Literature DB >> 11849443

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

Iekuni Ichikawa1, Fumiyo Kuwayama, John C Pope, F Douglas Stephens, Yoichi Miyazaki.   

Abstract

Ectopic budding of the ureter from the Wolffian duct is the first ontogenic misstep that leads to many-if not all-congenital anomalies of the kidney and urinary tract (CAKUT). The ectopia results in hypoplastic kidney, ectopia of ureterovesical orifice, urinary outflow obstruction and/or reflux. Studies in several mutant mouse models have verified that ectopic ureteric budding indeed precedes formation of CAKUT. Often, the genes involved in navigating ureteric budding to the correct site also regulate later ontogenic events of the kidney and urinary tract. The wide spectrum of CAKUT, for example, multicystic dysplastic kidney, megaureter and atretic ureter, portray the additional important functions of these same genes that are activated at multiple sites and stages during the normal morphogenesis of the kidney and urinary tract

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Year:  2002        PMID: 11849443     DOI: 10.1046/j.1523-1755.2002.00188.x

Source DB:  PubMed          Journal:  Kidney Int        ISSN: 0085-2538            Impact factor:   10.612


  79 in total

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

Authors:  Asaf Vivante; Marc-Jens Kleppa; Julian Schulz; Stefan Kohl; Amita Sharma; Jing Chen; Shirlee Shril; Daw-Yang Hwang; Anna-Carina Weiss; Michael M Kaminski; Rachel Shukrun; Markus J Kemper; Anja Lehnhardt; Rolf Beetz; Simone Sanna-Cherchi; Miguel Verbitsky; Ali G Gharavi; Helen M Stuart; Sally A Feather; Judith A Goodship; Timothy H J Goodship; Adrian S Woolf; Sjirk J Westra; Daniel P Doody; Stuart B Bauer; Richard S Lee; Rosalyn M Adam; Weining Lu; Heiko M Reutter; Elijah O Kehinde; Erika J Mancini; Richard P Lifton; Velibor Tasic; Soeren S Lienkamp; Harald Jüppner; Andreas Kispert; Friedhelm Hildebrandt
Journal:  Am J Hum Genet       Date:  2015-07-30       Impact factor: 11.025

2.  Familial multicystic dysplastic kidney.

Authors:  Toru Watanabe; Akira Yamazaki; Takumi Kurabayashi; Jin-ichi Hanaoka
Journal:  Pediatr Nephrol       Date:  2005-05-24       Impact factor: 3.714

Review 3.  MR urography in children.

Authors:  J Damien Grattan-Smith; Richard A Jones
Journal:  Pediatr Radiol       Date:  2006-06-22

4.  A genome-wide scan for genes involved in primary vesicoureteric reflux.

Authors:  H Kelly; C M Molony; J M Darlow; M E Pirker; A Yoneda; A J Green; P Puri; D E Barton
Journal:  J Med Genet       Date:  2007-07-27       Impact factor: 6.318

Review 5.  Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans.

Authors:  Asaf Vivante; Stefan Kohl; Daw-Yang Hwang; Gabriel C Dworschak; Friedhelm Hildebrandt
Journal:  Pediatr Nephrol       Date:  2014-01-08       Impact factor: 3.714

6.  Targeted sequencing of 96 renal developmental microRNAs in 1213 individuals from 980 families with congenital anomalies of the kidney and urinary tract.

Authors:  Stefan Kohl; Jing Chen; Asaf Vivante; Daw-Yang Hwang; Shirlee Shril; Gabriel C Dworschak; Amelie Van Der Ven; Simone Sanna-Cherchi; Stuart B Bauer; Richard S Lee; Neveen A Soliman; Elijah O Kehinde; Heiko M Reutter; Velibor Tasic; Friedhelm Hildebrandt
Journal:  Nephrol Dial Transplant       Date:  2016-01-29       Impact factor: 5.992

Review 7.  Genetics of vesicoureteral reflux.

Authors:  Prem Puri; Jan-Hendrik Gosemann; John Darlow; David E Barton
Journal:  Nat Rev Urol       Date:  2011-08-23       Impact factor: 14.432

8.  Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.

Authors:  Amelie T van der Ven; Dervla M Connaughton; Hadas Ityel; Nina Mann; Makiko Nakayama; Jing Chen; Asaf Vivante; Daw-Yang Hwang; Julian Schulz; Daniela A Braun; Johanna Magdalena Schmidt; David Schapiro; Ronen Schneider; Jillian K Warejko; Ankana Daga; Amar J Majmundar; Weizhen Tan; Tilman Jobst-Schwan; Tobias Hermle; Eugen Widmeier; Shazia Ashraf; Ali Amar; Charlotte A Hoogstraaten; Hannah Hugo; Thomas M Kitzler; Franziska Kause; Caroline M Kolvenbach; Rufeng Dai; Leslie Spaneas; Kassaundra Amann; Deborah R Stein; Michelle A Baum; Michael J G Somers; Nancy M Rodig; Michael A Ferguson; Avram Z Traum; Ghaleb H Daouk; Radovan Bogdanović; Natasa Stajić; Neveen A Soliman; Jameela A Kari; Sherif El Desoky; Hanan M Fathy; Danko Milosevic; Muna Al-Saffar; Hazem S Awad; Loai A Eid; Aravind Selvin; Prabha Senguttuvan; Simone Sanna-Cherchi; Heidi L Rehm; Daniel G MacArthur; Monkol Lek; Kristen M Laricchia; Michael W Wilson; Shrikant M Mane; Richard P Lifton; Richard S Lee; Stuart B Bauer; Weining Lu; Heiko M Reutter; Velibor Tasic; Shirlee Shril; Friedhelm Hildebrandt
Journal:  J Am Soc Nephrol       Date:  2018-08-24       Impact factor: 10.121

9.  Whole-exome sequencing identifies mutations of TBC1D1 encoding a Rab-GTPase-activating protein in patients with congenital anomalies of the kidneys and urinary tract (CAKUT).

Authors:  Anne Kosfeld; Martin Kreuzer; Christoph Daniel; Frank Brand; Anne-Kathrin Schäfer; Alexandra Chadt; Anna-Carina Weiss; Vera Riehmer; Cécile Jeanpierre; Michael Klintschar; Jan Hinrich Bräsen; Kerstin Amann; Lars Pape; Andreas Kispert; Hadi Al-Hasani; Dieter Haffner; Ruthild G Weber
Journal:  Hum Genet       Date:  2015-11-16       Impact factor: 4.132

10.  Kidney development in the absence of Gdnf and Spry1 requires Fgf10.

Authors:  Odyssé Michos; Cristina Cebrian; Deborah Hyink; Uta Grieshammer; Linda Williams; Vivette D'Agati; Jonathan D Licht; Gail R Martin; Frank Costantini
Journal:  PLoS Genet       Date:  2010-01-15       Impact factor: 5.917

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