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{{Template:Science for Ukraine}} | {{Template:Science for Ukraine}} | ||
2023 Week | 2023 Week 38 | ||
*'''Sep- | *'''Sep- 18 Mo''' | ||
:{| | :{| | ||
| width=" | | width="100" align="center" | [[File:World Mitochondrial Disease Week logo.jpg|130px|link=https://www.mitochondrialdiseaseweek.org/]] | ||
|''' | | '''World Mitochondrial Disease Week''' – Sep 18-24<br> | ||
World Mitochondrial Disease Week raises awareness of mitochondrial disease through educational, fundraising and advocacy activities.<br> | |||
<br> | '''[https://mitochondrialdiseaseweek.org/events/ »See what is happening near you«]''' | ||
|} | |} | ||
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*'''Sep- | *'''Sep- 19 Tu''' | ||
:{| | :{| | ||
| width="100" align="center" |[[Image:O2k-Publications.jpg|70px|link=http://wiki.oroboros.at/index.php/O2k-Publications:_Topics |O2k-Publications in the MiPMap]] | | width="100" align="center" |[[Image:O2k-Publications.jpg|70px|link=http://wiki.oroboros.at/index.php/O2k-Publications:_Topics |O2k-Publications in the MiPMap]] | ||
|''' | |'''In 1962, the first report of a patient with a mitochondrial disease was published.''' <br> | ||
* | * 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. [[Luft 1962 J Clin Invest|»Bioblast link«]] | ||
|} | |} | ||
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*'''Sep- | *'''Sep- 20 We''' | ||
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*'''Sep- 21 Th''' | |||
:{| | :{| | ||
| width="100" align="center" |[[ | | width="100" align="center" |[[File:O2k-Network.png|75px|link=https://wiki.oroboros.at/index.php/O2k-Network]] | ||
|''' | |'''The first mitochondrial DNA mutations associated with disease were described in 1988.''' <br> | ||
* | These discoveries were a game changer in the field of mitochondrial diseases. <br> | ||
* Holt IJ, Harding A E, Morgan-Hughes JA (1988) Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies. [[Holt 1988 Nature|»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. [[Wallace 1988 Science|»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. [[Zeviani 1988 Neurology|»Bioblast link«]] | |||
|} | |} | ||
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*'''Sep- 22 Fr''' | |||
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Revision as of 07:47, 18 September 2023
- Oroboros declares solidarity against the Russian aggression-war in Ukraine and against all aggression-wars worldwide. - »More details
- -» A future for Ukraine is the future of its science
2023 Week 38
- Sep- 18 Mo
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
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
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