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A descriptive and functional study of zebrafish Connexin43
by Zhang, Danhua, M.S.  Iowa State University. 2009: 66 pages; 1464413.
6.
Innovation and nonmarket strategies in environments with dominant firms: The case of the non-dominant firms in the Latin American telecommunications market
by Gonzalez Rodriguez, Nancy Patricia, Ph.D.  Instituto Tecnologico y de Estudios Superiores de Monterrey (Mexico). 2013: 129 pages; 3585549.
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Keeping the Red Queen in Check: Dynamic Mutation-Selection Balance in Evolving Populations
by Balick, Daniel J., Ph.D.  University of California, Santa Barbara. 2012: 264 pages; 3553705.
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Genetic Approach to Discover ARMC4 as a Novel NF-κB Negative Regulator and Tumor Suppressor in Colorectal Cancer
by Martin, Matthew Peter, Ph.D.  Indiana University - Purdue University Indianapolis. 2020: 128 pages; 27830485.
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Negative Regulation of Plant Stress Signaling by the EDR1 Protein Kinase
by Neubauer, Matthew Paul, Ph.D.  Indiana University. 2020: 161 pages; 27742261.
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Synaptotagmin in Asynchronous Neurotransmitter Release and Synaptic Disease
by Shields, Mallory Catherine, Ph.D.  Colorado State University. 2018: 195 pages; 10838850.
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CAPER as a Therapeutic Target for Triple Negative Breast Cancer
by Campbell, Mallory Christine, Ph.D.  University of the Sciences in Philadelphia. 2018: 123 pages; 10904829.
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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.
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Biochemical basis of human disease-causing actin mutations
by Bergeron, Sarah E., Ph.D.  The University of Iowa. 2011: 220 pages; 3516596.
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The Effect of Dynamic Kinetic Selection on an Evolving Ribozyme Population
by Poletti, Patrick David, Ph.D.  Portland State University. 2019: 144 pages; 13422098.
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Exploring Retromer Deficiency as a Mechanism of LRRK2-Induced Parkinson’s Disease
by Cunningham, Lindsey Aubrey, Ph.D.  Van Andel Research Institute. 2020: 174 pages; 27740362.
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Cowden Syndrome and PTEN Promoter Regulation Dissertation
by Teresi, Rosemary E., Ph.D.  The Ohio State University. 2008: 140 pages; 10631295.
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A Peptide-based Interaction Screen on Disease-related Mutations
by Meyer, Katrina, Ph.D.  Humboldt Universitaet zu Berlin (Germany). 2019: 125 pages; 27732541.
26.
Familial Cortical Myoclonus Caused by Mutation in NOL3
by Russell, Jonathan Foster, Ph.D.  University of California, San Francisco. 2013: 248 pages; 3558440.
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Efficient identification of disease causative mutations with next generation sequencing technologies
by Maranhao, Bruno, Ph.D.  University of California, San Diego. 2015: 836 pages; 3718508.
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Statistical Modeling and Analysis for Biomedical Applications
by Ho, Christine, Ph.D.  University of California, Berkeley. 2016: 131 pages; 10248676.
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Exome sequencing uncovers somatic drivers of endocrine tumorigenesis
by Cromer, Michael Kyle, Ph.D.  Yale University. 2014: 146 pages; 3580657.
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Big Data Approaches to Decipher Non-coding Cancer Driver Mutations
by Liu, Minwei, Ph.D.  Weill Medical College of Cornell University. 2019: 296 pages; 13902177.
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