Hi, I have a couple of questions, firstly,
say you wanted to insert a gene like the gene for healthy CFPR channel protein, you spray you insert it into harmless adenovirus etc and spray into nostrils, however, they say it would be more effective if the could get it to stem cells, which would provide a more long-term solution, but how? Once stem cells have divided, they're not replaced with new stem cells, so does the treatment have to be repeated for the stem cells? I'm a bit confused with this...can anyone help?