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Items: 1 to 20 of 49

1.
Age-related gene expression signatures from limb skeletal muscles and the diaphragm in mice and rats reveal common and species-specific changes
Tea Shavlakadze, Kun Xiong, Shawn Mishra, Corissa McEwen, Abhilash Gadi, Matthew Wakai, Hunter Salmon, Michael J. Stec, Nicole Negron, Min Ni, Yi Wei, Gurinder S. Atwal, Yu Bai, David J. Glass
Skelet Muscle. 2023; 13: 11. Published online 2023 Jul 12. doi: 10.1186/s13395-023-00321-3
PMCID:
PMC10337157
ArticlePDF–3.4M
2.
Loss of FoxOs in muscle increases strength and mitochondrial function during aging
Christie M. Penniman, Gourav Bhardwaj, Colette J. Nowers, Chandler U. Brown, Taylor L. Junck, Cierra K. Boyer, Jayashree Jena, Jordan D. Fuqua, Vitor A. Lira, Brian T. O'Neill
J Cachexia Sarcopenia Muscle. 2023 Feb; 14(1): 243–259. Published online 2022 Nov 28. doi: 10.1002/jcsm.13124
PMCID:
PMC9891940
ArticlePDF–4.8M
3.
Hypothalamic–pituitary–adrenal axis activation and glucocorticoid‐responsive gene expression in skeletal muscle and liver of Apc mice
Agnès Martin, Josiane Castells, Valentine Allibert, Andréa Emerit, Cindy Zolotoff, Victoire Cardot‐Ruffino, Yann S. Gallot, Barbara Vernus, Véronique Chauvet, Laurent Bartholin, Laurent Schaeffer, Anne‐Cécile Durieux, Christophe Hourdé, François B. Favier, Laetitia Mazelin, Damien Freyssenet
J Cachexia Sarcopenia Muscle. 2022 Jun; 13(3): 1686–1703. Published online 2022 Mar 11. doi: 10.1002/jcsm.12939
PMCID:
PMC9178358
ArticlePDF–6.1M
4.
The beneficial effect of chronic muscular exercise on muscle fragility is increased by Prox1 gene transfer in dystrophic mdx muscle
Alexandra Monceau, Clément Delacroix, Mégane Lemaitre, Gaelle Revet, Denis Furling, Onnik Agbulut, Arnaud Klein, Arnaud Ferry
PLoS One. 2022; 17(4): e0254274. Published online 2022 Apr 18. doi: 10.1371/journal.pone.0254274
PMCID:
PMC9015141
ArticlePDF–2.0M
5.
Sepsis induces interleukin 6, gp130/JAK2/STAT3, and muscle wasting
Lukas Zanders, Melanie Kny, Alexander Hahn, Sibylle Schmidt, Sebastian Wundersitz, Mihail Todiras, Ines Lahmann, Arnab Bandyopadhyay, Tobias Wollersheim, Lars Kaderali, Friedrich C. Luft, Carmen Birchmeier, Steffen Weber‐Carstens, Jens Fielitz
J Cachexia Sarcopenia Muscle. 2022 Feb; 13(1): 713–727. Published online 2021 Nov 24. doi: 10.1002/jcsm.12867
PMCID:
PMC8818599
ArticlePDF–7.6M
6.
A form of muscular dystrophy associated with pathogenic variants in JAG2
Sandra Coppens, Alison M. Barnard, Sanna Puusepp, Sander Pajusalu, Katrin Õunap, Dorianmarie Vargas-Franco, Christine C. Bruels, Sandra Donkervoort, Lynn Pais, Katherine R. Chao, Julia K. Goodrich, Eleina M. England, Ben Weisburd, Vijay S. Ganesh, Sanna Gudmundsson, Anne O’Donnell-Luria, Mait Nigul, Pilvi Ilves, Payam Mohassel, Teepu Siddique, Margherita Milone, Stefan Nicolau, Reza Maroofian, Henry Houlden, Michael G. Hanna, Ros Quinlivan, Mehran Beiraghi Toosi, Ehsan Ghayoor Karimiani, Sabine Costagliola, Nicolas Deconinck, Hazim Kadhim, Erica Macke, Brendan C. Lanpher, Eric W. Klee, Anna Łusakowska, Anna Kostera-Pruszczyk, Andreas Hahn, Bertold Schrank, Ichizo Nishino, Masashi Ogasawara, Rasha El Sherif, Tanya Stojkovic, Isabelle Nelson, Gisèle Bonne, Enzo Cohen, Anne Boland-Augé, Jean-François Deleuze, Yao Meng, Ana Töpf, Catheline Vilain, Christina A. Pacak, Marie L. Rivera-Zengotita, Carsten G. Bönnemann, Volker Straub, Penny A. Handford, Isabelle Draper, Glenn A. Walter, Peter B. Kang
Am J Hum Genet. 2021 May 6; 108(5): 840–856. Published online 2021 Apr 15. doi: 10.1016/j.ajhg.2021.03.020
Correction in:
Am J Hum Genet. 2021 Jun 3; 108(6): 1164.
PMCID:
PMC8206160
ArticlePDF–2.8M
7.
Preclinical Systemic Delivery of Adeno-Associated α-Sarcoglycan Gene Transfer for Limb-Girdle Muscular Dystrophy
Danielle A. Griffin, Eric R. Pozsgai, Kristin N. Heller, Rachael A. Potter, Ellyn L. Peterson, Louise R. Rodino-Klapac
Hum Gene Ther. April 2021; 32(7-8): 390–404. Published online 2021 Apr 19. doi: 10.1089/hum.2019.199
PMCID:
PMC8066346
ArticlePDF–1.9M
8.
FoxP1 is a transcriptional repressor associated with cancer cachexia that induces skeletal muscle wasting and weakness
Daria Neyroud, Rachel L. Nosacka, Chandler S. Callaway, Jose G. Trevino, Hui Hu, Sarah M. Judge, Andrew R. Judge
J Cachexia Sarcopenia Muscle. 2021 Apr; 12(2): 421–442. Published online 2021 Feb 1. doi: 10.1002/jcsm.12666
PMCID:
PMC8061399
ArticlePDF–45M
9.
Lifelong Ulk1-Mediated Autophagy Deficiency in Muscle Induces Mitochondrial Dysfunction and Contractile Weakness
Anna S. Nichenko, Jacob R. Sorensen, W. Michael Southern, Anita E. Qualls, Albino G. Schifino, Jennifer McFaline-Figueroa, Jamie E. Blum, Kayvan F. Tehrani, Hang Yin, Luke J. Mortensen, Anna E. Thalacker-Mercer, Sarah M. Greising, Jarrod A. Call
Int J Mol Sci. 2021 Feb; 22(4): 1937. Published online 2021 Feb 16. doi: 10.3390/ijms22041937
PMCID:
PMC7919824
ArticlePDF–26M
10.
Clinical features and genotypes of Laing distal myopathy in a group of Chinese patients, with in-frame deletions of MYH7 as common mutations
Meng Yu, Ying Zhu, Yuanyuan Lu, He Lv, Wei Zhang, Yun Yuan, Zhaoxia Wang
Orphanet J Rare Dis. 2020; 15: 344. Published online 2020 Dec 9. doi: 10.1186/s13023-020-01626-y
PMCID:
PMC7727133
ArticlePDF–1.4M
11.
A case report: identification of a novel exon 1 deletion mutation in the GNE gene in a Chinese patient with GNE myopathy
Jing Miao, Xiao-jing Wei, Xu Wang, Xiang Yin, Xue-fan Yu
Medicine (Baltimore) 2020 Oct 9; 99(41): e22663. Published online 2020 Oct 9. doi: 10.1097/MD.0000000000022663
PMCID:
PMC7544422
ArticlePDF–511K
12.
Skeletal muscle regeneration in facioscapulohumeral muscular dystrophy is correlated with pathological severity
Christopher R S Banerji, Don Henderson, Rabi N Tawil, Peter S Zammit
Hum Mol Genet. 2020 Aug 15; 29(16): 2746–2760. Published online 2020 Aug 3. doi: 10.1093/hmg/ddaa164
PMCID:
PMC7530526
ArticlePDF–1.2M
13.
Magnetic Resonance Imaging characteristics in case of TOR1AIP1 muscular dystrophy
Aashim Bhatia, Bret C. Mobley, Joy Cogan, Mary E. Koziura, Elly Brokamp, John Phillips, John Newman, Undiagnosed Diseases Network (UDN), Steven A. Moore, Rizwan Hamid, Undiagnosed Diseases Network
Clin Imaging. Author manuscript; available in PMC 2019 Dec 5.
Published in final edited form as: Clin Imaging. 2019 Nov-Dec; 58: 108–113. Published online 2019 Jun 21. doi: 10.1016/j.clinimag.2019.06.010
PMCID:
PMC6893088
ArticlePDF–946K
14.
Knee osteoarthritis induces atrophy and neuromuscular junction remodeling in the quadriceps and tibialis anterior muscles of rats
Jonathan Emanuel Cunha, Germanna Medeiros Barbosa, Paula Aiello Tomé de Souza Castro, Beatriz Leite Ferreira Luiz, Andreza Cristine Arcari Silva, Thiago Luiz Russo, Fernando Augusto Vasilceac, Thiago Mattar Cunha, Fernando Queiróz Cunha, Tania Fátima Salvini
Sci Rep. 2019; 9: 6366. Published online 2019 Apr 24. doi: 10.1038/s41598-019-42546-7
PMCID:
PMC6482306
ArticlePDF–1.6M
15.
RNA-sequencing reveals altered skeletal muscle contraction, E3 ligases, autophagy, apoptosis, and chaperone expression in patients with critical illness myopathy
Monica Llano-Diez, Wen Fury, Haruka Okamoto, Yu Bai, Jesper Gromada, Lars Larsson
Skelet Muscle. 2019; 9: 9. Published online 2019 Apr 16. doi: 10.1186/s13395-019-0194-1
PMCID:
PMC6466682
ArticlePDF–1.2M
16.
Muscle‐specific Perilipin2 down‐regulation affects lipid metabolism and induces myofiber hypertrophy
Maria Conte, Andrea Armani, Giuseppe Conte, Andrea Serra, Claudio Franceschi, Marcello Mele, Marco Sandri, Stefano Salvioli
J Cachexia Sarcopenia Muscle. 2019 Feb; 10(1): 95–110. Published online 2018 Oct 4. doi: 10.1002/jcsm.12355
PMCID:
PMC6438344
ArticlePDF–724K
17.
GNE Myopathy: Etiology, Diagnosis, and Therapeutic Challenges
Nuria Carrillo, May C. Malicdan, Marjan Huizing
Neurotherapeutics. 2018 Oct; 15(4): 900–914. Published online 2018 Oct 18. doi: 10.1007/s13311-018-0671-y
PMCID:
PMC6277305
ArticlePDF–7.3M
18.
miR‐424‐5p reduces ribosomal RNA and protein synthesis in muscle wasting
Martin Connolly, Richard Paul, Roser Farre‐Garros, Samantha A. Natanek, Susannah Bloch, Jen Lee, Jose P. Lorenzo, Harnish Patel, Cyrus Cooper, Avan A. Sayer, Stephen J. Wort, Mark Griffiths, Michael I. Polkey, Paul R. Kemp
J Cachexia Sarcopenia Muscle. 2018 Apr; 9(2): 400–416. Published online 2017 Dec 7. doi: 10.1002/jcsm.12266
PMCID:
PMC5879973
ArticlePDF–885K
19.
A Novel AGRN Mutation Leads to Congenital Myasthenic Syndrome Only Affecting Limb-girdle Muscle
Ying Zhang, Yi Dai, Jing-Na Han, Zhao-Hui Chen, Li Ling, Chuan-Qiang Pu, Li-Ying Cui, Xu-Sheng Huang
Chin Med J (Engl) 2017 Oct 5; 130(19): 2279–2282. doi: 10.4103/0366-6999.215332
PMCID:
PMC5634075
ArticlePDF–1.1M
20.
Natural disease history of mouse models for limb girdle muscular dystrophy types 2D and 2F
S. Pasteuning-Vuhman, K. Putker, C. L. Tanganyika-de Winter, J. W. Boertje-van der Meulen, L. van Vliet, M. Overzier, J. J. Plomp, A. Aartsma-Rus, M. van Putten
PLoS One. 2017; 12(8): e0182704. Published online 2017 Aug 10. doi: 10.1371/journal.pone.0182704
PMCID:
PMC5552258
ArticlePDF–8.4M

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