Ok, thanks for that, I pretty much always wonder if your posts are an attempt to be funny, since they contain so much bullshit that I always wonder if you're serious or not. But then again, they're never funny either.
So, if you're not trying to be funny, then why all that childish talk about foreskin ? Jahoda grew follicles on foreskin, since that's easily available in the medical world (donations after circumcision) and then transplanted that human skin onto SCID mice. Not sure what that has to with Dr Nigams ? He's going to try to repeat what Jahoda did, grow the cells in a 3d enviroment and then inject them into people's scalps instead of human (fore)skin on a SCID mouse. You do understand that they grew the cells in vitro ? So again, why the talk about foreskin ? It has exactly 0 to do with Nigams. So what's your point exactly ?
Dr Nigam, my own experience
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Optimism?
Okay - let me read your link and let me conclude what Dr. Nigam has to do (according to Dr. Jahoda's findings) to make you happy:
Step 1
Due to the lack of the (natural) micro environmental and anatomical context of natural and INTACT DP's, you have to grow cultured DP-CELLS in "hanging drops", which results in the formation of 1 DP spheroid = 1 dermal papilla. The latter means, you have to build up a "plantation" / "farm" of such "hanging drops" to get sufficient DP spheroids for implantation - and finally for step 2...
Step 2
After the formation of sufficient DP spheroids in your "hanging drops farm", the doctor has to genetically "recombine" these grown DP spheroids with tissue from your ****/dick - or more specific from your foreskin. That means, the doctor has to harvest as much tissue from your dick, as much as you have DP spheroids in your lab, or simply as much as you need DP spheroids for the (recombined) implantation into the bald scalp; that means, for let's say 1000 hair follicle producing DP spheroids, the doctor must almost amputate your dick to get sufficient dick-tissue for the genetically recombination with the grown DP spheroids - to get this to work FOR HUMANS at all, and as explained by Jahoda.
Step 3
Implantation of your genetically recombined penis- and DP spheroid parts into your bald areas.
Yeah, that's how it works - according to Jahoda.
Oh, by the way: If you think step 1-3 is just a joke - it is not.Leave a comment:
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Jahoda et al managed to biogenerate a human hair follicle and grew it on human skin, transplanted onto SCID mice earlier this year. Now Dr Nigams is going to try it on humans. That's pretty much the reason for the optimism. Read: http://www.baldtruthtalk.com/showpos...&postcount=116
Okay - let me read your link and let me conclude what Dr. Nigam has to do (according to Dr. Jahoda's findings) to make you happy:
Step 1
Due to the lack of the (natural) micro environmental and anatomical context of natural and INTACT DP's, you have to grow cultured DP-CELLS in "hanging drops", which results in the formation of 1 DP spheroid = 1 dermal papilla. The latter means, you have to build up a "plantation" / "farm" of such "hanging drops" to get sufficient DP spheroids for implantation - and finally for step 2...
Step 2
After the formation of sufficient DP spheroids in your "hanging drops farm", the doctor has to genetically "recombine" these grown DP spheroids with tissue from your ****/dick - or more specific from your foreskin. That means, the doctor has to harvest as much tissue from your dick, as much as you have DP spheroids in your lab, or simply as much as you need DP spheroids for the (recombined) implantation into the bald scalp; that means, for let's say 1000 hair follicle producing DP spheroids, the doctor must almost amputate your dick to get sufficient dick-tissue for the genetically recombination with the grown DP spheroids - to get this to work FOR HUMANS at all, and as explained by Jahoda.
Step 3
Implantation of your genetically recombined penis- and DP spheroid parts into your bald areas.
Yeah, that's how it works - according to Jahoda.
Oh, by the way: If you think step 1-3 is just a joke - it is not.Leave a comment:
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Hate to be the pessimist here, but what is all this dr nigam frenzy about?? Is there one iota of evidence that shows any substantial results? If the top hair researchers in the world at follica, anderans, etc. can't figure it out yet, what does dr nigam have that they don't? Better training? Hard to believe. I appreciate his passion, but I can't help but remain strongly skeptical, as there is absolutely no hard EVIDENCE to suggest otherwiseLeave a comment:
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Tom my friend. How are you? I've been here eight days in Paris, I try to enjoy .... but my brother, here is heat stroke, and I'm in a ****ing hotel without air conditioning :-) Do you travel tomorrow in Mumbai? How much you pay for a plane ticket from France to Mumbai? Have a safe trip and good luck!
Thanks for allLeave a comment:
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Tom my friend. How are you? I've been here eight days in Paris, I try to enjoy .... but my brother, here is heat stroke, and I'm in a ****ing hotel without air conditioning :-) Do you travel tomorrow in Mumbai? How much you pay for a plane ticket from France to Mumbai? Have a safe trip and good luck!Leave a comment:
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Sorry for the late update guys,
I'm I'm very occupied here, and since I'm for a limited time in Mumbai, I have to make priorities.
In short:
-My cells are in culture in different protocols (check page 85 for more info).
Tomorrow, we will check the cell growth of, and make possible adjustments to the medium.
-Probably within 3 weeks, we will try to create neofolcile in vitro (just for fun)...
The inverted scope has ability to take pictures, so I will arrange some if you guys want.
This week I will also do some touring in Mumbai, to see the beautiful places..Leave a comment:
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thanks for the update boldy . looking forward to the next updates .. and having this done myself.hope all is well
Leave a comment:
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I'm I'm very occupied here, and since I'm for a limited time in Mumbai, I have to make priorities.
In short:
-My cells are in culture in different protocols (check page 85 for more info).
Tomorrow, we will check the cell growth of, and make possible adjustments to the medium.
-Probably within 3 weeks, we will try to create neofolcile in vitro (just for fun)...
The inverted scope has ability to take pictures, so I will arrange some if you guys want.
This week I will also do some touring in Mumbai, to see the beautiful places..Leave a comment:
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Leave a comment: