From gene discovery to new biological mechanisms: heparanases and congenital urinary bladder disease

We present a scientific investigation into the pathogenesis of a urinary bladder disease. The disease in question is called urofacial syndrome (UFS), a congenital condition inherited in an autosomal recessive manner. UFS features incomplete urinary bladder emptying and vesicoureteric reflux, with a...

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Detalles Bibliográficos
Autores principales: Roberts, Neil A., Hilton, Emma N., Woolf, Adrian S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Cutting-Edge Renal Science
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4805131/
https://www.ncbi.nlm.nih.gov/pubmed/26315301
http://dx.doi.org/10.1093/ndt/gfv309

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4805131/
https://www.ncbi.nlm.nih.gov/pubmed/26315301
http://dx.doi.org/10.1093/ndt/gfv309

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