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Original Articles

Hereditary intermediate phenotypes in African American hypertension

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Pages 117-128 | Published online: 29 Apr 2010

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DANIEL T. O'CONNOR. (1999) Catecholamine storage vesicle protein expression in genetic hypertension. Blood Pressure 8:5-6, pages 285-295.
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Saiful A. Mir, Kuixing Zhang, Milos Milic, Yusu Gu, Timo Rieg, Michael Ziegler & Sucheta M. Vaingankar. (2016) Analysis and validation of traits associated with a single nucleotide polymorphism Gly364Ser in catestatin using humanized chromogranin A mouse models. Journal of Hypertension 34:1, pages 68-78.
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William Maixner, Joel D. Greenspan, Ronald Dubner, Eric Bair, Flora Mulkey, Vanessa Miller, Charles Knott, Gary D. Slade, Richard Ohrbach, Luda Diatchenko & Roger B. Fillingim. (2011) Potential Autonomic Risk Factors for Chronic TMD: Descriptive Data and Empirically Identified Domains from the OPPERA Case-Control Study. The Journal of Pain 12:11, pages T75-T91.
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Tiffany A. Greenwood, Fangwen Rao, Mats Stridsberg, Nitish R. Mahapatra, Manjula Mahata, Elizabeth O. Lillie, Sushil K. Mahata, Laurent Taupenot, Nicholas J. Schork & Daniel T. O’Connor. (2006) Pleiotropic effects of novel trans -acting loci influencing human sympathochromaffin secretion . Physiological Genomics 25:3, pages 470-479.
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Carol Moreno, Pierre Dumas, Mary L. Kaldunski, Peter J. Tonellato, Andrew S. Greene, Richard J. Roman, Qunli Cheng, Zhitao Wang, Howard J. Jacob & Allen W. CowleyJrJr. (2003) Genomic map of cardiovascular phenotypes of hypertension in female Dahl S rats. Physiological Genomics 15:3, pages 243-257.
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S W Chitbangonsyn, P Mahboubi, D Walker, B K Rana, K L Diggle, D S Timberlake, R J Parmer & D T O'Connor. (2003) Physical mapping of autonomic/sympathetic candidate genetic loci for hypertension in the human genome: a somatic cell radiation hybrid library approach. Journal of Human Hypertension 17:5, pages 319-324.
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ROBERT J. PARMER & OREN ZINDER. (2002) Catecholaminergic Pathways, Chromaffin Cells, and Human Disease. Annals of the New York Academy of Sciences 971:1, pages 497-505.
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Daniel T. O'Connor, Mala T. Kailasam, Brian P. Kennedy, Michael G. Ziegler, Noboru Yanaihara & Robert J. Parmer. (2002) Early decline in the catecholamine release-inhibitory peptide catestatin in humans at genetic risk of hypertension.. Journal of Hypertension 20:7, pages 1335-1345.
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Peng Fei Chang, Lars Arendt-Nielsen & Andrew C.N Chen. (2002) Dynamic changes and spatial correlation of EEG activities during cold pressor test in man. Brain Research Bulletin 57:5, pages 667-675.
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David S. Timberlake, Daniel T. O’Connor & Robert J. Parmer. (2001) Molecular genetics of essential hypertension: recent results and emerging strategies. Current Opinion in Nephrology and Hypertension 10:1, pages 71-79.
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Mala T. Kailasam, Robert J. Parmer, Elizabeth A. Tyrell, Robert R. Henry & Daniel T. OʼConnor. (2000) Circulating amylin in human essential hypertension. Journal of Hypertension 18:11, pages 1611-1620.
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M. Bravo-Luna, M. Orsatti & L. Poletto. (2000) Tachycardia: an autosomal, monogenic, biallelic, recessive trait. Medical Hypotheses 54:2, pages 307-309.
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Daniel T. O’Connor, Paul A. Insel, Michael G. Ziegler, Vivian Y. Hook, Douglas W. Smith, Bruce A. Hamilton, Palmer W. Taylor & Robert J. Parmer. (2000) Heredity and the autonomic nervous system in human hypertension. Current Hypertension Reports 2:1, pages 16-22.
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Oscar A. Carretero. 1999. Hormones and the Heart in Health and Disease. Hormones and the Heart in Health and Disease 137 158 .
T Teresa Dao, Mala T. Kailasam, Robert J. Parmer, Hiep V. Le, Roger Le Verge, Brian P. Kennedy, Michael G. Ziegler, Paul A. Insel, Fred A. Wright & Daniel T. OʼConnor. (1998) Expression of altered α2-adrenergic phenotypic traits in normotensive humans at genetic risk of hereditary (essential) hypertension. Journal of Hypertension 16:6, pages 779-792.
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