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Items: 1 to 20 of 133

1.

Ontogeny of congenital anomalies of the kidney and urinary tract, CAKUT.

Miyazaki Y, Ichikawa I.

Pediatr Int. 2003 Oct;45(5):598-604.

PMID:
14521544
2.

Embryogenesis of the congenital anomalies of the kidney and the urinary tract.

Kuwayama F, Miyazaki Y, Ichikawa I.

Nephrol Dial Transplant. 2002;17 Suppl 9:45-7.

PMID:
12386286
3.

Paradigm shift from classic anatomic theories to contemporary cell biological views of CAKUT.

Ichikawa I, Kuwayama F, Pope JC 4th, Stephens FD, Miyazaki Y.

Kidney Int. 2002 Mar;61(3):889-98. Review.

4.

Bone morphogenetic protein 4 regulates the budding site and elongation of the mouse ureter.

Miyazaki Y, Oshima K, Fogo A, Hogan BL, Ichikawa I.

J Clin Invest. 2000 Apr;105(7):863-73.

5.

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.

6.

Screening for mutations in BMP4 and FOXC1 genes in congenital anomalies of the kidney and urinary tract in humans.

Nakano T, Niimura F, Hohenfellner K, Miyakita E, Ichikawa I.

Tokai J Exp Clin Med. 2003 Oct;28(3):121-6.

PMID:
15055404
7.

How they begin and how they end: classic and new theories for the development and deterioration of congenital anomalies of the kidney and urinary tract, CAKUT.

Pope JC 4th, Brock JW 3rd, Adams MC, Stephens FD, Ichikawa I.

J Am Soc Nephrol. 1999 Sep;10(9):2018-28. Review.

8.
9.

Interkinetic nuclear migration in the mouse embryonic ureteric epithelium: Possible implication for congenital anomalies of the kidney and urinary tract.

Motoya T, Ogawa N, Nitta T, Rafiq AM, Jahan E, Furuya M, Matsumoto A, Udagawa J, Otani H.

Congenit Anom (Kyoto). 2016 May;56(3):127-34. doi: 10.1111/cga.12150.

PMID:
26710751
10.

Study of the association between the BMP4 gene and congenital anomalies of the kidney and urinary tract.

Reis GS, Simões E Silva AC, Freitas IS, Heilbuth TR, Marco LA, Oliveira EA, Miranda DM.

J Pediatr (Rio J). 2014 Jan-Feb;90(1):58-64. doi: 10.1016/j.jped.2013.06.004. Epub 2013 Oct 13.

11.

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. doi: 10.1002/bdrc.21084. Epub 2014 Nov 25. Review.

PMID:
25420794
12.

[Genetics of congenital anomalies of the kidney and urinary tract].

Zwolińska D, Polak-Jonkisz D, Makulska I.

Postepy Hig Med Dosw (Online). 2011 Dec 15;65:829-37. Review. Polish.

13.

Genetics of congenital anomalies of the kidney and urinary tract.

Song R, Yosypiv IV.

Pediatr Nephrol. 2011 Mar;26(3):353-64. doi: 10.1007/s00467-010-1629-4. Epub 2010 Aug 27. Review.

PMID:
20798957
14.

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; EUCAKUT consortium.

Nephrol Dial Transplant. 2011 Dec;26(12):3843-51. doi: 10.1093/ndt/gfr655. Review.

PMID:
22121240
15.

Congenital anomalies of the kidney and urinary tract--role of the loss of function mutation in the pluripotent angiotensin type 2 receptor gene.

Pope JC 4th, Brock JW 3rd, Adams MC, Miyazaki Y, Stephens FD, Ichikawa I.

J Urol. 2001 Jan;165(1):196-202. Review.

PMID:
11125405
16.

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. doi: 10.1681/ASN.2013101103. Epub 2014 Apr 3.

17.

Renal branching morphogenesis: morphogenetic and signaling mechanisms.

Blake J, Rosenblum ND.

Semin Cell Dev Biol. 2014 Dec;36:2-12. doi: 10.1016/j.semcdb.2014.07.011. Epub 2014 Jul 28. Review.

PMID:
25080023
18.

Changing concepts in urological management of the congenital anomalies of kidney and urinary tract, CAKUT.

Nakai H, Asanuma H, Shishido S, Kitahara S, Yasuda K.

Pediatr Int. 2003 Oct;45(5):634-41. Review.

PMID:
14521549
19.

Hnf1b and Pax2 cooperate to control different pathways in kidney and ureter morphogenesis.

Paces-Fessy M, Fabre M, Lesaulnier C, Cereghini S.

Hum Mol Genet. 2012 Jul 15;21(14):3143-55. doi: 10.1093/hmg/dds141. Epub 2012 Apr 17.

PMID:
22511595
20.

Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development.

Vivante A, Kleppa MJ, Schulz J, Kohl S, Sharma A, Chen J, Shril S, Hwang DY, Weiss AC, Kaminski MM, Shukrun R, Kemper MJ, Lehnhardt A, Beetz R, Sanna-Cherchi S, Verbitsky M, Gharavi AG, Stuart HM, Feather SA, Goodship JA, Goodship TH, Woolf AS, Westra SJ, Doody DP, Bauer SB, Lee RS, Adam RM, Lu W, Reutter HM, Kehinde EO, Mancini EJ, Lifton RP, Tasic V, Lienkamp SS, Jüppner H, Kispert A, Hildebrandt F.

Am J Hum Genet. 2015 Aug 6;97(2):291-301. doi: 10.1016/j.ajhg.2015.07.001. Epub 2015 Jul 30.

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