Bindels RJ - Search Results

1

Genetic renal disorders with hypomagnesemia and hypocalciuria.

Knoers NV, de Jong JC, Meij IC, Van Den Heuvel LP, Bindels RJ. Knoers NV, et al. Among authors: bindels rj. J Nephrol. 2003 Mar-Apr;16(2):293-6. J Nephrol. 2003. PMID: 12768080 Review.

2

Calbindin-D9k and parvalbumin are exclusively located along basolateral membranes in rat distal nephron.

Bindels RJ, Timmermans JA, Hartog A, Coers W, van Os CH. Bindels RJ, et al. J Am Soc Nephrol. 1991 Dec;2(6):1122-9. doi: 10.1681/ASN.V261122. J Am Soc Nephrol. 1991. PMID: 1777592

3

Immunocytochemical localization of calbindin-D28k, calbindin-D9k and parvalbumin in rat kidney.

Bindels RJ, Hartog A, Timmermans JA, van Os CH. Bindels RJ, et al. Contrib Nephrol. 1991;91:7-13. doi: 10.1159/000420150. Contrib Nephrol. 1991. PMID: 1800013

4

Epithelial calcium channel: gate-keeper of active calcium reabsorption.

Hoenderop JG, Müller D, Suzuki M, van Os CH, Bindels RJ. Hoenderop JG, et al. Among authors: bindels rj. Curr Opin Nephrol Hypertens. 2000 Jul;9(4):335-40. doi: 10.1097/00041552-200007000-00003. Curr Opin Nephrol Hypertens. 2000. PMID: 10926168 Review.

5

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. Among authors: bindels rj. Genomics. 2000 Jul 1;67(1):48-53. doi: 10.1006/geno.2000.6203. Genomics. 2000. PMID: 10945469

6

Dominant isolated renal magnesium loss is caused by misrouting of the Na(+),K(+)-ATPase gamma-subunit.

Meij IC, Koenderink JB, van Bokhoven H, Assink KF, Groenestege WT, de Pont JJ, Bindels RJ, Monnens LA, van den Heuvel LP, Knoers NV. Meij IC, et al. Among authors: bindels rj. Nat Genet. 2000 Nov;26(3):265-6. doi: 10.1038/81543. Nat Genet. 2000. PMID: 11062458

7

Functional implications of mutations in the human renal outer medullary potassium channel (ROMK2) identified in Bartter syndrome.

Starremans PG, van der Kemp AW, Knoers NV, van den Heuvel LP, Bindels RJ. Starremans PG, et al. Among authors: bindels rj. Pflugers Arch. 2002 Jan;443(3):466-72. doi: 10.1007/s004240100708. Epub 2001 Oct 16. Pflugers Arch. 2002. PMID: 11810218

8

Functional expression of mutations in the human NaCl cotransporter: evidence for impaired routing mechanisms in Gitelman's syndrome.

De Jong JC, Van Der Vliet WA, Van Den Heuvel LP, Willems PH, Knoers NV, Bindels RJ. De Jong JC, et al. Among authors: bindels rj. J Am Soc Nephrol. 2002 Jun;13(6):1442-8. doi: 10.1097/01.asn.0000017904.77985.03. J Am Soc Nephrol. 2002. PMID: 12039972

9

The structural unit of the thiazide-sensitive NaCl cotransporter is a homodimer.

de Jong JC, Willems PH, Mooren FJ, van den Heuvel LP, Knoers NV, Bindels RJ. de Jong JC, et al. Among authors: bindels rj. J Biol Chem. 2003 Jul 4;278(27):24302-7. doi: 10.1074/jbc.M303101200. Epub 2003 Apr 18. J Biol Chem. 2003. PMID: 12704198 Free article.

10

Mutations in the human Na-K-2Cl cotransporter (NKCC2) identified in Bartter syndrome type I consistently result in nonfunctional transporters.

Starremans PG, Kersten FF, Knoers NV, van den Heuvel LP, Bindels RJ. Starremans PG, et al. Among authors: bindels rj. J Am Soc Nephrol. 2003 Jun;14(6):1419-26. doi: 10.1097/01.asn.0000064948.39199.a0. J Am Soc Nephrol. 2003. PMID: 12761241

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