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Transformation of renal tubule epithelial cells by simian virus-40 is associated with emergence of Ca2+-insensitive K+ channels and altered mitogenic sensitivity to K+ channel blockers.
Published in:
Journal of Cellular Physiology, 1992, v. 151, n. 1, p. 113, doi. 10.1002/jcp.1041510116
By:
- Teulon, Jacques;
- Ronco, Pierre M.;
- Geniteau-Legendre, Monique;
- Baudouin, Béatrice;
- Estrade, Simone;
- Cassingena, Roland;
- Vandewalle, Alain
Publication type:
Article
Vasopressin-stimulated CFTR Cl− currents are increased in the renal collecting duct cells of a mouse model of Liddle's syndrome.
Published in:
Journal of Physiology, 2005, v. 562, n. 1, p. 271, doi. 10.1113/jphysiol.2004.077933
By:
- Chiz-Tzung Chang;
- Bens, Marcelle;
- Hummler, Edith;
- Boulkroun, Sheerazed;
- Schild, Laurent;
- Teulon, Jacques;
- Rossier, Bernard C.;
- Vandewalle, Alain
Publication type:
Article
An inward rectifier K+ channel at the basolateral membrane of the mouse distal convoluted tubule: similarities with Kir4-Kir5.1 heteromeric channels.
Published in:
Journal of Physiology, 2002, v. 538, n. 2, p. 391, doi. 10.1113/jphysiol.2001.012961
By:
- Lourdel, Stéphane;
- Paulais, Marc;
- Cluzeaud, Françoise;
- Bens, Marcelle;
- Tanemoto, Masayuki;
- Kurachi, Yoshihisa;
- Vandewalle, Alain;
- Teulon, Jacques
Publication type:
Article
A new regulator of the vacuolar H(+)-ATPase in the kidney.
Published in:
2011
By:
- Eladari D;
- Teulon J;
- Eladari, Dominique;
- Teulon, Jacques
Publication type:
journal article
A new regulator of the vacuolar H+-ATPase in the kidney.
Published in:
2011
By:
- Eladari, Dominique;
- Teulon, Jacques
Publication type:
Opinion
Novel CLCN5 mutations in patients with Dent’s disease result in altered ion currents or impaired exchanger processing.
Published in:
Kidney International, 2009, v. 76, n. 9, p. 999, doi. 10.1038/ki.2009.305
By:
- Grand, Teddy;
- Mordasini, David;
- L'Hoste, Sébastien;
- Pennaforte, Thomas;
- Genete, Mathieu;
- Biyeyeme, Marie-Jeanne;
- Vargas-Poussou, Rosa;
- Blanchard, Anne;
- Teulon, Jacques;
- Lourdel, Stéphane
Publication type:
Article
Phosphatidylinositol (4,5)-bisphosphate dynamically regulates the K2P background K+ channel TASK-2.
Published in:
Scientific Reports, 2017, p. 45407, doi. 10.1038/srep45407
By:
- Niemeyer, María Isabel;
- Cid, L. Pablo;
- Paulais, Marc;
- Teulon, Jacques;
- Sepúlveda, Francisco V.
Publication type:
Article
Piezo1-dependent stretch-activated channels are inhibited by Polycystin-2 in renal tubular epithelial cells.
Published in:
EMBO Reports, 2013, v. 14, n. 12, p. 1143, doi. 10.1038/embor.2013.170
By:
- Peyronnet, Rémi;
- Martins, Joana R;
- Duprat, Fabrice;
- Demolombe, Sophie;
- Arhatte, Malika;
- Jodar, Martine;
- Tauc, Michel;
- Duranton, Christophe;
- Paulais, Marc;
- Teulon, Jacques;
- Honoré, Eric;
- Patel, Amanda
Publication type:
Article
CLCNKB mutations causing mild Bartter syndrome profoundly alter the pH and Ca dependence of ClC-Kb channels.
Published in:
Pflügers Archiv: European Journal of Physiology, 2014, v. 466, n. 9, p. 1713, doi. 10.1007/s00424-013-1401-2
By:
- Andrini, Olga;
- Keck, Mathilde;
- L'Hoste, Sébastien;
- Briones, Rodolfo;
- Mansour-Hendili, Lamisse;
- Grand, Teddy;
- Sepúlveda, Francisco;
- Blanchard, Anne;
- Lourdel, Stéphane;
- Vargas-Poussou, Rosa;
- Teulon, Jacques
Publication type:
Article
ClC-5 mutations associated with Dent's disease: a major role of the dimer interface.
Published in:
Pflügers Archiv: European Journal of Physiology, 2012, v. 463, n. 2, p. 247, doi. 10.1007/s00424-011-1052-0
By:
- Lourdel, Stéphane;
- Grand, Teddy;
- Burgos, Johanna;
- González, Wendy;
- Sepúlveda, Francisco;
- Teulon, Jacques
Publication type:
Article
Identification and Functional Expression of a Glutamate- and Avermectin-Gated Chloride Channel from Caligus rogercresseyi, a Southern Hemisphere Sea Louse Affecting Farmed Fish.
Published in:
PLoS Pathogens, 2014, v. 10, n. 9, p. 1, doi. 10.1371/journal.ppat.1004402
By:
- Cornejo, Isabel;
- Andrini, Olga;
- Niemeyer, María Isabel;
- Marabolí, Vanessa;
- González-Nilo, F. Danilo;
- Teulon, Jacques;
- Sepúlveda, Francisco V.;
- Cid, L. Pablo
Publication type:
Article
Vasopressin‐stimulated chloride transport in transimmortalized mouse cell lines derived from the distal convoluted tubule and cortical and inner medullary collecting ducts.
Published in:
Nephrology Dialysis Transplantation, 2001, v. 16, n. 2, p. 238, doi. 10.1093/ndt/16.2.238
By:
- Duong Van Huyen, Jean‐Paul;
- Bens, Marcelle;
- Teulon, Jacques;
- Vandewalle, Alain
Publication type:
Article
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.
Published in:
Human Mutation, 2020, v. 41, n. 4, p. 774, doi. 10.1002/humu.23962
By:
- Bignon, Yohan;
- Sakhi, Imene;
- Bitam, Sara;
- Bakouh, Naziha;
- Keck, Mathilde;
- Frachon, Nadia;
- Paulais, Marc;
- Planelles, Gabrielle;
- Teulon, Jacques;
- Andrini, Olga
Publication type:
Article
Novel CLCNKB Mutations Causing Bartter Syndrome Affect Channel Surface Expression.
Published in:
Human Mutation, 2013, v. 34, n. 9, p. 1269, doi. 10.1002/humu.22361
By:
- Keck, Mathilde;
- Andrini, Olga;
- Lahuna, Olivier;
- Burgos, Johanna;
- Cid, L. Pablo;
- Sepúlveda, Francisco V.;
- L‘Hoste, Sébastien;
- Blanchard, Anne;
- Vargas‐Poussou, Rosa;
- Lourdel, Stéphane;
- Teulon, Jacques
Publication type:
Article
Heterogeneity in the processing of CLCN5 mutants related to Dent disease.
Published in:
Human Mutation, 2011, v. 32, n. 4, p. 476, doi. 10.1002/humu.21467
By:
- Grand, Teddy;
- L'Hoste, Sébastien;
- Mordasini, David;
- Defontaine, Nadia;
- Keck, Mathilde;
- Pennaforte, Thomas;
- Genete, Mathieu;
- Laghmani, Kamel;
- Teulon, Jacques;
- Lourdel, Stéphane
Publication type:
Article
Misprocessing of the CFTR protein leads to mild cystic fibrosis phenotype.
Published in:
Human Mutation, 2005, v. 25, n. 4, p. 360, doi. 10.1002/humu.20156
By:
- Clain, Jérôme;
- Lehmann-Che, Jacqueline;
- Duguépéroux, Ingrid;
- Arous, Nicole;
- Girodon, Emmanuelle;
- Legendre, Marie;
- Goossens, Michel;
- Edelman, Aleksander;
- de Braekeleer, Marc;
- Teulon, Jacques;
- Fanen, Pascale
Publication type:
Article
Acute genetic ablation of pendrin lowers blood pressure in mice.
Published in:
Nephrology Dialysis Transplantation, 2017, v. 32, n. 7, p. 1137, doi. 10.1093/ndt/gfw393
By:
- Trepiccione, Francesco;
- Soukaseum, Christelle;
- Baudrie, Veronique;
- Kumai, Yusuke;
- Teulon, Jacques;
- Villoutreix, Bruno;
- Cornière, Nicolas;
- Wangemann, Philine;
- Griffith, Andrew J.;
- Yoon Byung Choi;
- Hadchouel, Juliette;
- Chambrey, Regine;
- Eladari, Dominique
Publication type:
Article

Found: 17

Transformation of renal tubule epithelial cells by simian virus-40 is associated with emergence of Ca<sup>2+</sup>-insensitive K<sup>+</sup> channels and altered mitogenic sensitivity to K<sup>+</sup> channel blockers.

Vasopressin-stimulated CFTR Cl<sup>−</sup> currents are increased in the renal collecting duct cells of a mouse model of Liddle's syndrome.

An inward rectifier K<sup>+</sup> channel at the basolateral membrane of the mouse distal convoluted tubule: similarities with Kir4-Kir5.1 heteromeric channels.

A new regulator of the vacuolar H(+)-ATPase in the kidney.

A new regulator of the vacuolar H<sup>+</sup>-ATPase in the kidney.

Novel CLCN5 mutations in patients with Dent’s disease result in altered ion currents or impaired exchanger processing.

Phosphatidylinositol (4,5)-bisphosphate dynamically regulates the K<sub>2P</sub> background K<sup>+</sup> channel TASK-2.

Piezo1-dependent stretch-activated channels are inhibited by Polycystin-2 in renal tubular epithelial cells.

CLCNKB mutations causing mild Bartter syndrome profoundly alter the pH and Ca dependence of ClC-Kb channels.

ClC-5 mutations associated with Dent's disease: a major role of the dimer interface.

Identification and Functional Expression of a Glutamate- and Avermectin-Gated Chloride Channel from Caligus rogercresseyi, a Southern Hemisphere Sea Louse Affecting Farmed Fish.

Vasopressin‐stimulated chloride transport in transimmortalized mouse cell lines derived from the distal convoluted tubule and cortical and inner medullary collecting ducts.

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.

Novel CLCNKB Mutations Causing Bartter Syndrome Affect Channel Surface Expression.

Heterogeneity in the processing of CLCN5 mutants related to Dent disease.

Misprocessing of the CFTR protein leads to mild cystic fibrosis phenotype.

Acute genetic ablation of pendrin lowers blood pressure in mice.