Hahn MK - Search Results

1

Multivariate permutation analysis associates multiple polymorphisms with subphenotypes of major depression.

Hahn MK, Blackford JU, Haman K, Mazei-Robison M, English BA, Prasad HC, Steele A, Hazelwood L, Fentress HM, Myers R, Blakely RD, Sanders-Bush E, Shelton R. Hahn MK, et al. Genes Brain Behav. 2008 Jun;7(4):487-95. doi: 10.1111/j.1601-183X.2007.00384.x. Epub 2007 Dec 6. Genes Brain Behav. 2008. PMID: 18081710 Free PMC article.

2

Monoamine transporter gene structure and polymorphisms in relation to psychiatric and other complex disorders.

Hahn MK, Blakely RD. Hahn MK, et al. Pharmacogenomics J. 2002;2(4):217-35. doi: 10.1038/sj.tpj.6500106. Pharmacogenomics J. 2002. PMID: 12196911

3

Genetic basis of clinical catecholamine disorders.

Garland EM, Hahn MK, Ketch TP, Keller NR, Kim CH, Kim KS, Biaggioni I, Shannon JR, Blakely RD, Robertson D. Garland EM, et al. Among authors: hahn mk. Ann N Y Acad Sci. 2002 Oct;971:506-14. doi: 10.1111/j.1749-6632.2002.tb04515.x. Ann N Y Acad Sci. 2002. PMID: 12438171 Review.

4

A mutation in the human norepinephrine transporter gene (SLC6A2) associated with orthostatic intolerance disrupts surface expression of mutant and wild-type transporters.

Hahn MK, Robertson D, Blakely RD. Hahn MK, et al. J Neurosci. 2003 Jun 1;23(11):4470-8. doi: 10.1523/JNEUROSCI.23-11-04470.2003. J Neurosci. 2003. PMID: 12805287 Free PMC article.

5

Single nucleotide polymorphisms in the human norepinephrine transporter gene affect expression, trafficking, antidepressant interaction, and protein kinase C regulation.

Hahn MK, Mazei-Robison MS, Blakely RD. Hahn MK, et al. Mol Pharmacol. 2005 Aug;68(2):457-66. doi: 10.1124/mol.105.011270. Epub 2005 May 13. Mol Pharmacol. 2005. PMID: 15894713

6

A genetic screen in Caenorhabditis elegans for dopamine neuron insensitivity to 6-hydroxydopamine identifies dopamine transporter mutants impacting transporter biosynthesis and trafficking.

Nass R, Hahn MK, Jessen T, McDonald PW, Carvelli L, Blakely RD. Nass R, et al. Among authors: hahn mk. J Neurochem. 2005 Aug;94(3):774-85. doi: 10.1111/j.1471-4159.2005.03205.x. Epub 2005 Jun 30. J Neurochem. 2005. PMID: 15992384 Free article.

7

The functional impact of SLC6 transporter genetic variation.

Hahn MK, Blakely RD. Hahn MK, et al. Annu Rev Pharmacol Toxicol. 2007;47:401-41. doi: 10.1146/annurev.pharmtox.47.120505.105242. Annu Rev Pharmacol Toxicol. 2007. PMID: 17067279 Review.

8

A polymorphism in the norepinephrine transporter gene alters promoter activity and is associated with attention-deficit hyperactivity disorder.

Kim CH, Hahn MK, Joung Y, Anderson SL, Steele AH, Mazei-Robinson MS, Gizer I, Teicher MH, Cohen BM, Robertson D, Waldman ID, Blakely RD, Kim KS. Kim CH, et al. Among authors: hahn mk. Proc Natl Acad Sci U S A. 2006 Dec 12;103(50):19164-9. doi: 10.1073/pnas.0510836103. Epub 2006 Dec 4. Proc Natl Acad Sci U S A. 2006. PMID: 17146058 Free PMC article.

9

Novel and functional norepinephrine transporter protein variants identified in attention-deficit hyperactivity disorder.

Hahn MK, Steele A, Couch RS, Stein MA, Krueger JJ. Hahn MK, et al. Neuropharmacology. 2009 Dec;57(7-8):694-701. doi: 10.1016/j.neuropharm.2009.08.002. Epub 2009 Aug 19. Neuropharmacology. 2009. PMID: 19698724 Free PMC article.

10

Genetic variation in the presynaptic norepinephrine transporter is associated with blood pressure responses to exercise in healthy humans.

Kohli U, Hahn MK, English BA, Sofowora GG, Muszkat M, Li C, Blakely RD, Stein CM, Kurnik D. Kohli U, et al. Among authors: hahn mk. Pharmacogenet Genomics. 2011 Apr;21(4):171-8. doi: 10.1097/FPC.0b013e328344f63e. Pharmacogenet Genomics. 2011. PMID: 21412203 Free PMC article.

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