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Difference between revisions of "Template:Current week ecosystem agenda"

From Bioblast
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World Mitochondrial Disease Week raises awareness of mitochondrial disease through educational, fundraising and advocacy activities.<br>
World Mitochondrial Disease Week raises awareness of mitochondrial disease through educational, fundraising and advocacy activities.<br>
'''[https://mitochondrialdiseaseweek.org/events/ »See what is happening near you«]'''
'''[https://mitochondrialdiseaseweek.org/events/ »See what is happening near you«]'''
Visit of our distributor Huawei in China.<br>
'''[https://wiki.oroboros.at/index.php/CN_Beijing_Huawei«]'''
[[File:Visit Huawei.jpg|250px|Huawei and Oroboros]]
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Revision as of 16:18, 18 September 2023

Gentle Science
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A future for Ukraine is the future of its science
2023 Week 38
  • Sep- 18 Mo
World Mitochondrial Disease Week logo.jpg World Mitochondrial Disease Week – Sep 18-24

World Mitochondrial Disease Week raises awareness of mitochondrial disease through educational, fundraising and advocacy activities.
»See what is happening near you«


  • Sep- 19 Tu
O2k-Publications in the MiPMap In 1962, the first report of a patient with a mitochondrial disease was published.
  • Luft R, Ikkos D, Palmieri G, Ernster L, Afzelius B (1962). A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical, and morphological study. »Bioblast link«

  • Sep- 20 We

  • Sep- 21 Th
O2k-Network.png The first mitochondrial DNA mutations associated with disease were described in 1988.

These discoveries were a game changer in the field of mitochondrial diseases. 

  • Holt IJ, Harding A E, Morgan-Hughes JA (1988) Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies. »Bioblast link«
  • Wallace DC, Singh G, Lott MT, Hodge JA, Schurr TG, Lezza AM, Elsas LJ 2nd, Nikoskelainen EK (1988) Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy. »Bioblast link«
  • Zeviani M, Moraes CT, DiMauro S, Nakase H, Bonilla E, Schon EA, Rowland LP (1988) Deletions of mitochondrial DNA in Kearns-Sayre syndrome. »Bioblast link«

  • Sep- 22 Fr