Literature DB >> 17928823

Down the tube of obstructive nephropathies: the importance of tissue interactions during ureter development.

R Airik1, A Kispert.   

Abstract

Congenital obstructive malformations of the ureter are amongst the most common human birth defects. To date, the etiology of these diseases has remained largely unexplored, which has preempted any rational approach for therapeutic intervention. Here, we describe that obstructive ureter defects can arise from genetic insults affecting various subprograms of ureter development including formation and patterning of the ureteric bud, differentiation of tissue compartments of the ureter, and junction formation with the bladder and pelvis. New experimental findings have highlighted the importance of epithelial-mesenchymal tissue interactions in all of these subprograms and provided unique insights into the molecular nature of the transcriptional regulators and signaling pathways involved.

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Year:  2007        PMID: 17928823     DOI: 10.1038/sj.ki.5002589

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


  30 in total

1.  The transcription factors Etv4 and Etv5 mediate formation of the ureteric bud tip domain during kidney development.

Authors:  Satu Kuure; Xuan Chi; Benson Lu; Frank Costantini
Journal:  Development       Date:  2010-05-12       Impact factor: 6.868

2.  3-Dimensional morphometric analysis of murine bladder development and dysmorphogenesis.

Authors:  Ashley Carpenter; Andrew Paulus; Melissa Robinson; Carlton M Bates; Michael L Robinson; David Hains; David Kline; Kirk M McHugh
Journal:  Dev Dyn       Date:  2012-01-31       Impact factor: 3.780

3.  Six1 regulates Grem1 expression in the metanephric mesenchyme to initiate branching morphogenesis.

Authors:  Xuguang Nie; Jinshu Xu; Ahmed El-Hashash; Pin-Xian Xu
Journal:  Dev Biol       Date:  2011-01-31       Impact factor: 3.582

4.  Developmental Programming of Branching Morphogenesis in the Kidney.

Authors:  Rosemary V Sampogna; Laura Schneider; Qais Al-Awqati
Journal:  J Am Soc Nephrol       Date:  2015-02-02       Impact factor: 10.121

5.  Using mouse models to understand normal and abnormal urogenital tract development.

Authors:  Cathy Mendelsohn
Journal:  Organogenesis       Date:  2009-01       Impact factor: 2.500

6.  Reciprocal Spatiotemporally Controlled Apoptosis Regulates Wolffian Duct Cloaca Fusion.

Authors:  Masato Hoshi; Antoine Reginensi; Matthew S Joens; James A J Fitzpatrick; Helen McNeill; Sanjay Jain
Journal:  J Am Soc Nephrol       Date:  2018-01-11       Impact factor: 10.121

7.  Copy-number variation associated with congenital anomalies of the kidney and urinary tract.

Authors:  Georgina Caruana; Milagros N Wong; Amanda Walker; Yves Heloury; Nathalie Webb; Lilian Johnstone; Paul A James; Trent Burgess; John F Bertram
Journal:  Pediatr Nephrol       Date:  2014-10-01       Impact factor: 3.714

8.  Conditional loss of kidney microRNAs results in congenital anomalies of the kidney and urinary tract (CAKUT).

Authors:  Malte P Bartram; Martin Höhne; Claudia Dafinger; Linus A Völker; Marc Albersmeyer; Julia Heiss; Heike Göbel; Hella Brönneke; Volker Burst; Max C Liebau; Thomas Benzing; Bernhard Schermer; Roman-Ulrich Müller
Journal:  J Mol Med (Berl)       Date:  2013-01-24       Impact factor: 4.599

Review 9.  Mechanisms of renal injury and progression of renal disease in congenital obstructive nephropathy.

Authors:  Robert L Chevalier; Barbara A Thornhill; Michael S Forbes; Susan C Kiley
Journal:  Pediatr Nephrol       Date:  2009-10-21       Impact factor: 3.714

10.  Histochemical analysis of renal dysplasia with ureteral atresia.

Authors:  Toyoko Kawate; Ryuki Kawamura; Takenori Uchida; Kyosuke Takahashi; Tomohiro Hasegawa; Haruo Futamata; Ryohei Katoh; Sen Takeda
Journal:  Acta Histochem Cytochem       Date:  2009-04-25       Impact factor: 1.938

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