Ion Transport and Channel Regulation

TopicLeading institutions, researchers & key papers

This cluster of papers explores the molecular mechanisms, physiological roles, and pathophysiological implications of aquaporins, a family of water channel proteins involved in ion transport across cell membranes. The research covers various aspects such as brain edema, kidney function, regulation, and the role of aquaporins in disease.

226

Works

IDs:OpenAlex

How has Ion Transport and Channel Regulation's publication output changed over time?

ScholarIQpublication output · 1996–2016

Output grew0% over the shown period — from 1 works in 1996 to 1 in 2016.

1996199719982000200120022007200920122016

What are the most-cited papers on Ion Transport and Channel Regulation?

ScholarIQmost cited works

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III

David B. Simon, Ranjit S. Bindra, Traci A. Mansfield, Carol Nelson‐Williams, Érica Mendonça, Rosário Stone, Scott J. Schurman, Ahmet Nayır, Harika Alpay, A Bakkaloğlu, Juan Rodríguez‐Soriano, José Manuel Morales, Sami A. Sanjad, Carol M. Taylor, Daniela T. Pilz, Andrew S. Brem, Howard Trachtman, William R. Griswold, George A. Richard, Eunice John, Richard P. Lifton

S137905309. 1997870 Citations

Genetic heterogeneity of Barter's syndrome revealed by mutations in the K+ channel, ROMK

David B. Simon, Fiona E. Karet, Juan Rodríguez‐Soriano, Jahed Hamdan, Antonio DiPietro, Howard Trachtman, Sami A. Sanjad, Richard P. Lifton

S137905309. 1996827 Citations

Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities

Lynn M. Boyden, Murim Choi, Keith A. Choate, Carol Nelson‐Williams, Anita Farhi, Hakan R. Toka, Irina R. Tikhonova, Robert Bjornson, Shrikant Mane, Giacomo Colussi, Marcel Lebel, Richard D. Gordon, Ben A. Semmekrot, A. Poujol, Matti Välimäki, Maria Elisabetta De Ferrari, Sami A. Sanjad, Michael Gutkin, Fiona E. Karet, Joseph Tucci, Jim Stockigt, Kim M. Keppler‐Noreuil, Craig Porter, Sudhir Anand, Margo L. Whiteford, Ira D. Davis, Stephanie Dewar, Alberto Bettinelli, Jeffrey J. Fadrowski, Craig W. Belsha, Tracy E. Hunley, Raoul D. Nelson, Howard Trachtman, Trevor Cole, Maury Pinsk, Detlef Böckenhauer, Mohan Shenoy, Priya Vaidyanathan, John W. Foreman, Majid Rasoulpour, Farook Thameem, Hania Z. Al-Shahrouri, Jai Radhakrishnan, Ali G. Gharavi, Béatrice Goilav, Richard P. Lifton

Nature. 2012638 Citations

Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, and <i>KCNJ10</i> Mutations

Detlef Böckenhauer, Sally Feather, Horia Stanescu, Sascha Bandulik, Anselm A. Zdebik, Markus Reichold, Jonathan L. Tobin, Evelyn Lieberer, Christina Sterner, Guida Landouré, Ruchi Arora, Tony Sirimanna, Dorothy Thompson, J. Helen Cross, William van’t Hoff, Omar Masri, Kjell Tullus, Stella Yeung, Yair Anikster, Enriko Klootwijk, Michael Hubank, Michael J. Dillon, Dirk Heitzmann, Mauricio Arcos‐Burgos, Mark A. Knepper, Angus Dobbie, William A. Gahl, Richard Warth, Eamonn Sheridan, Robert Kleta

New England Journal of Medicine. 2009585 CitationsOPEN ACCESS

Pharmacological chaperones rescue cell-surface expression and function of misfolded V2 vasopressin receptor mutants

Jean-Pierre Morello, Ali Salahpour, André Laperrière, Virginie Bernier, Marie‐Françoise Arthus, Michèle Lonergan, Ulla E. Petäjä‐Repo, Stéphane Angers, Denis Morin, Daniel G. Bichet, Michel Bouvier

S114430552. 2000564 CitationsOPEN ACCESS