, Zhenguo Zhang, Yufang Zheng, Yufei Zhu, Zejun Wei, Heng Xu, Quan Tang, Xiangyin Kong, Landian Hu
J Cell Mol Med. 2011 Apr; 15(4): 783–795. Published online 2010 Mar 9. doi: 10.1111/j.1582-4934.2010.01048.x
PMCID:
PMC3922667
ArticlePDF–1.3M
9.
Inactivation of Heat Shock Factor Hsf4 Induces Cellular Senescence and Suppresses Tumorigenesis In Vivo
Xiongjie Jin, Binnur Eroglu, Wonkyoung Cho, Yukihiro Yamaguchi, Demetrius Moskophidis, Nahid F. Mivechi
Mol Cancer Res. Author manuscript; available in PMC 2013 Jun 24.
Published in final edited form as: Mol Cancer Res. 2012 Apr; 10(4): 523–534. Published online 2012 Feb 21. doi: 10.1158/1541-7786.MCR-11-0530
PMCID:
PMC3690822
ArticlePDF–4.2M
10.
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
ArticlePDF–2.7M
11.
Cell-type-dependent access of HSF1 and HSF4 to αB-crystallin promoter during heat shock
Zhe Jing, Rajendra K. Gangalum, Josh Z. Lee, Dennis Mock, Suraj P. Bhat
Cell Stress Chaperones. 2013 May; 18(3): 377–387. Published online 2012 Dec 23. doi: 10.1007/s12192-012-0386-7
Correction in:
Cell Stress Chaperones. 2013 May; 18(3): 389–390.
PMCID:
PMC3631099
ArticlePDF–817K
12.
N-myc regulates growth and fiber cell differentiation in lens development
Gabriel R. Cavalheiro, Gabriel E. Matos-Rodrigues, Yilin Zhao, Anielle L. Gomes, Deepti Anand, Danilo Predes, Silmara de Lima, Jose G. Abreu, Deyou Zheng, Salil A. Lachke, Ales Cvekl, Rodrigo A. P. Martins
Dev Biol. Author manuscript; available in PMC 2017 Sep 6.
Published in final edited form as: Dev Biol. 2017 Sep 1; 429(1): 105–117. Published online 2017 Jul 14. doi: 10.1016/j.ydbio.2017.07.002
PMCID:
PMC5586101
ArticlePDF–2.9M
13.
Pitx3 controls multiple aspects of lens development
Olga Medina-Martinez, Rina Shah, Milan Jamrich
Dev Dyn. Author manuscript; available in PMC 2010 Nov 10.
Published in final edited form as: Dev Dyn. 2009 Sep; 238(9): 2193–2201. doi: 10.1002/dvdy.21924
PMCID:
PMC2978039
ArticlePDF–2.3M
14.
Chromatin remodeling enzyme Snf2h regulates embryonic lens differentiation and denucleation
Shuying He, Saima Limi, Rebecca S. McGreal, Qing Xie, Lisa A. Brennan, Wanda Lee Kantorow, Juraj Kokavec, Romit Majumdar, Harry Hou, Jr, Winfried Edelmann, Wei Liu, Ruth Ashery-Padan, Jiri Zavadil, Marc Kantorow, Arthur I. Skoultchi, Tomas Stopka, Ales Cvekl
Development. 2016 Jun 1; 143(11): 1937–1947. doi: 10.1242/dev.135285
PMCID:
PMC4920164
Article
15.
HSF4 is required for normal cell growth and differentiation during mouse lens development
Mitsuaki Fujimoto, Hanae Izu, Keisuke Seki, Ken Fukuda, Teruo Nishida, Shu-ichi Yamada, Kanefusa Kato, Shigenobu Yonemura, Sachiye Inouye, Akira Nakai
EMBO J. 2004 Oct 27; 23(21): 4297–4306. Published online 2004 Oct 14. doi: 10.1038/sj.emboj.7600435
PMCID:
PMC524399
ArticlePDF–399K
16.
Analysis of HSF4 Binding Regions Reveals Its Necessity for Gene Regulation during Development and Heat Shock Response in Mouse Lenses
Mitsuaki Fujimoto, Koji Oshima, Toyohide Shinkawa, Bei Bei Wang, Sachiye Inouye, Naoki Hayashida, Ryosuke Takii, Akira Nakai
J Biol Chem. 2008 Oct 31; 283(44): 29961–29970. doi: 10.1074/jbc.M804629200
PMCID:
PMC2662063
ArticlePDF–929K
17.
A Systems Approach Reveals that the Myogenesis Genome Network Is Regulated by the Transcriptional Repressor RP58
Shigetoshi Yokoyama, Yoshiaki Ito, Hiroe Ueno-Kudoh, Hirohito Shimizu, Kenta Uchibe, Sonia Albini, Kazuhiko Mitsuoka, Shigeru Miyaki, Minako Kiso, Akane Nagai, Tomohiro Hikata, Tadahiro Osada, Noritsugu Fukuda, Satoshi Yamashita, Daisuke Harada, Valeria Mezzano, Masataka Kasai, Pier Lorenzo Puri, Yoshihide Hayashizaki, Haruo Okado, Megumi Hashimoto, Hiroshi Asahara
Dev Cell. Author manuscript; available in PMC 2011 Jun 7.
Published in final edited form as: Dev Cell. 2009 Dec; 17(6): 836–848. doi: 10.1016/j.devcel.2009.10.011
PMCID:
PMC3110151
ArticlePDF–2.0M
18.
High-throughput discovery of novel developmental phenotypes
Mary E. Dickinson, Ann M. Flenniken, Xiao Ji, Lydia Teboul, Michael D. Wong, Jacqueline K. White, Terrence F. Meehan, Wolfgang J. Weninger, Henrik Westerberg, Hibret Adissu, Candice N. Baker, Lynette Bower, James M. Brown, L. Brianna Caddle, Francesco Chiani, Dave Clary, James Cleak, Mark J. Daly, James M. Denegre, Brendan Doe, Mary E. Dolan, Sarah M. Edie, Helmut Fuchs, Valerie Gailus-Durner, Antonella Galli, Alessia Gambadoro, Juan Gallegos, Shiying Guo, Neil R. Horner, Chih-wei Hsu, Sara J. Johnson, Sowmya Kalaga, Lance C. Keith, Louise Lanoue, Thomas N. Lawson, Monkol Lek, Manuel Mark, Susan Marschall, Jeremy Mason, Melissa L. McElwee, Susan Newbigging, Lauryl M.J. Nutter, Kevin A. Peterson, Ramiro Ramirez-Solis, Douglas J. Rowland, Edward Ryder, Kaitlin E. Samocha, John R. Seavitt, Mohammed Selloum, Zsombor Szoke-Kovacs, Masaru Tamura, Amanda G Trainor, Ilinca Tudose, Shigeharu Wakana, Jonathan Warren, Olivia Wendling, David B. West, Leeyean Wong, Atsushi Yoshiki, The International Mouse Phenotyping Consortium, Daniel G. MacArthur, Glauco P. Tocchini-Valentini, Xiang Gao, Paul Flicek, Allan Bradley, William C. Skarnes, Monica J. Justice, Helen E. Parkinson, Mark Moore, Sara Wells, Robert E. Braun, Karen L. Svenson, Martin Hrabe de Angelis, Yann Herault, Tim Mohun, Ann-Marie Mallon, R. Mark Henkelman, Steve D.M. Brown, David J. Adams, K.C. Kent Lloyd, Colin McKerlie, Arthur L. Beaudet, Maja Bucan, Stephen A. Murray
Nature. Author manuscript; available in PMC 2017 Mar 14.
Published in final edited form as: Nature. 2016 Sep 22; 537(7621): 508–514. Published online 2016 Sep 14. doi: 10.1038/nature19356
Correction in:
Nature. 2017 Nov 16; 551(7680): 398.
PMCID:
PMC5295821
ArticlePDF–3.0M
19.
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
ArticlePDF–5.7M
20.
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
ArticlePDF–1.1M

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