The International Journal of Clinical Practice
Posted on Wiley DOI: 10.1111/ijcp.13795
Written by Timothy Cardozo
Department of Biochemistry and Molecular Pharmacology,
NYU Langone Health, New York, NY”
“Supported by NIH award R21AI157604 (to TC).”
“Informed consent disclosure to vaccine trial subjects of risk of
COVID-19 vaccines worsening clinical disease”
https://onlinelibrary.wiley.com/doi/epdf/10.1111/ijcp.13795
“Results of the study: COVID-19 vaccines designed to elicit neutralising antibodies may sensitise vaccine recipients to more severe dis-ease than if they were not vaccinated.
Vaccines for SARS, MERS and RSV have never been approved, and the data generated in the development and testing of these vaccines suggest a serious mechanistic concern: that vaccines designed empirically using the traditional approach (consisting of the unmodified or minimally modified coronavirus viral spike to elicit neutralising antibodies), be they composed of protein, viral vector, DNA or RNA and irrespective of delivery method, may worsen COVID-19 disease via antibody-dependent enhancement (ADE).
This risk is sufficiently obscured in clinical trial protocols and consent forms for ongoing COVID-19 vaccine trials that adequate patient comprehension of this risk is unlikely to occur, obviating truly informed consent by subjects in these trials.
Conclusions drawn from the study and clinical implications: The specific and significant COVID-19 risk of ADE should have been and should be prominently and independently disclosed to research subjects currently in vaccine trials, as well as those being recruited for the trials and future patients after vaccine approval, in order to meet the medical ethics standard of patient comprehension for informed consent.”
Pre-planned Graphene Oxide Cyborgization of billions of humans through COVID-19 shots of Graphene to criminally trick and medically transhuman its victims instead of a vaccine designed to treat or cure seen via even just “PROVIDE ME WITH JUST ONE EXAMPLE” criteria, in the deployment of what will be 42,000 plus 5G satellites via SpaceX alone?:
https://spacenews.com/spacex-submits-paperwork-for-30000-more-starlink-satellites/
“SpaceX submits paperwork for 30,000 more Starlink satellites
by Caleb Henry — October 15, 2019
Updated Oct. 15 at 6:18 p.m. Eastern to include a statement from SpaceX.
WASHINGTON — SpaceX has asked the International Telecommunication Union to arrange spectrum for 30,000 additional Starlink satellites.
SpaceX, which is already planning the world’s largest low-Earth-orbit broadband constellation by far, filed paperwork in recent weeks for up to 30,000 additional Starlink satellites on top of the 12,000 already approved by the U.S. Federal Communications Commission.
…In its filings, SpaceX said the additional 30,000 satellites would operate in low Earth orbit at altitudes ranging from 328 kilometers to 580 kilometers.
SpaceX said the satellites will have steerable spot beams to link with customers, and “omnidirectional” beams for spacecraft telemetry, tracking and control functions.”
Then from Since before the fall of 2019, after reading the following Medical Journal Paper, you too can also conclude with reasoning and thinking on all the information of Parts 1 - 4 on "Don't take the Shot(s)" that I have provided you, that
with at least 2 years planning minimum for the 5G assembly of Graphene
Shots or right after Trump was legally elected and General Flynn taken
out to prevent disclosure of the Big Tech & Pharmaceutical Industry
TREASON, this entire medical tyranny takeover with the corrupt DNC &
the RINOS was already in place, laid out, and given a green light by
the Rockefeller Empire Financiers of the US Government Elites.
Aggregate
Aggregate published by South China University of Technology; 2021;2:e18.
Republished in English under WILEY:
AIE Institute and John Wiley & Sons Australia, Ltd.
“Self-assembled magnetic nanomaterials: Versatile theranostics
nanoplatforms for cancer”
“Received: 1 November 2020 Revised: 7 December 2020 Accepted: 18 December 2020”
https://onlinelibrary.wiley.com/doi/epdf/10.1002/agt2.18
by Shuren Wang, Zhiyi Wang, Yanglong Hou
“Abstract
Self-assembled magnetic nanomaterials (MNMs) are a class of promising biomaterials possessing excellent physiochemical and biological characteristics, making them highly attractive in biomedical applications. A myriad of magnetic nanosystems can be created by using self-assembly as a synthetic tool.
Favorable nano-bio interfacial properties are shown in these promising self-assembled magnetic nanosystems, while still retaining their physical/chemical functionalities. This review aims to provide a systematical overview of the self-assembled MNMs.”
“Nanomaterials with pharmaceutical properties could be prepared by using many kinds of materials, including liposomes, polymers, biomacromolecules, and many other inorganic nanomaterials.
…the activity of these nanomaterials can be adjusted and improved by surface modification… the self-assembly process is based on the energy minimization trend from disordered state to ordered state, and it is a strategy different from covalent conjugation…
which depends on some relatively weak noncovalent interactions, including hydrogen bonding, van der Waals, electrostatic interaction, and hydrophobic interaction.
…There are many examples of self-assembled nanomaterials according to this classification, including DNA, proteins, lipid vesicles, and superlattice nanocrystals.
…The self-assembly process can be realized by the external magnetic fields.”
[The reason for 5G Coverage by towers and 30,000 low orbit satellites is apparent when the authors state:]
“Magnetic field–induced self-assembly simplifies the operation steps, but requires accurate magnetic field control equipment to achieve, which increases the dependence on the equipment.”
“Molecular switches are expected to realize the reversible remote control of the aggregation behavior of nanocrystals by light-induced structural isomerization.
For example, azobenzene in trans isomers became cis under ultraviolet (UV) irradiation (Figure 3(A)). The cis state was slowly converted back to trans at room temperature, which could be accelerated by thermal or blue light….”
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