π’ƒ²π’Œ‹π’…—π’†ͺπ’‰πŸœπŸ’© πŸ’›

@ultimape
586 Followers
230 Following
8.7K Posts

Creativity, insight, and questionable poots.
The ants seem to like it. #nobot follows plz.

Mostly talking to myself, or others who think like me.

Pronouns[Subject-pronoun] / [Reflexive]
Twitter Althttps://twitter.com/ultimape
Blog@[email protected]
Blueskyhttps://bsky.app/profile/ultimape.bsky.wovensoup.com

Happy to announce that patreon has approved my account at the current funding tier.

With this, I have successfully achieved "autistic citizen scientist bootstrapped a crowd-sourced basic income by eating dog shit"

My next life goal is my own lab.
https://glif.app/@UltimApe/runs/xuiveqktv82cdwsoaz214nen

Thank you everyone, especially @rw & moon

The [[Agora]] is a free knowledge commons that complements social networks:

https://anagora.org/agora

[[agora]] at anagora.org

The Agora is a free knowledge commons: anagora.org.

"To our knowledge, this is the first successful demonstration of direct decoding of full words from the brain activity of someone who is paralyzed and cannot speak"
https://developer.nvidia.com/blog/transforming-brain-waves-into-words-with-ai/

Sorry I haven't been very active here.

I've been really enjoying Bluesky though, so if you happen to have an account there you're welcome to follow me.

If you want to understand my content better consider this thread from a year ago about sperm banks and animal husbandry.
https://bsky.app/profile/ultimape.bsky.wovensoup.com/post/3jvxwii3jy22m

Nicholas (@ultimape) Perry (@ultimape.bsky.wovensoup.com)

Thinking about sperm banks and IFV in Denmark. https://time.com/5491636/denmark-ivf-storkklinik-fertility/

Bluesky Social

The absolutely infuriating thing about Tumblr potentially starting to silently sell off your posts unless you affirmatively check a deeply-hidden opt-out box you can only find out about through word of mouth is, if I bring up my *own* Tumblr and try to scroll back more than a few posts, it stops me literally saying "Stop: Classified". So I don't get access to my posts, but OpenAI does.

https://chat.noelle.codes/@noelle/112005577930056541

Ellie πŸβ˜ƒοΈ :blobsnowedin:​ (@[email protected])

If you have a Tumblr and you'd like them to not share the stuff you post with predictive algorithmic generators^W^W^W^H "AI", there's now a toggle in each blog's settings that tells them not to: https://www.tumblr.com/yutaleks/743510553034719232

Hoc quoque abibit.

Looks like @darius made it not suck anymore! https://github.com/mastodon/mastodon/pull/22048

Thanks!

Add exclusive lists by dariusk Β· Pull Request #22048 Β· mastodon/mastodon

This adds a checkbox to the list editor modal that lets you say a list is "Exclusive". If this is checked, the posts that appear in this list timeline do not get rendered in the user'...

GitHub

Is it still a thing where If I add people to lists It also forces me to follow them in the home feed?

The entire reason I used lists on twitter is to remove noise from home feed there.

Friendly reminder that if you are feeling sad this winter that you might be under the effects of low vitamin D. Vitamin D + Omega 3s + Tryptophan has been shown to be effective at boosting serotonin: https://www.sciencedaily.com/releases/2014/02/140226110836.htm
https://www.sciencedaily.com/releases/2015/02/150225094109.htm

In addition, there is the possibility that those 3 nutrients play a role in helping to avoid non-alcoholic fatty liver disease thru action on the microbiome. https://www.sciencedirect.com/science/article/pii/S2211124718304856

Causal link found between vitamin D, serotonin synthesis and autism in new study

Serotonin and vitamin D have been proposed to play a role in autism, however, no causal mechanism has been established. Now, researchers show that serotonin, oxytocin, and vasopressin, three brain hormones that affect social behavior related to autism, are all activated by vitamin D hormone. Supplementation with vitamin D and tryptophan would be a practical and affordable solution to help prevent autism and possibly ameliorate some symptoms of the disorder.

Jesus fuck

I wrote a paper in 2019 https://doi.org/10.1136/bmjopen-2019-034306

And the whole point of my paper is that drug repurposing doesn't save effort/cost

Khan et al cites me, saying:

> It is common for pharmaceutical companies to trial medicines for indications beyond the initially approved indication (Reference Carlisle, Doussau and Kimmelman). This significantly reduces the drug development timeline and saves cost.

https://doi.org/10.1017/S0266462323000491

Patient burden and clinical advances associated with postapproval monotherapy cancer drug trials: a retrospective cohort study

Objectives After regulatory approval, drug companies, public funding agencies and academic researchers often pursue trials aimed at extending the uses of a new drug by testing it in new non-approved indications. Patient burden and clinical impact of such research are not well understood. Design and setting We conducted a retrospective cohort study of postapproval clinical trials launched within 5 years after the drug’s first approval, testing anticancer drugs in monotherapy in indications that were first pursued after a drug’s first Food and Drug Administration (FDA) license, for all 12 anticancer drugs approved between 2005 and 2007. FDA, Medline and Embase search date 2019 February 12. Primary and secondary outcome measures Our primary objective was to measure burden and clinical impact for patients enrolling in these trials. Each trial was sorted into a β€˜trajectory’ defined by the drug and cancer indication. The risk was operationalised by proportions of grade 3–4 severe adverse events and deaths. The clinical impact was measured by estimating the proportion of patients participating in trajectories that resulted in FDA approval, uptake into National Comprehensive Cancer Network (NCCN) clinical practice guidelines or advancement to randomised controlled trials within 8 years. Results Our search captured 104 published trials exploring monotherapy, including 69 unique trajectories. In total, trials in our sample enrolled 4699 patients. Grade 3–4 adverse events were experienced by 19.6% of patients; grade 5 events were experienced by 2.8% of patients. None of the trajectories launched after initial drug approval received FDA approval. Five trajectories were recommended by the NCCN within 8 years of the first trial within that trajectory. Eleven trajectories were advanced to randomised controlled testing. Conclusions The challenges associated with unlocking new applications for drugs that first received approval from 2005 to 2007 were similar to those for developing new drugs altogether. Our findings can help inform priority setting in research and provide a basis for calibrating expectations when considering enrolment in label-extending trials.

BMJ Open

What can end up happening is that if you and said 'as-if' actor disagree on a point.

You may want to reposition the discussion back to the 'real world' and reject their imagined reality based on a disagreement on how things could have proceeded.

This suddenly cause an inherent argument, because at a fundamental level we are suddenly playing a game of "imagine this to be true, now we can imagine how it can be true in the real world". hence it feeling like sophistry.

In that case, bow out.