Revision history of "Genetic and molecular study of hereditary renal tubulopathies" (Q3190798)

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7 March 2024

20 December 2023

12 June 2023

10 June 2023

18 August 2022

  • curprev 07:2407:24, 18 August 2022DG Regio talk contribs 67,135 bytes +45,309 Changed label, description and/or aliases in el, da, fi, mt, lv, sk, ga, cs, pt, et, hu, bg, lt, hr, sv, ro, sl, pl, nl, fr, de, it, es, and other parts: Adding translations: el, da, fi, mt, lv, sk, ga, cs, pt, et, hu, bg, lt, hr, sv, ro, sl, pl,

16 January 2022

17 December 2021

9 December 2021

4 December 2021

12 October 2021

  • curprev 21:5121:51, 12 October 2021DG Regio talk contribs 12,180 bytes +2,136 Created claim: summary (P836): The general objectives of the project are to identify the genetic causes of renal tubulopathies in the paediatric age and to know the consequences of mutations on the cellular fate of the protein or on the processing of mRNA. In particular, we intend to: (1) determine the cell location of ClC-5 mutant proteins encoded by the p.G65R, p.G462S and p.G466D mutations by fluorescence microscopy with a confocal microscope; (2) Set the functional meanin...
  • curprev 21:5121:51, 12 October 2021DG Regio talk contribs 10,044 bytes −2,136 Removed claim: summary (P836): The general objectives of the project are to identify the genetic causes of renal tubulopathies in the paediatric age and to know the consequences of mutations on the cellular fate of the protein or on the processing of mRNA. In particular, we intend to: (1) determine the cell location of ClC-5 mutant proteins encoded by the p.G65R, p.G462S and p.G466D mutations by fluorescence microscopy with a confocal microscope; (2) Set the functional mean...
  • curprev 21:1821:18, 12 October 2021DG Regio talk contribs 12,180 bytes +120 Changed label, description and/or aliases in en: translated_label
  • curprev 21:1821:18, 12 October 2021DG Regio talk contribs 12,060 bytes +2,136 Created claim: summary (P836): The general objectives of the project are to identify the genetic causes of renal tubulopathies in the paediatric age and to know the consequences of mutations on the cellular fate of the protein or on the processing of mRNA. In particular, we intend to: (1) determine the cell location of ClC-5 mutant proteins encoded by the p.G65R, p.G462S and p.G466D mutations by fluorescence microscopy with a confocal microscope; (2) Set the functional meanin...

11 October 2021

10 October 2021

8 October 2021