Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Celine Grenier"'
Autor:
Filipa M Lopes, Celine Grenier, Benjamin W Jarvis, Sara Al Mahdy, Adrian Lène-McKay, Alison M Gurney, William G Newman, Simon N Waddington, Adrian S Woolf, Neil A Roberts
Publikováno v:
eLife, Vol 13 (2024)
Rare early-onset lower urinary tract disorders include defects of functional maturation of the bladder. Current treatments do not target the primary pathobiology of these diseases. Some have a monogenic basis, such as urofacial, or Ochoa, syndrome (U
Externí odkaz:
https://doaj.org/article/c7e0ce9ab0724cbca7d1f7f2cbe62eae
Autor:
Celine Grenier, Filipa M. Lopes, Anna M. Cueto-González, Eulàlia Rovira-Moreno, Romy Gander, Benjamin W. Jarvis, Karen D. McCloskey, Alison M. Gurney, Glenda M. Beaman, William G. Newman, Adrian S. Woolf, Neil A. Roberts
Publikováno v:
Kidney International Reports.
Autor:
Celine Grenier, Filipa M. Lopes, Anna M Cueto-González, Eulàlia Rovira-Moreno, Romy Gander, Benjamin W Jarvis, Karen D. McCloskey, Alison M. Gurney, Glenda M. Beaman, William G. Newman, Adrian S. Woolf, Neil A. Roberts
Urinary tract malformations account for half of all children with kidney failure, and some have defined monogenic causes. One such disorder is urofacial, or Ochoa, syndrome (UFS), an autosomal recessive disease featuring a dyssynergic bladder with de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35e49d20332dfbc5e75ea504b3170f62
https://doi.org/10.1101/2022.12.06.22283097
https://doi.org/10.1101/2022.12.06.22283097
Publikováno v:
The FASEB Journal. 36
Autor:
Hannah M Costello, Georgios Krilis, Celine Grenier, David Severs, Alicja Czopek, Jessica R Ivy, Mark Nixon, Megan C Holmes, Dawn E W Livingstone, Ewout J Hoorn, Neeraj Dhaun, Matthew A Bailey
Publikováno v:
Costello, H, Krilis, G, Grenier, C, Severs, D, Czopek, A, Ivy, J R, Nixon, M, Holmes, M C, Livingstone, D E W, Hoorn, E J, Dhaun, N & Bailey, M A 2022, ' High salt intake activates the hypothalamic-pituitary-adrenal axis, amplifies the stress response, and alters tissue glucocorticoid exposure in mice ', Cardiovascular Research . https://doi.org/10.1093/cvr/cvac160
Aims High salt intake is common and contributes to poor cardiovascular health. Urinary sodium excretion correlates directly with glucocorticoid excretion in humans and experimental animals. We hypothesized that high salt intake activates the hypothal
Autor:
Hannah M. Costello, Jessica R. Ivy, Neeraj Dhaun, Celine Grenier, Ailsa F. Ralph, Kevin Stewart, Matthew A. Bailey
Publikováno v:
Hypertension (Dallas, Tex. : 1979)
Supplemental Digital Content is available in the text.
Global salt intake averages >8 g/person per day, over twice the limit advocated by the American Heart Association. Dietary salt excess leads to hypertension, and this partly mediates its poo
Global salt intake averages >8 g/person per day, over twice the limit advocated by the American Heart Association. Dietary salt excess leads to hypertension, and this partly mediates its poo
Autor:
Neeraj Dhaun, Celine Grenier, Ailsa F. Ralph, Matthew A. Bailey, Kevin Stewart, Hannah M. Costello
Publikováno v:
The FASEB Journal. 33
Autor:
Hannah M. Costello, Kevin Stewart, Natalie Jones, Neeraj Dhaun, Dawn E W Livingstone, Matthew A. Bailey, Megan C. Holmes, Celine Grenier
Publikováno v:
Journal of Hypertension. 39:e222
Publikováno v:
Archives of Cardiovascular Diseases Supplements. 8(3)
On vascular endothelium, shear stress produces vasorelaxation and outward arterial remodeling. A chronic increase in blood flow induces arterial diameter expansion (normalizing shear stress), and is associated with a compensatory hypertrophy to norma
Autor:
Phuc Minh Chau Nguyen, Celine Grenier, Eric Lelievre, Linda Grimaud, Emilie Vessieres, Emmanuelle Sarzi, Dominique Bonneau, Pascal Reynier, Celine Fassot, Guy Lenaers, Daniel Henrion, Laurent Loufrani
Publikováno v:
Hypertension. 66
Background: Defects in mitochondrial dynamics have been associated with various disorders, including cardiovascular diseases. OPA1 is essential for mitochondrial inner membrane fusion and mutation in OPA1 is associated with autosomal dominant optic a