Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Michèle Lonergan"'
Autor:
Alexandre Leduc-Nadeau, Daniel G. Bichet, Jean-Yves Lapointe, Michèle Lonergan, Anatoly Tiulpakov, Yoann Lussier, Rafael Bedoya Perez, Marie-Françoise Arthus, Cécile Guyon, Pierre Bissonnette
Publikováno v:
American Journal of Physiology-Renal Physiology. 297:F489-F498
Aquaporin-2 (AQP2) is a water channel responsible for the final water reabsorption in renal collecting ducts. Alterations in AQP2 function induce nephrogenic diabetes insipidus (NDI), a condition characterized by severe polyuria and polydipsia. Three
Autor:
Daniel G. Bichet, Pascale Bardoux, Marie-Françoise Arthus, Michel Marre, Lise Bankir, Michèle Lonergan, Hélène Martin, Yves Gallois, Nicole Ruel, Nadine Bouby
Publikováno v:
Nephrology Dialysis Transplantation. 18:497-506
Background. An increase in urinary albumin excretion (UAE) represents an early predictor of glomerular damage in diabetes mellitus (DM) and a risk factor for cardiovascular complications in hypertension. Vasopressin is elevated in DM and in some form
Autor:
Nannette Marr, Fabrizio De Mattia, Nine V A M Knoers, Michèle Lonergan, T. Mary Fujiwara, Paul J.M. Savelkoul, Dominik N. Müller, Alexander Oksche, William J Balfe, Marie-Françoise Arthus, Irene B.M. Konings, Carel H. van Os, Michael P. J. Graat, Walter Rosenthal, Daniel Landau, Susan Hoefs, Peter M.T. Deen, Daniel G. Bichet
Publikováno v:
Journal of the American Society of Nephrology. 13:2267-2277
Mutations in the Aquaporin-2 gene, which encodes a renal water channel, have been shown to cause autosomal nephrogenic diabetes insipidus (NDI), a disease in which the kidney is unable to concentrate urine in response to vasopressin. Most AQP2 missen
Autor:
Daniel G. Bichet, Michèle Lonergan, Shih-Hua Lin, Michio Kuwahara, Sei Sasaki, Marie Françoise Arthus, Yuh Feng Lin
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 87:2694-2700
Mutations in the aquaporin-2 gene (AQP2), encoding the vasopressin-regulated water channel of the renal collecting duct, are responsible for the autosomal recessive or dominant forms of congenital nephrogenic diabetes insipidus. We describe two new f
Autor:
Yoshio Terada, Yuriko Katsushima, Daniel G. Bichet, Marie-Françoise Arthus, Michio Kuwahara, Michèle Lonergan, Toru Ooeda, Itsuki Shinbo, Eishin Ogawa, Sei Sasaki, Fumiaki Marumo, Shinichi Uchida, Kazuyuki Iwai, T. Mary Fujiwara, Takashi Igarashi
Publikováno v:
The American Journal of Human Genetics. 69:738-748
The vasopressin-regulated water channel aquaporin-2 (AQP2) is known to tetramerize in the apical membrane of the renal tubular cells and contributes to urine concentration. We identified three novel mutations, each in a single allele of exon 4 of the
Autor:
André Laperrière, Ulla E. Petäjä-Repo, Ivan R. Nabi, Daniel G. Bichet, Ali Salahpour, Jean-Pierre Morello, Michel Bouvier, Marie-Françoise Arthus, Michèle Lonergan
Publikováno v:
Biochemistry. 40:6766-6775
Over 155 mutations within the V2 vasopressin receptor (AVPR2) gene are responsible for nephrogenic diabetes insipidus (NDI). The expression and subcellular distribution of four of these was investigated in transfected cells. These include a point mut
Autor:
Marie-Françoise Arthus, Pierre Bissonnette, Yoann Lussier, Jessica Matar, Michèle Lonergan, Daniel G. Bichet, Abdulah El Tarazi, Detlef Bockenhauer
Publikováno v:
Clinical Kidney Journal
It is clinically useful to distinguish between two types of hereditary nephrogenic diabetes insipidus (NDI): a ‘pure’ type characterized by loss of water only and a complex type characterized by loss of water and ions. Patients with congenital ND
Autor:
Alexandre Leduc-Nadeau, Pierre Bissonnette, Marie-Françoise Arthus, Daniel G. Bichet, Eva Riveira-Munoz, Olivier Devuyst, Alejandro Martinez-Aguayo, Michèle Lonergan, Yoann Lussier
Aquaporin-2 (AQP2), located at the luminal side of the collecting duct principal cells, is a water channel responsible for the final concentration of urine. Lack of function, often occurring through mistargeting of mutated proteins, induces nephrogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a5a871cf67ba0290fcda8b243224512
https://europepmc.org/articles/PMC2911221/
https://europepmc.org/articles/PMC2911221/
Autor:
M. Monteagudo, Norishi Ueda, Kazuyoshi Watanabe, Aureliano Rocchi, J.V. Barbas, Giuseppe Curatola, Quirino Maggiore, Sojiro Ogino, Miiko Fujisawa, Fumiaki Marumo, Andrea Buscaroli, C. Bru, H. Nohno, C. Ronco, Yutaka Furumitsu, N. Koçak, Dino Docci, Eyal Raz, Salim K. Mujais, P. Conz, Takashi Inoue, Laura Gurioli, K. Nakatsuka, J. Lima, Sisca S, Nicole Ruel, A. Torras, Hideo Nakagawa, Stanley Nahman, H. Kawakami, E. Vilella, J.M. Simó, F. Marumo, G. Buccianti, Tsutomu Tabata, Y.E. Sönmez, P.A. Bevilacqua, Maria Giovanna Cirolla, Anna Cadario, J. Camps, Mikio Okamura, K. Jojima, Daniel G. Bichet, Dos Santos, Mayer Brezis, Alfonso Pacitti, Michèle Lonergan, Yusuke Tsukamoto, G. Valenti, Bruno Balbi, Kazuo Kumano, Zbigniew W. Hruby, Radwan al-Kiek, Marco Forni, Fumitake Gejyo, Sandra McEachrane, Takashi Morita, Carlo Feletti, Naftali Kaminski, S. Cantaro, Richard Dicker, Audrey V. Cybulsky, L. Masana, Earl Nielsen, L. Revert, E. Ponz, H. Iwamoto, Renzo Bilancioni, M.I. Sonnekus, Shigemi Kinoshita, Mhd Zaher Sahloul, Bahrain Azadeh, L. Bonfante, C. Villabona, Yuichiro Maruyama, Masaaki Arakawa, F. Garcia-Bragado, H. Itoh, P.R. Turner, A.E. Smyth, Jun Fujita, M. Vilardell, Saleh H. Abu-Romeh, H. Matsuzaki, Hiroyuki Shimada, Michele Portigliatti, Atsuko Morita, Yoshiharu Kanayama, Noriyuki Honma, M. Feriani, L. Calò, E.N. Wardle, Takami Miki, J. Joven, Takatoshi Inoue, Shinichi Nishi, Tadanao Takeda, Eros Malara, Massimiliano Bianchi, Hiromi Inariba, Carlo Viglino, Carmine Zoccali, Leopoldo Baldrati, S. Meli, Fernando G. Cosio, Maurizio Postorino, M. Valles, R. Dell’Aquila, Sebastiano Cutrupi, A.M. Meyers, G. Pietribiasi, Osamu Ishida, M.M. Praia, F.T. Sousa, M.Ş. Sever, M. Shichiri, Yoshiki Nishizawa, Masanori Emoto, G. La Greca, Silvia Mengozzi, Shigeru Iwanami, D. Cresseri, A. Piccoli, Marie-Françoise Arthus, Satoshi Saka, Rosa Giordano, Giuseppe Enia, A. Brendolan, M. Lorenz, García García, Hirotoshi Morii, Caterina Canavese, Y. Hirata, Robin P. Lowry, Fausto Turci, N.A. Laminski, Claudio Capponcini, Sergio Costantini, Vivette D. D'Agati, Nobuo Negoro, S. Favaro, M. Carrera, A. Borsatti, Peter Ivanovich, T. Murakami, J.M. Campistol, Awad Rashed
Publikováno v:
Nephron. 56:I-VI
Autor:
Virginie Bernier, Michèle Lonergan, Daniel G. Bichet, Michel Bouvier, Marie-Françoise Arthus, Monique Lagacé
Publikováno v:
Molecular endocrinology (Baltimore, Md.). 18(8)
In most cases, nephrogenic diabetes insipidus results from mutations in the V2 vasopressin receptor (V2R) gene that cause intracellular retention of improperly folded receptors. We previously reported that cell permeable V2R antagonists act as pharma