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374 open access dissertations and theses found for:
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1.
Systems Analysis of Eukaryotic Proteomic Regulatory Mechanisms
by Samir, Parimal, Ph.D.  Vanderbilt University. 2016: 294 pages; 13834909.
3.
Translation initiation and secondary structure of the fragile X mental retardation 1 mRNA
by Ludwig, Anna L., Ph.D.  University of California, Davis. 2009: 164 pages; 3397071.
4.
Pathogenic pathways and preclincial testing in mouse models of muscular dystrophy
by Gardner, Brandon Barnett, Ph.D.  The University of Chicago. 2016: 165 pages; 10129504.
5.
The role of histone acetylation in CAG /CTG repeat stability
by Yang, Jiahui, Ph.D.  Tufts University. 2010: 186 pages; 3396546.
6.
New Congenital Mouse Model to Study Laminin Protein Therapy for Muscular Dystrophy
by Coffey, Caroline B. M., Ph.D.  University of Nevada, Reno. 2015: 350 pages; 10001052.
7.
Characterization of UBIAD1 and its role in Schnyder corneal dystrophy
by Nickerson, Michael L., Ph.D.  The George Washington University. 2011: 148 pages; 3422895.
8.
SMAD signaling drives heart and muscle dysfunction in muscular dystrophy
by Goldstein, Jeffery Adam, Ph.D.  The University of Chicago. 2012: 149 pages; 3526242.
9.
Role of Mitochondria in Plasma Membrane Repair and Pathogenesis of Muscular Dystrophy
by Horn, Adam, Ph.D.  The George Washington University. 2018: 226 pages; 10845492.
10.
Efficacy of glucocorticoids in muscular dystrophy: Signaling, hormonal activities, and muscle inflammation
by Baudy, Andreas R., Ph.D.  The George Washington University. 2010: 171 pages; 3417954.
12.
Development of Dual Functional DNA/RNA Nanostructures for Drug Delivery
by Valsangkar, Vibhav A., Ph.D.  State University of New York at Albany. 2020: 121 pages; 27964522.
15.
Myogenesis Is Perturbed By Asynchronous Regeneration
by Johnston-Carey, Helen K., Ph.D.  The George Washington University. 2014: 172 pages; 3631374.
17.
The Use of Emerin-Null and EDMD-Causing Emerin Mutant Myogenic Progenitors to Elucidate the EDMD Mechanism
by Iyer, Ashvin, Ph.D.  University of the Sciences in Philadelphia. 2020: 216 pages; 27998882.
18.
It's a Jungle Out There: Myoblasts, Matrix, and MMPs
by Lund, Dane, Ph.D.  University of Missouri - Columbia. 2015: 135 pages; 10182609.
19.
nNos localization, muscle function and atrophy in skeletal muscle disorders
by Simmers, Jessica L., Ph.D.  The Johns Hopkins University. 2013: 107 pages; 3573097.
20.
Human Skeletal Muscle Study Through 2D and 3D Model Design
by Fibben, Kirby Sinclair, M.S.  University of California, Irvine. 2019: 30 pages; 13898360.
21.
23.
Understanding the Pathogenesis of Muscle Diseases Using In vivo SILAC Proteomic Strategy
by Rayavarapu, Sree Veera VSS, Ph.D.  The George Washington University. 2013: 156 pages; 3588601.
24.
Quantification and tracking of transplanted satellite cells
by Elster, Jennifer L., Ph.D.  The University of Arizona. 2009: 142 pages; 3369686.
25.
Genetics of inherited retinal degeneration
by Schindler, Emily Isaak, Ph.D.  The University of Iowa. 2011: 192 pages; 3461416.
26.
The identification and study of known and novel variants in spinocerebellar ataxia
by Reed, Patrick Jennings, Ph.D.  The University of Chicago. 2015: 158 pages; 3718546.
27.
Campus Crossings
by Black, Spencer, M.A.  University of Louisiana at Lafayette. 2017: 184 pages; 10273011.
28.
The Role of Group I Paks in Postnatal Muscle Development and Homeostasis
by Joseph, Giselle A., Ph.D.  Icahn School of Medicine at Mount Sinai. 2017: 170 pages; 10640750.
29.
Characterization of the CELF6 RNA Binding Protein: Effects on Mouse Vocal Behavior and Biochemical Function
by Rieger, Michael A., Ph.D.  Washington University in St. Louis. 2018: 290 pages; 10824444.
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