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Originally posted by Starwise
reply to post by ErroneousDylan
S&F!!!!
WHAT A FIND!! I HOPE ITS REAL!!!!!!!!!
I was just diagnosed with MS and this could lead to a real cure!
*Happy Dancing* Well not literally, but I am in my mind
Originally posted by Diggz
Great read. Hopefully this could actually be applied to humans.
I wonder if those are the actual scissors they used in the experiment.
Mutations in SPG4, the gene that encodes spastin in humans, are the most common cause of HSP, but adult onset of degeneration is difficult to explain based on studies of spastin function. Most phenotypes that have been identified in model organisms or cultured neurons with reduced levels of spastin are developmental. For example, knockdown of spastin in zebrafish embryos leads to axon outgrowth defects (Wood et al., 2006), knockdown in mammalian cultured neurons leads to axon branching defects (Yu et al., 2008), and Drosophila mutants have synaptic defects at the neuromuscular junction (Sherwood et al., 2004; Trotta et al., 2004) and dendrite branching defects (Jinushi-Nakao et al., 2007). However, in human disease, developmental defects do not seem to be present in many cases. Instead, disease onset occurs after several asymptomatic decades of life.
Originally posted by Wolfenz
reply to post by ErroneousDylan
Now if Only Superman AKA Christopher Reaves Could see this Now ...
I have severe MS. Secondary progressive to be more specific. If this will help to reattach the nerves destroyed or damaged, than please put me in line for the trials. It took me 3+ hours to be able to walk today. I am soooo tired of this crud!
Originally posted by The X
I just gave this news to my girlfriend who has MS, she was very excited about it, but, i guess it wil be 5 - 10 years before a viable gene therapy treatment is going to be available.
Nevertheless, there are millions of people who are blighted by such disease who will benefit from this research, if not now, in the future generations.
Professor rolls, well done chap, thank you!!.
Originally posted by Propulsion
I have severe MS. Secondary progressive to be more specific. If this will help to reattach the nerves destroyed or damaged, than please put me in line for the trials. It took me 3+ hours to be able to walk today. I am soooo tired of this crud!
Originally posted by The X
I just gave this news to my girlfriend who has MS, she was very excited about it, but, i guess it wil be 5 - 10 years before a viable gene therapy treatment is going to be available.
Nevertheless, there are millions of people who are blighted by such disease who will benefit from this research, if not now, in the future generations.
Professor rolls, well done chap, thank you!!.