Ya know when stupid USA charges 15,K. for a month of dialysis for the millions suffering kidney disease caused by gene sharing stealth infections they refuse to treat,
when you can get it in SA for 1000 a month what part of robbing you while they murder you in denial of real treatment for the cause do you just not unnerstand??? http://www.ploscompbiol.org/article/info:doi/...
Previously, we had developed a pipeline for rapidly identifying LGT between Wolbachia and its hosts by using NUCMER (Figure 1A). BLASTN against NT was used to further validate such transfers. http://f1000.com/12877956...
Researchers in Italy and subsequently in the UK have recently (October and November 2011) published findings that demonstrate Bartonella heslslae
transferring DNA to human endothelial cells.
Endothelial cells are the thin layer of cells that line the interior of blood vessels.
Just because its not expressed never meant it was not there.
Two main conclusions can be derived from our studies. First, we show that when B. burgdorferi come in direct contact with epithelial cells
the spirochetes can extract cholesterol from epithelial cell membranes.
Second, both cholesterol and the antigenic cholesterol-glycolipids of B. burgdorferi
are transferred to epithelial cells
through direct contact between the spirochete and the plasma membrane and through released OMV. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3...
Recombinant expression of soluble murine Prion protein for C-terminal modification. http://www.ncbi.nlm.nih.gov/pubmed/23337878
FEBS Lett. 2013 Jan 18. pii: S0014-5793(13)00021-5. doi: 10.1016/j.febslet.2012.12.026. [Epub ahead of print]
It really cannot get any worse unless they add something that goes very viralent to the mix.
"Prior exposure to LPS induces "endotoxin tolerance"
that reprograms TLR4 responses
to subsequent LPS challenge by altering expression
of inflammatory mediators.
Endotoxin tolerance is thought to limit the excessive cytokine storm and prevent tissue damage during sepsis
but renders the host immunocompromised
and susceptible to secondary infections.
Tolerance initiated via one TLR can affect cellular responses to challenge via the same TLR ("homotolerance") or through different TLRs ("heterotolerance"). " http://www.ncbi.nlm.nih.gov/pubmed/23695305
And what infections do we already know can give you that immune suppression that causes you to tolerize multiple infections in the immune suppression junk DNA in vaccines have caused? http://www.biomedcentral.com/1471-2180/9/137
Genome sequencing of diverse bacterial species has revealed widespread distribution of conserved gene products with as-yet unknown functions. Among these are a family of small proteins with approximate molecular masses of 12 kDa, which have been variously classed as
"domain of unknown function" (DUF) 149, Pfam 2575 and COG-0718 .
Such genes have been identified in a wide variety of bacterial phyla,
a list that includes many significant pathogens of humans, domestic animals and plants (Fig. 1).
thumbnailFigure 1. Alignment of the predicted amino acid sequences of YbaB/EbfC orthologs of
H. influenzae (Hi),
E. coli (Ec),
Vibrio cholerae (Vc),
Pseudomonas putida (Pp),
Rickettsia rickettsiae (Rr),
Neisseria gonorrhoeae (Ng),
Bdellovibrio bacteriovorus (Bba),
Clostridium perfringens (Cp),
Bacillus subtilis (Bs),
Enterococcus faecalis (Ef),
Streptococcus pneumoniae (Sp),
Mycobacterium tuberculosis (Mt),
Bacteroides capillosus (Bc), and
B. burgdorferi (Bbu).
Identical amino acids are boxed and shaded. Amino acid residues of YbaBEc and YbaBHi that comprise αlpha-helices 1 and 3 of their determined protein structures are identified.