Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Emma N. Hilton"'
Autor:
Eamon Dubaissi, Emma N. Hilton, Sarah Lilley, Richard Collins, Charlotte Holt, Peter March, Henry Danahay, Martin Gosling, Richard K Grencis, Ian S Roberts, David J Thornton
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-16 (2024)
Abstract The TMEM16A chloride channel is proposed as a therapeutic target in cystic fibrosis, where activation of this ion channel might restore airway surface hydration and mitigate respiratory symptoms. While TMEM16A is associated with increased mu
Externí odkaz:
https://doaj.org/article/862848294a45463c8ad8b0615eb98903
Autor:
Emad A. Hindi, Craig J. Williams, Leo A. H. Zeef, Filipa M. Lopes, Katie Newman, Martha M. M. Davey, Nigel W. Hodson, Emma N. Hilton, Jennifer L. Huang, Karen L. Price, Neil A. Roberts, David A. Long, Adrian S. Woolf, Natalie J. Gardiner
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-16 (2021)
Abstract Diabetes mellitus (DM) is the leading cause of chronic kidney disease and diabetic nephropathy is widely studied. In contrast, the pathobiology of diabetic urinary bladder disease is less understood despite dysfunctional voiding being common
Externí odkaz:
https://doaj.org/article/3d05190d673047aca307800a35df1323
Publikováno v:
Kidney International
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=r3c4b2081b22::913bd585a6d963910cb1900d03d860d6
From gene discovery to new biological mechanisms: heparanases and congenital urinary bladder disease
Publikováno v:
Nephrology Dialysis Transplantation
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 b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5f6d9cd0d084168079b0536efeba122c
https://pubmed.ncbi.nlm.nih.gov/26315301
https://pubmed.ncbi.nlm.nih.gov/26315301