Key processes in genetic biochemistry

Two key processes are:

1) the clinically introduced New Gene (NG) is able to in a Cell (C1) replace the Old Gene (OG) that is in the cell by nature; and,

2) the clinically introduced New Gene (NG) cause cellss (C1, C2 C3 C4 etc etc) outside of C1 which the NG has entered, to become infected with the NG.

Process 1 is more basic that Process 2 because the NG has to displace the OG in C1 before C1 can transmit it to C2 C3 C4 etc.; and, the NG can be transmitted directly to C2 C3 C4 etc., in the absence of the ability of C1 to infect other cells with the NG.

The NG replacing the OG in cells, requires:

Process A: the entry of NG into C; and,

Process B: the dominance of NG over OG in C.

B can be accomplished without A

A can be accomplished without B

Process A in and of itself accomplishes nothing, if the NG is unable to assert its dominance over the OG in the cell; process B however, in and of itself can accomplish something, by acting to destroy the influence of the OG in cells from without without entering the cells, thereby decreasing the influence of the NG compared to the OG in cells (NG zero OG zero is a tie). Thus Process B is more basic than process A. Process A and Process B are part of Process 1, which is more basic than process 2. Thus the basis of biochemistry is process B, the war to increase the influence of the NG relative to the OG in cells.

Nevertheless to my surprise, I was able to find little about process B while compiling a new timeline of genetic biochemistry ( http://www.angelfire.com/ma/vincemoon/biochemtimeline.htm ) from 14 different timelines of biochemical gene therapy that I found on the internet.





@2005 David Virgil Hobbs This represents my opinion at the present time, which may not coincide with reality