Mázala DA - Search Results

1

NAD+ repletion improves muscle function in muscular dystrophy and counters global PARylation.

Ryu D, Zhang H, Ropelle ER, Sorrentino V, Mázala DA, Mouchiroud L, Marshall PL, Campbell MD, Ali AS, Knowels GM, Bellemin S, Iyer SR, Wang X, Gariani K, Sauve AA, Cantó C, Conley KE, Walter L, Lovering RM, Chin ER, Jasmin BJ, Marcinek DJ, Menzies KJ, Auwerx J. Ryu D, et al. Among authors: mazala da. Sci Transl Med. 2016 Oct 19;8(361):361ra139. doi: 10.1126/scitranslmed.aaf5504. Sci Transl Med. 2016. PMID: 27798264 Free PMC article.

2

Perturbations in intracellular Ca2+ handling in skeletal muscle in the G93A*SOD1 mouse model of amyotrophic lateral sclerosis.

Chin ER, Chen D, Bobyk KD, Mázala DA. Chin ER, et al. Among authors: mazala da. Am J Physiol Cell Physiol. 2014 Dec 1;307(11):C1031-8. doi: 10.1152/ajpcell.00237.2013. Epub 2014 Sep 24. Am J Physiol Cell Physiol. 2014. PMID: 25252949 Free PMC article.

3

The role of proteases in excitation-contraction coupling failure in muscular dystrophy.

Mázala DA, Grange RW, Chin ER. Mázala DA, et al. Am J Physiol Cell Physiol. 2015 Jan 1;308(1):C33-40. doi: 10.1152/ajpcell.00267.2013. Epub 2014 Oct 8. Am J Physiol Cell Physiol. 2015. PMID: 25298424 Free PMC article.

4

SERCA1 overexpression minimizes skeletal muscle damage in dystrophic mouse models.

Mázala DA, Pratt SJP, Chen D, Molkentin JD, Lovering RM, Chin ER. Mázala DA, et al. Am J Physiol Cell Physiol. 2015 May 1;308(9):C699-709. doi: 10.1152/ajpcell.00341.2014. Epub 2015 Feb 4. Am J Physiol Cell Physiol. 2015. PMID: 25652448 Free PMC article.

5

The SH3 and cysteine-rich domain 3 (Stac3) gene is important to growth, fiber composition, and calcium release from the sarcoplasmic reticulum in postnatal skeletal muscle.

Cong X, Doering J, Mazala DA, Chin ER, Grange RW, Jiang H. Cong X, et al. Among authors: mazala da. Skelet Muscle. 2016 Apr 11;6:17. doi: 10.1186/s13395-016-0088-4. eCollection 2016. Skelet Muscle. 2016. PMID: 27073615 Free PMC article.

6

Calcium dysregulation, functional calpainopathy, and endoplasmic reticulum stress in sporadic inclusion body myositis.

Amici DR, Pinal-Fernandez I, Mázala DA, Lloyd TE, Corse AM, Christopher-Stine L, Mammen AL, Chin ER. Amici DR, et al. Among authors: mazala da. Acta Neuropathol Commun. 2017 Mar 22;5(1):24. doi: 10.1186/s40478-017-0427-7. Acta Neuropathol Commun. 2017. PMID: 28330496 Free PMC article.

7

Defects in sarcolemma repair and skeletal muscle function after injury in a mouse model of Niemann-Pick type A/B disease.

Michailowsky V, Li H, Mittra B, Iyer SR, Mazála DAG, Corrotte M, Wang Y, Chin ER, Lovering RM, Andrews NW. Michailowsky V, et al. Skelet Muscle. 2019 Jan 5;9(1):1. doi: 10.1186/s13395-018-0187-5. Skelet Muscle. 2019. PMID: 30611303 Free PMC article.

8

STAT3 in Skeletal Muscle Function and Disorders.

Guadagnin E, Mázala D, Chen YW. Guadagnin E, et al. Int J Mol Sci. 2018 Aug 2;19(8):2265. doi: 10.3390/ijms19082265. Int J Mol Sci. 2018. PMID: 30072615 Free PMC article. Review.

9

TGF-β-driven muscle degeneration and failed regeneration underlie disease onset in a DMD mouse model.

Mázala DA, Novak JS, Hogarth MW, Nearing M, Adusumalli P, Tully CB, Habib NF, Gordish-Dressman H, Chen YW, Jaiswal JK, Partridge TA. Mázala DA, et al. JCI Insight. 2020 Mar 26;5(6):e135703. doi: 10.1172/jci.insight.135703. JCI Insight. 2020. PMID: 32213706 Free PMC article.

10

Dysregulation of Mitochondrial Ca²⁺ Uptake and Sarcolemma Repair Underlie Muscle Weakness and Wasting in Patients and Mice Lacking MICU1.

Debattisti V, Horn A, Singh R, Seifert EL, Hogarth MW, Mazala DA, Huang KT, Horvath R, Jaiswal JK, Hajnóczky G. Debattisti V, et al. Among authors: mazala da. Cell Rep. 2019 Oct 29;29(5):1274-1286.e6. doi: 10.1016/j.celrep.2019.09.063. Cell Rep. 2019. PMID: 31665639 Free PMC article.

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