10 results for author:"Lippiat J." in Literature citations
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| Constitutively active TRPC channels of adipocytes confer a mechanism for sensing dietary fatty acids and regulating adiponectin. Sukumar P., Sedo A., Li J., Wilson L.A., O'Regan D., Lippiat J.D., Porter K.E., Kearney M.T., Ainscough J.F., Beech D.J. Circ. Res. 111:191-200(2012) · Mapped (7) |
| Voltage-dependent charge movement associated with activation of the CLC-5 2Cl-/1H+ exchanger. Smith A.J., Lippiat J.D. FASEB J. 24:3696-3705(2010) · Mapped (3) |
| Direct endosomal acidification by the outwardly rectifying CLC-5 Cl(-)/H(+) exchanger. Smith A.J., Lippiat J.D. J. Physiol. (Lond.) 588:2033-2045(2010) · Mapped (3) |
| CLC-5 and KIF3B interact to facilitate CLC-5 plasma membrane expression, endocytosis, and microtubular transport: relevance to pathophysiology of Dent's disease. Reed A.A., Loh N.Y., Terryn S., Lippiat J.D., Partridge C., Galvanovskis J., Williams S.E., Jouret F., Wu F.T., Courtoy P.J. et al. Am. J. Physiol. Renal Physiol. 298:F365-80(2010) · Mapped (12) |
| Mutational analysis of CLC-5, cofilin and CLC-4 in patients with Dent's disease. Wu F., Reed A.A., Williams S.E., Loh N.Y., Lippiat J.D., Christie P.T., Large O., Bettinelli A., Dillon M.J., Goldraich N.P. et al. Nephron Physiol 112:p53-62(2009) · Mapped (12) |
| Characterization of Dent's disease mutations of CLC-5 reveals a correlation between functional and cell biological consequences and protein structure. Smith A.J., Reed A.A., Loh N.Y., Thakker R.V., Lippiat J.D. Am. J. Physiol. 296:F390-F397(2009) · UniProtKB (1) · Mapped (2) |
| Mutations at the same residue (R50) of Kir6.2 (KCNJ11) that cause neonatal diabetes produce different functional effects. Shimomura K., Girard C.A.J., Proks P., Nazim J., Lippiat J.D., Cerutti F., Lorini R., Ellard S., Hattersely A.T., Barbetti F. et al. Diabetes 55:1705-1712(2006) · UniProtKB (1) |
| A genetic and physiological study of impaired glucose homeostasis control in C57BL/6J mice. Toye A.A., Lippiat J.D., Proks P., Shimomura K., Bentley L., Hugill A., Mijat V., Goldsworthy M., Moir L., Haynes A. et al. Diabetologia 48:675-686(2005) · Mapped (34) |
| Molecular basis of Kir6.2 mutations associated with neonatal diabetes or neonatal diabetes plus neurological features. Proks P., Antcliff J.F., Lippiat J., Gloyn A.L., Hattersley A.T., Ashcroft F.M. Proc. Natl. Acad. Sci. U.S.A. 101:17539-17544(2004) · UniProtKB (1) · Mapped (2) |
| ATP-dependent interaction of the cytosolic domains of the inwardly rectifying K+ channel Kir6.2 revealed by fluorescence resonance energy transfer. Tsuboi T., Lippiat J.D., Ashcroft F.M., Rutter G.A. Proc. Natl. Acad. Sci. U.S.A. 101:76-81(2004) · Mapped (3) |