Similar articles for PMID: 11929850

Year	Number of Results
1967	1
1994	2
1995	3
1996	4
1997	5
1998	13
1999	9
2000	10
2001	9
2002	8
2003	8
2004	10
2005	5
2006	9
2007	5
2008	7
2009	12
2010	5
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2012	7
2013	3
2014	6
2015	6
2016	3
2017	1
2018	4
2019	8
2020	6
2021	11
2022	3
2023	4
2024	0

1

Heteroligomerization of an Aquaporin-2 mutant with wild-type Aquaporin-2 and their misrouting to late endosomes/lysosomes explains dominant nephrogenic diabetes insipidus.

Marr N, Bichet DG, Lonergan M, Arthus MF, Jeck N, Seyberth HW, Rosenthal W, van Os CH, Oksche A, Deen PM. Marr N, et al. Hum Mol Genet. 2002 Apr 1;11(7):779-89. doi: 10.1093/hmg/11.7.779. Hum Mol Genet. 2002. PMID: 11929850

2

A novel mechanism in recessive nephrogenic diabetes insipidus: wild-type aquaporin-2 rescues the apical membrane expression of intracellularly retained AQP2-P262L.

de Mattia F, Savelkoul PJ, Bichet DG, Kamsteeg EJ, Konings IB, Marr N, Arthus MF, Lonergan M, van Os CH, van der Sluijs P, Robertson G, Deen PM. de Mattia F, et al. Hum Mol Genet. 2004 Dec 15;13(24):3045-56. doi: 10.1093/hmg/ddh339. Epub 2004 Oct 27. Hum Mol Genet. 2004. PMID: 15509592

3

An impaired routing of wild-type aquaporin-2 after tetramerization with an aquaporin-2 mutant explains dominant nephrogenic diabetes insipidus.

Kamsteeg EJ, Wormhoudt TA, Rijss JP, van Os CH, Deen PM. Kamsteeg EJ, et al. EMBO J. 1999 May 4;18(9):2394-400. doi: 10.1093/emboj/18.9.2394. EMBO J. 1999. PMID: 10228154 Free PMC article.

4

Cell-biologic and functional analyses of five new Aquaporin-2 missense mutations that cause recessive nephrogenic diabetes insipidus.

Marr N, Bichet DG, Hoefs S, Savelkoul PJ, Konings IB, De Mattia F, Graat MP, Arthus MF, Lonergan M, Fujiwara TM, Knoers NV, Landau D, Balfe WJ, Oksche A, Rosenthal W, Müller D, Van Os CH, Deen PM. Marr N, et al. J Am Soc Nephrol. 2002 Sep;13(9):2267-77. doi: 10.1097/01.asn.0000027355.41663.14. J Am Soc Nephrol. 2002. PMID: 12191971

5

Three families with autosomal dominant nephrogenic diabetes insipidus caused by aquaporin-2 mutations in the C-terminus.

Kuwahara M, Iwai K, Ooeda T, Igarashi T, Ogawa E, Katsushima Y, Shinbo I, Uchida S, Terada Y, Arthus MF, Lonergan M, Fujiwara TM, Bichet DG, Marumo F, Sasaki S. Kuwahara M, et al. Am J Hum Genet. 2001 Oct;69(4):738-48. doi: 10.1086/323643. Epub 2001 Aug 30. Am J Hum Genet. 2001. PMID: 11536078 Free PMC article.

6

Reversed polarized delivery of an aquaporin-2 mutant causes dominant nephrogenic diabetes insipidus.

Kamsteeg EJ, Bichet DG, Konings IB, Nivet H, Lonergan M, Arthus MF, van Os CH, Deen PM. Kamsteeg EJ, et al. J Cell Biol. 2003 Dec 8;163(5):1099-109. doi: 10.1083/jcb.200309017. J Cell Biol. 2003. PMID: 14662748 Free PMC article.

7

Importance of aquaporin-2 expression levels in genotype -phenotype studies in nephrogenic diabetes insipidus.

Kamsteeg EJ, Deen PM. Kamsteeg EJ, et al. Am J Physiol Renal Physiol. 2000 Oct;279(4):F778-84. doi: 10.1152/ajprenal.2000.279.4.F778. Am J Physiol Renal Physiol. 2000. PMID: 10997928 Free article.

8

Defective processing and trafficking of water channels in nephrogenic diabetes insipidus.

Kamsteeg EJ, Deen PM, van Os CH. Kamsteeg EJ, et al. Exp Nephrol. 2000 Nov-Dec;8(6):326-31. doi: 10.1159/000020686. Exp Nephrol. 2000. PMID: 11014929 Review.

9

Lack of arginine vasopressin-induced phosphorylation of aquaporin-2 mutant AQP2-R254L explains dominant nephrogenic diabetes insipidus.

de Mattia F, Savelkoul PJ, Kamsteeg EJ, Konings IB, van der Sluijs P, Mallmann R, Oksche A, Deen PM. de Mattia F, et al. J Am Soc Nephrol. 2005 Oct;16(10):2872-80. doi: 10.1681/ASN.2005010104. Epub 2005 Aug 24. J Am Soc Nephrol. 2005. PMID: 16120822

10

Pathogenesis of nephrogenic diabetes insipidus by aquaporin-2 C-terminus mutations.

Asai T, Kuwahara M, Kurihara H, Sakai T, Terada Y, Marumo F, Sasaki S. Asai T, et al. Kidney Int. 2003 Jul;64(1):2-10. doi: 10.1046/j.1523-1755.2003.00049.x. Kidney Int. 2003. PMID: 12787389 Free article.

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