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HDAC9 and TWIST1 are the two candidate genes at that locus, but again TWIST1 IMO is more likely the causal gene for basically the same reasons.
Knocking out Twist1 in mice -> infinite anagen. (source)
HDAC 4 Is most likely the cause of our suffering
- Thread starter EndlessPossibilities
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HDAC9 and TWIST1 are the two candidate genes at that locus, but again TWIST1 IMO is more likely the causal gene for basically the same reasons.
Knocking out Twist1 in mice -> infinite anagen. (source)
You aren’t figuring out anything, anything said here doesn’t go past conjecture.
Do you know what they teach in basic elementary science?
The funny thing is you’re getting offended when I present an opposing view to your conjectures and the data doesn’t even confirm your bone hairloss theory.
So are several others, this isn’t the be all end all.
Nope. Twist1 might be though
Wtf are you really taking rapamycin??
Of course. I'm going to stop when I take CHIR/VPA because mTOR mediates the reprogramming
You’re crazy. Exposing yourself to health risks like that and playing with your immune system, wow.
You must be NW0 by now looking at your crazy regime…sheesh even CsA!
I'm not taking rapamycin for hair, I take it for health. Low dose rapamycin doesn't suppress the immune system. What it does is suppress mTOR and mimics caloric restriction to slow aging. Incidentally it may prevent stem cell depletion in HFs due to Wnt overactivation.
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if your regime didn't cure you already its over for me
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What's your protocol for hair?
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Mines is shemale drugs
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I’m finding you everywhere
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people like you clog the threads and make it difficult for people to read and learn. You make a name for yourself as someone to ignore
get a life
good one, got me there. Proving my point
hahaha
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Great work as always mods.
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@pegasus2 So I think hdac4 is associated with vertex balding. And hdac9 causes frontal balding. Together. U go fully bald. Why do I think that. Well apparently hdac4 is overexpressed in prostate cancer. and prostate cancer is only associated with vertex balding. This could really explain alot of things.
but I am not sure. I looked at diseases with lack of twist2 expression. Most of them have vertex balding.
one thing is for sure. Twist 1 and 2 control skull shape. And this explains why we see balding people it’s bad skull shapes
looking at twist1 and what it does. I am starting to understand something. We need twist1. Just not too much. Too much and we get hairloss.
too low and we get bone abnormalities growing up.
low enough to I believe is The key. So that group buy u about to do. Keep dosage low.
but I am not sure. I looked at diseases with lack of twist2 expression. Most of them have vertex balding.
one thing is for sure. Twist 1 and 2 control skull shape. And this explains why we see balding people it’s bad skull shapes
looking at twist1 and what it does. I am starting to understand something. We need twist1. Just not too much. Too much and we get hairloss.
too low and we get bone abnormalities growing up.
low enough to I believe is The key. So that group buy u about to do. Keep dosage low.
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@pegasus2 yo check this out. TWIST1 haploinsuffecieny results in craniostenosis
look at this bottom photos. https://www.drderderian.com/sagittal-craniosynostosis
Saethre-Chotzen have twist 1 dysfunction. And low hairlines. Interestingly low twist 2 function related disease also seems relate to low hairlines. But they often have sparse hair.
look at this bottom photos. https://www.drderderian.com/sagittal-craniosynostosis
Saethre-Chotzen have twist 1 dysfunction. And low hairlines. Interestingly low twist 2 function related disease also seems relate to low hairlines. But they often have sparse hair.
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Proposed solution. Upregulate twist2. Downregulate twist1. Problem solved. Could it be that easy.
hdac9 upregulated twist1. But if hdac9 is too low. Strokes are more likely.
so lower hdac9 . Class 2a hdac inhibitor should do it.
twist2 is most def necessary more than twist1. But I am unsure if we need to lower it or increase it or how hdac4 actually interacts with it.
perhaos focusing just on the twists instead of the heads is the solution
hdac9 upregulated twist1. But if hdac9 is too low. Strokes are more likely.
so lower hdac9 . Class 2a hdac inhibitor should do it.
twist2 is most def necessary more than twist1. But I am unsure if we need to lower it or increase it or how hdac4 actually interacts with it.
perhaos focusing just on the twists instead of the heads is the solution
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Saethra chotzen disease. Low and or dysfunctioning twist1. Results in zero recession in all including adult males at least based on all the online presentations.
we just need to figure out a few things. how do the hdacs regulate these twists and how can we regulate them ourselves. And we need to figure out what do with twist2.
we just need to figure out a few things. how do the hdacs regulate these twists and how can we regulate them ourselves. And we need to figure out what do with twist2.
