Post by lilsissy on Nov 11, 2009 8:54:04 GMT -5
This is how genes put into a virus and given to us can affect us.
www.youtube.com/watch?v=v7uRFVR9BPU
edboyden.org/07.08.opticalcontrol.comment.nytimes.pdf
cut,
proof that a new generation of
genetic and optical technology can give
researchers unprecedented power to
turn on and off targeted sets of cells in
the brain, and to do so by remote control.
This virus can be put in Retinal cells which can then be put in us .
Retinal cells are said to be in the H1N1 Vaccine,
cut,
And in Detroit, investigators at Wayne State University used blind mice lacking
photoreceptors in their eyes and injected a virus carrying the channelrhodopsin gene into
surviving retinal cells. Later, shining a light into the animals’ eyes, the scientists detected
electrical signals registering in the visual cortex. But they are still investigating whether
the treatment actually brings back vision, said Zhuo-Hua Pan, a neuroscientist.
Tells how it can be done with a virus,
www.wired.com/magazine/2009/10/mf_optigenetics/all/1
Two Genes are used ChR2 and NhPR.
Chamydomonas (ChR2) had been found in numerous Morgellons samples.
This shows the human expression of the NhPR protein and how they get it into us.
Optical Inhibition: Halorhodopsin (NpHR)
The NpHR sequence here has been optimized for mammalian expression. The NpHR-EYFP inframe fusion genes are made via a NotI site with the linker GCGGCCGCC. The start codon on EYFP has been deliberately removed. To reduce membrane blebbing or other toxicity at high levels of expression, we have generated a modified eNpHR by adding signaling peptides to enhance membrane translocation and ER export.
tinyurl.com/ya9n3as
cut,
Note: Due to ease of recombination, AAV and lentivirus vectors should be amplified in a recombination deficient bacteria strain such as Invitrogen's OneShot Stbl3 cells.
Three point-mutants of humanized ChR2 convert a brief pulse of light into a stable step in membrane potential. The lentiviral vectors were created by site-directed mutagenesis of the C128 position in ChR2. All three mutants are activated by blue (470nm) light. Photocurrents generated by ChR2(C128A) and ChR2(C128S) can be effectively terminated by a pulse of green (542nm) light
Hallow hair that was
discovered by
Mark Darrah Scientist.
Reply 6.
lymebusters.proboards.com/index.cgi?board=research&action=display&thread=10186&page=1
Only polar bears have hallow hair.
Did Mark find of evidence of fiber optic's growing in Morgellon's Patient's.
ami.usc.edu/projects/ami/projects/sencil/
cut,
The external end of the fiber will be attached to a photonic analyzer by means of a connector that accepts the free end of the fiber. The analyzer sends excitation light through the fiber to reach the biosensor element and receives returning fluorescent emissions from the biosensing element through the same fiber.
This next article shows how they can use Invisible Radio waves instead of visible light for accessing our brain.
www.nature.com/nrn/journal/v8/n8/full/nrn2192.html
The optical fibre can be coupled to a bright light source such as a diode laser16. Alternative solutions may involve
high intensity light-emitting diodes (LEDs)
the LEDs could even be powered wirelessly by radio frequency or magnetic induction.
I believe I am finding some linkage between this system using these two genes that allow for the eletrically enhancement of animals and the H1N1 vaccine,
The retinal cells mentioned in the next article may be related to this , they are light encoding cells , related to the former mentioned technology.
Seems they have attached these Retinal cells to immortal cells (Mutated CANCER CELLS) to allow for endless duplication of cells that may be activated by light.
Also polymers are being used in the H1N1 vaccine.
www.elreporterosf.com/editions/?q=node/3785
Now I will show that polymers can be absorbed throught the skin and grow right in our cells and are used by the government in Areial Scattering techniques.
This thread shows how polymer can be absorbed throught the skin,
lymebusters.proboards.com/index.cgi?board=rash&action=display&thread=12597
Can be grown in our own cells,
www.iop.org/EJ/abstract/1741-2552/4/2/L02
cut,
. Nano and microscale PEDOT filaments extend out from electrode sites, presumably forming within extracellular spaces. The cloud of PEDOT filaments penetrates out into the tissue far enough that it should be possible to bypass fibrous scar tissue and contact surrounding healthy neurons. These electrically functional, diffuse conducting polymer networks grown directly within tissue signify a new paradigm for creating soft, low impedance implantable electrodes.
Are used in Government Spraying,
tinyurl.com/yjyb2rn
cut,
nanofibers and nanoporus absorbents will protect against CB threats while minimizing heat burdens and providing chameleon like color adaptation for chamouflage. The small size of the nanodevices will limit the volume,weight,and power burdens.
.....we need new weapons for this war on insecurity.
These are new scientific and technological areas that deal with structures the size of large individual molecules.
These structures , roughly 50,000 times smaller than the width of a human hair cannot be seem or felt,
...... they are invisible, they are remarkably potent.
......this is not just the technology of tommarrow - nanotechnology applications are already reality.
www.dtic.mil/cgi-bin/GetTRDoc?AD=ADA394560&Location=U2&doc=GetTRDoc.pdf
This is why we are wired ,
And this by IEEE EXPLORE,
Conductive polymer "molecular wires" increase conductance across artificial cell membranes
ieeexplore.ieee.org/xpl/freeabs_all.jsp?arnumber=1404205
color=Yellow]Highly intimate contact between an electrode and a living neuron is strongly desired by both basic neuroscientists and engineers seeking to develop more effective neural prostheses[/color]. The net resistance between electrode and cell must be decreased in order to improve the quality of recordings and deliver the minimum necessary stimulating current specifically to the target cell. The ideal situation would be to establish chronic intracellular contact, bypassing the resistance of the cell membrane and the surrounding tissue. We present here evidence that regioregular polythiophene conductive polymers increase the electrical conductance of an artificial lipid bilayer that simulates a cell membrane. Our initial data on its behavior suggest that the polymer is freely diffusing within the lipid phase. This implies that these polymers, if tethered to a larger microelectrode, could permit long-term sustainable intracellular stimulation and recording. We therefore believe that this new molecule, when further developed, has the potential to significantly improve the performance of existing chronic electrode systems and possibly to enable new types of biosensors.
This is where this all is heading,
The
HUMAN BRAIN MACHINE INTERFACE
lymebusters.proboards.com/index.cgi?board=rash&action=display&thread=12467
this shows the patent our Government has certain rights to and explains how they grow an artificial nervous system in our vascular bed .
This matches the findings of Randy Wymore From he University of Oklahoma who found,
in patient's that self diagnose as having Morgellons there exists a subcutaneous network of fibers that when teased out is a single fiber.
www.youtube.com/watch?v=mfoidtKEpqc&feature=related
This fiber network attaches ot every brain neuron which can then be remotely access via the fiber optic hair to computer software resulting in,
www.wired.com/wiredscience/2009/04/lasercontrolledhumans/
www.youtube.com/watch?v=v7uRFVR9BPU
edboyden.org/07.08.opticalcontrol.comment.nytimes.pdf
cut,
proof that a new generation of
genetic and optical technology can give
researchers unprecedented power to
turn on and off targeted sets of cells in
the brain, and to do so by remote control.
This virus can be put in Retinal cells which can then be put in us .
Retinal cells are said to be in the H1N1 Vaccine,
cut,
And in Detroit, investigators at Wayne State University used blind mice lacking
photoreceptors in their eyes and injected a virus carrying the channelrhodopsin gene into
surviving retinal cells. Later, shining a light into the animals’ eyes, the scientists detected
electrical signals registering in the visual cortex. But they are still investigating whether
the treatment actually brings back vision, said Zhuo-Hua Pan, a neuroscientist.
Tells how it can be done with a virus,
www.wired.com/magazine/2009/10/mf_optigenetics/all/1
Two Genes are used ChR2 and NhPR.
Chamydomonas (ChR2) had been found in numerous Morgellons samples.
This shows the human expression of the NhPR protein and how they get it into us.
Optical Inhibition: Halorhodopsin (NpHR)
The NpHR sequence here has been optimized for mammalian expression. The NpHR-EYFP inframe fusion genes are made via a NotI site with the linker GCGGCCGCC. The start codon on EYFP has been deliberately removed. To reduce membrane blebbing or other toxicity at high levels of expression, we have generated a modified eNpHR by adding signaling peptides to enhance membrane translocation and ER export.
tinyurl.com/ya9n3as
cut,
Note: Due to ease of recombination, AAV and lentivirus vectors should be amplified in a recombination deficient bacteria strain such as Invitrogen's OneShot Stbl3 cells.
Three point-mutants of humanized ChR2 convert a brief pulse of light into a stable step in membrane potential. The lentiviral vectors were created by site-directed mutagenesis of the C128 position in ChR2. All three mutants are activated by blue (470nm) light. Photocurrents generated by ChR2(C128A) and ChR2(C128S) can be effectively terminated by a pulse of green (542nm) light
Hallow hair that was
discovered by
Mark Darrah Scientist.
Reply 6.
lymebusters.proboards.com/index.cgi?board=research&action=display&thread=10186&page=1
Only polar bears have hallow hair.
Did Mark find of evidence of fiber optic's growing in Morgellon's Patient's.
ami.usc.edu/projects/ami/projects/sencil/
cut,
The external end of the fiber will be attached to a photonic analyzer by means of a connector that accepts the free end of the fiber. The analyzer sends excitation light through the fiber to reach the biosensor element and receives returning fluorescent emissions from the biosensing element through the same fiber.
This next article shows how they can use Invisible Radio waves instead of visible light for accessing our brain.
www.nature.com/nrn/journal/v8/n8/full/nrn2192.html
The optical fibre can be coupled to a bright light source such as a diode laser16. Alternative solutions may involve
high intensity light-emitting diodes (LEDs)
the LEDs could even be powered wirelessly by radio frequency or magnetic induction.
I believe I am finding some linkage between this system using these two genes that allow for the eletrically enhancement of animals and the H1N1 vaccine,
The retinal cells mentioned in the next article may be related to this , they are light encoding cells , related to the former mentioned technology.
Seems they have attached these Retinal cells to immortal cells (Mutated CANCER CELLS) to allow for endless duplication of cells that may be activated by light.
Also polymers are being used in the H1N1 vaccine.
www.elreporterosf.com/editions/?q=node/3785
Now I will show that polymers can be absorbed throught the skin and grow right in our cells and are used by the government in Areial Scattering techniques.
This thread shows how polymer can be absorbed throught the skin,
lymebusters.proboards.com/index.cgi?board=rash&action=display&thread=12597
Can be grown in our own cells,
www.iop.org/EJ/abstract/1741-2552/4/2/L02
cut,
. Nano and microscale PEDOT filaments extend out from electrode sites, presumably forming within extracellular spaces. The cloud of PEDOT filaments penetrates out into the tissue far enough that it should be possible to bypass fibrous scar tissue and contact surrounding healthy neurons. These electrically functional, diffuse conducting polymer networks grown directly within tissue signify a new paradigm for creating soft, low impedance implantable electrodes.
Are used in Government Spraying,
tinyurl.com/yjyb2rn
cut,
nanofibers and nanoporus absorbents will protect against CB threats while minimizing heat burdens and providing chameleon like color adaptation for chamouflage. The small size of the nanodevices will limit the volume,weight,and power burdens.
.....we need new weapons for this war on insecurity.
These are new scientific and technological areas that deal with structures the size of large individual molecules.
These structures , roughly 50,000 times smaller than the width of a human hair cannot be seem or felt,
...... they are invisible, they are remarkably potent.
......this is not just the technology of tommarrow - nanotechnology applications are already reality.
www.dtic.mil/cgi-bin/GetTRDoc?AD=ADA394560&Location=U2&doc=GetTRDoc.pdf
This is why we are wired ,
And this by IEEE EXPLORE,
Conductive polymer "molecular wires" increase conductance across artificial cell membranes
ieeexplore.ieee.org/xpl/freeabs_all.jsp?arnumber=1404205
color=Yellow]Highly intimate contact between an electrode and a living neuron is strongly desired by both basic neuroscientists and engineers seeking to develop more effective neural prostheses[/color]. The net resistance between electrode and cell must be decreased in order to improve the quality of recordings and deliver the minimum necessary stimulating current specifically to the target cell. The ideal situation would be to establish chronic intracellular contact, bypassing the resistance of the cell membrane and the surrounding tissue. We present here evidence that regioregular polythiophene conductive polymers increase the electrical conductance of an artificial lipid bilayer that simulates a cell membrane. Our initial data on its behavior suggest that the polymer is freely diffusing within the lipid phase. This implies that these polymers, if tethered to a larger microelectrode, could permit long-term sustainable intracellular stimulation and recording. We therefore believe that this new molecule, when further developed, has the potential to significantly improve the performance of existing chronic electrode systems and possibly to enable new types of biosensors.
This is where this all is heading,
The
HUMAN BRAIN MACHINE INTERFACE
lymebusters.proboards.com/index.cgi?board=rash&action=display&thread=12467
this shows the patent our Government has certain rights to and explains how they grow an artificial nervous system in our vascular bed .
This matches the findings of Randy Wymore From he University of Oklahoma who found,
in patient's that self diagnose as having Morgellons there exists a subcutaneous network of fibers that when teased out is a single fiber.
www.youtube.com/watch?v=mfoidtKEpqc&feature=related
This fiber network attaches ot every brain neuron which can then be remotely access via the fiber optic hair to computer software resulting in,
www.wired.com/wiredscience/2009/04/lasercontrolledhumans/