Template:Current week ecosystem agenda: Difference between revisions

From Bioblast
No edit summary
No edit summary
Line 9: Line 9:
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/ ยปSee what is happening near youยซ]'''
'''[https://mitochondrialdiseaseweek.org/events/ ยปSee what is happening near youยซ]'''
Visit of our distributor Huawei in China.<br>
'''[https://wiki.oroboros.at/index.php/CN_Beijing_Huaweiยซ]'''
[[File:Visit Huawei.jpg|250px|Huawei and Oroboros]]
|}
|}



Revision as of 16:18, 18 September 2023

Gentle Science
Oroboros declares solidarity against the Russian aggression-war in Ukraine and against all aggression-wars worldwide. -  ยปMore details
-ยป 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 โ€“ Sep 18-24

World Mitochondrial Disease Week raises awareness of mitochondrial disease through educational, fundraising and advocacy activities.
ยปSee what is happening near youยซ


  • 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. ยปBioblast linkยซ

  • 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. ยปBioblast linkยซ
  • 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. ยปBioblast linkยซ
  • Zeviani M, Moraes CT, DiMauro S, Nakase H, Bonilla E, Schon EA, Rowland LP (1988) Deletions of mitochondrial DNA in Kearns-Sayre syndrome. ยปBioblast linkยซ

  • Sep- 22 Fr

Cookies help us deliver our services. By using our services, you agree to our use of cookies.