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B

Bandulik, S. and Tauber, P. and Penton, D. and Stindl, J. and Tegtmeier, I. and Sterner, C. and Beuschlein, F. and Reincke, M. and Barnahin, J. and Warth, R. (2014) Functional and pharmacological consequences of adenoma-associated KCNJ5 mutations in adrenocortical cells. WILEY-BLACKWELL, HOBOKEN.

Broeker, C. and Reichold, M. and Klootwijk, E. and Reinders, J. and Assmann, N. and Oefner, P. and Kleta, R. and Warth, R. (2014) Mitochondrial malfunction caused by protein mistargeting. WILEY-BLACKWELL, HOBOKEN.

Q

Quintanova, C. and Afonso, S. and Forst, A. -L. and Konrad, M. and Warth, R. (2016) Heteromeric KCNJ10 and KCNJ16 potassium channels: Functional consequences of the rare KCNJ16 variant p.R35Q. WILEY-BLACKWELL, HOBOKEN.

Quintanova, C. and Sterner, C. and Afonso, S. and Meier, C. and Forst, A. -L. and Warth, R. (2016) Expression and localization of KCNJ16 in various mouse tissues. WILEY-BLACKWELL, HOBOKEN.

S

Schmitt, R. and Wiesner, J. and Christ, C. and Albrecht, A. and Reichold, M. (2016) High-resolution respirometry on proximal tubules from mice. WILEY-BLACKWELL, HOBOKEN.

Stindl, J. and Tauber, P. and Penton, D. and Sterner, C. and Tegtmeier, I. and Beuschlein, F. and Reincke, M. and Williams, T. and Mulatero, P. and Warth, R. and Bandulik, S. (2014) Physiology and pathophysiology of ATPases in aldosterone secretion. WILEY-BLACKWELL, HOBOKEN.

T

Thompson, Dorothy A. and Feather, Sally and Stanescu, Horia C. and Freudenthal, Bernard and Zdebik, Anselm A. and Warth, Richard and Ognjanovic, Milos and Hulton, Sally A. and Wassmer, Evangeline and van't Hoff, William and Russell-Eggitt, Isabelle and Dobbie, Angus and Sheridan, Eamonn and Kleta, Robert and Bockenhauer, Detlef (2011) Altered electroretinograms in patients with KCNJ10 mutations and EAST syndrome. JOURNAL OF PHYSIOLOGY-LONDON, 589 (7). pp. 1681-1689. ISSN 0022-3751, 1469-7793

Tondorf, F. and Ratermann, A. and Scherl, F. and Humberg, E. and Reichold, M. and Bockenhauer, D. and Zdebik, A. and Kleta, R. and Warth, R. (2014) Pathophysiology of the p.A167V Mutation of KCNJ10 in mammalian cells. WILEY-BLACKWELL, HOBOKEN.

W

Warth, R. (2014) Molecular mechanisms of an autosomal dominant form of renal Fanconi syndrome. WILEY-BLACKWELL, HOBOKEN.

Warth, R. (2016) Regulation of aldosterone release by potassium. WILEY-BLACKWELL, HOBOKEN.

Warth, R. and Tauber, P. and Stindl, J. and Bandulik, S. (2014) A difficult task - the regulation of adrenal aldosterone secretion. WILEY-BLACKWELL, HOBOKEN.

Warth, Richard (2015) Defects of plasma membrane proteins: The first step to hyperaldosteronism? WILEY-BLACKWELL, HOBOKEN.