Revision history of "ANIMAL MODELS FOR RETINAL DYSTROPHY: STRATEGIES OF GENOMIC EDITION, PHENOTYPING AND NANOTHERAPY" (Q3140799)

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10 October 2024

  • curprev 09:3809:38, 10 October 2024DG Regio talk contribs 114,305 bytes +3 Changed label, description and/or aliases in pt
  • curprev 09:3809:38, 10 October 2024DG Regio talk contribs 114,302 bytes +33 Set a claim value: summary (P836): A DESFUNÇÃO E A MORTE DOS FOTORECEPTORES É A PRINCIPAL CAUSA DE PERDA DE VISÃO NA DESSTROPIA RETINAL HEREDITÁRIA (IRDS), UM GRUPO DE DOENÇAS DA RETINA, FENÓTIPO VÁRIO E MUITO HETEROGÉNEO. Após mais de 30 anos de investigação, conhecem-se cerca de 300 genes causadores, mas continua a existir um corpo de conhecimentos que correlaciona de forma integrada os genes e as suas mutações (genótipo) com a sua função fisiológica na saúde e a sua desfunção na d...

20 March 2024

20 December 2023

12 June 2023

10 June 2023

17 August 2022

  • curprev 20:0320:03, 17 August 2022DG Regio talk contribs 112,273 bytes +79,824 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

2 December 2021

  • curprev 11:5711:57, 2 December 2021DG Regio talk contribs 19,952 bytes +4,223 Created claim: summary (P836): LA DYSFONCTION ET LA MORT DES PHOTORÉCEPTEURS SONT LA PRINCIPALE CAUSE DE PERTE DE VISION DANS LA DYSTROPHIE RÉTINIENNE HÉRÉDITAIRE (IRD), UN GROUPE DE MALADIES DE LA RÉTINE, UN PHÉNOTYPE SÉVÈRE ET TRÈS HÉTÉROGÈNE. APRÈS PLUS DE 30 ANS DE RECHERCHE, PRÈS DE 300 GÈNES CAUSALS SONT CONNUS, MAIS IL EXISTE ENCORE UN CORPUS DE CONNAISSANCES QUI CORRÉLE DE MANIÈRE INTÉGRÉE LES GÈNES IRD ET LEURS MUTATIONS (GÉNOTYPE) AVEC LEUR FONCTION PHYSIOLOGIQUE EN...
  • curprev 11:5711:57, 2 December 2021DG Regio talk contribs 15,729 bytes +173 Changed label, description and/or aliases in fr: translated_label

12 October 2021

  • curprev 13:2113:21, 12 October 2021DG Regio talk contribs 15,556 bytes +154 Changed label, description and/or aliases in en: translated_label
  • curprev 13:2113:21, 12 October 2021DG Regio talk contribs 15,402 bytes +3,830 Created claim: summary (P836): DYSFUNCTION AND DEATH OF PHOTORECEPTORS IS THE MAIN CAUSE OF LOSS OF VISION IN HEREDITARY RETINAL DYSTROPHY (IRDS), A GROUP OF DISEASES OF THE RETINA, SEVERE PHENOTYPE AND VERY HETEROGENEOUS. AFTER MORE THAN 30 YEARS OF RESEARCH, NEARLY 300 CAUSATIVE GENES ARE KNOWN BUT THERE IS STILL A CORPUS OF KNOWLEDGE THAT CORRELATES IN AN INTEGRATED WAY THE IRD GENES AND THEIR MUTATIONS (GENOTYPE) WITH THEIR PHYSIOLOGICAL FUNCTION IN HEALTH AND THEIR DYSFU...

10 October 2021

9 October 2021

7 October 2021