'gene-cloning' means gene-copy, natch

does your physique cause nightmares?

stemcells won't help-see GENE-CULTURE

 

 

OFF LIMITS

*

KINDLY LEAVE THIS SITE ALONE - IT'S UNDER REVIEW

PARALLEL PLOTLINE:

see blog for lowdown

the website is on 'virtual' genes - see blog under 'epigenomes' - the way the body 'programs' genes can be related to environment

'Human-oriented' includes iPS reprogramming of adult skin cells, adult stemcells from bone-marrow & population-sampling for gene-variants. 'Non-human-oriented' comes down to 'breeding genes' from embryonic stemcells (ESC).

It may strike you as odd to classify ESCs 'non-human-oriented' research but similarities with hybrid-cloning (breeding human genes in non-human cells -see next page) makes it apparent both are ways of 'breeding genes'

As we know, genes are distressingly similar - what the website's dealing in is the way genes are 'programmed' by the body. In other words, it's bio-centric as opposed to techno-centric

GET YOUR JARGON HERE

ESC*  - EMBRYONIC STEMCELLS

iPSC - INDUCED PLURIPOTENT STEMCELLS

(reprogrammed genetically from adult skin cells)

piPS -PROTEIN-INDUCED PLURIPOTENT STEMCELLS

(the very latest and potentially safest technology - see link on left)

ADULT STEMCELLS -from bone marrow that grow into blood-types

HYBRID-CLONES*  -breeding human genes in non-human cells (abandoned following protest in UK - see this link!)


* THESE 2 ARE NON-HUMAN-ORIENTED RESEARCH 

Relating these 2 together makes a point that both are a type of technology for breeding of genes - using a host as a type of 'factory breeding', whatever technical term you care to give it. Since this website is talking genes, both carry human genes & in that respect are identical regardless of the 'host'.

The idea of 'virtual' genes is it is half of the equation. This is why ESC is classified here 'non-human-oriented' research - you're only looking at genes & not how they relate to human physique. If you read on, what we're dealing in is how ultra-precise that type of human-oriented research can be!

ease of 'reprogramming'

SC BLOGS:

Pragmatically, how much genetic-info is in ESCs as opposed to iPSCs which have gene-identity?

 

iPS is an in vivo protocol that uses adult skin cells: you already know how the genes will grow in nerve & muscle, so you know the disease profile (this is in addition to well-advertized downsides to ESC - auto-immune rejection-response to foreign cells).

Though claims are made for ESC, many more genuine advances & therapies are made with the other types of research listed. There are 2 problems: lack of gene-identity means immuno-suppresants may always be necessary for transplants to counter rejection. The second factor is even more vital to future studies: at this early stage there are no diseases so there are no disease-gene profiles to study!

 

The idea of the website is you can regard genes as 'virtual' which become animated only when key control-sequences are 'programmed' & a stemcell grows into nerve or muscle. Basically, the program is what counts & we know it affects only a very few control-genes.

We also know genes are easy to program - here by proteins (piPS).

CONSERVATIVE BLOGS:

(all these are opposed to ESC. I reckon there's a wider issue: 'transhumanism' & what you might call a biotech 'takeover' of the human. This might also go in 'non-human-oriented' research - see blog)

US CONSERVATIVE

URBAN CONSERVATIVE

CONSERVATIVE CULTURE

EXO-Genetic

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