Regulation of the vasopressin V2 receptor by vasopressin in polarized renal collecting duct cells von Robben, J H, Knoers, N V A M, Deen, P M T

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Congenital myopathy caused by a novel missense mutation in the CFL2 gene von Ockeloen, C.W, Gilhuis, H.J, Pfundt, R, Kamsteeg, E.J, Agrawal, P.B, Beggs, A.H, Dara Hama-Amin, A, Diekstra, A, Knoers, N.V.A.M, Lammens, M, van Alfen, N

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From Karyotyping to Array-CGH in Prenatal Diagnosis von Lichtenbelt, K.D., Knoers, N.V.A.M., Schuring-Blom, G.H.

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Rescue of vasopressin V2 receptor mutants by chemical chaperones: specificity and mechanism von Robben, J H, Sze, M, Knoers, N V A M, Deen, P M T

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POS-421 KIDNEYNETWORK: A NEW METHOD TO PREDICT KIDNEY DISEASE GENES USING KIDNEY DERIVED GENE EXPRESSION DATA IDENTIFIES A NEW CANDIDATE GENE FOR MILD ADPKD / PCLD von Boulogne, F., CLAUS, L., Wiersma, H., Schukking, F., de Klein, N., Li, S., Westra, H.J., Genomics England Research Consortium, U.K., Deelen, P., Knoers, N.V.A.M., van Eerde, A.M., Franke, L.

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Aetiology of hypospadias: a systematic review of genes and environment von van der Zanden, L F M, van Rooij, I A L M, Feitz, W F J, Franke, B, Knoers, N V A M, Roeleveld, N

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Spinocerebellar ataxias in the Netherlands: Prevalence and age at onset variance analysis von VAN DE WARRENBURG, B. P. C, SINKE, R. J, KNOERS, N. V. A. M, KREMER, H. P. H, VERSCHUUREN-BEMELMANS, C. C, SCHEFFER, H, BRUNT, E. R, IPPEL, P. F, MAAT-KIEVIT, J. A, DOOIJES, D, NOTERMANS, N. C, LINDHOUT, D

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Kinderurologie en etiologie: Radboudumc AGORA data- en biobank von Feitz, W.F.J., van Rooij, I.A.L.M., Bongers, E.M.H.F., Renkema, K.Y., Knoers, N.V.A.M., Dokter, E.M.J., de Gier, R., Kortmann, B., Schreuder, M.F., Brunner, H.G., van der Zanden, L.F.M., Roeleveld, N.

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Molecular Cloning, Tissue Distribution, and Chromosomal Mapping of the Human Epithelial Ca2+ Channel (ECAC1) von Müller, D., Hoenderop, J.G.J., Meij, I.C., van den Heuvel, L.P.J., Knoers, N.V.A.M., den Hollander, A.I., Eggert, P., Garcı&́a-Nieto, V., Claverie-Martı&́n, F., Bindels, R.J.M.

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N.P.2 04 Patients with spinal muscular atrophy (SMA) and healthy siblings sharing homozygous deletions of the SMN1 gene reveal an identical number of SMN2 gene copies but different... von Lemmink, H.H., Vos, Y.J., Plaza de Menacho, I., Dijkhuis, J., Knoers, N.V.A.M., de Visser, M., Buys, C.H.C.M.

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KidneyNetwork: using kidney-derived gene expression data to predict and prioritize novel genes involved in kidney disease von Boulogne, F., Claus, L.R., Wiersma, H., Oelen, R., Schukking, F., Klein, N. de, Li, S., Westra, H.J., Zwaag, B. van der, Reekum, F. van, Sierks, D., Schönauer, R., Li, Z.G., Bijlsma, E.K., Bos, W.J.W., Halbritter, J., Knoers, N.V.A.M., Besse, W., Deelen, P., Franke, L., Eerde, A.M. van

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An update on the use of tolvaptan for autosomal dominant polycystic kidney disease: consensus statement on behalf of the ERA Working Group on Inherited Kidney Disorders, the Europe... von Müller, R.-U, Lianne Messchendorp, A, Birn, H, Capasso, G, Cornec-Le Gall, E, Devuyst, O, Eerde, A.V, Guirchoun, P, Harris, T, Hoorn, E.J, Knoers, N.V.A.M, Korst, U, Mekahli, D, Le Meur, Y, Nijenhuis, T, Ong, A.C.M, Sayer, J.A, Schaefer, F, Servais, A, Tesar, V, Torra, R, Walsh, S.B, Gansevoort, R.T

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An update on the use of tolvaptan for autosomal dominant polycystic kidney disease: consensus statement on behalf of the ERA Working Group on Inherited Kidney Disorders, the Europe... von Müller, R.-U, Messchendorp, A.L, Birn, H, Capasso, G, Cornec-Le Gall, E, Devuyst, O, van Eerde, A, Guirchoun, P, Harris, T, Hoorn, E.J, Knoers, N.V.A.M, Korst, U, Mekahli, D, Le Meur, Y, Nijenhuis, T, Ong, A.C.M, Sayer, J.A, Schaefer, F, Servais, A, Tesar, V, Torra, R, Walsh, S.B, Gansevoort, R.T

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The von Hippel-Lindau gene is required to maintain renal proximal tubule and glomerulus integrity in zebrafish larvae von van Rooijen, E, van de Hoek, G, Logister, I, Ajzenberg, H, Knoers, N.V.A.M, van Eeden, F, Voest, E.E, Schulte-Merker, S, Giles, R.H

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Supplementary Material for: Importance of Genetic Diagnostics in Adult-Onset Focal Segmental Glomerulosclerosis von Snoek, R., Nguyen, T.Q., VanderZwaag, B., VanZuilen, A.D., Kruis H.M.E., VanGils-Verrij, L.A., Goldschmeding, R., Knoers N.V.A.M., Rookmaaker, M.B., VanEerde, A.M.

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Supplementary Material for: The von Hippel-Lindau Gene Is Required to Maintain Renal Proximal Tubule and Glomerulus Integrity in Zebrafish Larvae von Van Rooijen, E., Van De Hoek, G., Logister, I., Ajzenberg, H., Knoers N.V.A.M., Van Eeden, F., Voest, E.E., Schulte-Merker, S., Giles, R.H.

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Dominant isolated renal magnesium loss is caused by misrouting of the Na + ,K + -ATPase γ-subunit von Knoers, Nine V.A.M, van Bokhoven, Hans, Koenderink, Jan B, Tiel Groenestege, Wouter, de Pont, Jan Joep H.H.M, van den Heuvel, Lambert P.W.J, Meij, Iwan C, Monnens, Leo A.H, Assink, Karin F.H, Bindels, René J.M

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Molecular and cellular defects in nephrogenic diabetes insipidus von KNOERS, Nine V. A. M, DEEN, Peter M. T

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Nail-patella syndrome. Overview on clinical and molecular findings von Bongers, Ernie M H F, Gubler, Marie-Claire, Knoers, Nine V A M

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Kidney development out of tune : Genetic and functional aspects of congenital renal anomalies von Nicolaou, N

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