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Publications

In chronological order

  • Magnesium homeostasis: the balancing act of TRPM6.
    van der Wijst J, Bindels RJ and Hoenderop JG.
    documentCurr Opinion Nephrol Hypertension 23: 361-369, 2014
  • β1-Adrenergic receptor signaling activates the epithelial calcium channel, TRPV5, via the protein kinase A pathway.
    van der Hagen EA, Tudpor K, Verkaart S, Lavrijsen M, van der Kemp A, van Zeeland F, Bindels RJ and Hoenderop JG.
    documentJ Biol Chem 289: 18489-18496, 2014
  • CNNM2 mutations cause impaired brain development and seizures in patients with hypomagnesemia.
    Arjona FJ, de Baaij JH, Schlingmann KP, Lameris AL, van Wijk E, Flik G, Regele S, Korenke GC, Neophytou, Rust S, Reintjes N, Konrad M, Bindels RJ and Hoenderop JG.
    documentPLoS Genet 4: e1004267, 2014
  • Kinase and channel activity of TRPM6 are coordinated by a dimerization motif and pocket interaction.
    van der Wijst J, Blanchard MG, Woodroof HI, Macartney TJ, Gourlay R, Hoenderop JG, Bindels RJ and Alessi DR.
    documentBiochem J 460: 165-75, 2014
  • A novel KCNA1 mutation causing episodic ataxia type I.
    Lassche S, Lainez S, Bloem BR, van de Warrenburg BP, Hofmeijer J, Lemmink HH, Hoenderop JG, Bindels RJ and Drost G.
    documentMuscle nerve 50: 289-291, 2014
  • Coordinated regulation of TRPV5-mediated Ca2+ transport in primary distal convolution cultures.
    van der Hagen EA, Lavrijsen M, van Zeeland F, Praetorius J, Bonny O, Bindels RJ and Hoenderop JG.
    documentPflügers Archiv 466: 2077-2087, 2014
  • Function and regulation of the Na+-Ca2+ exchanger NCX3 splice variants in brain and skeletal muscle.
    Michel LY, Verkaart S, Koopman WJ, Willems PH, Hoenderop JG and Bindels RJ.
    documentJ Biol Chem 289: 11293-303, 2014
  • Importance of dietary calcium and vitamin D in the treatment of hypercalcaemia in Williams-Beuren syndrome.
    Lameris AL, Geesing CL, Hoenderop JG and Schreuder MF.
    documentJ Pediatr Endocr Met 27: 757-761, 2014
  • P2X4 receptor regulation of transient receptor potential melastatin type 6 (TRPM6) Mg2+ channels.
    de Baaij JHF, Blanchard MG, Lavrijsen M, Leipziger J, Bindels RJ, Hoenderop JG.
    documentPflügers Archiv 466: 1941-1952, 2014
  • Mutations in PCBD1 cause hypomagnesemia and renal magnesium wasting.
    Ferrè S, de Baaij JH, Ferreira P, Germann R, de Klerk JB, Lavrijsen M, van Zeeland F, Venselaar H, Kluijtmans LA, Hoenderop JG and Bindels RJ.
    documentJ Am Soc Nephrol 25: 574-586, 2014


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