Hoenderop JGJ - Search Results

1

Possible role for rare TRPM7 variants in patients with hypomagnesaemia with secondary hypocalcaemia.

Vargas-Poussou R, Claverie-Martin F, Prot-Bertoye C, Carotti V, van der Wijst J, Perdomo-Ramirez A, Fraga-Rodriguez GM, Hureaux M, Bos C, Latta F, Houillier P, Hoenderop JGJ, de Baaij JHF. Vargas-Poussou R, et al. Among authors: hoenderop jgj. Nephrol Dial Transplant. 2023 Feb 28;38(3):679-690. doi: 10.1093/ndt/gfac182. Nephrol Dial Transplant. 2023. PMID: 35561741 Free PMC article.

2

Molecular cloning, tissue distribution, and chromosomal mapping of the human epithelial Ca2+ channel (ECAC1).

Müller D, Hoenderop JG, Meij IC, van den Heuvel LP, Knoers NV, den Hollander AI, Eggert P, García-Nieto V, Claverie-Martín F, Bindels RJ. Müller D, et al. Genomics. 2000 Jul 1;67(1):48-53. doi: 10.1006/geno.2000.6203. Genomics. 2000. PMID: 10945469

3

Epithelial Ca(2+) channel (ECAC1) in autosomal dominant idiopathic hypercalciuria.

Müller D, Hoenderop JG, Vennekens R, Eggert P, Harangi F, Méhes K, Garcia-Nieto V, Claverie-Martin F, Os CH, Nilius B, J M Bindels R. Müller D, et al. Nephrol Dial Transplant. 2002 Sep;17(9):1614-20. doi: 10.1093/ndt/17.9.1614. Nephrol Dial Transplant. 2002. PMID: 12198212

4

Tissue kallikrein-deficient mice display a defect in renal tubular calcium absorption.

Picard N, Van Abel M, Campone C, Seiler M, Bloch-Faure M, Hoenderop JG, Loffing J, Meneton P, Bindels RJ, Paillard M, Alhenc-Gelas F, Houillier P. Picard N, et al. J Am Soc Nephrol. 2005 Dec;16(12):3602-10. doi: 10.1681/ASN.2004110923. Epub 2005 Oct 26. J Am Soc Nephrol. 2005. PMID: 16251243

5

Tissue kallikrein stimulates Ca(2+) reabsorption via PKC-dependent plasma membrane accumulation of TRPV5.

Gkika D, Topala CN, Chang Q, Picard N, Thébault S, Houillier P, Hoenderop JG, Bindels RJ. Gkika D, et al. EMBO J. 2006 Oct 18;25(20):4707-16. doi: 10.1038/sj.emboj.7601357. Epub 2006 Sep 28. EMBO J. 2006. PMID: 17006539 Free PMC article.

6

Impaired basolateral sorting of pro-EGF causes isolated recessive renal hypomagnesemia.

Groenestege WM, Thébault S, van der Wijst J, van den Berg D, Janssen R, Tejpar S, van den Heuvel LP, van Cutsem E, Hoenderop JG, Knoers NV, Bindels RJ. Groenestege WM, et al. J Clin Invest. 2007 Aug;117(8):2260-7. doi: 10.1172/JCI31680. J Clin Invest. 2007. PMID: 17671655 Free PMC article. Clinical Trial.

7

RACK1 inhibits TRPM6 activity via phosphorylation of the fused alpha-kinase domain.

Cao G, Thébault S, van der Wijst J, van der Kemp A, Lasonder E, Bindels RJ, Hoenderop JG. Cao G, et al. Curr Biol. 2008 Feb 12;18(3):168-76. doi: 10.1016/j.cub.2007.12.058. Curr Biol. 2008. PMID: 18258429 Free article.

8

The beta-glucuronidase klotho exclusively activates the epithelial Ca2+ channels TRPV5 and TRPV6.

Lu P, Boros S, Chang Q, Bindels RJ, Hoenderop JG. Lu P, et al. Nephrol Dial Transplant. 2008 Nov;23(11):3397-402. doi: 10.1093/ndt/gfn291. Epub 2008 May 21. Nephrol Dial Transplant. 2008. PMID: 18495742

9

TRPV5 gene polymorphisms in renal hypercalciuria.

Renkema KY, Lee K, Topala CN, Goossens M, Houillier P, Bindels RJ, Hoenderop JG. Renkema KY, et al. Nephrol Dial Transplant. 2009 Jun;24(6):1919-24. doi: 10.1093/ndt/gfn735. Epub 2009 Jan 8. Nephrol Dial Transplant. 2009. PMID: 19131347 Free article.

10

A missense mutation in the Kv1.1 voltage-gated potassium channel-encoding gene KCNA1 is linked to human autosomal dominant hypomagnesemia.

Glaudemans B, van der Wijst J, Scola RH, Lorenzoni PJ, Heister A, van der Kemp AW, Knoers NV, Hoenderop JG, Bindels RJ. Glaudemans B, et al. J Clin Invest. 2009 Apr;119(4):936-42. doi: 10.1172/JCI36948. Epub 2009 Mar 23. J Clin Invest. 2009. PMID: 19307729 Free PMC article.

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