Pharmacological chaperone action on G-protein-coupled receptors
Bernier, Virginie, Bichet, Daniel G, Bouvier, Michel
Published in Current opinion in pharmacology (01.10.2004)
Published in Current opinion in pharmacology (01.10.2004)
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Molecular biology of hereditary diabetes insipidus
FUJIWARA, T. Mary, BICHET, Daniel G
Published in Journal of the American Society of Nephrology (01.10.2005)
Published in Journal of the American Society of Nephrology (01.10.2005)
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Pharmacological chaperones: potential treatment for conformational diseases
Bernier, Virginie, Lagacé, Monique, Bichet, Daniel G, Bouvier, Michel
Published in Trends in endocrinology and metabolism (01.07.2004)
Published in Trends in endocrinology and metabolism (01.07.2004)
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Pharmacological chaperones rescue cell-surface expression and function of misfolded V2 vasopressin receptor mutants
Morello, J P, Salahpour, A, Laperrière, A, Bernier, V, Arthus, M F, Lonergan, M, Petäjä-Repo, U, Angers, S, Morin, D, Bichet, D G, Bouvier, M
Published in The Journal of clinical investigation (01.04.2000)
Published in The Journal of clinical investigation (01.04.2000)
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Pharmacological chaperones: a new twist on receptor folding
Morello, Jean-Pierre, Bouvier, Michel, Petäjä-Repo, Ulla E., Bichet, Daniel G.
Published in Trends in pharmacological sciences (Regular ed.) (01.12.2000)
Published in Trends in pharmacological sciences (Regular ed.) (01.12.2000)
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Functional Rescue of the Constitutively Internalized V2 Vasopressin Receptor Mutant R137H by the Pharmacological Chaperone Action of SR49059
Bernier, Virginie, Lagacé, Monique, Lonergan, Michèle, Arthus, Marie-Françoise, Bichet, Daniel G, Bouvier, Michel
Published in Molecular endocrinology (Baltimore, Md.) (01.08.2004)
Published in Molecular endocrinology (Baltimore, Md.) (01.08.2004)
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Secondary nephrogenic diabetes insipidus as a complication of inherited renal diseases
Bockenhauer, D, van't Hoff, W, Dattani, M, Lehnhardt, A, Subtirelu, M, Hildebrandt, F, Bichet, D G
Published in Nephron (01.01.2010)
Published in Nephron (01.01.2010)
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Reversed Polarized Delivery of an Aquaporin-2 Mutant Causes Dominant Nephrogenic Diabetes Insipidus
Kamsteeg, Erik-Jan, Bichet, Daniel G., Irene B. M. Konings, Nivet, Hubert, Lonergan, Michelle, Arthus, Marie-Françoise, van Os, Carel H., Peter M. T. Deen
Published in The Journal of cell biology (08.12.2003)
Published in The Journal of cell biology (08.12.2003)
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Hyponatremia in cirrhosis: From pathogenesis to treatment
Ginés, Pere, Berl, Tomas, Bernardi, Mauro, Bichet, Daniel G., Hamon, Guilles, Jiménez, Wladimiro, Liard, Jean‐François, Martin, Pierre‐Yves, Schrier, Robert W.
Published in Hepatology (Baltimore, Md.) (01.09.1998)
Published in Hepatology (Baltimore, Md.) (01.09.1998)
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Heteroligomerization of an Aquaporin-2 mutant with wild-type Aquaporin-2 and their misrouting to late endosomes/lysosomes explains dominant nephrogenic diabetes insipidus
Marr, Nannette, Bichet, Daniel G, Lonergan, Michele, Arthus, Marie-Francoise, Jeck, Nikola, Seyberth, Hannsjörg W., Rosenthal, Walter, van Os, Carel H., Oksche, Alexander, Deen, Peter M. T.
Published in Human molecular genetics (01.04.2002)
Published in Human molecular genetics (01.04.2002)
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Three Families with Autosomal Dominant Nephrogenic Diabetes Insipidus Caused by Aquaporin-2 Mutations in the C-Terminus
Kuwahara, Michio, Iwai, Kazuyuki, Ooeda, Toru, Igarashi, Takashi, Ogawa, Eishin, Katsushima, Yuriko, Shinbo, Itsuki, Uchida, Shinichi, Terada, Yoshio, Arthus, Marie-Francoise, Lonergan, Michele, Fujiwara, T. Mary, Bichet, Daniel G., Marumo, Fumiaki, Sasaki, Sei
Published in American journal of human genetics (01.10.2001)
Published in American journal of human genetics (01.10.2001)
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Journal Article
An aquaporin-2 water channel mutant which causes autosomal dominant nephrogenic diabetes insipidus is retained in the Golgi complex
Mulders, S M, Bichet, D G, Rijss, J P, Kamsteeg, E J, Arthus, M F, Lonergan, M, Fujiwara, M, Morgan, K, Leijendekker, R, van der Sluijs, P, van Os, C H, Deen, P M
Published in The Journal of clinical investigation (01.07.1998)
Published in The Journal of clinical investigation (01.07.1998)
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Cell-biologic and functional analyses of five new Aquaporin-2 missense mutations that cause recessive nephrogenic diabetes insipidus
MARR, Nannette, BICHET, Daniel G, KNOERS, Nine V. A. M, LANDAU, Daniel, BALFE, William J, OKSCHE, Alexander, ROSENTHAL, Walter, MÜLLER, Dominik, VAN OS, Carel H, DEEN, Peter M. T, HOEFS, Susan, SAVELKOUL, Paul J. M, KONINGS, Irene B. M, DE MATTIA, Fabrizio, GRAAT, Michael P. J, ARTHUS, Marie-Francoise, LONERGAN, Michele, FUJIWARA, T. Mary
Published in Journal of the American Society of Nephrology (01.09.2002)
Published in Journal of the American Society of Nephrology (01.09.2002)
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Journal Article
Urinary Excretion of Aquaporin-2 in Patients with Diabetes Insipidus
Kanno, Kazuo, Sasaki, Sei, Hirata, Yukio, Ishikawa, San-e, Fushimi, Kiyohide, Nakanishi, Setsuko, Bichet, Daniel G, Marumo, Fumiaki
Published in The New England journal of medicine (08.06.1995)
Published in The New England journal of medicine (08.06.1995)
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Report of 33 novel AVPR2 mutations and analysis of 117 families with X-linked nephrogenic diabetes insipidus
ARTHUS, M.-F, LONERGAN, M, BICHET, D. G, FUJIWARA, T. M, CRUMLEY, M. J, NAUMOVA, A. K, MORIN, D, DE MARCO, L. A, KAPLAN, B. S, ROBERTSON, G. L, SASAKI, S, MORGAN, K
Published in Journal of the American Society of Nephrology (01.06.2000)
Published in Journal of the American Society of Nephrology (01.06.2000)
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