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Results: 1-25 | 26-43
Results: 1-25/43
Dinucleating hybrid ligands providing a "soft" P boolean AND N and an adjacent N-rich coordination pocket - Controlled synthesis of unsymmetric homodinuclear and heterodinuclear complexes
Authors: Konrad, M Wuthe, S Meyer, F Kaifer, E
Citation: M. Konrad et al., Dinucleating hybrid ligands providing a "soft" P boolean AND N and an adjacent N-rich coordination pocket - Controlled synthesis of unsymmetric homodinuclear and heterodinuclear complexes, EUR J INORG, (9), 2001, pp. 2233-2240
Difunctional pyrazole derivatives - Key compounds en route to multidentatepyrazolate ligands
Authors: Roder, JC Meyer, F Konrad, M Sandhofner, S Kaifer, E Pritzkow, H
Citation: Jc. Roder et al., Difunctional pyrazole derivatives - Key compounds en route to multidentatepyrazolate ligands, EUR J ORG C, (23), 2001, pp. 4479-4487
Conceiving persons: ethnographies of procreation, fertility and growth
Authors: Konrad, M
Citation: M. Konrad, Conceiving persons: ethnographies of procreation, fertility and growth, J ROY ANTHR, 7(3), 2001, pp. 591-592
Extending the boundaries of care: medical ethics & caring practices
Authors: Konrad, M
Citation: M. Konrad, Extending the boundaries of care: medical ethics & caring practices, J ROY ANTHR, 7(3), 2001, pp. 603-604
Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure
Authors: Birkenhager, R Otto, E Schurmann, MJ Vollmer, M Ruf, EM Maier-Lutz, I Beekmann, F Fekete, A Omran, H Feldmann, D Milford, DV Jeck, N Konrad, M Landau, D Knoers, NVAM Antignac, C Sudbrak, R Kispert, A Hildebrandt, F
Citation: R. Birkenhager et al., Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure, NAT GENET, 29(3), 2001, pp. 310-314
Novel paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis
Authors: Weber, S Schneider, L Peters, M Misselwitz, J Ronnefarth, G Boswald, M Bonzel, KE Seeman, T Sulakova, T Kuwertz-Broking, E Gregoric, A Palcoux, JB Tasic, V Manz, F Scharer, K Seyberth, HW Konrad, M
Citation: S. Weber et al., Novel paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis, J AM S NEPH, 12(9), 2001, pp. 1872-1881
Primary gene structure and expression studies of rodent paracellin-1
Authors: Weber, S Schlingmann, KP Peters, M Nejsum, LN Nielsen, S Engel, H Grzeschik, KH Seyberth, HW Grone, HJ Nusing, R Konrad, M
Citation: S. Weber et al., Primary gene structure and expression studies of rodent paracellin-1, J AM S NEPH, 12(12), 2001, pp. 2664-2672
Hereditary hypokalemic salt-losing tubulopathies: Bartter-like syndromes
Authors: Peters, M Jeck, N Seyberth, HW Konrad, M
Citation: M. Peters et al., Hereditary hypokalemic salt-losing tubulopathies: Bartter-like syndromes, CONTR NEPHR, 136, 2001, pp. 157-173
Functional heterogeneity of ROMK mutations linked to hyperprostaglandin E syndrome
Authors: Jeck, N Derst, C Wischmeyer, E Ott, H Weber, S Rudin, C Seyberth, HW Daut, J Karschin, A Konrad, M
Citation: N. Jeck et al., Functional heterogeneity of ROMK mutations linked to hyperprostaglandin E syndrome, KIDNEY INT, 59(5), 2001, pp. 1803-1811
Surface reconstruction of an ordered fluid: An analogy with crystal surfaces - art. no. 035505
Authors: Rehse, N Knoll, A Konrad, M Magerle, R Krausch, G
Citation: N. Rehse et al., Surface reconstruction of an ordered fluid: An analogy with crystal surfaces - art. no. 035505, PHYS REV L, 8703(3), 2001, pp. 5505-NIL_80
Hypokalemic salt-losing tubulopathy with chronic renal failure and sensorineural deafness
Authors: Jeck, N Reinalter, SC Henne, T Marg, W Mallmann, R Pasel, K Vollmer, M Klaus, G Leonhardt, A Seyberth, HW Konrad, M
Citation: N. Jeck et al., Hypokalemic salt-losing tubulopathy with chronic renal failure and sensorineural deafness, PEDIATRICS, 108(1), 2001, pp. NIL_23-NIL_31
Evaluation of long-term treatment with indomethacin in hereditary hypokalemic salt-losing tubulopathies
Authors: Reinalter, SC Grone, HJ Konrad, M Seyberth, HW Klaus, G
Citation: Sc. Reinalter et al., Evaluation of long-term treatment with indomethacin in hereditary hypokalemic salt-losing tubulopathies, J PEDIAT, 139(3), 2001, pp. 398-406
YLR209c encodes Saccharomyces cerevisiae purine nucleoside phosphorylase
Authors: Lecoq, K Belloc, I Desgranges, C Konrad, M Daignan-Fornier, B
Citation: K. Lecoq et al., YLR209c encodes Saccharomyces cerevisiae purine nucleoside phosphorylase, J BACT, 183(16), 2001, pp. 4910-4913
Structural and catalytic properties and homology modelling of the human nucleoside diphosphate kinase C, product of the DRnm23 gene
Authors: Erent, M Gonin, P Cherfils, J Tissier, P Raschella, G Giartosio, A Agou, F Sarger, C Lacombe, ML Konrad, M Lascu, I
Citation: M. Erent et al., Structural and catalytic properties and homology modelling of the human nucleoside diphosphate kinase C, product of the DRnm23 gene, EUR J BIOCH, 268(7), 2001, pp. 1972-1981
Regulatory properties of tropomyosin effects of length, isoform, and N-terminal sequence
Authors: Maytum, R Konrad, M Lehrer, SS Geeves, MA
Citation: R. Maytum et al., Regulatory properties of tropomyosin effects of length, isoform, and N-terminal sequence, BIOCHEM, 40(24), 2001, pp. 7334-7341
Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome
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
Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene
Authors: Weber, S Hoffmann, K Jeck, N Saar, K Boeswald, M Kuwertz-Broeking, E Meij, IIC Knoers, NVAM Cochat, P Sulakova, T Bonzel, KE Soergel, M Manz, F Schaerer, K Seyberth, HW Reis, A Konrad, M
Citation: S. Weber et al., Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene, EUR J HUM G, 8(6), 2000, pp. 414-422
Insights into the phosphoryltransfer mechanism of human thymidylate kinasegained from crystal structures of enzyme complexes along the reaction coordinate
Authors: Ostermann, N Schlichting, I Brundiers, R Konrad, M Reinstein, J Veit, T Goody, RS Lavie, A
Citation: N. Ostermann et al., Insights into the phosphoryltransfer mechanism of human thymidylate kinasegained from crystal structures of enzyme complexes along the reaction coordinate, STRUCT F D, 8(6), 2000, pp. 629-642
Cellular and synaptic effect of substance P on neonatal phrenic motoneurons
Authors: Ptak, K Konrad, M Di Pasquale, E Tell, F Hilaire, G Monteau, R
Citation: K. Ptak et al., Cellular and synaptic effect of substance P on neonatal phrenic motoneurons, EUR J NEURO, 12(1), 2000, pp. 126-138
Antenatal Bartter syndrome with sensorineural deafness: refinement of the locus on chromosome 1p31
Authors: Vollmer, M Jeck, N Lemmink, HH Vargas, R Feldmann, D Konrad, M Beekmann, F van den Heuvel, LPWJ Deschenes, G Guay-Woodford, LM Antignac, C Seyberth, HW Hildebrandt, F Knoers, NVAM
Citation: M. Vollmer et al., Antenatal Bartter syndrome with sensorineural deafness: refinement of the locus on chromosome 1p31, NEPH DIAL T, 15(7), 2000, pp. 970-974
The diuretic- and Bartter-like salt-losing tubulopathies
Authors: Jeck, N Konrad, M Hess, M Seyberth, HW
Citation: N. Jeck et al., The diuretic- and Bartter-like salt-losing tubulopathies, NEPH DIAL T, 15, 2000, pp. 19-20
Atypical distal renal tubular acidosis confirmed by mutation analysis
Authors: Weber, S Soergel, M Jeck, N Konrad, M
Citation: S. Weber et al., Atypical distal renal tubular acidosis confirmed by mutation analysis, PED NEPHROL, 15(3-4), 2000, pp. 201-204
Adopting a middle-class attitude of nobility for Jews in mid-nineteenth-century Hungary - Reinforcing opposition to the emancipation and social integration of Hungarian Jewry
Authors: Konrad, M
Citation: M. Konrad, Adopting a middle-class attitude of nobility for Jews in mid-nineteenth-century Hungary - Reinforcing opposition to the emancipation and social integration of Hungarian Jewry, REV ETUD J, 159(1-2), 2000, pp. 145-184
Mutations in the chloride channel gene, CLCNKB, leading to a mixed Bartter-Gitelman phenotype
Authors: Jeck, N Konrad, M Peters, M Weber, S Bonzel, KE Seyberth, HW
Citation: N. Jeck et al., Mutations in the chloride channel gene, CLCNKB, leading to a mixed Bartter-Gitelman phenotype, PEDIAT RES, 48(6), 2000, pp. 754-758
Volume imaging of an ultrathin SBS triblock copolymer film
Authors: Konrad, M Knoll, A Krausch, G Magerle, R
Citation: M. Konrad et al., Volume imaging of an ultrathin SBS triblock copolymer film, MACROMOLEC, 33(15), 2000, pp. 5518-5523
Risultati: 1-25 | 26-43