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Journal of the American Society of Nephrology : JASN
|
April 12, 2014
A copeptin-based classification of the osmoregulatory defects in the syndrome of inappropriate antidiuresis
Wiebke Kristin Fenske, Mirjam Christ-Crain, Anna Hörning, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 10, 2014
Comparison between copeptin and vasopressin in a population from the community and in people with chronic kidney disease
Ronan Roussel, Léopold Fezeu, Michel Marre, et al.
American Journal of Physiology. Renal Physiology
|
May 22, 2009
Characterization of D150E and G196D aquaporin-2 mutations responsible for nephrogenic diabetes insipidus: importance of a mild phenotype
Cécile Guyon, Yoann Lussier, Pierre Bissonnette, et al.
Physiological Reports
|
June 13, 2021
Further evidence for functional recovery of AQP2 mutations associated with nephrogenic diabetes insipidus
Pierre Bissonnette, Yoann Lussier, Jessica Matar, et al.
The Journal of Cell Biology
|
December 10, 2003
Reversed polarized delivery of an aquaporin-2 mutant causes dominant nephrogenic diabetes insipidus
Erik-Jan Kamsteeg, Daniel G Bichet, Irene B M Konings, et al.
Journal of the American Society of Nephrology : JASN
|
June 12, 2016
MAP17 Is a Necessary Activator of Renal Na+/Glucose Cotransporter SGLT2
Michael J Coady, Abdulah El Tarazi, René Santer, et al.
Journal of the American Society of Nephrology : JASN
|
December 2, 2005
Pharmacologic chaperones as a potential treatment for X-linked nephrogenic diabetes insipidus
Virginie Bernier, Jean-Pierre Morello, Alexandro Zarruk, et al.
Journal of Medical Genetics
|
March 13, 2020
Use of a rare disease registry for establishing phenotypic classification of previously unassigned <i>GLA</i> variants: a consensus classification system by a multispecialty Fabry disease genotype-phenotype workgroup
Dominique P Germain, João Paulo Oliveira, Daniel G Bichet, et al.
Human Molecular Genetics
|
April 4, 2002
Heteroligomerization of an Aquaporin-2 mutant with wild-type Aquaporin-2 and their misrouting to late endosomes/lysosomes explains dominant nephrogenic diabetes insipidus
Nannette Marr, Daniel G Bichet, Michele Lonergan, et al.
Nephron. Physiology
|
December 5, 2012
Response of the renal inner medulla to hypoxia: possible defense mechanisms
Namhee Kim, Laura Voicu, Gregory M T Hare, et al.
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of 15
Search research articles
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Showing results (101-110 of 144) with videos related to
Sort By:
Page
of 15
Journal of the American Society of Nephrology : JASN
|
April 12, 2014
A copeptin-based classification of the osmoregulatory defects in the syndrome of inappropriate antidiuresis
Wiebke Kristin Fenske, Mirjam Christ-Crain, Anna Hörning, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 10, 2014
Comparison between copeptin and vasopressin in a population from the community and in people with chronic kidney disease
Ronan Roussel, Léopold Fezeu, Michel Marre, et al.
American Journal of Physiology. Renal Physiology
|
May 22, 2009
Characterization of D150E and G196D aquaporin-2 mutations responsible for nephrogenic diabetes insipidus: importance of a mild phenotype
Cécile Guyon, Yoann Lussier, Pierre Bissonnette, et al.
Physiological Reports
|
June 13, 2021
Further evidence for functional recovery of AQP2 mutations associated with nephrogenic diabetes insipidus
Pierre Bissonnette, Yoann Lussier, Jessica Matar, et al.
The Journal of Cell Biology
|
December 10, 2003
Reversed polarized delivery of an aquaporin-2 mutant causes dominant nephrogenic diabetes insipidus
Erik-Jan Kamsteeg, Daniel G Bichet, Irene B M Konings, et al.
Journal of the American Society of Nephrology : JASN
|
June 12, 2016
MAP17 Is a Necessary Activator of Renal Na+/Glucose Cotransporter SGLT2
Michael J Coady, Abdulah El Tarazi, René Santer, et al.
Journal of the American Society of Nephrology : JASN
|
December 2, 2005
Pharmacologic chaperones as a potential treatment for X-linked nephrogenic diabetes insipidus
Virginie Bernier, Jean-Pierre Morello, Alexandro Zarruk, et al.
Journal of Medical Genetics
|
March 13, 2020
Use of a rare disease registry for establishing phenotypic classification of previously unassigned <i>GLA</i> variants: a consensus classification system by a multispecialty Fabry disease genotype-phenotype workgroup
Dominique P Germain, João Paulo Oliveira, Daniel G Bichet, et al.
Human Molecular Genetics
|
April 4, 2002
Heteroligomerization of an Aquaporin-2 mutant with wild-type Aquaporin-2 and their misrouting to late endosomes/lysosomes explains dominant nephrogenic diabetes insipidus
Nannette Marr, Daniel G Bichet, Michele Lonergan, et al.
Nephron. Physiology
|
December 5, 2012
Response of the renal inner medulla to hypoxia: possible defense mechanisms
Namhee Kim, Laura Voicu, Gregory M T Hare, et al.
Page
of 15