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Subject Changing Your Behaviour by Introducing a Single Gene via a Virus or Nanoparticle to Your Brain! HAPPENING NOW!
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Original Message i came across this by accident last night because i was researching voles (they are like mice) because i have them in my yard and they are driving me nuts eating my vegetables.

anyway, from wiki on voles:

[link to en.wikipedia.org]

"Genetics and sexual behavior

The prairie vole is a notable animal model for its monogamous sexual fidelity, since the male is usually faithful to the female, and shares in the raising of pups. (The woodland vole is also usually monogamous.)

Another species from the same genus, the meadow vole, has promiscuously mating males, and scientists have changed adult male meadow voles' behavior to resemble that of prairie voles in experiments in which a single gene was introduced into the brain via a virus.[4]

The behavior is influenced by the number of repetitions of a particular string of microsatellite DNA, and the same DNA sequence is found in humans. Male prairie voles with the longest DNA strings spend more time with their mates and pups than male prairie voles with shorter strings.[5] However, other scientists have disputed the gene's relationship to monogamy, and cast doubt on whether the human version plays an analogous role.[6] Physiologically, pair-bonding behavior has been shown to be connected to vasopressin, dopamine, and oxytocin levels, with the genetic influence apparently arising via the number of receptors for these substances in the brain; the pair-bonding behavior has also been shown in experiments to be strongly modifiable by administering some of these substances directly."


source:
[link to www.scientificamerican.com]

"The manipulation of a single gene is enough to cure the wandering eye of a meadow vole. According to a report published today in the journal Nature, gene therapy that increases levels of a specific protein in the brain turned the promiscuous creatures into monogamous mates."


"gene therapy" nice way to put it, eh?


"Miranda M. Lim of Emory University and her colleagues inserted a gene that encodes for the vasopressin receptor protein directly into the brains of male meadow voles. The researchers then observed the animals' behavior as they were introduced to a variety of potential partners....


According to study co-author Larry J. Young of Emory University, the results provide evidence in a comparatively simple animal model that changes in the activity of a single gene profoundly can change a fundamental social behavior of animals within a species.



"Of course, it's a big step from voles to people, but the researchers hope the results will contribute to a better understanding of how human attachments form"


this is frightening, imo.

they can change behaviour PROFOUNDLY by giving you a virus which changes your DNA.
they can do this NOW.

horrifying.
what are they doing to us?

gene therapy:
[link to en.wikipedia.org]

"Gene therapy is the use of DNA as a pharmaceutical agent to treat disease. It derives its name from the idea that DNA can be used to supplement or alter genes within an individual's cells as a therapy to treat disease. The most common form of gene therapy involves using DNA that encodes a functional, therapeutic gene in order to replace a mutated gene. Other forms involve directly correcting a mutation, or using DNA that encodes a therapeutic protein drug (rather than a natural human gene) to provide treatment. In gene therapy, DNA that encodes a therapeutic protein is packaged within a "vector", which is used to get the DNA inside cells within the body. Once inside, the DNA becomes expressed by the cell machinery, resulting in the production of therapeutic protein, which in turn treats the patient's disease."

"Gene therapy using an Adenovirus vector. A new gene is inserted into an adenovirus. If the treatment is successful, the new gene will make functional protein to treat a disease."

define "dis-ease"

what do YOU need to be "cured" of in their eyes?

+++


"Vectors in gene therapy

Main article: Vectors in Gene Therapy
Gene therapy utilizes the delivery of DNA into cells, which can be accomplished by a number of methods. The two major classes of methods are those that use recombinant viruses (sometimes called biological nanoparticles or viral vectors) and those that use naked DNA or DNA complexes (non-viral methods).
[edit]Viruses
Main article: Viral vector
All viruses bind to their hosts and introduce their genetic material into the host cell as part of their replication cycle. Therefore this has been recognized as a plausible strategy for gene therapy, by removing the viral DNA and using the virus as a vehicle to deliver the therapeutic DNA.
A number of viruses have been used for human gene therapy, including retrovirus, adenovirus, lentivirus, herpes simplex virus, vaccinia, pox virus, and adeno-associated virus.[3]"

methods of delivery of "gene therapy, both viral and non viral:

[link to en.wikipedia.org]

"Gene Gun
The use of particle bombardment, or the gene gun, is another physical method of DNA transfection. In this technique, DNA is coated with gold particles and loaded into a device which generates a force to achieve penetration of DNA/gold into the cells."

"Inorganic Nanoparticles
Inorganic nanoparticles, such as gold, silica, iron oxide (ex. magnetofection) and calcium phosphates have been shown to be capable of gene delivery.[7] Some of the benefits of inorganic vectors is in their storage stability, low manufacturing cost and often time, low immunogenicity, and resistance to microbial attack. Nanosized materials less than 100 nm have been shown to efficiently trap the DNA or RNA and allows its escape from the endosome without degradation. Inorganics have also been shown to exhibit improved in vitro transfection for attached cell lines due to their increased density and preferential location on the base of the culture dish. Quantum dots have also been used successfully and permits the coupling of gene therapy with a stable fluorescence marker."

all they have to do is spray the air with nanoparticles.
and they can profoundly change your behaviour.
your very DNA.
and pass it on to your children changing the human race forever.


Hybrid methods

Due to every method of gene transfer having shortcomings, there have been some hybrid methods developed that combine two or more techniques. Virosomes are one example; they combine liposomes with an inactivated HIV or influenza virus.

then something "triggers" it. it remains "unactivated" until the trigger for it is released and tells it to start doing it's thing.

talk about "sleeper cells"

link to online.liebertpub.com]

"tissue engineering"

release date january 2012.


"The anticipated growth in the aging population will drastically increase medical needs of society; of which, one of the largest components will undoubtedly be from orthopedic-related pathologies. There are several proposed solutions being investigated to cost-effectively prepare for the future—pharmaceuticals, implant devices, cell and gene therapies, or some combination thereof. Gene therapy is one of the more promising possibilities because it seeks to correct the root of the problem, thereby minimizing treatment duration and cost. Currently, viral vectors have shown the highest efficacies, but immunological concerns remain. Nonviral methods show reduced immune responses but are regarded as less efficient. The nonviral paradigms consist of mechanical and chemical approaches. While organic-based materials have been used more frequently in particle-based methods, inorganic materials capable of delivery have distinct advantages, especially advantageous in orthopedic applications. The inorganic gene therapy field is highly interdisciplinary in nature, and requires assimilation of knowledge across the broad fields of cell biology, biochemistry, molecular genetics, materials science, and clinical medicine. This review provides an overview of the role each area plays in orthopedic gene therapy as well as possible future directions for the field."


(these are comments i made after this post. see my comments in this thread to for the link to these sources)
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