Cosa ti cambia se vedi la foto vediamo Lo hanno detto tutti che vai in dm a cercare aiuto E poi si capisce subito come quando avete preso di mira Pepito Oppure "siamo tutti pinzie" Guarda caso i soliti 4 malleabili. Poi perché scrivi romano? Io te lo ripeto, tu hai gravi disturbi

This study revealed that cases of myocarditis have surged by 620% among people who received Covid mRNA injections. It also found that Covid shots caused a 175% spike in pericarditis. nature.com/articles/s41467-0…

Most cancer drugs approved by European regulators lack a high clinical benefit, analysis finds statnews.com/pharmalot/2026/…

Chart 11 - Cancer Excess Mortality Ages 0-54 (USA - No PFE) Steady escalation through 57.2% elevated versus 2010-2019 historic baseline. This is a 20-sigma event, or 60,700 excess deaths from cancer since Week 14 of 2021. This excess cancer mortality composes 37% of the total cancer excess mortality the US has experienced since Week 14 of 2021. This age bracket normally contributes only 8 to 11% of all cancer mortality ...so the post-vax novel risk to this age bracket is now 360% higher than it was in 2020 and prior. The 2020 dry tinder surge in cancers for this age bracket is NOT TREND DATA. This was early capture of persons already dying from cancer - contributing a later pull-forward effect (PFE) in the signal data, which is not even taken into account in this inflection chart. Note: One CANNOT manipulate the baseline in this analysis (paltering) in order to get this inflection to disappear. The baseline is corroborated by 2010 - 2019 per-100K Age-Standardized CDC/NCHS Cancer Mortality data. Do not allow fraudsters to deceive you on this principle inside a DFT-Inflection chart. This analytical method is superior to trend analysis, and is how we detected the excess cancer mortality signal in July of 2021 - and alerted the world over it. 😔

Scientists discover a surprising link between vitamin C and cancer survival sciencedaily.com/releases/20…

Appreciate very interesting presentation this morning by Professor Shengliang Zhang @shengliang15 at #eldeirylab group meeting of an interesting paper in the October 1, 2026 issue of @ScienceMagazine Loss of the tumor suppressor p53 generates a signaling gradient that drives epithelial clonal expansion “p53 restrains epithelial colonization by maintaining a network that controls both the strength and spatial organization of Wnt signaling. Its loss creates a radial Wnt activity gradient that is associated with sustained progenitor self-­ renewal and rapid clonal expansion. These findings show that the spatial pattern of a growth signal, not only its overall level, can determine how mutant cells spread through normal tissue.” “Trp53−/− clones sustain a higher rate of progenitor renewal at the center than at the edges and in surrounding WT cells, enabling sustained expansion over time. This mode of growth contrasts with that of HrasG12V mutant clones, which exhibit lower renewal at the center than at the edge.” science.org/doi/10.1126/scie… I am reminded of a classical paper in Science in 2000 “Hematopoietic stem cell quiescence maintained by p21cip1/waf1” pubmed.ncbi.nlm.nih.gov/1071… and would suspect that loss of p21(WAF1) regulation by p53 in a state of p53 deficiency might contribute to a more proliferative state in the presence of Wnt activation. I am also reminded of a paper from 3 decades ago “p53-independent transcriptional activation of p21 by vitamin D3 “Transcriptional activation of the Cdk inhibitor p21 by vitamin D3 leads to the induced differentiation of the myelomonocytic cell line U937” genesdev.cshlp.org/content/1… Such control as summarized in “Vitamin D and the skin: Physiology and pathophysiology” pmc.ncbi.nlm.nih.gov/article… “Regulation of these actions is exerted by a number of different coregulator complexes including the coactivators vitamin D receptor interacting protein (DRIP) complex also known as Mediator and the steroid receptor coactivator (SRC) family (of which SRC 2 and 3 are found in keratincytes), the inhibitor hairless (Hr), and β-catenin whose impact on VDR function is complex.” Thus there is complex regulation of skin proliferation and one would hope future studies will investigate and discuss in more depth the complex regulatory networks that involve, growth, differentiation and cancer in p53-dependent and -independent pathways in epidermis and other tissues that also look at role of p53 family members. science.org/doi/10.1126/scie… @theNCI @AACR @AmericanCancer @BrownUniversity @ASCO @WIN_Consortium @Dr_R_Kurzrock @AACRPres @VivekSubbiah @SewantiLimaye @NCIDirector

In new study, we show that SARS-CoV-2 has evolved decreased inherent antigenicity in humans, as quantified by a ~3-fold decrease in the number of naïve human B cells that can bind the spike RBD. doi.org/10.64898/2026.10.15.…

BREAKING STUDY: Intramuscular mRNA Injections Distribute to Vital Organs, Resulting in Systemic Spike Protein Production Spike protein expression observed in critical organs, including the liver, spleen, lungs, heart, head, and kidneys. Even at low doses (0.0005 mg/kg), systemic distribution of LNPs and translated mRNA was measurable. These data demonstrate that COVID-19 mRNA injection LNPs systemically circulate and are taken up into vital organ systems resulting in body-wide toxic Spike protein production. Biodistribution studies should have been performed BEFORE mass ‘vaccination’ of the entire world’s population. These invasive gene therapy injections must be pulled from global markets immediately. nature.com/articles/s41587-0…

🚨 BREAKING: CAN AN ALGORITHM TELL THE DIFFERENCE BETWEEN NATURE’S DNA AND HUMAN-MADE CODE? WE JUST PROVED IT CAN - BLINDLY! 🧬🔍💥 New Version v8 (v14.7) is LIVE on Zenodo (11K+ views, 3K+ downloads!): 👉 doi.org/10.5281/zenodo.23287… Let’s explain what we just discovered in plain, simple language: 👇 When humans engineer synthetic DNA in a lab, they usually check only one thing: "Does this sequence translate into the right protein?" (the static letters). They don’t see that living nature writes DNA using a hidden, medium-range grammatical rhythm - a 30-codon sequential program that guides how the ribosome builds life in real time. So we ran a blind forensic test on Craig Venter’s famous synthetic cells (JCVI-syn1.0 and JCVI-syn3.0) against wild natural Mycoplasma. We forbade our script from reading any gene names or annotations. We just fed it raw DNA letters and asked: "Find what doesn't belong." 🎯 THE RESULT WAS A FORENSIC BULLSEYE: 1️⃣ Out of 789 genes in JCVI-syn1.0, our algorithm flagged 12 genes where the natural syntactic program completely collapsed (d3b < 0). When we opened the labels, those exact outliers were the FOREIGN VECTOR GENES artificially stitched in by human engineers: • E. coli beta-galactosidase lacZ (d3b = -0.4564) • Yeast marker HIS3 (d3b = -0.4286) • Plasmid ampicillin-resistance gene bla (d3b = -0.2353) • Synthetic assembly cassettes (d3b = -0.5294)! 2️⃣ Even crazier: Venter’s team hid secret ASCII "watermarks" inside the genome (their names and quotes from James Joyce & Richard Feynman). Our scanner flagged 10 out of 10 watermark regions as total syntactic voids across all reading frames (d3b down to -0.4825)! 3️⃣ And when we tested JCVI-syn3.0 - where engineers deleted those foreign markers and kept only 412 essential natural Mycoplasma genes - 0 out of 412 genes failed! 100% of nature’s core genes kept their positive program intact! 🌋 BONUS FRONTIER TESTS IN THIS RELEASE: • Giant DNA Viruses (Mimivirus, Megavirus, 2.47-Mb Pandoravirus, and 30,000-year Siberian permafrost Pithovirus): 4/4 pass our strict 7/7 cellular test! They are NOT "genetic junk" - they carry a full, ancient cellular-grade software architecture. • "Hell Boreholes" & 122°C Abyssal Extremophiles (Desulforudis audaxviator living 2.8 km underground on uranium radiation in total isolation, and Methanopyrus kandleri at 122°C): 4/4 pass 7/7! The 30-codon program is universal across the biosphere. ⚙️ SIMPLE TO RUN - RUTHLESS DISCRETE MATHEMATICS UNDER THE HOOD: To the user, it is a single command line in Python. Behind that simplicity stands a rock-solid discrete mathematical apparatus: • 64×64 Markov transition operators in true reading frame; • A strict 10-level hierarchy of null models (H0–H7) stripping away GC isochores, order-2 nucleotide trigrams, amino-acid bigrams, synonymous multisets, and all 32 Watson–Crick reverse-complement mirror pairs (Jean-Claude Perez’s parity law); • Exact support across 8 genetic code tables & non-parametric bootstrap confidence intervals. 🔓 100% OPEN SOURCE & SELF-TESTING: No black boxes. No "trust me, bro." Download the 31-page preprint, the autonomous Python pipelines (super_codon_autonomous_v14.py, super_codon_proof_v14_6.py, super_codon_proof_v14_7.py), and 1 MB of full execution logs - and verify every single number on your own machine in minutes! 💻🔥 Researchgate: researchgate.net/publication… #Bioinformatics #Genomics #SyntheticBiology #OpenSource #DiscreteMath #DNA #Python #Science