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Jacques Teulon

Showing results (31-40 of 39) with videos related to

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EMBO Reports|October 26, 2013
Piezo1-dependent stretch-activated channels are inhibited by Polycystin-2 in renal tubular epithelial cellsRémi Peyronnet, Joana R Martins, Fabrice Duprat, et al.
Human Mutation|May 25, 2013
Novel CLCNKB mutations causing Bartter syndrome affect channel surface expressionMathilde Keck, Olga Andrini, Olivier Lahuna, et al.
Pflugers Archiv : European Journal of Physiology|November 26, 2013
CLCNKB mutations causing mild Bartter syndrome profoundly alter the pH and Ca2+ dependence of ClC-Kb channelsOlga Andrini, Mathilde Keck, Sébastien L'Hoste, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 3, 2011
Renal phenotype in mice lacking the Kir5.1 (Kcnj16) K+ channel subunit contrasts with that observed in SeSAME/EAST syndromeMarc Paulais, May Bloch-Faure, Nicolas Picard, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 9, 2017
Acute genetic ablation of pendrin lowers blood pressure in miceFrancesco Trepiccione, Christelle Soukaseum, Veronique Baudrie, et al.
The Journal of Biological Chemistry|August 30, 2013
Mutations in SLC2A2 gene reveal hGLUT2 function in pancreatic β cell developmentAurélien Michau, Ghislaine Guillemain, Alexandra Grosfeld, et al.
Journal of the American Society of Nephrology : JASN|June 24, 2016
The ClC-K2 Chloride Channel Is Critical for Salt Handling in the Distal NephronJ Christopher Hennings, Olga Andrini, Nicolas Picard, et al.
Journal of Molecular Biology|June 1, 2016
Rattlesnake Phospholipase A2 Increases CFTR-Chloride Channel Current and Corrects ∆F508CFTR Dysfunction: Impact in Cystic FibrosisGrazyna Faure, Naziha Bakouh, Stéphane Lourdel, et al.
Journal of the American Society of Nephrology : JASN|April 7, 2017
Clinical and Genetic Spectrum of Bartter Syndrome Type 3Elsa Seys, Olga Andrini, Mathilde Keck, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
EMBO Reports|October 26, 2013
Piezo1-dependent stretch-activated channels are inhibited by Polycystin-2 in renal tubular epithelial cellsRémi Peyronnet, Joana R Martins, Fabrice Duprat, et al.
Human Mutation|May 25, 2013
Novel CLCNKB mutations causing Bartter syndrome affect channel surface expressionMathilde Keck, Olga Andrini, Olivier Lahuna, et al.
Pflugers Archiv : European Journal of Physiology|November 26, 2013
CLCNKB mutations causing mild Bartter syndrome profoundly alter the pH and Ca2+ dependence of ClC-Kb channelsOlga Andrini, Mathilde Keck, Sébastien L'Hoste, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 3, 2011
Renal phenotype in mice lacking the Kir5.1 (Kcnj16) K+ channel subunit contrasts with that observed in SeSAME/EAST syndromeMarc Paulais, May Bloch-Faure, Nicolas Picard, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 9, 2017
Acute genetic ablation of pendrin lowers blood pressure in miceFrancesco Trepiccione, Christelle Soukaseum, Veronique Baudrie, et al.
The Journal of Biological Chemistry|August 30, 2013
Mutations in SLC2A2 gene reveal hGLUT2 function in pancreatic β cell developmentAurélien Michau, Ghislaine Guillemain, Alexandra Grosfeld, et al.
Journal of the American Society of Nephrology : JASN|June 24, 2016
The ClC-K2 Chloride Channel Is Critical for Salt Handling in the Distal NephronJ Christopher Hennings, Olga Andrini, Nicolas Picard, et al.
Journal of Molecular Biology|June 1, 2016
Rattlesnake Phospholipase A2 Increases CFTR-Chloride Channel Current and Corrects ∆F508CFTR Dysfunction: Impact in Cystic FibrosisGrazyna Faure, Naziha Bakouh, Stéphane Lourdel, et al.
Journal of the American Society of Nephrology : JASN|April 7, 2017
Clinical and Genetic Spectrum of Bartter Syndrome Type 3Elsa Seys, Olga Andrini, Mathilde Keck, et al.
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