Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Abdulah El Tarazi"'
Autor:
Michael J. Coady, Abdulah El Tarazi, Pierre Bissonnette, Yoann Lussier, René Santer, Daniel G. Bichet, Jean-Yves Lapointe, Joaquim Calado, Christopher Dumayne, Louis J. Sasseville
Publikováno v:
Journal of the American Society of Nephrology. 28:85-93
The renal proximal tubule reabsorbs 90% of the filtered glucose load through the Na+-coupled glucose transporter SGLT2, and specific inhibitors of SGLT2 are now available to patients with diabetes to increase urinary glucose excretion. Using expressi
Publikováno v:
Scientific Reports
Aquaporin-2 (AQP2) is a homotetrameric water channel responsible for the final water reuptake in the kidney. Mutations in the protein induce nephrogenic diabetes insipidus (NDI), which challenges the water balance by producing large urinary volumes.
Autor:
Daniel G. Bichet, Abdulah El Tarazi, Rikard Blunck, Yoann Lussier, Hugo McGuire, Pierre Bissonnette
Publikováno v:
The FASEB Journal. 28
Mutations in Aquaporin-2 (AQP2) induce nephrogenic diabetes insipidus, a water reabsorption defect of the kidney. Using co-immunoprecipitation and functional assays, we have recently shown that (at...
Autor:
Daniel G. Bichet, Michael J. Coady, Pierre Bissonnette, Abdulah El Tarazi, Jean-Yves Lapointe
Publikováno v:
The FASEB Journal. 28
Publikováno v:
The FASEB Journal. 28
Autor:
Marie-Françoise Arthus, Pierre Bissonnette, Yoann Lussier, Jessica Matar, Michèle Lonergan, Daniel G. Bichet, Abdulah El Tarazi, Detlef Bockenhauer
Publikováno v:
Clinical Kidney Journal
It is clinically useful to distinguish between two types of hereditary nephrogenic diabetes insipidus (NDI): a ‘pure’ type characterized by loss of water only and a complex type characterized by loss of water and ions. Patients with congenital ND