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Results: 1-5 |
Results: 5

Authors: Konrad, M Vollmer, M Lemmink, HH Van den Heuvel, LPWJ Jeck, N Vargas-Poussou, R Lakings, A Ruf, R Deschenes, G Antignac, C Guay-Woodford, L Knoers, NVAM Seyberth, HW Feldmann, D Hildebrandt, F
Citation: M. Konrad et al., Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome, J AM S NEPH, 11(8), 2000, pp. 1449-1459

Authors: Kunzelmann, K Hubner, M Vollmer, M Ruf, R Hildebrandt, F Greger, R Schreiber, R
Citation: K. Kunzelmann et al., A Bartter's syndrome mutation of ROMK1 exerts dominant negative effects onK+ conductance, CELL PHYS B, 10(3), 2000, pp. 117-124

Authors: Vollmer, M Kremer, M Ruf, R Miot, S Nothwang, HG Wirth, J Otto, E Krapf, R Hildebrandt, F
Citation: M. Vollmer et al., Molecular cloning of the critical region for glomerulopathy with fibronectin deposits (GFND) and evaluation of candidate genes, GENOMICS, 68(2), 2000, pp. 127-135

Authors: Martin, MD Vina, L Ruf, R Mendez, EE
Citation: Md. Martin et al., Spin polarization dynamics in a semiconductor microcavity, PHYS ST S-A, 178(1), 2000, pp. 539-543

Authors: Vollmer, M Jung, M Ruschendorf, F Ruf, R Wienker, T Reis, A Krapf, R Hildebrandt, F
Citation: M. Vollmer et al., The gene for human fibronectin glomerulopathy maps to 1q32, in the region of the regulation of complement activation gene cluster, AM J HU GEN, 63(6), 1998, pp. 1724-1731
Risultati: 1-5 |