Genetic modifiers of the phenotype of mice deficient in mitochondrial superoxide dismutase von Huang, Ting-Ting, Naeemuddin, Mohammed, Elchuri, Sailaja, Yamaguchi, Mutsuo, Kozy, Heather M., Carlson, Elaine J., Epstein, Charles J.

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Natural Variation in Human Membrane Transporter Genes Reveals Evolutionary and Functional Constraints von Leabman, Maya K., Huang, Conrad C., DeYoung, Joseph, Carlson, Elaine J., Taylor, Travis R., de la Cruz, Melanie, Johns, Susan J., Stryke, Doug, Kawamoto, Michiko, Urban, Thomas J., Kroetz, Deanna L., Ferrin, Thomas E., Clark, Andrew G., Risch, Neil, Herskowitz, Ira, Giacomini, Kathleen M., Pharmacogenetics of Membrane Transporters Investigators

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A flexible estimating equations approach for mapping function-valued traits von Xiong, Hao, Goulding, Evan H, Carlson, Elaine J, Tecott, Laurence H, McCulloch, Charles E, Sen, Saunak

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Primary afferent tachykinins are required to experience moderate to intense pain von Basbaum, Allan I, Cao, Yu Qing, Mantyh, Patrick W, Carlson, Elaine J, Gillespie, Anne-Marie, Epstein, Charles J

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Dilated cardiomyopathy and neonatal lethality in mutant mice lacking manganese superoxide dismutase von Li, Yibing, Huang, Ting-Ting, Carlson, Elaine J, Melov, Simon, Ursell, Philip C, Olson, Jean L, Noble, Linda J, Yoshimura, Midori P, Berger, Christoph, Chan, Pak H, Wallace, Douglas C, Epstein, Charles J

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Ts1Cje, a Partial Trisomy 16 Mouse Model for down Syndrome, Exhibits Learning and Behavioral Abnormalities von Sago, Haruhiko, Carlson, Elaine J., Smith, Desmond J., Kilbridge, Joshua, Rubin, Edward M., Mobley, William C., Epstein, Charles J., Huang, Ting-Ting

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The uptake and fate of vanadyl ion in ascidian blood cells and a detailed hypothesis for the mechanism and location of biological vanadium reduction. A visible and X-ray absorption... von Frank, Patrick, Carlson, Elaine J., Carlson, Robert M.K., Hedman, Britt, Hodgson, Keith O.

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Genetic variants of human organic anion transporter 4 demonstrate altered transport of endogenous substrates von Shima, James E, Komori, Takafumi, Taylor, Travis R, Stryke, Doug, Kawamoto, Michiko, Johns, Susan J, Carlson, Elaine J, Ferrin, Thomas E, Giacomini, Kathleen M

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The human organic anion transporter 3 (OAT3; SLC22A8): genetic variation and functional genomics von Erdman, Andrew R, Mangravite, Lara M, Urban, Thomas J, Lagpacan, Leah L, Castro, Richard A, de la Cruz, Melanie, Chan, Wendy, Huang, Conrad C, Johns, Susan J, Kawamoto, Michiko, Stryke, Douglas, Taylor, Travis R, Carlson, Elaine J, Ferrin, Thomas E, Brett, Claire M, Burchard, Esteban G, Giacomini, Kathleen M

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Biological sulfur in the blood cells of Ascidia ceratodes: XAS spectroscopy and a cellular-enzymatic hypothesis for vanadium reduction in the ascidians von Frank, Patrick, Carlson, Robert M.K., Carlson, Elaine J., Hedman, Britt, Hodgson, Keith O.

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Functional analysis of polymorphisms in the organic anion transporter, SLC22A6 (OAT1) von Fujita, Tomoe, Brown, Chaline, Carlson, Elaine J, Taylor, Travis, de la Cruz, Melanie, Johns, Susan J, Stryke, Doug, Kawamoto, Michiko, Fujita, Kazumi, Castro, Richard, Chen, Chung-Wen, Lin, Emil T, Brett, Claire M, Burchard, Esteban Gonzalez, Ferrin, Thomas E, Huang, Conrad C, Leabman, Maya K, Giacomini, Kathleen M

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Functional Genetic Diversity in the High-Affinity Carnitine Transporter OCTN2 (SLC22A5) von Urban, Thomas J, Gallagher, Renata C, Brown, Chaline, Castro, Richard A, Lagpacan, Leah L, Brett, Claire M, Taylor, Travis R, Carlson, Elaine J, Ferrin, Thomas E, Burchard, Esteban G, Packman, Seymour, Giacomini, Kathleen M

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Functional effects of protein sequence polymorphisms in the organic cation/ergothioneine transporter OCTN1 (SLC22A4) von Urban, Thomas J, Yang, Chen, Lagpacan, Leah L, Brown, Chaline, Castro, Richard A, Taylor, Travis R, Huang, Conrad C, Stryke, Douglas, Johns, Susan J, Kawamoto, Michiko, Carlson, Elaine J, Ferrin, Thomas E, Burchard, Esteban G, Giacomini, Kathleen M

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Functional and Genetic Diversity in the Concentrative Nucleoside Transporter, CNT1, in Human Populations von Gray, Jennifer H., Mangravite, Lara M., Owen, Ryan P., Urban, Thomas J., Chan, Wendy, Carlson, Elaine J., Huang, Conrad C., Kawamoto, Michiko, Johns, Susan J., Stryke, Douglas, Ferrin, Thomas E., Giacomini, Kathleen M.

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Sequence diversity and haplotype structure in the human ABCB1 (MDR1, multidrug resistance transporter) gene von KROETZ, Deanna L, PAULI-MAGNUS, Christiane, CARLSON, Elaine J, HERSKOWITZ, Ira, GIACOMINI, Kathleen M, CLARK, Andrew G, HODGES, Laura M, HUANG, Conrad C, KAWAMOTO, Michiko, JOHNS, Susan J, STRYKE, Doug, FERRIN, Thomas E, DEYOUNG, Joseph, TAYLOR, Travis

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Genetic analysis and functional characterization of polymorphisms in the human concentrative nucleoside transporter, CNT2 von Owen, Ryan P, Gray, Jennifer H, Taylor, Travis R, Carlson, Elaine J, Huang, Conrad C, Kawamoto, Michiko, Johns, Susan J, Stryke, Doug, Ferrin, Thomas E, Giacomini, Kathleen M

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Failed Retrograde Transport of NGF in a Mouse Model of Down's Syndrome: Reversal of Cholinergic Neurodegenerative Phenotypes Following NGF Infusion von Cooper, Jonathan D., Salehi, Ahmad, Delcroix, Jean-Dominique, Howe, Charles L., Belichenko, Pavel V., Chua-Couzens, Jane, Kilbridge, Joshua F., Carlson, Elaine J., Epstein, Charles J., Mobley, William C.

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Defective Secretion of Saliva in Transgenic Mice Lacking Aquaporin-5 Water Channels von Ma, T, Song, Y, Gillespie, A, Carlson, E J, Epstein, C J, Verkman, A S

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App Gene Dosage Modulates Endosomal Abnormalities of Alzheimer's Disease in a Segmental Trisomy 16 Mouse Model of Down Syndrome von Cataldo, Anne M, Petanceska, Suzana, Peterhoff, Corrinne M, Terio, Nicole B, Epstein, Charles J, Villar, Angela, Carlson, Elaine J, Staufenbiel, Matthias, Nixon, Ralph A

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Nephrogenic Diabetes Insipidus in Mice Lacking Aquaporin-3 Water Channels von Ma, Tonghui, Song, Yuanlin, Yang, Baoxue, Gillespie, Annemarie, Carlson, Elaine J., Epstein, Charles J., Verkman, A. S.

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