Accorsi A - Search Results

1

p38α Regulates Expression of DUX4 in a Model of Facioscapulohumeral Muscular Dystrophy.

Rojas LA, Valentine E, Accorsi A, Maglio J, Shen N, Robertson A, Kazmirski S, Rahl P, Tawil R, Cadavid D, Thompson LA, Ronco L, Chang AN, Cacace AM, Wallace O. Rojas LA, et al. Among authors: accorsi a. J Pharmacol Exp Ther. 2020 Sep;374(3):489-498. doi: 10.1124/jpet.119.264689. Epub 2020 Jun 23. J Pharmacol Exp Ther. 2020. PMID: 32576599

2

Safety and efficacy of losmapimod in facioscapulohumeral muscular dystrophy (ReDUX4): a randomised, double-blind, placebo-controlled phase 2b trial.

Tawil R, Wagner KR, Hamel JI, Leung DG, Statland JM, Wang LH, Genge A, Sacconi S, Lochmüller H, Reyes-Leiva D, Diaz-Manera J, Alonso-Perez J, Muelas N, Vilchez JJ, Pestronk A, Gibson S, Goyal NA, Hayward LJ, Johnson N, LoRusso S, Freimer M, Shieh PB, Subramony SH, van Engelen B, Kools J, Leinhard OD, Widholm P, Morabito C, Moxham CM, Cadavid D, Mellion ML, Odueyungbo A, Tracewell WG, Accorsi A, Ronco L, Gould RJ, Shoskes J, Rojas LA, Jiang JG. Tawil R, et al. Among authors: accorsi a. Lancet Neurol. 2024 May;23(5):477-486. doi: 10.1016/S1474-4422(24)00073-5. Lancet Neurol. 2024. PMID: 38631764 Clinical Trial.

3

Fibrogenesis in LAMA2-Related Muscular Dystrophy Is a Central Tenet of Disease Etiology.

Accorsi A, Cramer ML, Girgenrath M. Accorsi A, et al. Front Mol Neurosci. 2020 Feb 4;13:3. doi: 10.3389/fnmol.2020.00003. eCollection 2020. Front Mol Neurosci. 2020. PMID: 32116541 Free PMC article. Review.

4

Optimization of Xenografting Methods for Generating Human Skeletal Muscle in Mice.

O'Neill A, Martinez AL, Mueller AL, Huang W, Accorsi A, Kane MA, Eyerman D, Bloch RJ. O'Neill A, et al. Among authors: accorsi a. Cell Transplant. 2024 Jan-Dec;33:9636897241242624. doi: 10.1177/09636897241242624. Cell Transplant. 2024. PMID: 38600801 Free PMC article.

5

Dysregulation of matricellular proteins is an early signature of pathology in laminin-deficient muscular dystrophy.

Mehuron T, Kumar A, Duarte L, Yamauchi J, Accorsi A, Girgenrath M. Mehuron T, et al. Among authors: accorsi a. Skelet Muscle. 2014 Jul 2;4:14. doi: 10.1186/2044-5040-4-14. eCollection 2014. Skelet Muscle. 2014. PMID: 25075272 Free PMC article.

6

Do's and don'ts in the preparation of muscle cryosections for histological analysis.

Kumar A, Accorsi A, Rhee Y, Girgenrath M. Kumar A, et al. Among authors: accorsi a. J Vis Exp. 2015 May 15;(99):e52793. doi: 10.3791/52793. J Vis Exp. 2015. PMID: 26066009 Free PMC article.

7

Magnetic Resonance Imaging Is Sensitive to Pathological Amelioration in a Model for Laminin-Deficient Congenital Muscular Dystrophy (MDC1A).

Vohra R, Accorsi A, Kumar A, Walter G, Girgenrath M. Vohra R, et al. Among authors: accorsi a. PLoS One. 2015 Sep 17;10(9):e0138254. doi: 10.1371/journal.pone.0138254. eCollection 2015. PLoS One. 2015. PMID: 26379183 Free PMC article.

8

miR-410 and miR-495 Are Dynamically Regulated in Diverse Cardiomyopathies and Their Inhibition Attenuates Pathological Hypertrophy.

Clark AL, Maruyama S, Sano S, Accorsi A, Girgenrath M, Walsh K, Naya FJ. Clark AL, et al. Among authors: accorsi a. PLoS One. 2016 Mar 21;11(3):e0151515. doi: 10.1371/journal.pone.0151515. eCollection 2016. PLoS One. 2016. PMID: 26999812 Free PMC article.

9

IGF-1/GH axis enhances losartan treatment in Lama2-related muscular dystrophy.

Accorsi A, Kumar A, Rhee Y, Miller A, Girgenrath M. Accorsi A, et al. Hum Mol Genet. 2016 Oct 24;25(21):4624–4634. doi: 10.1093/hmg/ddw291. Hum Mol Genet. 2016. PMID: 27798092

10

Integrin dysregulation as a possible driver of matrix remodeling in Laminin-deficient congenital muscular dystrophy (MDC1A).

Accorsi A, Mehuron T, Kumar A, Rhee Y, Girgenrath M. Accorsi A, et al. J Neuromuscul Dis. 2015;2(1):51-61. J Neuromuscul Dis. 2015. PMID: 28198706

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