Human Anatomy, Physiology, and Medicine. Anything human!
Thank you for all the information. I am starting to go through it and I hate to say what u alreay know..but this is FUBAR.
Is this correct? Because this thing is a hybrid, and every person is different,
what ultimately develops can be wildly different from person to person?
back to reading and again my thanks
Hi, I am rather dense at times. Did I do something wrong and if so, would you mind explaining it to me? I'd appreciate it.
To all: Ever heard of programmable atoms?http://tinyurl.com/y5agny
or this from wikipedia? It's called HACKING MATTER......
or PROGAMMABLE MATTER??????
here, try another one.....
Last edited by London on Fri Dec 15, 2006 12:22 am, edited 2 times in total.
Christ desires for man to be relieved of the curse of sin, which includes sickness. Therefore, in His atoning work on the cross of Calvary He made provision for man’s healing and, “...with His stripes we are healed” (Isaiah 53:5).
“Jesus Christ (is) the same yesterday, and today, and for ever” (Hebrews 13:8). He is still Jehovah-Rophe, “the Lord that healeth thee,” today!
Faith is a verb, exercise it and be well,
THANKS MARCOS....I WILL.
A while back (about a month) I asked "Have you ever heard atoms move?" I mentioned the "whiskers" of steel!!! I believe we are a magnet for them.....it is the things in you that look like hair but is not.
They are trying to make sunlight in a tube.
They used the plants to poison us with,,,,the herbs....too much of a good thing.....can be bad. Mushsrooms anyone? Trippin! J. acid? Oh I think so....
They went thru the phone lines and cable lines too. No, I don;t understand all of it, not do I intend to. Govt is doing experiments on us for their gain. Intel and Dupont is involved and that is a fact. It is doc. in a post w/ hyperlink of mine from yesterday.
So where are the vampires?
Im well aware of the vampire plants.....CAN YOU SAY DODDER???? WELL IF YOU CAN, LOOK IT UP DAMMIT....GUESS WHAT IT DOES....???? IT WRAPS AND WRAPS IT SELF AROUND WHAT IT IS ATTACKING JUST LIKE THE FIBERS FROM HELL.
THEY ARE ALL SATANIC A-HOLES AND MY ANGELS AND MY GOD WILL STRIKE THEM DOWN WITH A VENGENCE.
THERE, THE PHUCKIN END.
hey thank Puck, Pan, Gog,and Magog for that. the avatar that provides the entropy dost have only one moon and it has been borne of its self.... a most Fubar situation indeed ......
the latest wave of empathy could probably be traced to that dank cannibus that trafficks the plane... or it could be some plotted points on the ELF/GWEN haarp logorythems..... not matter its the thought that counts right...
after dwelling for many hours on the angle of approach that must undertaken to undo all this evil... and at the apex of hopelessness i stumbled apon a rash system of asysmetrical logic... what if ... like the geometrically electrical, active atmosphere on Jupiters moon Titan .....the planetoid synaptic process under goes a layering like humans put on clothes..... soo if Titan were a naked baby ....and the true core of our earth were acually a highly charged superconducting plasma , with its neurons "trees" mature ,lush with dendridic spins reaching, regulating, obsorbing, charging, dispersing all function in our atmosphere ..... forming a reflective cognating olfactory system we call "clouds" ... further skipping a few chapters we get to microbal symbiosis... "humans"
like the few toying around with attempting to controll microbial functions ...should we assume that this great vessal has perfected that art...
like every single atom the flows thru a human brain has been cultured,selected and delegated to the human by the earth.. .so from all pervading non local time domains perspective the human influance on the
environment is completely dependant upon the signal of the earth for all actions... and to rationlize the disgrace of humanities landfill habit....
maybe we are forming a GEOFILM, an elastic membrane of HPDE,and long chain polymers to cover an adult planetoids private plasma parts.
enough of this northern lights ... . . weres that damn G13?
ps on a less lighter note.....
MSC is this that Magnusson you spoke of?
http://peir.path.uab.edu/pathgrad/publi ... geting.pdf
Adenoviruses (Ads) are a family of over 50 viral mammalian
pathogens, whose nonenveloped protein capsids embody a sin-
gle copy of double-stranded DNA genome (36). Based on their
ability to agglutinate red blood cells and the homology of their
genomes, Ads have been classified into species A through F.
The vast majority of the studies of Ad biology have been done
on human Ad serotype 2 (Ad2) and Ad5, respectively, both
belonging to species C.
The well-understood life cycle of these viruses, combined
with relatively simple methods for the generation, propagation,
and purification of recombinants derived from Ad2 and Ad5,
made them attractive candidates as gene delivery vectors for
human gene therapy. However, two decades of the extensive
use of Ad-based vectors as prototypes of future gene thera-
peutics has revealed a number of limitations of this vector
system, which have hampered its rapid transition into the
clinic. One of these drawbacks is the relative inefficiency of
gene delivery by Ad vectors to certain types of diseased human
tissues. On the other hand, the susceptibility of many normal
tissues to Ad infection makes them random targets for Ad
vectors and results in the suboptimal distribution of the viruses
upon administration to patients.
Attempts to rectify this deficiency of Ad vectors have been
rationalized by the identification of the molecular determi-
nants of the virus tropism. A typical Ad capsid is an icosahe-
dron, whose planes are formed by the Ad hexon protein,
whereas the vertices are occupied by a penton assembly
formed by the penton base and protruding fiber proteins (9).
The cell entry mechanism used by the majority of human Ad
serotypes involves two sequential interactions between an Ad
particle and a cell. According to this concept, the first of the
two contacts involves the Ad fiber protein (17, 26) and the
so-called coxsackievirus and Ad receptor (CAR) (4, 39). Spe-
cifically, the carboxy-terminal knob domain of the fiber binds
to the immunoglobulin-like D1 domain of CAR (5, 13), result-
ing in the tight association of the virus with the cell. The
presence of CAR on a target cell is thus recognized as a critical
prerequisite of efficient infection. This binding step is followed
by the secondary contact, which involves the arginine-glycine-
aspartic acid (RGD) sequence found in the Ad penton base
protein and the cellular integrins v 3 and v 5 (45, 46). This
interaction triggers the internalization of the virion within a
clathrin-coated endosome (44). Acidification of the endosome
is believed to lead to the release of the virus into the cytoplasm,
followed by its translocation to the nucleus, where the repli-
cation of the virus begins. It has been reported that, whereas
CAR is used by the majority of human Ads as a primary
receptor (34), other cell surface molecules are also exploited in
this capacity by certain Ad serotypes (1, 10, 24, 35). This
observation suggests that the receptor specificity of a given Ad
serotype may be modified by redirecting the virus to alternative
This targeting concept has been realized by using the fol-
lowing strategies. In adapter-mediated targeting, the tropism
of the virus is modified by an extraneous targeting moiety, the
ligand, which associates with the Ad virion either covalently or
noncovalently. Adapters or adapter-ligand complexes success-
fully used for Ad targeting include bispecific antibody (Ab)
conjugates, genetic fusions of single-chain Ab (scFv) with
CAR, or scFv-scFv diabodies (reviewed in reference 21).
Adapter-mediated targeting is rather versatile and technically
simple, it may use a wide range of targeting ligands, and it
allows for the rapid generation of analytical amounts of tar-
geted complexes and their fast validation. However, it requires
the production and purification of at least two different com-
ponents (the virus and targeting ligand), their subsequent con-
jugation in a targeting complex, and the purification of that
complex from nonreacted components. These requirements
substantially complicate the large-scale production of the vec-
tor complex, which may result in significant batch-to-batch
variations and complicate the regulatory approval of the vector
for clinical use.
In contrast, genetic targeting, which is based on the genetic
incorporation of the ligand into the Ad capsid (reviewed in
reference 22) results in a one-component, self-assembling, and
self-replicating vector, which, once made and validated, may be
amplified to any desired scale. The choice of ligands in this
strategy, however, is limited to proteins only. Furthermore,
additional limitations may be imposed by the potential struc-
tural or biosynthetic incompatibility of the ligand with the
protein components of Ad capsid. For instance, recent studies
by Magnusson et al. (27) have shown that protein ligands, such
as the epidermal growth factor or scFvs, whose correct folding
requires the formation of disulfide bonds, cannot be used for
genetic targeting of Ad.
http://www.arl.army.mil/main/main/Downl ... 06_pt2.pdf
https://dspace.mit.edu/bitstream/1721.1 ... BCS016.pdf.
Thanks Hippyass Soul, you are the man!
Hey MSC.....you prob. already know but Lewis Acids/ Lewis base....
see: Lewis base
From Wikipedia, the free encyclopedia
A Lewis base is any molecule or ion that can form a new coordinate covalent bond, by donating a pair of electrons, named after the American chemist Gilbert Lewis. The term base is ambiguous. This is one interpretation. To put it another way, any molecule with an electron lone pair in a bonding orbital may act as a Lewis base, as it is capable of accepting an ion with a single positive charge. Lewis bases are also generally capable of forming hydrogen bonds.
A nucleophile is a Lewis base. Lewis bases do not require a hydroxide ion as the electron acceptor. Some common examples include ammonia and amides. Many anions can also be considered Lewis bases such as F-.
When a Lewis acid and Lewis base form a complex ion the Lewis base is always the ligand.
Now MCS, can you point us into stoping this?
Nad, can you?
Was not trying to scare you nor was I kidding. Now check this out re: space.
It's called the Space Elevator.......Funny, why doesent the army try it or Jurvetson or someone. How bout Mr. and Ms. Dupont?
Maybe if they use it first then I would not be so against it. What do you say Jurvetson? Duponts? Bill? George? I mean, there is nothing to be worried about right? Tell you what, if something goes awry, we will document and know not to send others there. No biggy!
PS: Or how unthoughtful of me....How bout you MothLady, Griselda?
oops! nearly forgot, you might want to take this with ya.....sorrybouthat!
http://en.wikipedia.org/wiki/Artificial ... xoskeleton
Here's some trivia facts for you guys:
Along with General Motors, DuPont was the inventor of CFCs (chlorofluorocarbons), and the largest producer of these ozone depleting chemicals (used primarily in aerosol sprays and refrigerants) in the world, with a 25% market share in the late 1980s.
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