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La ricerca find articoli where authors phrase all words 'Jeck, N' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 16 riferimenti
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    1. 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
      Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure

      NATURE GENETICS
    2. Peters, M; Jeck, N; Seyberth, HW; Konrad, M
      Hereditary hypokalemic salt-losing tubulopathies: Bartter-like syndromes

      RARE KIDNEY DISEASES
    3. Jeck, N; Derst, C; Wischmeyer, E; Ott, H; Weber, S; Rudin, C; Seyberth, HW; Daut, J; Karschin, A; Konrad, M
      Functional heterogeneity of ROMK mutations linked to hyperprostaglandin E syndrome

      KIDNEY INTERNATIONAL
    4. Jeck, N; Reinalter, SC; Henne, T; Marg, W; Mallmann, R; Pasel, K; Vollmer, M; Klaus, G; Leonhardt, A; Seyberth, HW; Konrad, M
      Hypokalemic salt-losing tubulopathy with chronic renal failure and sensorineural deafness

      PEDIATRICS
    5. 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
      Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome

      JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
    6. 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
      Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene

      EUROPEAN JOURNAL OF HUMAN GENETICS
    7. 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
      Antenatal Bartter syndrome with sensorineural deafness: refinement of the locus on chromosome 1p31

      NEPHROLOGY DIALYSIS TRANSPLANTATION
    8. Jeck, N; Konrad, M; Hess, M; Seyberth, HW
      The diuretic- and Bartter-like salt-losing tubulopathies

      NEPHROLOGY DIALYSIS TRANSPLANTATION
    9. Weber, S; Soergel, M; Jeck, N; Konrad, M
      Atypical distal renal tubular acidosis confirmed by mutation analysis

      PEDIATRIC NEPHROLOGY
    10. Jeck, N; Konrad, M; Peters, M; Weber, S; Bonzel, KE; Seyberth, HW
      Mutations in the chloride channel gene, CLCNKB, leading to a mixed Bartter-Gitelman phenotype

      PEDIATRIC RESEARCH
    11. Scharnagl, H; Schliack, M; Loser, R; Nauck, M; Gierens, H; Jeck, N; Wieland, H; Gross, W; Marz, W
      The effects of lifibrol (K12.148) on the cholesterol metabolism of cultured cells: evidence for sterol independent stimulation of the LDL receptor pathway

      ATHEROSCLEROSIS
    12. Jeck, N; Konrad, M; Seyberth, HW
      Hereditary hypokalemic salt-losing tubulopathies

      CHANNELOPATHIES - COMMON MECHANISMS IN AURA, ARRHYTHMIA AND ALKALOSIS
    13. Schulte, U; Hahn, H; Konrad, M; Jeck, N; Derst, C; Wild, K; Weidemann, S; Ruppersberg, JP; Fakler, B; Ludwig, J
      pH gating of ROMK (K(ir)1.1) channels: Control by an Arg-Lys-Arg triad disrupted in antenatal Bartter syndrome

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    14. Derst, C; Doring, F; Preisig-Muller, R; Daut, J; Karschin, A; Jeck, N; Weber, S; Engel, H; Grzeschik, KH
      Partial gene structure and assignment to chromosome 2q37 of the human inwardly rectifying K+ channel (K(ir)7.1) gene (KCNJ13)

      GENOMICS
    15. JECK N; KONRAD M; WEBER S; REINALTER S; SEYBERTH HW
      MUTATIONS IN CLCKB-CHANNEL CAUSE BARTTER-SYNDROME

      Naunyn-Schmiedeberg's archives of pharmacology
    16. DERST C; WISCHMEYER E; PREISIGMULLER R; SPAUSCHUS A; KONRAD M; HENSEN P; JECK N; SEYBERTH HW; DAUT J; KARSCHIN A
      A HYPERPROSTAGLANDIN-E SYNDROME MUTATION IN KIR1.1 (RENAL OUTER MEDULLARY POTASSIUM) CHANNELS REVEALS A CRUCIAL RESIDUE FOR CHANNEL FUNCTION IN KIR1.3 CHANNELS

      The Journal of biological chemistry


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 21/10/20 alle ore 04:53:04