Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS043264-02
Application #
6660816
Study Section
Special Emphasis Panel (ZNS1-SRB-K (01))
Program Officer
Chen, Daofen
Project Start
2002-09-20
Project End
2005-07-31
Budget Start
2003-08-01
Budget End
2004-07-31
Support Year
2
Fiscal Year
2003
Total Cost
$1,121,658
Indirect Cost
Name
University of Utah
Department
Neurology
Type
Schools of Medicine
DUNS #
009095365
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
Weiss, Robert B; Vieland, Veronica J; Dunn, Diane M et al. (2018) Long-range genomic regulators of THBS1 and LTBP4 modify disease severity in duchenne muscular dystrophy. Ann Neurol 84:234-245
Mayer, O H; Finkel, R S; Rummey, C et al. (2015) Characterization of pulmonary function in Duchenne Muscular Dystrophy. Pediatr Pulmonol 50:487-94
Findlay, Andrew R; Wein, Nicolas; Kaminoh, Yuuki et al. (2015) Clinical phenotypes as predictors of the outcome of skipping around DMD exon 45. Ann Neurol 77:668-74
Vulin, Adeline; Wein, Nicolas; Strandjord, Dana M et al. (2014) The ZZ domain of dystrophin in DMD: making sense of missense mutations. Hum Mutat 35:257-64
Anthony, Karen; Arechavala-Gomeza, Virginia; Taylor, Laura E et al. (2014) Dystrophin quantification: Biological and translational research implications. Neurology 83:2062-9
Wein, Nicolas; Vulin, Adeline; Falzarano, Maria S et al. (2014) Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice. Nat Med 20:992-1000
Thrush, Philip T; Edward, Neeraj; Flanigan, Kevin M et al. (2013) Precordial R wave height does not correlate with echocardiographic findings in boys with Duchenne muscular dystrophy. Congenit Heart Dis 8:561-7
Flanigan, Kevin M; Ceco, Ermelinda; Lamar, Kay-Marie et al. (2013) LTBP4 genotype predicts age of ambulatory loss in Duchenne muscular dystrophy. Ann Neurol 73:481-8
Viollet, Laurence; Thrush, Philip T; Flanigan, Kevin M et al. (2012) Effects of angiotensin-converting enzyme inhibitors and/or beta blockers on the cardiomyopathy in Duchenne muscular dystrophy. Am J Cardiol 110:98-102
Flanigan, Kevin M; Dunn, Diane; Larsen, C Aaron et al. (2011) Becker muscular dystrophy due to an inversion of exons 23 and 24 of the DMD gene. Muscle Nerve 44:822-5

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