
Epid @UNCpublichealth | Biostats @usfcoph | Math/CS @XavierU | Biochem @TulaneCBE || đ Ascending beyond just healthy aging mandates https://teapawt.org/t.co/JE2bhVjCml đ
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Joined October 2023
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NIASCEND | Dr. Dmitry Kats retweeted
Trillions wasted into AI drug discovery isnât solving disease but simply accelerating biopharmaâs ongoing cash grab for patentable downstream analogues. It is deeply concerning that @Google for one is co-conspiring in fraud, this naive, or under coercion?
share.gemini.google/VWUcV0MPâŚ
NIASCEND | Dr. Dmitry Kats retweeted
I will keep going until @Googleâs move:
share.gemini.google/92aXGT1HâŚ
share.gemini.google/20RhHfTrâŚ
share.gemini.google/QxQ64oOGâŚ
share.gemini.google/XXdMx6HzâŚ
share.gemini.google/HEiafUx6âŚ
share.gemini.google/mfvF4CJfâŚ
share.gemini.google/5ArvCPzfâŚ
share.gemini.google/W53pOALJâŚ
share.gemini.google/FSiMaLTyâŚ
Get your đżâŚ
NIASCEND | Dr. Dmitry Kats retweeted
Such^ groundbreaking medical advancements only collect dust in top journals like @Nature. Naturallyâlike their partnersâthey prefer the wealth and acclaim per their role in the âracing to find answersâ archetype vs. being rendered useless if they ever promoted even mentioned them
Replying to @NIASCEND
As they conveniently "ignored" 99.4 of relatively needed nicotinic acid mass! But don't worry -- because the BRILLIANT investigators at UC Berkeley teamed up with the most advanced AI drug discovery capabilities to provide you the fix for that... you see how they do it?
Suckers
NIASCEND | Dr. Dmitry Kats retweeted
These fundamentals have already been disentangled to realize not just safe, effective but THE CAUSAL intervention, however, thereâs no $ in their transparencyâwhereas merely hyping ânext-genâ AI to inevitably lead to rinse-repeat âdiscoveringâ futile analogues of them strikes oil
Imagine when AI consistently generatesânot some estimateâbut the EXACT causal effect of ANY intervention on ANY outcome possibleâdown to the VERY DAY it happens!
By 2020, I already did.
Weâ@OpenAI, @Merck, & Iâseek fellow frontierists ready to leadâŚ
đŻ aging-us.com/article/102916/âŚ
NIASCEND | Dr. Dmitry Kats retweeted
Donât let on the one hand my below excerpt go over your head but AI digitizing tryptophan degrading out proteins along pellagra on the other hand charm you
realize the exponentially amplified oxidative degradation of tryptophan coupled to niacinâs lack driving protein misfolding
Replying to @NIASCEND @SmartScience
8/9 Historic investigations uncovered ultimately how w/o adequate nicotinic acid supplementation, tryptophan is left exposed for inflammation to accelerate its oxidative degradation along the kynurenine pathway, diminishing the pool left for protein turnover and tissue repair.
NIASCEND | Dr. Dmitry Kats retweeted
Replying to @AlanaDLevin
Wonder whyâŚ
Early-life antibiotic dysbiosis impairs microbial tryptophan-nicotinic acid metabolism exacerbating food allergy in adulthood
sciencedirect.com/science/arâŚ
NIASCEND | Dr. Dmitry Kats retweeted
That they donât even realize what tryptophan is for?
Early-life antibiotic dysbiosis impairs microbial tryptophan-nicotinic acid metabolism exacerbating food allergy in adulthood
sciencedirect.com/science/arâŚ
NIASCEND | Dr. Dmitry Kats retweeted
Replying to @AlanaDLevin
But not this eh?
Early-life antibiotic dysbiosis impairs microbial tryptophan-nicotinic acid metabolism exacerbating food allergy in adulthood
sciencedirect.com/science/arâŚ
NIASCEND | Dr. Dmitry Kats retweeted
Imagine when AI consistently generatesânot some estimateâbut the EXACT causal effect of ANY intervention on ANY outcome possibleâdown to the VERY DAY it happens!
By 2020, I already did.
Weâ@OpenAI, @Merck, & Iâseek fellow frontierists ready to leadâŚ
đŻ aging-us.com/article/102916/âŚ
đ¤ Made with AI
NIASCEND | Dr. Dmitry Kats retweeted
NA proves itâs the ONLY NAD choice BY the flushânot balk but SIGN of enough potential energy flux as NAADP through NAD/NADP for excess energy expenditure vs accrual along aging/disease thatâs STRONGER than exerciseâshaking potential energy out storesâexposing NAM/NMN/NR as futile
Replying to @NIASCEND @j0ssyoursalad
The [anti-inflammatory] flush [which for those more pellagric from the start is far less hostile coming w/ necessary tryptophans to restore tissue niacin binds toâGPR109Aâthat grew fried away as a result of decades w/o niacin]ârememberâis nothing more than a random âside effectâ!
NIASCEND | Dr. Dmitry Kats retweeted
I would take HOM3OSTASIS.com/NIASCEND seriouslyâand monogamously
Tryptophan-Nicotinic Acid Metabolism in Patients with Tumours of the Bladder and Kidney
pmc.ncbi.nlm.nih.gov/articleâŚ
Cheers!
NIASCEND | Dr. Dmitry Kats retweeted
Replying to @TradesByJacob @CaseySapp
Not cures. But many treatments can get you back to a functional human.
Have you tried Niacin therapy?
Helped me bigtime in 2020 then they wiped @NIASCEND off the social medias
NIASCEND | Dr. Dmitry Kats retweeted
Marketing amides over nicotinic acid defies logic. NMN, NR, and NAM start behind, choked by deamidation bottlenecks that can never yield or realize high-level NA flux. Paying a premium for amides buys an inherently throttled pathway that fails where direct NA succeeds.
NIASCEND | Dr. Dmitry Kats retweeted
Mainstream longevity marketing reframed the harmless flush as a structural flaw to push patented, non-flushing amides like NMN & NR, steering public focus away from direct nicotinic acid, locking consumers into fruitless derivative pathways, and hiding the kinetic reality. (1/6)
NIASCEND | Dr. Dmitry Kats retweeted
Commercial amides hit strict low-capacity NAMPT limits, requiring slow, rate-limited deamidation just to yield free nicotinic acid, meaning they deliver only a weak, metered trickle instead of the uncompromised metabolic surge required for real disease reversal. (2/6)
NIASCEND | Dr. Dmitry Kats retweeted
While conventional studies track static, superficial biomarker snapshots, my advanced MCMC-simulated Bayesian joint models of life-course ARIC cohort dataârigorously accounting for non-ignorable attritionâproved uncompromised nicotinic acid flux is completely irreplaceable. (3/6)
NIASCEND | Dr. Dmitry Kats retweeted
Chronic cellular stress creates an unrelenting metabolic demand for NAD+, rapidly draining and degrading natural tryptophan reserves through inflammatory cascades, leaving cellular engines completely underpowered when patched with dead-end amides. (4/6)
NIASCEND | Dr. Dmitry Kats retweeted
Achieving complete metabolic restoration requires precise structural pairing: combining direct nicotinic acid with a rare, free-form L- and D-tryptophan fraction where the D-enantiomer acts as a vital kinetic shield against enzymatic degradation. (5/6)
NIASCEND | Dr. Dmitry Kats retweeted
Direct nicotinic acid instantly surges the Preiss-Handler pathway, driving high-velocity NAD+ to NAADP+ flux while utilizing the temporary physical flush as the definitive boundary marker proving peak endolysosomal potential energy release and homeostatic mastery. (6/6)
NIASCEND | Dr. Dmitry Kats retweeted
Replying to @dantawfik
Incorrect. ULK1 is totally downstream, subsidiary, just one of many sub proteins dependent on nicotinic acid binding to properlyâw/ enough d-tryptophanâmodulated GPR109A protein:
mdpi.com/1422-0067/21/9/3321
pmc.ncbi.nlm.nih.gov/articleâŚ
academia.edu/127710430/NicotâŚ
pmc.ncbi.nlm.nih.gov/articleâŚ










































