Revision history of "Optimisation of genomic editing for application to gene therapy of monogenic diseases" (Q3167757)

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11 October 2024

  • curprev 09:3909:39, 11 October 2024DG Regio talk contribs 78,915 bytes 0 Changed label, description and/or aliases in pt
  • curprev 09:3909:39, 11 October 2024DG Regio talk contribs 78,915 bytes +56 Set a claim value: summary (P836): O medicamento ideal para o tratamento de doenças monogénicas seria aquele que poderia corrigir as mutações que causam a patologia. Este objetivo é algo que está a ser abordado recentemente graças ao desenvolvimento de vários sistemas de edição genómica, especialmente aqueles baseados em nucleases específicas (NE), como ZFNs ou o sistema CRISPR. Estas técnicas permitem reescrever a sequência de ADN das células-alvo de uma forma suficientemente eficaz...

7 March 2024

20 December 2023

12 June 2023

10 June 2023

4 August 2022

  • curprev 10:0210:02, 4 August 2022DG Regio talk contribs 77,587 bytes +53,398 Changed label, description and/or aliases in et, lt, hr, el, sk, fi, pl, hu, cs, lv, ga, sl, bg, mt, pt, da, ro, sv, nl, fr, de, it, es, and other parts: Adding translations: et, lt, hr, el, sk, fi, pl, hu, cs, lv, ga, sl, bg, mt, pt, da, ro, sv,

16 January 2022

17 December 2021

9 December 2021

4 December 2021

12 October 2021

  • curprev 17:3717:37, 12 October 2021DG Regio talk contribs 12,898 bytes +2,427 Created claim: summary (P836): The ideal medicine for the treatment of monogenic diseases would be one that could correct the mutations that cause the pathology. This objective is something that is recently being addressed thanks to the development of various genomic editing systems, especially those based on specific nucleases (NE) such as ZFNs or the CRISPR system. These techniques allow to rewrite the DNA sequence of target cells in a sufficiently effective and specific wa...
  • curprev 17:3717:37, 12 October 2021DG Regio talk contribs 10,471 bytes −2,427 Removed claim: summary (P836): The ideal medicine for the treatment of monogenic diseases would be one that could correct the mutations that cause the pathology. This objective is something that is recently being addressed thanks to the development of various genomic editing systems, especially those based on specific nucleases (NE) such as ZFNs or the CRISPR system. These techniques allow to rewrite the DNA sequence of target cells in a sufficiently effective and specific...
  • curprev 16:2316:23, 12 October 2021DG Regio talk contribs 12,898 bytes +144 Changed label, description and/or aliases in en: translated_label
  • curprev 16:2316:23, 12 October 2021DG Regio talk contribs 12,754 bytes +2,427 Created claim: summary (P836): The ideal medicine for the treatment of monogenic diseases would be one that could correct the mutations that cause the pathology. This objective is something that is recently being addressed thanks to the development of various genomic editing systems, especially those based on specific nucleases (NE) such as ZFNs or the CRISPR system. These techniques allow to rewrite the DNA sequence of target cells in a sufficiently effective and specific wa...

10 October 2021

9 October 2021

8 October 2021