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You searched for: Author/Creator Planelles, Gabrielle

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1. 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. Issue 4 (24th December 2019)

2. Characterization of SLC26A9 in Patients with CF‐Like Lung Disease. Issue 10 (13th August 2013)

3. Functional and electrophysiological characterization of four non‐truncating mutations responsible for creatine transporter (SLC6A8) deficiency syndrome. Issue 1 (30th May 2012)

4. Rattlesnake Phospholipase A2 Increases CFTR-Chloride Channel Current and Corrects ∆ F508CFTR Dysfunction: Impact in Cystic Fibrosis. Issue 14 (17th July 2016)