Mutflash - Medizinische Argumentationen und Studiensammlungen
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https://t.me/Mutflash

P.s.: Leute die ohne eine vernünftige Grundlagenargumentation gegen Biom/ Virom argumentieren sind UNwillkommen!
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Impfterror

Die Krankenkasse werten die Daten aus und terrorisieren ihre Mitglieder mit dem Hinweis angeblicher Impflücken.

So sollen alle brav zur nächsten spritze marschieren. Bratwurst gibt es diesmal keine, der Brief reicht. 🤡


Die vollständige Vernichtung von Ungeimlften wurde bisher von den selbsternannten Faktencheckern als Verschwörungstheorie abgehen. Stimmt sogar, war bis dahin nur eine Theorie und nun wird die Theorie zur Realität.

Faktencheckern sind nur eine System Einrichtung um Warner zu diskreditieren. Hätte es diese Faktenchecker schon 1776 gegeben, hätten diese die Meldung, "General Washington, die Engländer kommen" als Fakenews abgetan und behauptet diese Meldung ist falsch, es kommen nicht alle Engländer sondern nur Teile der englischen Armee.


@CovidiotenTV


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https://www.youtube.com/watch?v=DJ2zE2qKd_E

Der Dummschwätzer ist zurück!

The blood-brain barrier and glutamate

"Facilitative carriers exist only in luminal membranes, and Na+-dependent glutamate cotransporters (excitatory amino acid transporters; EAATs) exist exclusively in abluminal membranes. The EAATs are secondary transporters that couple the Na+ gradient between the ECF and the endothelial cell to move glutamate against the existing electrochemical gradient. Thus, the EAATs in the abluminal membrane shift glutamate from the ECF to the endothelial cell where glutamate is free to diffuse into blood on facilitative carriers. This organization does not allow net glutamate entry to the brain; rather, it promotes the removal of glutamate and the maintenance of low glutamate concentrations in the ECF."


Chronic Glutamate Toxicity in Neurodegenerative Diseases—What is the Evidence?


"Chronically increased input via iGluRs, even if it is only moderate, has the propensity to induce neuronal degeneration, so-called chronic excitotoxicity. In many neurodegenerative diseases, including HD, AD, and ALS, multilayered evidence suggests that glutamatergic dysregulation is an important contributor to disease pathology although the molecular basis for this varies widely and might be distinct for each disease and most likely does not represent the only pathway that leads to neurodegeneration."

Glutamate Neurotoxicity and Destruction of the Blood–Brain Barrier: Key Pathways for the Development of Neuropsychiatric Consequences of TBI and Their Potential Treatment Strategies

"Thus, we novelly hypothesize that it is the integrity of the BBB that is the key factor in the context of the control of glutamate in CSF and ECF after brain damage. Specifically, this occurs after TBI, in which neurotoxicity involving high levels of glutamate causes neurodegenerative processes which ultimately lead to mental disorders"

The Role of monosodium glutamate (MSG) in Epilepsy and other Neurodegenerative Diseases: Phytochemical-based Therapeutic Approaches and Mechanisms

"MSG acts on glutamate receptors, specifically NMDA and AMPA receptors, leading to an imbalance between excitatory glutamate and inhibitory GABA neurotransmission."

Glutamate-induced and NMDA receptor-mediated neurodegeneration entails P2Y1 receptor activation

"This P2Y1R-driven neuromodulation seems to be prominent in pathological conditions, and was shown to control neuronal damage in ischemia. The contribution of ATP to neuropathological conditions may further entail other P2Rs12."

The Role of monosodium glutamate (MSG) in Epilepsy and other Neurodegenerative Diseases: Phytochemical-based Therapeutic Approaches and Mechanisms

An excessive increase in glutamate contributes to glucose-toxicity in β-cells via activation of pancreatic NMDA receptors in rodent diabetes

"Glutamate receptors, which include more than twenty subtypes, have been classified into two major categories: the ionotropic glutamate receptors (that function as ion channels) and the metabotropic glutamate receptors. Glutamate neurotoxicity is primarily mediated by N-methyl-D-aspartate (NMDA) receptors, which belong to the family of ionotropic glutamate receptors9. Recently, NMDARs have been found in peripheral non-neuronal tissues and cells, including the kidney, lung, urogenital tract and pancreatic β-cells."

"These data suggested that glutamate released from β-cells under high-glucose conditions increased the production of ROS and promoted the activation of NF-κB and NLRP3 inflammasomes, accelerating the dysfunction of β-cells through excessive activation of NMDA receptors."!

Das war mal wieder die Krzewrze in Janos Face-Version
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Wissenschaftliche Freiheit aus der Perspektive von Neugierigen
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https://www.youtube.com/watch?v=VYDe5-U9qyw

Wie wäre mit mal eine Minute mitdenken?:

N + S = IgG bei nat. Infizierten (Bevölkerung ist größtenteils durchseucht!)

+ Shedding geimpft S = igG memory durch B-Zellgedächtnis! -> Schneller und höhere Antikörpertiter!

Geimpfter hat nur Spike ohne N? Das wird euren Gedächtnis-B-Zellen sowas von scheißegal sein!

Was sagt dann ein IgG-Titer-Test?! GAR NICHTS! Sorry......

Hey... Bezahlt ruhig 25 Euro für diese simple Logik.
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Mutflash - Medizinische Argumentationen und Studiensammlungen
https://www.youtube.com/watch?v=VYDe5-U9qyw Wie wäre mit mal eine Minute mitdenken?: N + S = IgG bei nat. Infizierten (Bevölkerung ist größtenteils durchseucht!) + Shedding geimpft S = igG memory durch B-Zellgedächtnis! -> Schneller und höhere Antikörpertiter!…
Und ich mach es jetzt ganz offiziell: Jemand der von EUCH Kohle dafür haben will, dass er SEINE Studie angeblich durchziehen kann, verarscht euch nach Strich und Faden. Aber hey: Das lest ihr im Lehrbuch 8. Klasse, wo "Pseudouridyl"™(by S. Stebel) direkt neben "Eukaryotische Initiationsfaktoren" steht und Proteinfaltung losgelöst von sekundärer und tertiärer mRNA-Faltung nachzulesen ist... -_-

Sorry: Aber es sind eure 25 Euro

https://www.youtube.com/watch?v=VYDe5-U9qyw

Und wer noch Fragen nach ACEII-Rezeptor hat: Lesen was der Unterschied zw. Spaltenzymen und Rezeptoren ist!

Na Gott sei Dank ist Acetylierung und Methylierung eine Frage eures Mindsets und nicht etwa die, nach wie böse habt ihr MAPK-ERK-Signale Downstream zerkleistert?!

Nur um das ganze noch etwas näher zu erklären:

"In contrast, COVID-19 vaccines targeting the spike protein do not induce an anti-N antibody response. Therefore, anti-N antibodies can be used to detect the response to COVID-19 in those who have received a COVID-19 spike-based vaccine. However, COVID-19 spike-based vaccination has been reported to reduce the anti-N seroconversion rate if received prior to SARS-CoV-2 infection, impacting the reliability of population-level serosurveys."

(...) "In addition, the anti-N seroconversion rate was reduced following a complete course of vaccinations in those with mild or moderate symptoms, while those with the most severe symptoms had 100% anti-N seroconversion in both groups."

https://www.journalofinfection.com/article/S0163-4453(25)00030-1/fulltext

-> Ein Großteil der Bevölkerung hatte bereits Gedächtniszellen, weil er vorher durchseucht war. Gerade bei den sog. "Durchbruchsinfektionen" (trademark by Pfizer) ist davon auszugehen.

Und wer mit "restriktierte B-Zell-Anitkörperepitope" argumentieren will:

Sry:

"A recent study [41] demonstrates one mechanism through which MBC antibodies may be more adaptable to the levels of variation seen with viral point mutations or seen between ‘nearly conserved’ epitopes present on more distantly related viral strains. After analyzing several hundred recombinant antibodies cloned from plasmablasts and MBCs induced by influenza infection or vaccination, a minor subset of haemagglutinin (HA)-specific antibodies was shown to be polyreactive as defined by reactivity with a panel of diverse antigens. The majority of these HA-specific polyreactive antibodies bound the most conserved—but still variant—regions of HA, principally to the HA stalk region but also to the more conserved RBS region of the usually variable HA head. This suggested that polyreactivity is a common feature of antibodies that can bind related epitopes."

https://www.mdpi.com/1999-4915/13/4/565

-> 41:

Polyreactive Broadly Neutralizing B cells Are Selected to Provide Defense against Pandemic Threat Influenza Viruses

https://www.cell.com/immunity/fulltext/S1074-7613(20)30446-5
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