296 related articles for article (PubMed ID: 17357069)
1. 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. PubMed ID: 17357069
[TBL] [Abstract][Full Text] [Related]
2. New congenital anomalies of the kidney and urinary tract and outcomes in Robo2 mutant mice with the inserted piggyBac transposon.
Liu J; Sun L; Shen Q; Wu X; Xu H
BMC Nephrol; 2016 Jul; 17(1):98. PubMed ID: 27460642
[TBL] [Abstract][Full Text] [Related]
3. ROBO2 gene variants are associated with familial vesicoureteral reflux.
Bertoli-Avella AM; Conte ML; Punzo F; de Graaf BM; Lama G; La Manna A; Polito C; Grassia C; Nobili B; Rambaldi PF; Oostra BA; Perrotta S
J Am Soc Nephrol; 2008 Apr; 19(4):825-31. PubMed ID: 18235093
[TBL] [Abstract][Full Text] [Related]
4. ROBO2 gene variants in children with primary nonsyndromic vesicoureteral reflux with or without renal hypoplasia/dysplasia.
Mitsioni AG; Siomou E; Bouba I; Petridi S; Siamopoulou A; Georgiou I
Pediatr Res; 2016 Jul; 80(1):72-6. PubMed ID: 27002985
[TBL] [Abstract][Full Text] [Related]
5. Mutations in the ROBO2 and SLIT2 genes are rare causes of familial vesico-ureteral reflux.
Zu S; Bartik Z; Zhao S; Sillen U; Nordenskjöld A
Pediatr Nephrol; 2009 Aug; 24(8):1501-8. PubMed ID: 19350278
[TBL] [Abstract][Full Text] [Related]
6. Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tract.
Münch J; Engesser M; Schönauer R; Hamm JA; Hartig C; Hantmann E; Akay G; Pehlivan D; Mitani T; Coban Akdemir Z; Tüysüz B; Shirakawa T; Dateki S; Claus LR; van Eerde AM; ; Smol T; Devisme L; Franquet H; Attié-Bitach T; Wagner T; Bergmann C; Höhn AK; Shril S; Pollack A; Wenger T; Scott AA; Paolucci S; Buchan J; Gabriel GC; Posey JE; Lupski JR; Petit F; McCarthy AA; Pazour GJ; Lo CW; Popp B; Halbritter J
Kidney Int; 2022 May; 101(5):1039-1053. PubMed ID: 35227688
[TBL] [Abstract][Full Text] [Related]
7. Genes in the ureteric budding pathway: association study on vesico-ureteral reflux patients.
van Eerde AM; Duran K; van Riel E; de Kovel CG; Koeleman BP; Knoers NV; Renkema KY; van der Horst HJ; Bökenkamp A; van Hagen JM; van den Berg LH; Wolffenbuttel KP; van den Hoek J; Feitz WF; de Jong TP; Giltay JC; Wijmenga C
PLoS One; 2012; 7(4):e31327. PubMed ID: 22558067
[TBL] [Abstract][Full Text] [Related]
8. Mutations of the SLIT2-ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract.
Hwang DY; Kohl S; Fan X; Vivante A; Chan S; Dworschak GC; Schulz J; van Eerde AM; Hilger AC; Gee HY; Pennimpede T; Herrmann BG; van de Hoek G; Renkema KY; Schell C; Huber TB; Reutter HM; Soliman NA; Stajic N; Bogdanovic R; Kehinde EO; Lifton RP; Tasic V; Lu W; Hildebrandt F
Hum Genet; 2015 Aug; 134(8):905-16. PubMed ID: 26026792
[TBL] [Abstract][Full Text] [Related]
9. Genetics of vesicoureteral reflux and congenital anomalies of the kidney and urinary tract.
Lee KH; Gee HY; Shin JI
Investig Clin Urol; 2017 Jun; 58(Suppl 1):S4-S13. PubMed ID: 28612055
[TBL] [Abstract][Full Text] [Related]
10. 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. PubMed ID: 21731775
[TBL] [Abstract][Full Text] [Related]
11. Responsible genes in children with primary vesicoureteral reflux: findings from the Chinese Children Genetic Kidney Disease Database.
Liu JL; Shen Q; Wu MY; Zhu GH; Li YF; Wang XW; Tang XS; Bi YL; Gong YN; Chen J; Fang XY; Zhai YH; Wu BB; Li GM; Sun YB; Gao XJ; Liu CH; Jiang XY; Hao S; Kang YL; Gong YL; Rong LP; Li D; Wang S; Ma D; Rao J; Xu H;
World J Pediatr; 2021 Aug; 17(4):409-418. PubMed ID: 34059960
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 17881463
[TBL] [Abstract][Full Text] [Related]
13. Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.
van der Ven AT; Connaughton DM; Ityel H; Mann N; Nakayama M; Chen J; Vivante A; Hwang DY; Schulz J; Braun DA; Schmidt JM; Schapiro D; Schneider R; Warejko JK; Daga A; Majmundar AJ; Tan W; Jobst-Schwan T; Hermle T; Widmeier E; Ashraf S; Amar A; Hoogstraaten CA; Hugo H; Kitzler TM; Kause F; Kolvenbach CM; Dai R; Spaneas L; Amann K; Stein DR; Baum MA; Somers MJG; Rodig NM; Ferguson MA; Traum AZ; Daouk GH; Bogdanović R; Stajić N; Soliman NA; Kari JA; El Desoky S; Fathy HM; Milosevic D; Al-Saffar M; Awad HS; Eid LA; Selvin A; Senguttuvan P; Sanna-Cherchi S; Rehm HL; MacArthur DG; Lek M; Laricchia KM; Wilson MW; Mane SM; Lifton RP; Lee RS; Bauer SB; Lu W; Reutter HM; Tasic V; Shril S; Hildebrandt F
J Am Soc Nephrol; 2018 Sep; 29(9):2348-2361. PubMed ID: 30143558
[TBL] [Abstract][Full Text] [Related]
14. 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. PubMed ID: 15200408
[TBL] [Abstract][Full Text] [Related]
15. Gene discovery and vesicoureteric reflux.
Murawski IJ; Gupta IR
Pediatr Nephrol; 2008 Jul; 23(7):1021-7. PubMed ID: 18253765
[TBL] [Abstract][Full Text] [Related]
16. Noninvasive assessment of antenatal hydronephrosis in mice reveals a critical role for Robo2 in maintaining anti-reflux mechanism.
Wang H; Li Q; Liu J; Mendelsohn C; Salant DJ; Lu W
PLoS One; 2011; 6(9):e24763. PubMed ID: 21949750
[TBL] [Abstract][Full Text] [Related]
17. 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. PubMed ID: 22729463
[TBL] [Abstract][Full Text] [Related]
18. Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract.
Hwang DY; Dworschak GC; Kohl S; Saisawat P; Vivante A; Hilger AC; Reutter HM; Soliman NA; Bogdanovic R; Kehinde EO; Tasic V; Hildebrandt F
Kidney Int; 2014 Jun; 85(6):1429-33. PubMed ID: 24429398
[TBL] [Abstract][Full Text] [Related]
19. Intrauterine low-protein diet aggravates developmental abnormalities of the urinary system via the Akt/Creb3 pathway in
Yu M; Tan L; Li Y; Chen J; Zhai Y; Rao J; Fang X; Wu X; Xu H; Shen Q
Am J Physiol Renal Physiol; 2020 Jan; 318(1):F43-F52. PubMed ID: 31630547
[TBL] [Abstract][Full Text] [Related]
20. Lower urinary tract development and disease.
Rasouly HM; Lu W
Wiley Interdiscip Rev Syst Biol Med; 2013; 5(3):307-42. PubMed ID: 23408557
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
