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The Journal of Biological Chemistry|November 11, 1994
Mutations along transmembrane segment II of the NK-1 receptor affect substance P competition with non-peptide antagonists but not substance P bindingM M Rosenkilde, M Cahir, U Gether, et al.
Journal of Chromatography|March 13, 1987
High-performance liquid chromatography of phenylthiocarbamyl derivatives of amino acids and side-chain derivatized amino acidsM M O'Hare, O Tortora, U Gether, et al.
Biochemistry|December 22, 2000
Structural probing of a microdomain in the dopamine transporter by engineering of artificial Zn2+ binding sitesL Norregaard, I Visiers, C J Loland, et al.
The EMBO Journal|January 10, 1998
Agonists induce conformational changes in transmembrane domains III and VI of the beta2 adrenoceptorU Gether, S Lin, P Ghanouni, et al.
The Journal of Biological Chemistry|August 31, 2001
Engineered Zn(2+) switches in the gamma-aminobutyric acid (GABA) transporter-1. Differential effects on GABA uptake and currentsN MacAulay, A Bendahan, C J Loland, et al.
Molecular and Cellular Endocrinology|February 1, 1993
Efficient amidation of C-peptide deleted NPY precursors by non-endocrine cells is affected by the presence of Lys-Arg at the C-terminusB S Wulff, B Catipovic, H Okamoto, et al.
The Journal of Biological Chemistry|January 31, 1997
Structural instability of a constitutively active G protein-coupled receptor. Agonist-independent activation due to conformational flexibilityU Gether, J A Ballesteros, R Seifert, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry|January 29, 2026
Impulsivity and attentional dysfunction in DAT-AAA knock-in miceC M Fitzpatrick, J C McGirr, A Petersen, et al.
Nature|March 25, 1993
Different binding epitopes on the NK1 receptor for substance P and non-peptide antagonistU Gether, T E Johansen, R M Snider, et al.
The Journal of Biological Chemistry|March 28, 1998
Different effects of Gsalpha splice variants on beta2-adrenoreceptor-mediated signaling. The beta2-adrenoreceptor coupled to the long splice variant of Gsalpha has properties of a constitutively active receptorR Seifert, K Wenzel-Seifert, T W Lee, et al.
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