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CLDN16 genotype predicts renal decline in familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
Konrad M, Hou J, Weber S, Dötsch J, Kari JA, Seeman T, Kuwertz-Bröking E, Peco-Antic A, Tasic V, Dittrich K, Alshaya HO, von Vigier RO, Gallati S, Goodenough DA, Schaller A. Konrad M, et al. Among authors: schaller a. J Am Soc Nephrol. 2008 Jan;19(1):171-81. doi: 10.1681/ASN.2007060709. Epub 2007 Nov 14. J Am Soc Nephrol. 2008. PMID: 18003771 Free PMC article.
Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement.
Konrad M, Schaller A, Seelow D, Pandey AV, Waldegger S, Lesslauer A, Vitzthum H, Suzuki Y, Luk JM, Becker C, Schlingmann KP, Schmid M, Rodriguez-Soriano J, Ariceta G, Cano F, Enriquez R, Juppner H, Bakkaloglu SA, Hediger MA, Gallati S, Neuhauss SC, Nurnberg P, Weber S. Konrad M, et al. Among authors: schaller a. Am J Hum Genet. 2006 Nov;79(5):949-57. doi: 10.1086/508617. Epub 2006 Sep 19. Am J Hum Genet. 2006. PMID: 17033971 Free PMC article.
Heterologous expression from the human D-Loop in organello.
Jackson CB, Zbinden C, Gallati S, Schaller A. Jackson CB, et al. Among authors: schaller a. Mitochondrion. 2014 Jul;17:67-75. doi: 10.1016/j.mito.2014.05.011. Epub 2014 Jun 6. Mitochondrion. 2014. PMID: 24911383
Cardiopulmonary bypass reduces atrial Na+-K+-ATPase expression in children.
Pavlovic M, Schaller A, Ammann RA, Sanz J, Pfammatter JP, Carrel T, Berdat P, Gallati S. Pavlovic M, et al. Among authors: schaller a. Biochem Biophys Res Commun. 2005 Sep 30;335(3):700-4. doi: 10.1016/j.bbrc.2005.07.134. Biochem Biophys Res Commun. 2005. PMID: 16087159
402 results