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Items: 1 to 20 of 29

1.
A potent and selective small molecule inhibitor of myoferlin attenuates colorectal cancer progression
Yuan He, Weiqiong Kan, Yunqi Li, Yun Hao, Anling Huang, Haijun Gu, Minna Wang, Qingqing Wang, Jinlian Chen, Zhenliang Sun, Mingyao Liu, Yihua Chen, Zhengfang Yi
Clin Transl Med. 2021 Feb; 11(2): e289. Published online 2021 Feb 7. doi: 10.1002/ctm2.289
PMCID:
PMC7868085
AbstractArticlePDF–12M
2.
Ferlin proteins in myoblast fusion and muscle growth
Avery D. Posey, Jr, Alexis Demonbreun, Elizabeth M McNally
Curr Top Dev Biol. Author manuscript; available in PMC 2015 Jun 13.
Published in final edited form as: Curr Top Dev Biol. 2011; 96: 203–230. doi: 10.1016/B978-0-12-385940-2.00008-5
PMCID:
PMC4464798
AbstractArticlePDF–535K
3.
Myoferlin regulation by NFAT in muscle injury, regeneration and repair
Alexis R. Demonbreun, Karen A. Lapidos, Konstantina Heretis, Samantha Levin, Rodney Dale, Peter Pytel, Eric C. Svensson, Elizabeth M. McNally
J Cell Sci. 2010 Jul 15; 123(14): 2413–2422. Published online 2010 Jun 22. doi: 10.1242/jcs.065375
PMCID:
PMC2894657
AbstractArticle
4.
Lysosomal retargeting of Myoferlin mitigates membrane stress to enable pancreatic cancer growth
Suprit Gupta, Julian Yano, Vincent Mercier, Htet Htwe Htwe, Hijai R. Shin, Gilles Rademaker, Zeynep Cakir, Thomas Ituarte, Kwun W. Wen, Grace E. Kim, Roberto Zoncu, Aurelien Roux, David W. Dawson, Rushika M. Perera
Nat Cell Biol. Author manuscript; available in PMC 2022 Sep 6.
Published in final edited form as: Nat Cell Biol. 2021 Mar; 23(3): 232–242. Published online 2021 Mar 8. doi: 10.1038/s41556-021-00644-7
PMCID:
PMC9446896
AbstractArticlePDF–7.0M
5.
Loss of dysferlin or myoferlin results in differential defects in excitation–contraction coupling in mouse skeletal muscle
David Y. Barefield, Jordan J. Sell, Ibrahim Tahtah, Samuel D. Kearns, Elizabeth M. McNally, Alexis R. Demonbreun
Sci Rep. 2021; 11: 15865. Published online 2021 Aug 5. doi: 10.1038/s41598-021-95378-9
PMCID:
PMC8342512
AbstractArticlePDF–6.5M
6.
Myoferlin Regulates Wnt/β-Catenin Signaling-Mediated Skeletal Muscle Development by Stabilizing Dishevelled-2 Against Autophagy
Shunshun Han, Can Cui, Haorong He, Xiaoxu Shen, Yuqi Chen, Yan Wang, Diyan Li, Qing Zhu, Huadong Yin
Int J Mol Sci. 2019 Oct; 20(20): 5130. Published online 2019 Oct 16. doi: 10.3390/ijms20205130
PMCID:
PMC6829482
AbstractArticlePDF–3.7M
7.
Normal myoblast fusion requires myoferlin
Katherine R. Doherty, Andrew Cave, Dawn Belt Davis, Anthony J. Delmonte, Avery Posey, Judy U. Earley, Michele Hadhazy, Elizabeth M. McNally
Development. Author manuscript; available in PMC 2014 Jun 23.
Published in final edited form as: Development. 2005 Dec; 132(24): 5565–5575. Published online 2005 Nov 9. doi: 10.1242/dev.02155
PMCID:
PMC4066872
AbstractArticlePDF–1.2M
8.
Myoferlin is required for insulin-like growth factor response and muscle growth
Alexis R. Demonbreun, Avery D. Posey, Konstantina Heretis, Kayleigh A. Swaggart, Judy U. Earley, Peter Pytel, Elizabeth M. McNally
FASEB J. 2010 Apr; 24(4): 1284–1295. doi: 10.1096/fj.09-136309
PMCID:
PMC2845429
AbstractArticle
9.
The Endocytic Recycling Protein EHD2 Interacts with Myoferlin to Regulate Myoblast Fusion
Katherine R. Doherty, Alexis R. Demonbreun, Gregory Q. Wallace, Andrew Cave, Avery D. Posey, Konstantina Heretis, Peter Pytel, Elizabeth M. McNally
J Biol Chem. 2008 Jul 18; 283(29): 20252–20260. doi: 10.1074/jbc.M802306200
PMCID:
PMC2459265
AbstractArticlePDF–474K
10.
Impairment of APPL1/Myoferlin facilitates adipogenic differentiation of mesenchymal stem cells by blocking autophagy flux in osteoporosis
Yunhui Zhang, Wenjie Liu, Weiquan Yuan, Zhaopeng Cai, Guiwen Ye, Guan Zheng, Chenhao Xu, Xinglang Wang, Chenying zeng, Rujia Mi, Pei Feng, Fenglei Chen, Yanfeng Wu, Huiyong Shen, Peng Wang
Cell Mol Life Sci. 2022 Sep; 79(9): 488. Published online 2022 Aug 19. doi: 10.1007/s00018-022-04511-y
PMCID:
PMC9391247
AbstractArticlePDF–16M
11.
Dysferlin and Myoferlin Regulate Transverse Tubule Formation and Glycerol Sensitivity
Alexis R. Demonbreun, Ann E. Rossi, Manuel G. Alvarez, Kaitlin E. Swanson, H. Kieran Deveaux, Judy U. Earley, Michele Hadhazy, Ravneet Vohra, Glenn A. Walter, Peter Pytel, Elizabeth M. McNally
Am J Pathol. 2014 Jan; 184(1): 248–259. doi: 10.1016/j.ajpath.2013.09.009
PMCID:
PMC3873498
AbstractArticlePDF–3.0M
12.
WNT/β-catenin signaling plays a crucial role in myoblast fusion through regulation of nephrin expression during development
Akiko Suzuki, Ryohei Minamide, Junichi Iwata
Development. 2018 Dec 1; 145(23): dev168351. Published online 2018 Nov 27. doi: 10.1242/dev.168351
PMCID:
PMC6288386
AbstractArticle
13.
Endocytic recycling protein EHD1 regulates primary cilia morphogenesis and SHH signaling during neural tube development
Sohinee Bhattacharyya, Mark A Rainey, Priyanka Arya, Samikshan Dutta, Manju George, Matthew D. Storck, Rodney D. McComb, David Muirhead, Gordon L. Todd, Karen Gould, Kaustubh Datta, Janee Gelineau-van Waes, Vimla Band, Hamid Band
Sci Rep. 2016; 6: 20727. Published online 2016 Feb 17. doi: 10.1038/srep20727
Correction in:
Sci Rep. 2017; 7: 42320.
PMCID:
PMC4756679
AbstractArticlePDF–3.9M
14.
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
AbstractArticlePDF–929K
15.
The ubiquitin ligase Ubr4 controls stability of podocin/MEC-2 supercomplexes
Markus M. Rinschen, Puneet Bharill, Xiongwu Wu, Priyanka Kohli, Matthäus J. Reinert, Oliver Kretz, Isabel Saez, Bernhard Schermer, Martin Höhne, Malte P. Bartram, Sriram Aravamudhan, Bernard R. Brooks, David Vilchez, Tobias B. Huber, Roman-Ulrich Müller, Marcus Krüger, Thomas Benzing
Hum Mol Genet. 2016 Apr 1; 25(7): 1328–1344. Published online 2016 Jan 19. doi: 10.1093/hmg/ddw016
PMCID:
PMC4787903
AbstractArticlePDF–1.0M
16.
Phospho-proteomic analyses of B-Raf protein complexes reveal new regulatory principles
Anja E. Eisenhardt, Adrian Sprenger, Michael Röring, Ricarda Herr, Florian Weinberg, Martin Köhler, Sandra Braun, Joachim Orth, Britta Diedrich, Ulrike Lanner, Natalja Tscherwinski, Simon Schuster, Nicolas Dumaz, Enrico Schmidt, Ralf Baumeister, Andreas Schlosser, Jörn Dengjel, Tilman Brummer
Oncotarget. 2016 May 3; 7(18): 26628–26652. Published online 2016 Mar 28. doi: 10.18632/oncotarget.8427
PMCID:
PMC5042004
AbstractArticlePDF–7.5M
17.
Assembly, Verification, and Initial Annotation of the NIA Mouse 7.4K cDNA Clone Set
Vincent VanBuren, Yulan Piao, Dawood B. Dudekula, Yong Qian, Mark G. Carter, Patrick R. Martin, Carole A. Stagg, Uwem C. Bassey, Kazuhiro Aiba, Toshio Hamatani, George J. Kargul, Amber G. Luo, Janet Kelso, Winston Hide, Minoru S.H. Ko
Genome Res. 2002 Dec; 12(12): 1999–2003. doi: 10.1101/gr.633802
PMCID:
PMC187561
AbstractArticlePDF–431K
18.
LCP1 preferentially binds clasped αMβ2 integrin and attenuates leukocyte adhesion under flow
Hui-yuan Tseng, Anna V. Samarelli, Patricia Kammerer, Sarah Scholze, Tilman Ziegler, Roland Immler, Roy Zent, Markus Sperandio, Charles R. Sanders, Reinhard Fässler, Ralph T. Böttcher
J Cell Sci. 2018 Nov 15; 131(22): jcs218214. Published online 2018 Nov 21. doi: 10.1242/jcs.218214
PMCID:
PMC6262777
AbstractArticle
19.
Transcriptome Analysis of Mouse Stem Cells and Early Embryos
Alexei A Sharov, Yulan Piao, Ryo Matoba, Dawood B Dudekula, Yong Qian, Vincent VanBuren, Geppino Falco, Patrick R Martin, Carole A Stagg, Uwem C Bassey, Yuxia Wang, Mark G Carter, Toshio Hamatani, Kazuhiro Aiba, Hidenori Akutsu, Lioudmila Sharova, Tetsuya S Tanaka, Wendy L Kimber, Toshiyuki Yoshikawa, Saied A Jaradat, Serafino Pantano, Ramaiah Nagaraja, Kenneth R Boheler, Dennis Taub, Richard J Hodes, Dan L Longo, David Schlessinger, Jonathan Keller, Emily Klotz, Garnett Kelsoe, Akihiro Umezawa, Angelo L Vescovi, Janet Rossant, Tilo Kunath, Brigid L. M Hogan, Anna Curci, Michele D'Urso, Janet Kelso, Winston Hide, Minoru S. H Ko
PLoS Biol. 2003 Dec; 1(3): e74. Published online 2003 Dec 22. doi: 10.1371/journal.pbio.0000074
PMCID:
PMC300684
AbstractArticlePDF–572K
20.
BioID screening of biotinylation sites using the avidin-like protein Tamavidin 2-REV identifies global interactors of stimulator of interferon genes (STING)
Kou Motani, Hidetaka Kosako
J Biol Chem. 2020 Aug 7; 295(32): 11174–11183. Published online 2020 Jun 17. doi: 10.1074/jbc.RA120.014323
PMCID:
PMC7415991
AbstractArticlePDF–2.0M

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