>There is no such thing as qanon
Fellow qanoner, nobody cares is there is such thing.
For example, I don't consider Q as a signature.
<To hell with "Q".
Z
you think they're really opening up dimensions over there? Letting pandora out of the box?
DONT FUCK WITH ME I GOT NOTHING TO LOSE UNLIKE YOU.
The same bloodline that gave you the evolution theory, and says Earth is the only habitable planet, also gave you precisely the Abrahamic religions (the church, mosque, synagogue). The same ones have been sacrificing human children for over five thousand years on Earth.
This is why around eight million children a year are kidnapped and trafficked world wide. The vast majority of these children ending up in the hands of the dark elites, politicians, celebrities.
One of the main reasons why they demonized Donald Trump 24/7 is because he was shutting down their food supply, again, children/child trafficking.
The same entities have been pushing the transgender agenda, by paying certain people to go through sex changes and giving them media attention, thus manipulating confused people, who need healing, instead bringing them to hating the body their born into. It is the same ones who are trying to normalize pedophilia, and label it as a sexual preference.
https://www.washingtonexaminer.com/policy/twitter-to-ban-ads-that-contradict-authorities-on-climate-change
Twitter to ban ads that contradict authorities on climate change
by Nihal Krishan, Technology Reporter |
| April 22, 2022 05:12 PM
https://t.me/VigilantFox/5072
The Vigilant Fox 🦊, [02.07.22 14:35]
UFC Superstar Israel Adesanya Asks The One Question Everyone Wants To Know
https://www.redvoicemedia.com/2022/07/ufc-superstar-asks-the-one-question-everyone-wants-to-know-about-maxwell-epsteins-pedo-sex-ring-video/ref/8/
which past posts?
Any anons up for some mountain climbing?
https://www.nature.com/articles/nature22067
Human umbilical cord plasma proteins revitalize hippocampal function in aged mice
Ageing drives changes in neuronal and cognitive function, the decline of which is a major feature of many neurological disorders. The hippocampus, a brain region subserving roles of spatial and episodic memory and learning, is sensitive to the detrimental effects of ageing at morphological and molecular levels. With advancing age, synapses in various hippocampal subfields exhibit impaired long-term potentiation, an electrophysiological correlate of learning and memory. At the molecular level, immediate early genes are among the synaptic plasticity genes that are both induced by long-term potentiation, and downregulated in the aged brain. In addition to revitalizing other aged tissues exposure to factors in young blood counteracts age-related changes in these central nervous system parameters, although the identities of specific cognition-promoting factors or whether such activity exists in human plasma remains unknown. We hypothesized that plasma of an early developmental stage, namely umbilical cord plasma, provides a reservoir of such plasticity-promoting proteins. Here we show that human cord plasma treatment revitalizes the hippocampus and improves cognitive function in aged mice. Tissue inhibitor of metalloproteinases 2 (TIMP2), a blood-borne factor enriched in human cord plasma, young mouse plasma, and young mouse hippocampi, appears in the brain after systemic administration and increases synaptic plasticity and hippocampal-dependent cognition in aged mice. Depletion experiments in aged mice revealed TIMP2 to be necessary for the cognitive benefits conferred by cord plasma. We find that systemic pools of TIMP2 are necessary for spatial memory in young mice, while treatment of brain slices with TIMP2 antibody prevents long-term potentiation, arguing for previously unknown roles for TIMP2 in normal hippocampal function. Our findings reveal that human cord plasma contains plasticity-enhancing proteins of high translational value for targeting ageing- or disease-associated hippocampal dysfunction.