George G. Rodney

Baylor College of Medicine — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

32h-index3.4kcitations101works1.62yr avg
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Research Topics

Muscle Physiology and Disorders(33), Ion channel regulation and function(29), Genetic Neurodegenerative Diseases(16), Redox biology and oxidative stress(14), Autophagy in Disease and Therapy(12)

Publications101 total

Phosphorylation of RYR1 at Ser <sup>2902</sup> decreases Ca <sup>2+</sup> leak in skeletal muscle and susceptibility to malignant hyperthermia and heat stroke
Science Signaling·2025
Abstract Wed067: The microtubule network regulates NOX2-mediated oxidative stress and Cx43 remodelling in Duchenne Muscular Dystrophy
Circulation Research·2025
A novel mechanism of the cachexia-promoting action of chemotherapy drugs fluorouracil and cisplatin
2025Open Access
Impaired hydrogen sulfide biosynthesis underlies eccentric contraction–induced force loss in dystrophin-deficient skeletal muscle
Journal of Clinical Investigation·2025· 1 citedOpen Access
Mechanisms underlying dilated cardiomyopathy associated with FKBP12 deficiency
The Journal of General Physiology·2024· 3 citedOpen Access
Histone deacetylase 6 inhibition promotes microtubule acetylation and facilitates autophagosome–lysosome fusion in dystrophin‐deficient <i>mdx</i> mice
Acta Physiologica·2024· 7 citedOpen Access
Alternatively spliced MAP4 isoforms have key roles in maintaining microtubule organization and skeletal muscle function
iScience·2024· 2 citedOpen Access
Abstract Or101: Phospho-Mimic Mutation in Beta Tubulin Suppresses Arrhythmias and Improves Cardiac Connexin 43 Localization in Duchenne Muscular Dystrophy Mice
Circulation Research·2024
Abstract 16468: A Microtubule-Connexin 43 Regulatory Link Suppresses Cardiac Fibrosis and Arrhythmias in Duchenne Muscular Dystrophy Mice
Circulation·2023
Speg interactions that regulate the stability of excitation-contraction coupling protein complexes in triads and dyads
Communications Biology·2023· 10 citedOpen Access
The role of<i>Limch1</i>alternative splicing in skeletal muscle function
Life Science Alliance·2023· 6 citedOpen Access
Author Reply to Peer Reviews of The role of Limch1 alternative splicing in skeletal muscle function
2022
A deep redox proteome profiling workflow and its application to skeletal muscle of a Duchenne Muscular Dystrophy model
Free Radical Biology and Medicine·2022· 20 citedOpen Access
Correction: NADPH oxidase mediates microtubule alterations and diaphragm dysfunction in dystrophic mice
eLife·2022Open Access
UBR2 targets myosin heavy chain IIb and IIx for degradation: Molecular mechanism essential for cancer-induced muscle wasting
Proceedings of the National Academy of Sciences·2022· 29 citedOpen Access
Reduction of senescent fibro‐adipogenic progenitors in progeria‐aged muscle by senolytics rescues the function of muscle stem cells
Journal of Cachexia Sarcopenia and Muscle·2022· 33 citedOpen Access
A microtubule-connexin-43 regulatory link suppresses arrhythmias and cardiac fibrosis in Duchenne muscular dystrophy mice
American Journal of Physiology-Heart and Circulatory Physiology·2022· 5 citedOpen Access
The role of <i>Limch1</i> alternative splicing in skeletal muscle function
2022Open Access
A Deep Redox Proteome Profiling Workflow and Its Application to Skeletal Muscle of a Duchene Muscular Dystrophy Model
2022Open Access
Histone deacetylase 6 inhibition promotes microtubule acetylation and facilitates autophagosome-lysosome fusion in dystrophin-deficient <i>mdx</i> mice
2022· 2 citedOpen Access
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Frequent Co-authors

Rituraj Pal(12), Susan L. Hamilton(11), Marco Sardiello(7), Michela Palmieri(6), Tanner O. Monroe(6), Xander H.T. Wehrens(6), James A. Loehr(6), Reem Abo‐Zahrah(6), Joel R. Neilson(5), Barbara Williams(5), Arindam Chaudhury(4), Chang Seok Lee(4), Qiongling Wang(4), Martin F. Schneider(4), Parisa Lotfi(3), Gary Stinnett(3), Lakshya Bajaj(3), Vitaliy V. Bondar(3), Robia G. Pautler(3), Jia-Zheng Zhang(3)