R01 AR042423/AR/NIAMS NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2000	1
2002	2
2006	1
2007	1
2008	1
2009	3
2010	1
2011	1
2012	3
2013	3
2014	2
2015	3
2016	1
2018	7
2019	5
2020	2
2021	2
2022	2
2023	1
2024	0

1

Dystrophin As a Molecular Shock Absorber.

Le S, Yu M, Hovan L, Zhao Z, Ervasti J, Yan J. Le S, et al. ACS Nano. 2018 Dec 26;12(12):12140-12148. doi: 10.1021/acsnano.8b05721. Epub 2018 Nov 27. ACS Nano. 2018. PMID: 30457830 Free PMC article.

2

Xanthine oxidase is hyper-active in Duchenne muscular dystrophy.

Lindsay A, McCourt PM, Karachunski P, Lowe DA, Ervasti JM. Lindsay A, et al. Free Radic Biol Med. 2018 Dec;129:364-371. doi: 10.1016/j.freeradbiomed.2018.10.404. Epub 2018 Oct 10. Free Radic Biol Med. 2018. PMID: 30312761 Free PMC article.

3

Dystrophinopathy-associated dysfunction of Krebs cycle metabolism.

Lindsay A, Chamberlain CM, Witthuhn BA, Lowe DA, Ervasti JM. Lindsay A, et al. Hum Mol Genet. 2019 Mar 15;28(6):942-951. doi: 10.1093/hmg/ddy404. Hum Mol Genet. 2019. PMID: 30476171 Free PMC article.

4

Disease-proportional proteasomal degradation of missense dystrophins.

Talsness DM, Belanto JJ, Ervasti JM. Talsness DM, et al. Proc Natl Acad Sci U S A. 2015 Oct 6;112(40):12414-9. doi: 10.1073/pnas.1508755112. Epub 2015 Sep 21. Proc Natl Acad Sci U S A. 2015. PMID: 26392559 Free PMC article.

5

Contraction-Induced Loss of Plasmalemmal Electrophysiological Function Is Dependent on the Dystrophin Glycoprotein Complex.

Baumann CW, Lindsay A, Sidky SR, Ervasti JM, Warren GL, Lowe DA. Baumann CW, et al. Front Physiol. 2021 Oct 26;12:757121. doi: 10.3389/fphys.2021.757121. eCollection 2021. Front Physiol. 2021. PMID: 34764884 Free PMC article.

6

Dystrophin is a microtubule-associated protein.

Prins KW, Humston JL, Mehta A, Tate V, Ralston E, Ervasti JM. Prins KW, et al. J Cell Biol. 2009 Aug 10;186(3):363-9. doi: 10.1083/jcb.200905048. Epub 2009 Aug 3. J Cell Biol. 2009. PMID: 19651889 Free PMC article.

7

Some dystrophy phenotypes of dystrophin-deficient mdx mice are exacerbated by mild, repetitive daily stress.

Lindsay A, Holm J, Razzoli M, Bartolomucci A, Ervasti JM, Lowe DA. Lindsay A, et al. FASEB J. 2021 Apr;35(4):e21489. doi: 10.1096/fj.202002500R. FASEB J. 2021. PMID: 33734502

8

Social stress is lethal in the mdx model of Duchenne muscular dystrophy.

Razzoli M, Lindsay A, Law ML, Chamberlain CM, Southern WM, Berg M, Osborn J, Engeland WC, Metzger JM, Ervasti JM, Bartolomucci A. Razzoli M, et al. EBioMedicine. 2020 May;55:102700. doi: 10.1016/j.ebiom.2020.102700. Epub 2020 Mar 16. EBioMedicine. 2020. PMID: 32192914 Free PMC article.

9

Neopterin/7,8-dihydroneopterin is elevated in Duchenne muscular dystrophy patients and protects mdx skeletal muscle function.

Lindsay A, Schmiechen A, Chamberlain CM, Ervasti JM, Lowe DA. Lindsay A, et al. Exp Physiol. 2018 Jul;103(7):995-1009. doi: 10.1113/EP087031. Exp Physiol. 2018. PMID: 29791760 Free PMC article.

10

Functional substitution by TAT-utrophin in dystrophin-deficient mice.

Sonnemann KJ, Heun-Johnson H, Turner AJ, Baltgalvis KA, Lowe DA, Ervasti JM. Sonnemann KJ, et al. PLoS Med. 2009 May 26;6(5):e1000083. doi: 10.1371/journal.pmed.1000083. Epub 2009 May 26. PLoS Med. 2009. PMID: 19478831 Free PMC article.

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