	Jim Bogenpohl I’m originally from St. Charles, Missouri, and I went to undergrad at Washington University in St. Louis where I received a bachelor’s degree in biology in 2004. While at WU, I spent three years researching the mammalian circadian clock. Shortly after graduating, I joined Emory’s Neuroscience Program in the Fall of 2004. After a few rotations, I joined Yoland’s lab where I am currently studying new pharmacological treatments for Parkinson’s Disease involving antagonism of metabotropic glutamate receptors and adenosine receptors. I will also examine the cellular and sub-cellular localization of these receptors in the basal ganglia of monkeys using electron microscopy. Like a few other members of our lab, my project will involve a strong collaboration with the lab of Thomas Wichmann. I enjoy working with animals, and I spend a lot of time with the rhesus macaques here at the Yerkes Primate Center. Publications ABSTRACTS Bogenpohl J.W., Pare J.F., Smith Y. Subcellular Localization of Adenosine A2A Receptors in the Striatum and Globus Pallidus of Monkey and Rat. International Basal Ganglia Society 9th Triennial Meeting. P-056 (2007). J. W. BOGENPOHL, M. VERREAULT, A. GALVAN, J. LIU, Y. SMITH. The use of mGluR5 antagonists as antiparkinsonian therapy in MPTP-treated monkeys. Society for Neuroscience Abstracts, 175.3 (2006). H. A. MITCHELL, J. BOGENPOHL, L. LILES, D. BOZYCZKO-COYNE, M. WILLIAMS, D. WEINSHENKER. Dopamine beta-hydroxylase (DBH) knockout mice support a dual dopaminergic-noradrenergic mechanism of modafinil (MOD) action. Society for Neuroscience Abstracts, 157.26 (2006). RESEARCH PAPERS Kozlov SV, Bogenpohl JW, Howell MP, Wevrick R, Panda S, Hogenesch JB, Muglia LJ, Van Gelder RN, Herzog ED, Stewart CL. The imprinted gene Magel2 regulates normal circadian output. Nat Genet. 2007 Oct;39(10):1266-72. Slawson EE, Shaffer CD, Malone CD, Leung W, Kellmann E, Shevchek RB, Craig CA, Bloom SM, Bogenpohl J 2nd, Dee J, Morimoto ET, Myoung J, Nett AS, Ozsolak F, Tittiger ME, Zeug A, Pardue ML, Buhler J, Mardis ER, Elgin SC. Comparison of dot chromosome sequences from D. melanogaster and D. virilis reveals an enrichment of DNA transposon sequences in heterochromatic domains. Genome Biol. 2006;7(2):R15.

Jim Bogenpohl

I’m originally from St. Charles, Missouri, and I went to undergrad at Washington University in St. Louis where I received a bachelor’s degree in biology in 2004. While at WU, I spent three years researching the mammalian circadian clock. Shortly after graduating, I joined Emory’s Neuroscience Program in the Fall of 2004. After a few rotations, I joined Yoland’s lab where I am currently studying new pharmacological treatments for Parkinson’s Disease involving antagonism of metabotropic glutamate receptors and adenosine receptors. I will also examine the cellular and sub-cellular localization of these receptors in the basal ganglia of monkeys using electron microscopy. Like a few other members of our lab, my project will involve a strong collaboration with the lab of Thomas Wichmann. I enjoy working with animals, and I spend a lot of time with the rhesus macaques here at the Yerkes Primate Center.

Publications

ABSTRACTS
Bogenpohl J.W., Pare J.F., Smith Y. Subcellular Localization of Adenosine A2A Receptors in the Striatum and Globus Pallidus of Monkey and Rat. International Basal Ganglia Society 9th Triennial Meeting. P-056 (2007).

J. W. BOGENPOHL, M. VERREAULT, A. GALVAN, J. LIU, Y. SMITH. The use of mGluR5 antagonists as antiparkinsonian therapy in MPTP-treated monkeys. Society for Neuroscience Abstracts, 175.3 (2006).

H. A. MITCHELL, J. BOGENPOHL, L. LILES, D. BOZYCZKO-COYNE, M. WILLIAMS, D. WEINSHENKER. Dopamine beta-hydroxylase (DBH) knockout mice support a dual dopaminergic-noradrenergic mechanism of modafinil (MOD) action. Society for Neuroscience Abstracts, 157.26 (2006).

RESEARCH PAPERS
Kozlov SV, Bogenpohl JW, Howell MP, Wevrick R, Panda S, Hogenesch JB, Muglia LJ, Van Gelder RN, Herzog ED, Stewart CL. The imprinted gene Magel2 regulates normal circadian output. Nat Genet. 2007 Oct;39(10):1266-72.

Slawson EE, Shaffer CD, Malone CD, Leung W, Kellmann E, Shevchek RB, Craig CA, Bloom SM, Bogenpohl J 2nd, Dee J, Morimoto ET, Myoung J, Nett AS, Ozsolak F, Tittiger ME, Zeug A, Pardue ML, Buhler J, Mardis ER, Elgin SC. Comparison of dot chromosome sequences from D. melanogaster and D. virilis reveals an enrichment of DNA transposon sequences in heterochromatic domains. Genome Biol. 2006;7(2):R15.