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Regulatory polymorphisms in human DBH affect peripheral gene expression and sympathetic activity.
Barrie ES, Weinshenker D, Verma A, Pendergrass SA, Lange LA, Ritchie MD, Wilson JG, Kuivaniemi H, Tromp G, Carey DJ, Gerhard GS, Brilliant MH, Hebbring SJ, Cubells JF, Pinsonneault JK, Norman GJ, Sadee W. Barrie ES, et al. Among authors: cubells jf. Circ Res. 2014 Dec 5;115(12):1017-25. doi: 10.1161/CIRCRESAHA.116.304398. Epub 2014 Oct 17. Circ Res. 2014. PMID: 25326128 Free PMC article.
A revised allele frequency estimate and haplotype analysis of the DBH deficiency mutation IVS1+2T --> C in African- and European-Americans.
Zabetian CP, Romero R, Robertson D, Sharma S, Padbury JF, Kuivaniemi H, Kim KS, Kim CH, Köhnke MD, Kranzler HR, Gelernter J, Cubells JF. Zabetian CP, et al. Among authors: cubells jf. Am J Med Genet A. 2003 Dec 1;123A(2):190-2. doi: 10.1002/ajmg.a.20300. Am J Med Genet A. 2003. PMID: 14598346 No abstract available.
A single nucleotide polymorphism at DBH, possibly associated with attention-deficit/hyperactivity disorder, associates with lower plasma dopamine beta-hydroxylase activity and is in linkage disequilibrium with two putative functional single nucleotide polymorphisms.
Tang Y, Buxbaum SG, Waldman I, Anderson GM, Zabetian CP, Köhnke MD, Cubells JF. Tang Y, et al. Among authors: cubells jf. Biol Psychiatry. 2006 Nov 15;60(10):1034-8. doi: 10.1016/j.biopsych.2006.02.017. Epub 2006 Apr 17. Biol Psychiatry. 2006. PMID: 16616730
147 results