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Ryan S. Friese

University of California, San Diego

20

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341

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verificationpathway identification, and experimental A-null model of hypertension: transcriptomic Global metabolic consequences of the chromogranin

2015
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Role of the gluconeogenic/glycogenolytic enzyme G6Pase: Response to PST, GRP78, and inhibition of GRP78's ATPase enzymatic activity.

2014 PLOS ONE
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MicroRNA-22 and promoter motif polymorphisms at the Chga locus in genetic hypertension: functional and therapeutic implications for gene expression and the pathogenesis of hypertension

2013 Human Molecular Genetics
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Integrated Computational and Experimental Analysis of the Neuroendocrine Transcriptome in Genetic Hypertension Identifies Novel Control Points for the Cardiometabolic Syndrome

2012 Circulation-cardiovascular Genetics
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Genes and environment: novel, functional polymorphism in the human cathepsin L (CTSL1) promoter disrupts a xenobiotic response element (XRE) to alter transcription and blood pressure.

2012 Journal of Hypertension
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Systematic polymorphism discovery after genome-wide identification of potential susceptibility loci in a hereditary rodent model of human hypertension.

2011 Blood Pressure
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Catecholamine Storage Vesicles: Role of Core Protein Genetic Polymorphisms in Hypertension

2011 Current Hypertension Reports
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Conserved regulatory motifs at phenylethanolamine N-methyltransferase (PNMT) are disrupted by common functional genetic variation: an integrated computational/experimental approach.

2010 Mammalian Genome
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Genetic regulation of catecholamine synthesis, storage and secretion in the spontaneously hypertensive rat

2010 Human Molecular Genetics
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Naturally Occurring Genetic Variants in Human Chromogranin A (CHGA) Associated with Hypertension as well as Hypertensive Renal Disease

2010 Cellular and Molecular Neurobiology
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