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Analysis of CLCNKB mutations at dimer-interface, calcium-binding site, and pore reveals a variety of functional alterations in ClC-Kb channel leading to Bartter syndrome. [electronic resource] by
- Bignon, Yohan
- Sakhi, Imene
- Bitam, Sara
- Bakouh, Naziha
- Keck, Mathilde
- Frachon, Nadia
- Paulais, Marc
- Planelles, Gabrielle
- Teulon, Jacques
- Andrini, Olga
Producer: 20210722
In:
Human mutation vol. 41
Availability: No items available.
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In silico model of the human ClC-Kb chloride channel: pore mapping, biostructural pathology and drug screening. [electronic resource] by
- Louet, Maxime
- Bitam, Sara
- Bakouh, Naziha
- Bignon, Yohan
- Planelles, Gabrielle
- Lagorce, David
- Miteva, Maria A
- Eladari, Dominique
- Teulon, Jacques
- Villoutreix, Bruno O
Producer: 20190218
In:
Scientific reports vol. 7
Availability: No items available.
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The ClC-K2 Chloride Channel Is Critical for Salt Handling in the Distal Nephron. [electronic resource] by
- Hennings, J Christopher
- Andrini, Olga
- Picard, Nicolas
- Paulais, Marc
- Huebner, Antje K
- Cayuqueo, Irma Karen Lopez
- Bignon, Yohan
- Keck, Mathilde
- Cornière, Nicolas
- Böhm, David
- Jentsch, Thomas J
- Chambrey, Régine
- Teulon, Jacques
- Hübner, Christian A
- Eladari, Dominique
Producer: 20170602
In:
Journal of the American Society of Nephrology : JASN vol. 28
Availability: No items available.
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