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Items: 1 to 20 of 25

1.
Nuclear numbers in syncytial muscle fibers promote size but limit the development of larger myonuclear domains
Alyssa A. W. Cramer, Vikram Prasad, Einar Eftestøl, Taejeong Song, Kenth-Arne Hansson, Hannah F. Dugdale, Sakthivel Sadayappan, Julien Ochala, Kristian Gundersen, Douglas P. Millay
Nat Commun. 2020; 11: 6287. Published online 2020 Dec 8. doi: 10.1038/s41467-020-20058-7
PMCID:
PMC7722938
AbstractArticlePDF–3.6M
2.
Myonuclear accretion is a determinant of exercise-induced remodeling in skeletal muscle
Qingnian Goh, Taejeong Song, Michael J Petrany, Alyssa AW Cramer, Chengyi Sun, Sakthivel Sadayappan, Se-Jin Lee, Douglas P Millay
eLife. 2019; 8: e44876. Published online 2019 Apr 23. doi: 10.7554/eLife.44876
PMCID:
PMC6497442
AbstractArticlePDF–8.5M
3.
Insights into the localization and function of myomaker during myoblast fusion
Dilani G. Gamage, Eugenia Leikina, Malgorzata E. Quinn, Anthony Ratinov, Leonid V. Chernomordik, Douglas P. Millay
J Biol Chem. 2017 Oct 20; 292(42): 17272–17289. Published online 2017 Aug 31. doi: 10.1074/jbc.M117.811372
PMCID:
PMC5655506
AbstractArticlePDF–8.3M
4.
Structure–function analysis of myomaker domains required for myoblast fusion
Douglas P. Millay, Dilani G. Gamage, Malgorzata E. Quinn, Yi-Li Min, Yasuyuki Mitani, Rhonda Bassel-Duby, Eric N. Olson
Proc Natl Acad Sci U S A. 2016 Feb 23; 113(8): 2116–2121. Published online 2016 Feb 8. doi: 10.1073/pnas.1600101113
PMCID:
PMC4776501
AbstractArticlePDF–1.7M
5.
Myocyte-derived Myomaker expression is required for regenerative fusion but exacerbates membrane instability in dystrophic myofibers
Michael J. Petrany, Taejeong Song, Sakthivel Sadayappan, Douglas P. Millay
JCI Insight. 2020 May 7; 5(9): e136095. Published online 2020 May 7. doi: 10.1172/jci.insight.136095
PMCID:
PMC7253022
AbstractArticlePDF–20M
6.
Enveloped viruses pseudotyped with mammalian myogenic cell fusogens target skeletal muscle for gene delivery
Sajedah M. Hindi, Michael J. Petrany, Elena Greenfeld, Leah C. Focke, Alyssa A.W. Cramer, Michael A. Whitt, Ramzi J. Khairallah, Christopher W. Ward, Jeffrey S. Chamberlain, Vikram Prasad, Benjamin Podbilewicz, Douglas P. Millay
Cell. Author manuscript; available in PMC 2024 Jun 17.
Published in final edited form as: Cell. 2023 May 11; 186(10): 2062–2077.e17. Published online 2023 Apr 18. doi: 10.1016/j.cell.2023.03.033
PMCID:
PMC11181154
AbstractArticlePDF–2.2M
7.
The Trithorax protein Ash1L promotes myoblast fusion by activating Cdon expression
Ilaria Castiglioni, Roberta Caccia, Jose Manuel Garcia-Manteiga, Giulia Ferri, Giuseppina Caretti, Ivan Molineris, Kenichi Nishioka, Davide Gabellini
Nat Commun. 2018; 9: 5026. Published online 2018 Nov 28. doi: 10.1038/s41467-018-07313-8
PMCID:
PMC6262021
AbstractArticlePDF–2.7M
8.
Myomaker and Myomerger work independently to control distinct steps of membrane remodeling during myoblast fusion
Evgenia Leikina, Dilani G. Gamage, Vikram Prasad, Joanna Goykhberg, Michael Crowe, Jiajie Diao, Michael M. Kozlov, Leonid V. Chernomordik, Douglas P. Millay
Dev Cell. Author manuscript; available in PMC 2019 Sep 24.
Published in final edited form as: Dev Cell. 2018 Sep 24; 46(6): 767–780.e7. Published online 2018 Sep 6. doi: 10.1016/j.devcel.2018.08.006
PMCID:
PMC6203449
AbstractArticlePDF–1.6M
9.
A defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome
Silvio Alessandro Di Gioia, Samantha Connors, Norisada Matsunami, Jessica Cannavino, Matthew F. Rose, Nicole M. Gilette, Pietro Artoni, Nara Lygia de Macena Sobreira, Wai-Man Chan, Bryn D. Webb, Caroline D. Robson, Long Cheng, Carol Van Ryzin, Andres Ramirez-Martinez, Payam Mohassel, Mark Leppert, Mary Beth Scholand, Christopher Grunseich, Carlos R. Ferreira, Tyler Hartman, Ian M. Hayes, Tim Morgan, David M. Markie, Michela Fagiolini, Amy Swift, Peter S. Chines, Carlos E. Speck-Martins, Francis S. Collins, Ethylin Wang Jabs, Carsten G. Bönnemann, Eric N. Olson, Moebius Syndrome Research Consortium, John C. Carey, Stephen P. Robertson, Irini Manoli, Elizabeth C. Engle
Nat Commun. 2017; 8: 16077. Published online 2017 Jul 6. doi: 10.1038/ncomms16077
PMCID:
PMC5504296
AbstractArticlePDF–3.1M
10.
Requirement of myomaker-mediated stem cell fusion for skeletal muscle hypertrophy
Qingnian Goh, Douglas P Millay
eLife. 2017; 6: e20007. Published online 2017 Feb 10. doi: 10.7554/eLife.20007
PMCID:
PMC5338923
AbstractArticlePDF–9.2M
11.
In vivo myomaker-mediated heterologous fusion and nuclear reprogramming
Yasuyuki Mitani, Ronald J. Vagnozzi, Douglas P. Millay
FASEB J. 2017 Jan; 31(1): 400–411. Published online 2016 Oct 17. doi: 10.1096/fj.201600945R
PMCID:
PMC5161518
AbstractArticle
12.
Control of muscle formation by the fusogenic micropeptide myomixer
Pengpeng Bi, Andres Ramirez-Martinez, Hui Li, Jessica Cannavino, John R. McAnally, John M. Shelton, Efrain Sánchez-Ortiz, Rhonda Bassel-Duby, Eric N. Olson
Science. Author manuscript; available in PMC 2017 Jul 9.
Published in final edited form as: Science. 2017 Apr 21; 356(6335): 323–327. Published online 2017 Apr 6. doi: 10.1126/science.aam9361
PMCID:
PMC5502127
AbstractArticlePDF–1.6M
13.
Myomaker is essential for muscle regeneration
Douglas P. Millay, Lillian B. Sutherland, Rhonda Bassel-Duby, Eric N. Olson
Genes Dev. 2014 Aug 1; 28(15): 1641–1646. doi: 10.1101/gad.247205.114
PMCID:
PMC4117939
AbstractArticlePDF–1.9M
14.
Myomaker: A membrane activator of myoblast fusion and muscle formation
Douglas P. Millay, Jason R. O’Rourke, Lillian B. Sutherland, Svetlana Bezprozvannaya, John M. Shelton, Rhonda Bassel-Duby, Eric N. Olson
Nature. Author manuscript; available in PMC 2014 Jan 18.
Published in final edited form as: Nature. 2013 Jul 18; 499(7458): 301–305. doi: 10.1038/nature12343
PMCID:
PMC3739301
AbstractArticlePDF–2.7M
15.
Zfp422 promotes skeletal muscle differentiation by regulating EphA7 to induce appropriate myoblast apoptosis
Yaping Nie, Shufang Cai, Renqiang Yuan, Suying Ding, Xumeng Zhang, Luxi Chen, Yaosheng Chen, Delin Mo
Cell Death Differ. 2020 May; 27(5): 1644–1659. Published online 2019 Nov 4. doi: 10.1038/s41418-019-0448-9
PMCID:
PMC7206035
AbstractArticlePDF–6.1M
16.
Dysregulation of nuclear receptor COUP-TFII impairs skeletal muscle development
Hui-Ju Lee, Chung-Yang Kao, Shih-Chieh Lin, Mafei Xu, Xin Xie, Sophia Y. Tsai, Ming-Jer Tsai
Sci Rep. 2017; 7: 3136. Published online 2017 Jun 9. doi: 10.1038/s41598-017-03475-5
PMCID:
PMC5466650
AbstractArticlePDF–4.7M
17.
Analysis of the dynamics of limb transcriptomes during mouse development
Istvan Gyurján, Bernhard Sonderegger, Felix Naef, Denis Duboule
BMC Dev Biol. 2011; 11: 47. Published online 2011 Jul 29. doi: 10.1186/1471-213X-11-47
PMCID:
PMC3160909
AbstractArticlePDF–791K
18.
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
19.
Opposing gene regulatory programs governing myofiber development and maturation revealed at single nucleus resolution
Matthieu Dos Santos, Akansha M. Shah, Yichi Zhang, Svetlana Bezprozvannaya, Kenian Chen, Lin Xu, Weichun Lin, John R. McAnally, Rhonda Bassel-Duby, Ning Liu, Eric N. Olson
Nat Commun. 2023; 14: 4333. Published online 2023 Jul 19. doi: 10.1038/s41467-023-40073-8
PMCID:
PMC10356771
AbstractArticlePDF–4.9M
20.
Temporal regulation of the Mediator complex during muscle proliferation, differentiation, regeneration, aging, and disease
Dominic W. Kolonay, Kristina M. Sattler, Corinne Strawser, Jill Rafael-Fortney, Maria M. Mihaylova, Katherine E. Miller, Christoph Lepper, Kedryn K. Baskin
Front Cell Dev Biol. 2024; 12: 1331563. Published online 2024 Apr 16. doi: 10.3389/fcell.2024.1331563
PMCID:
PMC11058648
AbstractArticlePDF–3.8M

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