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Items: 1 to 20 of 35

1.
Filamin C is Essential for mammalian myocardial integrity
Tongbin Wu, Yujun Xu, Lunfeng Zhang, Zhengyu Liang, Xiaohai Zhou, Sylvia M. Evans, Ju Chen
PLoS Genet. 2023 Jan; 19(1): e1010630. Published online 2023 Jan 27. doi: 10.1371/journal.pgen.1010630
PMCID:
PMC9907827
AbstractArticlePDF–3.3M
2.
Comparative genomic analyses of multiple backcross mouse populations suggest SGCG as a novel potential obesity-modifier gene
Tanja Kuhn, Katharina Kaiser, Sandra Lebek, Delsi Altenhofen, Birgit Knebel, Ralf Herwig, Axel Rasche, Angela Pelligra, Sarah Görigk, Jenny Minh-An Khuong, Heike Vogel, Annette Schürmann, Matthias Blüher, Alexandra Chadt, Hadi Al-Hasani
Hum Mol Genet. 2022 Dec 1; 31(23): 4019–4033. Published online 2022 Jul 7. doi: 10.1093/hmg/ddac150
PMCID:
PMC9703946
AbstractArticlePDF–1.6M
3.
Novel γ-sarcoglycan interactors in murine muscle membranes
Tara C. Smith, Georgios Vasilakos, Scott A. Shaffer, Jason M. Puglise, Chih-Hsuan Chou, Elisabeth R. Barton, Elizabeth J. Luna
Skelet Muscle. 2022; 12: 2. Published online 2022 Jan 22. doi: 10.1186/s13395-021-00285-2
PMCID:
PMC8783446
AbstractArticlePDF–4.5M
4.
Dusp6 is a genetic modifier of growth through enhanced ERK activity
Andy H Vo, Kayleigh A Swaggart, Anna Woo, Quan Q Gao, Alexis R Demonbreun, Katherine S Fallon, Mattia Quattrocelli, Michele Hadhazy, Patrick G T Page, Zugen Chen, Ascia Eskin, Kevin Squire, Stanley F Nelson, Elizabeth M McNally
Hum Mol Genet. 2019 Jan 15; 28(2): 279–289. Published online 2018 Oct 5. doi: 10.1093/hmg/ddy349
PMCID:
PMC6322066
AbstractArticlePDF–6.0M
5.
Intermittent Glucocorticoid Dosing Improves Muscle Repair and Function in Mice with Limb-Girdle Muscular Dystrophy
Mattia Quattrocelli, Isabella M. Salamone, Patrick G. Page, James L. Warner, Alexis R. Demonbreun, Elizabeth M. McNally
Am J Pathol. 2017 Nov; 187(11): 2520–2535. doi: 10.1016/j.ajpath.2017.07.017
Correction in:
Am J Pathol. 2021 Nov; 191(11): 2039.
PMCID:
PMC5809598
AbstractArticle
6.
Fancd2 in vivo interaction network reveals a non-canonical role in mitochondrial function
Tingting Zhang, Wei Du, Andrew F. Wilson, Satoshi H. Namekawa, Paul R. Andreassen, Amom Ruhikanta Meetei, Qishen Pang
Sci Rep. 2017; 7: 45626. Published online 2017 Apr 5. doi: 10.1038/srep45626
PMCID:
PMC5381226
AbstractArticlePDF–1.4M
7.
HSPB7 interacts with dimerized FLNC and its absence results in progressive myopathy in skeletal muscles
Liang-Yi Juo, Wern-Chir Liao, Yen-Ling Shih, Bih-Ying Yang, An-Bang Liu, Yu-Ting Yan
J Cell Sci. 2016 Apr 15; 129(8): 1661–1670. doi: 10.1242/jcs.179887
PMCID:
PMC4852768
AbstractArticle
8.
Reengineering a transmembrane protein to treat muscular dystrophy using exon skipping
Quan Q. Gao, Eugene Wyatt, Jeff A. Goldstein, Peter LoPresti, Lisa M. Castillo, Alec Gazda, Natalie Petrossian, Judy U. Earley, Michele Hadhazy, David Y. Barefield, Alexis R. Demonbreun, Carsten Bönnemann, Matthew Wolf, Elizabeth M. McNally
J Clin Invest. 2015 Nov 2; 125(11): 4186–4195. Published online 2015 Oct 12. doi: 10.1172/JCI82768
PMCID:
PMC4639981
AbstractArticlePDF–4.9M
9.
Serum proteomic profiling reveals fragments of MYOM3 as potential biomarkers for monitoring the outcome of therapeutic interventions in muscular dystrophies
Jérémy Rouillon, Jérôme Poupiot, Aleksandar Zocevic, Fatima Amor, Thibaut Léger, Camille Garcia, Jean-Michel Camadro, Brenda Wong, Robin Pinilla, Jérémie Cosette, Anna M.L. Coenen-Stass, Graham Mcclorey, Thomas C. Roberts, Matthew J.A. Wood, Laurent Servais, Bjarne Udd, Thomas Voit, Isabelle Richard, Fedor Svinartchouk
Hum Mol Genet. 2015 Sep 1; 24(17): 4916–4932. Published online 2015 Jun 9. doi: 10.1093/hmg/ddv214
PMCID:
PMC4527491
AbstractArticlePDF–834K
10.
Biochemical and Functional Comparisons of mdx and Sgcg−/− Muscular Dystrophy Mouse Models
Nathan W. Roberts, Jenan Holley-Cuthrell, Magdalis Gonzalez-Vega, Aaron J. Mull, Ahlke Heydemann
Biomed Res Int. 2015; 2015: 131436. Published online 2015 May 3. doi: 10.1155/2015/131436
PMCID:
PMC4433636
AbstractArticlePDF–2.7M
11.
Gamma-sarcoglycan is required for the response of archvillin to mechanical stimulation in skeletal muscle
Janelle M. Spinazzola, Tara C. Smith, Min Liu, Elizabeth J. Luna, Elisabeth R. Barton
Hum Mol Genet. 2015 May 1; 24(9): 2470–2481. Published online 2015 Jan 20. doi: 10.1093/hmg/ddv008
PMCID:
PMC4383861
AbstractArticlePDF–785K
12.
Excess SMAD signaling contributes to heart and muscle dysfunction in muscular dystrophy
Jeffery A. Goldstein, Sasha Bogdanovich, Anastasia Beiriger, Lisa M. Wren, Ann E. Rossi, Quan Q. Gao, Brandon B. Gardner, Judy U. Earley, Jeffery D. Molkentin, Elizabeth M. McNally
Hum Mol Genet. 2014 Dec 20; 23(25): 6722–6731. Published online 2014 Jul 28. doi: 10.1093/hmg/ddu390
PMCID:
PMC4303797
AbstractArticlePDF–699K
13.
Annexin A6 modifies muscular dystrophy by mediating sarcolemmal repair
Kayleigh A. Swaggart, Alexis R. Demonbreun, Andy H. Vo, Kaitlin E. Swanson, Ellis Y. Kim, John P. Fahrenbach, Jenan Holley-Cuthrell, Ascia Eskin, Zugen Chen, Kevin Squire, Ahlke Heydemann, Abraham A. Palmer, Stanley F. Nelson, Elizabeth M. McNally
Proc Natl Acad Sci U S A. 2014 Apr 22; 111(16): 6004–6009. Published online 2014 Apr 9. doi: 10.1073/pnas.1324242111
PMCID:
PMC4000833
AbstractArticlePDF–1.4M
14.
Distinctive Serum miRNA Profile in Mouse Models of Striated Muscular Pathologies
Nicolas Vignier, Fatima Amor, Paul Fogel, Angélique Duvallet, Jérôme Poupiot, Sabine Charrier, Michel Arock, Marie Montus, Isabelle Nelson, Isabelle Richard, Lucie Carrier, Laurent Servais, Thomas Voit, Gisèle Bonne, David Israeli
PLoS One. 2013; 8(2): e55281. Published online 2013 Feb 13. doi: 10.1371/journal.pone.0055281
PMCID:
PMC3572119
AbstractArticlePDF–2.2M
15.
Proteomic Analysis Reveals New Cardiac-Specific Dystrophin-Associated Proteins
Eric K. Johnson, Liwen Zhang, Marvin E. Adams, Alistair Phillips, Michael A. Freitas, Stanley C. Froehner, Kari B. Green-Church, Federica Montanaro
PLoS One. 2012; 7(8): e43515. Published online 2012 Aug 24. doi: 10.1371/journal.pone.0043515
PMCID:
PMC3427372
AbstractArticlePDF–1.1M
16.
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
17.
Distinct pathophysiological mechanisms of cardiomyopathy in hearts lacking dystrophin or the sarcoglycan complex
DeWayne Townsend, Soichiro Yasuda, Elizabeth McNally, Joseph M. Metzger
FASEB J. 2011 Sep; 25(9): 3106–3114. doi: 10.1096/fj.10-178913
PMCID:
PMC3157690
AbstractArticle
18.
Identification of Anchor Genes during Kidney Development Defines Ontological Relationships, Molecular Subcompartments and Regulatory Pathways
Rathi D. Thiagarajan, Kylie M. Georgas, Bree A. Rumballe, Emmanuelle Lesieur, Han Sheng Chiu, Darrin Taylor, Dave T. P. Tang, Sean M. Grimmond, Melissa H. Little
PLoS One. 2011; 6(2): e17286. Published online 2011 Feb 28. doi: 10.1371/journal.pone.0017286
PMCID:
PMC3046260
AbstractArticlePDF–982K
19.
DOT1L regulates dystrophin expression and is critical for cardiac function
Anh T. Nguyen, Bin Xiao, Ronald L. Neppl, Eric M. Kallin, Juan Li, Taiping Chen, Da-Zhi Wang, Xiao Xiao, Yi Zhang
Genes Dev. 2011 Feb 1; 25(3): 263–274. doi: 10.1101/gad.2018511
PMCID:
PMC3034901
AbstractArticlePDF–863K
20.
SMAD signaling drives heart and muscle dysfunction in a Drosophila model of muscular dystrophy
Jeffery A. Goldstein, Sean M. Kelly, Peter P. LoPresti, Ahlke Heydemann, Judy U. Earley, Edwin L. Ferguson, Matthew J. Wolf, Elizabeth M. McNally
Hum Mol Genet. 2011 Mar 1; 20(5): 894–904. Published online 2010 Dec 6. doi: 10.1093/hmg/ddq528
PMCID:
PMC3033181
AbstractArticlePDF–413K

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