Search Results - "Meij, I.C."

The European Renal Genome Project: An Integrated Approach Towards Understanding the Genetics of Kidney Development and Disease by Willnow, T.E., Antignac, C., Brändli, A.W., Christensen, E.I., Cox, R.D., Davidson, D., Davies, J.A., Devuyst, O., Eichele, G., Hastie, N.D., Verroust, P.J., Schedl, A., Meij, I.C.

“…Rapid progress in genome research creates a wealth of information on the functional annotation of mammalian genome sequences. However, as we accumulate large…”
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Molecular Cloning, Tissue Distribution, and Chromosomal Mapping of the Human Epithelial Ca2+ Channel (ECAC1) by 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.

“…Functional and morphological analyses indicated that the epithelial Ca2+ channel (ECaC), which was recently cloned from rabbit kidney, exhibits the defining…”
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Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene by Weber, S, Hoffmann, K, Jeck, N, Saar, K, Boeswald, M, Kuwertz-Broeking, E, Meij, I I, Knoers, N V, Cochat, P, Suláková, T, Bonzel, K E, Soergel, M, Manz, F, Schaerer, K, Seyberth, H W, Reis, A, Konrad, M

“…Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis (FHHNC, MIM 248250) is a complex renal tubular disorder characterised by hypomagnesaemia,…”
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