259 related articles for article (PubMed ID: 14521546)
1. Genetic disorders of human congenital anomalies of the kidney and urinary tract (CAKUT).
Nakanishi K; Yoshikawa N
Pediatr Int; 2003 Oct; 45(5):610-6. PubMed ID: 14521546
[TBL] [Abstract][Full Text] [Related]
2. Mild recessive mutations in six Fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tract.
Kohl S; Hwang DY; Dworschak GC; Hilger AC; Saisawat P; Vivante A; Stajic N; Bogdanovic R; Reutter HM; Kehinde EO; Tasic V; Hildebrandt F
J Am Soc Nephrol; 2014 Sep; 25(9):1917-22. PubMed ID: 24700879
[TBL] [Abstract][Full Text] [Related]
3. Criteria for HNF1B analysis in patients with congenital abnormalities of kidney and urinary tract.
Raaijmakers A; Corveleyn A; Devriendt K; van Tienoven TP; Allegaert K; Van Dyck M; van den Heuvel L; Kuypers D; Claes K; Mekahli D; Levtchenko E
Nephrol Dial Transplant; 2015 May; 30(5):835-42. PubMed ID: 25500806
[TBL] [Abstract][Full Text] [Related]
4. [Genetic basis for malformation-associated uropathy and renal dysplasia].
Oppezzo C; Barberis V; Edefonti A; Cusi D; Marra G
G Ital Nefrol; 2003; 20(2):120-6. PubMed ID: 12746796
[TBL] [Abstract][Full Text] [Related]
5. Disruption of
Wang H; Zhang C; Wang X; Lian Y; Guo B; Han M; Zhang X; Zhu X; Xu S; Guo Z; Bi Y; Shen Q; Wang X; Liu J; Zhuang Y; Ni T; Xu H; Wu X
Int J Biol Sci; 2018; 14(1):10-20. PubMed ID: 29483821
[TBL] [Abstract][Full Text] [Related]
6. Novel perspectives for investigating congenital anomalies of the kidney and urinary tract (CAKUT).
Renkema KY; Winyard PJ; Skovorodkin IN; Levtchenko E; Hindryckx A; Jeanpierre C; Weber S; Salomon R; Antignac C; Vainio S; Schedl A; Schaefer F; Knoers NV; Bongers EM;
Nephrol Dial Transplant; 2011 Dec; 26(12):3843-51. PubMed ID: 22121240
[TBL] [Abstract][Full Text] [Related]
7. Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative gene.
Bekheirnia MR; Bekheirnia N; Bainbridge MN; Gu S; Coban Akdemir ZH; Gambin T; Janzen NK; Jhangiani SN; Muzny DM; Michael M; Brewer ED; Elenberg E; Kale AS; Riley AA; Swartz SJ; Scott DA; Yang Y; Srivaths PR; Wenderfer SE; Bodurtha J; Applegate CD; Velinov M; Myers A; Borovik L; Craigen WJ; Hanchard NA; Rosenfeld JA; Lewis RA; Gonzales ET; Gibbs RA; Belmont JW; Roth DR; Eng C; Braun MC; Lupski JR; Lamb DJ
Genet Med; 2017 Apr; 19(4):412-420. PubMed ID: 27657687
[TBL] [Abstract][Full Text] [Related]
8. Congenital anomalies of the kidney and urinary tract: an embryogenetic review.
dos Santos Junior AC; de Miranda DM; Simões e Silva AC
Birth Defects Res C Embryo Today; 2014 Dec; 102(4):374-81. PubMed ID: 25420794
[TBL] [Abstract][Full Text] [Related]
9. Novel Insights into the Pathogenesis of Monogenic Congenital Anomalies of the Kidney and Urinary Tract.
van der Ven AT; Vivante A; Hildebrandt F
J Am Soc Nephrol; 2018 Jan; 29(1):36-50. PubMed ID: 29079659
[TBL] [Abstract][Full Text] [Related]
10. Expression profiling of the AT2R mRNA in affected tissue from children with CAKUT.
Stanković A; Zivković M; Kostić M; Atanacković J; Krstić Z; Alavantić D
Clin Biochem; 2010 Jan; 43(1-2):71-5. PubMed ID: 19781541
[TBL] [Abstract][Full Text] [Related]
11. High frequency of kidney and urinary tract anomalies in asymptomatic first-degree relatives of patients with CAKUT.
Bulum B; Ozçakar ZB; Ustüner E; Düşünceli E; Kavaz A; Duman D; Walz K; Fitoz S; Tekin M; Yalçınkaya F
Pediatr Nephrol; 2013 Nov; 28(11):2143-7. PubMed ID: 23812353
[TBL] [Abstract][Full Text] [Related]
12. Genetics of congenital anomalies of the kidney and urinary tract.
Song R; Yosypiv IV
Pediatr Nephrol; 2011 Mar; 26(3):353-64. PubMed ID: 20798957
[TBL] [Abstract][Full Text] [Related]
13. Genetic, environmental, and epigenetic factors involved in CAKUT.
Nicolaou N; Renkema KY; Bongers EM; Giles RH; Knoers NV
Nat Rev Nephrol; 2015 Dec; 11(12):720-31. PubMed ID: 26281895
[TBL] [Abstract][Full Text] [Related]
14. Severe prenatal renal anomalies associated with mutations in HNF1B or PAX2 genes.
Madariaga L; Morinière V; Jeanpierre C; Bouvier R; Loget P; Martinovic J; Dechelotte P; Leporrier N; Thauvin-Robinet C; Jensen UB; Gaillard D; Mathieu M; Turlin B; Attie-Bitach T; Salomon R; Gübler MC; Antignac C; Heidet L
Clin J Am Soc Nephrol; 2013 Jul; 8(7):1179-87. PubMed ID: 23539225
[TBL] [Abstract][Full Text] [Related]
15. Genetics of Congenital Anomalies of the Kidney and Urinary Tract: The Current State of Play.
Capone VP; Morello W; Taroni F; Montini G
Int J Mol Sci; 2017 Apr; 18(4):. PubMed ID: 28398236
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Congenital anomalies of the kidney and urinary tract (CAKUT) associated with Hirschsprung's disease: a systematic review.
Hofmann AD; Duess JW; Puri P
Pediatr Surg Int; 2014 Aug; 30(8):757-61. PubMed ID: 24974188
[TBL] [Abstract][Full Text] [Related]
18. A molecular and genetic view of human renal and urinary tract malformations.
Woolf AS
Kidney Int; 2000 Aug; 58(2):500-12. PubMed ID: 10916073
[TBL] [Abstract][Full Text] [Related]
19. Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations.
Connaughton DM; Dai R; Owen DJ; Marquez J; Mann N; Graham-Paquin AL; Nakayama M; Coyaud E; Laurent EMN; St-Germain JR; Blok LS; Vino A; Klämbt V; Deutsch K; Wu CW; Kolvenbach CM; Kause F; Ottlewski I; Schneider R; Kitzler TM; Majmundar AJ; Buerger F; Onuchic-Whitford AC; Youying M; Kolb A; Salmanullah D; Chen E; van der Ven AT; Rao J; Ityel H; Seltzsam S; Rieke JM; Chen J; Vivante A; Hwang DY; Kohl S; Dworschak GC; Hermle T; Alders M; Bartolomaeus T; Bauer SB; Baum MA; Brilstra EH; Challman TD; Zyskind J; Costin CE; Dipple KM; Duijkers FA; Ferguson M; Fitzpatrick DR; Fick R; Glass IA; Hulick PJ; Kline AD; Krey I; Kumar S; Lu W; Marco EJ; Wentzensen IM; Mefford HC; Platzer K; Povolotskaya IS; Savatt JM; Shcherbakova NV; Senguttuvan P; Squire AE; Stein DR; Thiffault I; Voinova VY; Somers MJG; Ferguson MA; Traum AZ; Daouk GH; Daga A; Rodig NM; Terhal PA; van Binsbergen E; Eid LA; Tasic V; Rasouly HM; Lim TY; Ahram DF; Gharavi AG; Reutter HM; Rehm HL; MacArthur DG; Lek M; Laricchia KM; Lifton RP; Xu H; Mane SM; Sanna-Cherchi S; Sharrocks AD; Raught B; Fisher SE; Bouchard M; Khokha MK; Shril S; Hildebrandt F
Am J Hum Genet; 2020 Oct; 107(4):727-742. PubMed ID: 32891193
[TBL] [Abstract][Full Text] [Related]
20. Angiotensin-converting enzyme and angiotensin type 2 receptor gene genotype distributions in Italian children with congenital uropathies.
Rigoli L; Chimenz R; di Bella C; Cavallaro E; Caruso R; Briuglia S; Fede C; Salpietro CD
Pediatr Res; 2004 Dec; 56(6):988-93. PubMed ID: 15470205
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
