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Results: 1 to 20 of 99

Similar articles for PubMed (Select 23620400)

1.

TNXB mutations can cause vesicoureteral reflux.

Gbadegesin RA, Brophy PD, Adeyemo A, Hall G, Gupta IR, Hains D, Bartkowiak B, Rabinovich CE, Chandrasekharappa S, Homstad A, Westreich K, Wu G, Liu Y, Holanda D, Clarke J, Lavin P, Selim A, Miller S, Wiener JS, Ross SS, Foreman J, Rotimi C, Winn MP.

J Am Soc Nephrol. 2013 Jul;24(8):1313-22. doi: 10.1681/ASN.2012121148. Epub 2013 Apr 25.

2.

Vesicoureteral reflux: Association of TNXB mutations with vesicoureteral reflux.

Kelsey R.

Nat Rev Nephrol. 2013 Jul;9(7):370. doi: 10.1038/nrneph.2013.90. Epub 2013 May 14. No abstract available.

PMID:
23670083
3.

Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral reflux.

Lu W, van Eerde AM, Fan X, Quintero-Rivera F, Kulkarni S, Ferguson H, Kim HG, Fan Y, Xi Q, Li QG, Sanlaville D, Andrews W, Sundaresan V, Bi W, Yan J, Giltay JC, Wijmenga C, de Jong TP, Feather SA, Woolf AS, Rao Y, Lupski JR, Eccles MR, Quade BJ, Gusella JF, Morton CC, Maas RL.

Am J Hum Genet. 2007 Apr;80(4):616-32. Epub 2007 Feb 14.

4.

Mutations in DSTYK and dominant urinary tract malformations.

Sanna-Cherchi S, Sampogna RV, Papeta N, Burgess KE, Nees SN, Perry BJ, Choi M, Bodria M, Liu Y, Weng PL, Lozanovski VJ, Verbitsky M, Lugani F, Sterken R, Paragas N, Caridi G, Carrea A, Dagnino M, Materna-Kiryluk A, Santamaria G, Murtas C, Ristoska-Bojkovska N, Izzi C, Kacak N, Bianco B, Giberti S, Gigante M, Piaggio G, Gesualdo L, Kosuljandic Vukic D, Vukojevic K, Saraga-Babic M, Saraga M, Gucev Z, Allegri L, Latos-Bielenska A, Casu D, State M, Scolari F, Ravazzolo R, Kiryluk K, Al-Awqati Q, D'Agati VD, Drummond IA, Tasic V, Lifton RP, Ghiggeri GM, Gharavi AG.

N Engl J Med. 2013 Aug 15;369(7):621-9. doi: 10.1056/NEJMoa1214479. Epub 2013 Jul 17.

5.

Traditional and targeted exome sequencing reveals common, rare and novel functional deleterious variants in RET-signaling complex in a cohort of living US patients with urinary tract malformations.

Chatterjee R, Ramos E, Hoffman M, VanWinkle J, Martin DR, Davis TK, Hoshi M, Hmiel SP, Beck A, Hruska K, Coplen D, Liapis H, Mitra R, Druley T, Austin P, Jain S.

Hum Genet. 2012 Nov;131(11):1725-38. doi: 10.1007/s00439-012-1181-3. Epub 2012 Jun 23.

6.

Vesicoureteral reflux and other urinary tract malformations in mice compound heterozygous for Pax2 and Emx2.

Boualia SK, Gaitan Y, Murawski I, Nadon R, Gupta IR, Bouchard M.

PLoS One. 2011;6(6):e21529. doi: 10.1371/journal.pone.0021529. Epub 2011 Jun 24.

7.

Genetics of vesicoureteral reflux.

Puri P, Gosemann JH, Darlow J, Barton DE.

Nat Rev Urol. 2011 Aug 23;8(10):539-52. doi: 10.1038/nrurol.2011.113. Review.

PMID:
21862976
8.

Lower urinary tract development and disease.

Rasouly HM, Lu W.

Wiley Interdiscip Rev Syst Biol Med. 2013 May-Jun;5(3):307-42. doi: 10.1002/wsbm.1212. Epub 2013 Feb 13. Review.

9.

[Vesicoureteral reflux: a familial study].

Santavá A, Utíkalová A, Michálková K, Hanáková S, Santavý J.

Cesk Pediatr. 1992 Feb;47(2):80-4. Czech.

PMID:
1572017
10.

[Genetic basis for malformation-associated uropathy and renal dysplasia].

Oppezzo C, Barberis V, Edefonti A, Cusi D, Marra G.

G Ital Nefrol. 2003 Mar-Apr;20(2):120-6. Review. Italian.

PMID:
12746796
11.

Gene discovery and vesicoureteric reflux.

Murawski IJ, Gupta IR.

Pediatr Nephrol. 2008 Jul;23(7):1021-7. doi: 10.1007/s00467-007-0704-y. Epub 2008 Feb 6. Review.

PMID:
18253765
12.

Vesico-ureteric reflux and urinary tract development in the Pax2 1Neu+/- mouse.

Murawski IJ, Myburgh DB, Favor J, Gupta IR.

Am J Physiol Renal Physiol. 2007 Nov;293(5):F1736-45. Epub 2007 Sep 19.

13.

Vesicoureteral reflux and reflux nephropathy.

Thomsen HS.

Acta Radiol Diagn (Stockh). 1985 Jan-Feb;26(1):3-13. Review.

PMID:
3883698
14.

Extracellular microenvironment and cytokine profile of the ureterovesical junction in children with vesicoureteral reflux.

Schwentner C, Oswald J, Lunacek A, Pelzer AE, Fritsch H, Schlenck B, Karatzas A, Bartsch G, Radmayr C.

J Urol. 2008 Aug;180(2):694-700. doi: 10.1016/j.juro.2008.04.048. Epub 2008 Jun 13.

PMID:
18554644
15.

Absence of PAX2 gene mutations in patients with primary familial vesicoureteric reflux.

Choi KL, McNoe LA, French MC, Guilford PJ, Eccles MR.

J Med Genet. 1998 Apr;35(4):338-9.

16.

Urinary tract anomalies associated with high grade primary vesicoureteral reflux.

Hunziker M, Kutasy B, D'Asta F, Puri P.

Pediatr Surg Int. 2012 Feb;28(2):201-4. doi: 10.1007/s00383-011-2986-1.

PMID:
21994077
17.

Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1.

Feather SA, Malcolm S, Woolf AS, Wright V, Blaydon D, Reid CJ, Flinter FA, Proesmans W, Devriendt K, Carter J, Warwicker P, Goodship TH, Goodship JA.

Am J Hum Genet. 2000 Apr;66(4):1420-5. Epub 2000 Mar 17.

18.

Familial vesicoureteral reflux: testing replication of linkage in seven new multigenerational kindreds.

Sanna-Cherchi S, Reese A, Hensle T, Caridi G, Izzi C, Kim YY, Konka A, Murer L, Scolari F, Ravazzolo R, Ghiggeri GM, Gharavi AG.

J Am Soc Nephrol. 2005 Jun;16(6):1781-7. Epub 2005 Apr 13.

19.

Exome sequencing and linkage analysis identified tenascin-C (TNC) as a novel causative gene in nonsyndromic hearing loss.

Zhao Y, Zhao F, Zong L, Zhang P, Guan L, Zhang J, Wang D, Wang J, Chai W, Lan L, Li Q, Han B, Yang L, Jin X, Yang W, Hu X, Wang X, Li N, Li Y, Petit C, Wang J, Wang HY, Wang Q.

PLoS One. 2013 Jul 30;8(7):e69549. doi: 10.1371/journal.pone.0069549. Print 2013.

20.

Lack of major involvement of human uroplakin genes in vesicoureteral reflux: implications for disease heterogeneity.

Jiang S, Gitlin J, Deng FM, Liang FX, Lee A, Atala A, Bauer SB, Ehrlich GD, Feather SA, Goldberg JD, Goodship JA, Goodship TH, Hermanns M, Hu FZ, Jones KE, Malcolm S, Mendelsohn C, Preston RA, Retik AB, Schneck FX, Wright V, Ye XY, Woolf AS, Wu XR, Ostrer H, Shapiro E, Yu J, Sun TT.

Kidney Int. 2004 Jul;66(1):10-9.

PMID:
15200408
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