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Cell Metabolism
|
June 7, 2011
Insulin receptor-related receptor as an extracellular alkali sensor
Igor E Deyev, Fabien Sohet, Konstantin P Vassilenko, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 4, 2017
Multiplex epithelium dysfunction due to CLDN10 mutation: the HELIX syndrome
Smail Hadj-Rabia, Gaelle Brideau, Yasser Al-Sarraj, et al.
Frontiers in Immunology
|
March 17, 2018
Characterization of Renal Injury and Inflammation in an Experimental Model of Intravascular Hemolysis
Nicolas S Merle, Anne Grunenwald, Marie-Lucile Figueres, et al.
Journal of Medical Genetics
|
August 18, 2016
Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutations
Paulo Marcio Yamaguti, Francisco de Assis Rocha Neves, Dominique Hotton, et al.
Journal of the American Society of Nephrology : JASN
|
March 19, 2011
Spectrum of mutations in Gitelman syndrome
Rosa Vargas-Poussou, Karin Dahan, Diana Kahila, et al.
The Journal of Clinical Investigation
|
April 15, 2010
The Na+-dependent chloride-bicarbonate exchanger SLC4A8 mediates an electroneutral Na+ reabsorption process in the renal cortical collecting ducts of mice
Françoise Leviel, Christian A Hübner, Pascal Houillier, et al.
European Journal of Endocrinology
|
April 15, 2026
Risk of bone overstimulation in long-term PTH(1-34) therapy for hypoparathyroidism
Rebecca Fischler, Anne-Lise Lecoq, Pascal Houillier, et al.
Journal of the American Society of Nephrology : JASN
|
April 14, 2006
Genetic investigation of autosomal recessive distal renal tubular acidosis: evidence for early sensorineural hearing loss associated with mutations in the ATP6V0A4 gene
Rosa Vargas-Poussou, Pascal Houillier, Nelly Le Pottier, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 31, 2013
Targeting proximal tubule mitochondrial dysfunction attenuates the renal disease of methylmalonic acidemia
Irini Manoli, Justin R Sysol, Lingli Li, et al.
JCI Insight
|
June 22, 2018
Intravascular hemolysis activates complement via cell-free heme and heme-loaded microvesicles
Nicolas S Merle, Anne Grunenwald, Helena Rajaratnam, et al.
Page
of 18
Search research articles
Search
Showing results (151-160 of 176) with videos related to
Sort By:
Page
of 18
Cell Metabolism
|
June 7, 2011
Insulin receptor-related receptor as an extracellular alkali sensor
Igor E Deyev, Fabien Sohet, Konstantin P Vassilenko, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 4, 2017
Multiplex epithelium dysfunction due to CLDN10 mutation: the HELIX syndrome
Smail Hadj-Rabia, Gaelle Brideau, Yasser Al-Sarraj, et al.
Frontiers in Immunology
|
March 17, 2018
Characterization of Renal Injury and Inflammation in an Experimental Model of Intravascular Hemolysis
Nicolas S Merle, Anne Grunenwald, Marie-Lucile Figueres, et al.
Journal of Medical Genetics
|
August 18, 2016
Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutations
Paulo Marcio Yamaguti, Francisco de Assis Rocha Neves, Dominique Hotton, et al.
Journal of the American Society of Nephrology : JASN
|
March 19, 2011
Spectrum of mutations in Gitelman syndrome
Rosa Vargas-Poussou, Karin Dahan, Diana Kahila, et al.
The Journal of Clinical Investigation
|
April 15, 2010
The Na+-dependent chloride-bicarbonate exchanger SLC4A8 mediates an electroneutral Na+ reabsorption process in the renal cortical collecting ducts of mice
Françoise Leviel, Christian A Hübner, Pascal Houillier, et al.
European Journal of Endocrinology
|
April 15, 2026
Risk of bone overstimulation in long-term PTH(1-34) therapy for hypoparathyroidism
Rebecca Fischler, Anne-Lise Lecoq, Pascal Houillier, et al.
Journal of the American Society of Nephrology : JASN
|
April 14, 2006
Genetic investigation of autosomal recessive distal renal tubular acidosis: evidence for early sensorineural hearing loss associated with mutations in the ATP6V0A4 gene
Rosa Vargas-Poussou, Pascal Houillier, Nelly Le Pottier, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 31, 2013
Targeting proximal tubule mitochondrial dysfunction attenuates the renal disease of methylmalonic acidemia
Irini Manoli, Justin R Sysol, Lingli Li, et al.
JCI Insight
|
June 22, 2018
Intravascular hemolysis activates complement via cell-free heme and heme-loaded microvesicles
Nicolas S Merle, Anne Grunenwald, Helena Rajaratnam, et al.
Page
of 18