Telomerase Activator in humans, TA Science's ta-65 |
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Telomerase Activator in humans, TA Science's ta-65 |
Apr 12 2007, 12:08 AM
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#1
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Group: Member Threadstarter Joined: 15-February 07 Posts: 1,077 From: Atlanta, Ga |
TA Science announced that it will use Geron's license to develop and market non-therapeutic products using Geron's small molecule telomerase activators.
The compound is derived from a Chinese herb(Astragalus), and activates telomerase genes in human cells. Human studies have been underway since 2005. http://www.lef.org/news/LefDailyNews.htm?N...6&Section=AGING QUOTE New Product Scientifically Battles Aging at the Cellular Level-Exclusively licensed from the Geron Corporation, TA-65 is the world's first Telomerase Activator PR Newswire 04-09-07 NEW YORK, April 9, 2007 /PRNewswire via COMTEX/ -- Telomerase Activation Sciences, Inc. (TA Sciences) announced on March 12 its license with Geron to develop and market non-therapeutic products using Geron's small molecule telomerase activators. Now TA Sciences announces the opening of the TA Sciences Center in Manhattan where customers can purchase TA Sciences' first product, a nutraceutical containing the telomerase activating agent "TA-65." "TA Sciences welcomes our first customers and the launch of the world's first telomerase activator product," said Noel Thomas Patton, founder of TA Sciences. "A natural consequence of aging is the shortening of telomeres (caps of DNA located at the ends of all chromosomes), which ultimately results in loss of cell function. TA-65 offers the potential of reducing or reversing telomere shortening and battles tissue and organ degeneration by rejuvenating aging cells." TA-65 is the result of vigorous scientific research that began at Geron in 1992. Already the response from the scientific community to the news of TA Sciences' ground-breaking launch has been very enthusiastic: "Telomerase Activation is the single most promising approach to reversing the effects of aging," said Michael Fossel, MD, PhD., Clinical Professor of Medicine at Michigan State University, author, and recognized authority on aging and age- related clinical disease. And Dr. William H. Andrews, founder of Sierra Sciences, LLC and one of the principal discoverers of the telomerase genes, said: "Cleopatra, Ponce de Leon, and untold others throughout the ages have searched for the secrets of youth. That search has been futile, until now: Telomerase Activation is the first and only scientifically sound way to approach anti- aging. TA-65 is the first product in history that has been proven to slow or reverse cellular aging. Congratulations to TA Sciences and Geron!" On April 30, 2007 TA Sciences plans to publish the results of the Pivotal 2005 Anti-Aging Trial, which is the first ever human clinical trial of a telomerase activator. This trial shows statistical verification of the anti- aging benefits of telomerase activation. The TA Sciences Center is located at 24 E. 64th Street in New York. The company offers its telomerase-activating products as part of the 12 month "Patton Protocol." The driver of TA Sciences' product line is the telomerase- activating small molecule "TA-65," sold under license from Geron. For more information on TA Sciences visit http://www.TASciences.com or call 888-360-8886. For more information on Geron visit http://www.Geron.com. SOURCE TA Sciences Inc. CONTACT: Greta Blackburn of TA Sciences Inc., cell, +1-818-634-5941 URL: http://www.tasciences.com http://www.Geron.com http://www.prnewswire.com www.prnewswire.com Here is the full report of the 2005 study (I believe that I read somewhere that there is additional information that will be revealed from the study on the 30th of April). http://www.tasciences.com/ta/blum2.html QUOTE The Pivotal 2005 Anti-Aging Trial of TA-65 was a double blind, placebo controlled, 24 week study in which subjects consumed 2 or 4 tablets daily of a placebo control substance (placebo groups) for 12 weeks or 2 or 4 tablets daily of a TA-65 precursor molecule (TA-41) for 12 weeks (product groups). The product tablets each contained 10 mg of TA-41 (an Astragalus extract) along with other botanical extracts and excipients. The placebo control tablets were essentially indistinguishable from the product tablets in appearance and taste, even when the tablet was broken. The 12 week placebo or product use period was followed by a further 12 week follow-up period. To ascertain active substance in the blood (for compliance and to better understand the relationship between TA-41 and TA-65), analytical measurements of TA-41 and TA-65 (the presumed major metabolite of TA-41) were conducted at 6 weeks and 12 weeks. Thirty six male subjects aged 60-85 who expressed an interest in reducing the signs and symptoms of aging and who reported a gradual decline in overall energy levels at the screening visit were recruited. Subjects were randomly assigned to the placebo group (n=6 taking two placebo tablets, one in the morning, one in the evening; n=6 taking 4 placebo tablets, two in the morning, two in the evening) or the product treatment group (n=12 taking two product tablets, one in morning, one in evening; n=12 taking 4 product tablets, 2 in morning, 2 in evening). Subjects were assessed at baseline and at 6 weeks, 12 weeks and 24 weeks from the first dose of product. The full study design is described in Appendix A. Here is a paper with evidence saying telomerase is not an oncogene: http://www.nature.com/onc/journal/v21/n4/f...l/1205076a.html There is a thread on this topic in supplements, but where as it is particularly relevant to conversations occurring here in SENS, I thought that I would open this up for discussion. |
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Apr 17 2007, 03:06 AM
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#2
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Group: Registered User Joined: 3-April 07 Posts: 3 |
Here is the letter I received today, hey ... anyone have an extra $25000 sitting around? Maybe if we bought 1000 shares of GERN at $7.50 and and sold it at 40 in May, maybe we could make a good investment in our health and bank account.
Thank you for your recent inquiry and your interest in TA Sciences. The 12 month PATTON PROTOCOL TM is the first and only program in the exciting field of Telomere Biology designed to help optimize our individual health as we age, and to help prolong our "Healthspan". Here is how it works: Clients need to visit the TA Center in New York and have extensive blood work and other biomarkers of aging done prior to starting the PATTON PROTOCOL. This will establish your baseline condition. About two weeks later, when the test results are in, you will have an in-depth consultation with our associated Anti-Aging physician to discuss your results and assess your individual health situation. If you live outside of the New York area, it is possible to have your consultation over the phone. The price for this baseline program, which would normally cost close to $5000.00, is $2430 (our actual third party, discounted out-of-pocket costs). This baseline evaluation is very valuable on its own as a health and aging tool. After your initial biomarkers and consultation, you then decide if you actually want to start the 12 month PATTON PROTOCOL. The PATTON PROTOCOL consists of: - A year's supply of Telomerase Activator TA-65 TM (Patents Pending). This is a pulsed program taken daily for 3 months, then off for 3 months, and then taken again for the next 3 months, then off again for the final 3 months. - A repeat of the baseline blood work and biomarkers of aging at 3 months, 6 months, 9 months and 12 months, and follow-up consultations with the Anti-Aging physician at each of those time points to track your personal progress. -A year's supply of our proprietary packets of other nutritional supplements, vitamins, minerals, and herbs specially formulated for TA Sciences. These packets, taken 2 times a day, offer a comprehensive assortment of the most effective vitamins, minerals and herbs, available anywhere. - A series of monthly consultations with TA Sciences' expert Lifestyle Counselor is also available and included, to help you optimize your personal health and aging goals. The price for the 12 month Protocol is $22,570.00, payable in two 6 month installments of $11,285.00 each. We expect the benefits of Telomerase Activation to last well beyond the initial 12 month period, but this is leading edge technology and individual results will vary. We suggest that clients come back one year after finishing the Protocol to have their biomarkers re-tested and evaluated, and to discuss whether a TA Maintenance Program at a significantly lower cost would be beneficial. Please call me if you have any questions or would like to schedule your biomarkers. With Best Regards, Greta Blackburn, Marketing Director TA Sciences Inc. Phone: 212-588-8805 E-mail: gretabfit@aol.com |
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Apr 17 2007, 06:10 PM
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#3
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Group: Registered User Joined: 3-April 07 Posts: 65 |
Wow...
We all knew molecular therapies like this one would be expensive, but 25k! Though I suppose they're trying to reduce the brunt of the possibility that the therapy isn't going to be very successful, and if it it then they can safely market it on a much larger scale. It's a test of an anti-aging hypothesis that I've wondered about for some time: "If you make it, they will come." |
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Apr 17 2007, 06:33 PM
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#4
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Group: Member Joined: 28-January 06 Posts: 2,350 From: Rhode Island, USA |
QUOTE Clients need to visit the TA Center in New York and have extensive blood work and other biomarkers of aging done... I would love to know what these biomarkers are! QUOTE A year's supply of our proprietary packets of other nutritional supplements, vitamins, minerals, and herbs specially formulated for TA Sciences. These packets, taken 2 times a day, offer a comprehensive assortment of the most effective vitamins, minerals and herbs, available anywhere. Uhhh, this makes this sound like a major scam. Why would you introduce additional variables into a trial? |
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Apr 18 2007, 12:33 AM
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#5
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Group: Registered User Joined: 3-April 07 Posts: 65 |
I'm not sure if that counts as the addition of variables.
It makes sense to me that even in a trial, they're going to want to get people in as good of functional shape as they can get them, and biologically this means supplements and nutrition. By exposing the sample size to this constant set of positive supplements, they can measure the effect of telomere elongation/maintanence induced by the drug. In order for it to be a true 'test' of the like you are mentioning, they would need a double blind with a placebo, but that's definately not what they're looking for here. They want to show that their product can perform the task it was designed for, and that its function does not overlap with currently available supplements. PS: 25 grand for a placebo would suck! |
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Apr 18 2007, 01:15 AM
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#6
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Group: Advisor Joined: 19-September 02 Posts: 2,365 From: Mountain View, CA |
QUOTE PS: 25 grand for a placebo would suck! Not if it makes you live longer ;-) |
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Apr 19 2007, 02:40 PM
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#7
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Group: Registered User Joined: 21-February 05 Posts: 58 From: London, mobile: 0783 |
looks like a deception
http://groups.google.com/group/sci.life-ex...020fce84318ff2d http://groups.google.com.ar/group/sci.life...0eaeb100a092bc2 http://www.altbaldspot.com/forums/viewtopi...pic.php?p=96671 no scientific evidence |
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Apr 20 2007, 06:20 PM
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#8
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Group: Registered User Joined: 3-April 07 Posts: 65 |
Hmm....
This definately does deserve an eye of skepticism. This TA-65 enzyme they are touting is a telomerase activating protein, apparently originally found by Geron (I assume, since they seem to have the patents on the molecule and the patent has been 'leased' to TASciences). TA-65 is a purified extract from a plant that has been used safely as a Traditional Chinese herb for thousands of years. This powerful ingredient is the only substance commercially available that activates (turns on) telomerase. The herb is called Astragalus. I gave a fake phone number and real email address to the TA website so that I could poke around in it. http://www.tasciences.com/ta/blum.html I don't know if there are barriers to entry if you haven't registered but I encourage you to take a look. The problem I see is a lack of in vitro and biochemical assays. However, they were legitimate enough to do double blind palcebo experiments. I don't immediately dismiss it, but the product begs a few important questions. Concentration to be effective? Quantitative elongation of telomeres? How much is naturally present in the herb? BIOCHEMICAL ASSAYS? |
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Apr 22 2007, 12:00 AM
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#9
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Group: Member Threadstarter Joined: 15-February 07 Posts: 1,077 From: Atlanta, Ga |
QUOTE However, they were legitimate enough to do double blind palcebo experiments. The p-values of the expiriment were huge: some as high as .75 The big thing is that they haven't tested for telomere lengthening or telomerase activation directly in any study that I have read... |
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Apr 22 2007, 04:35 AM
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#10
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Group: Navigator Joined: 15-December 06 Posts: 6,285 From: Philadelphia |
QUOTE The p-values of the expiriment were huge: some as high as .75 The big thing is that they haven't tested for telomere lengthening or telomerase activation directly in any study that I have read... Well, they were pretty up-front about labeling the high p-value stuff as "trends" or some such. I didn't feel misled by it. The data wasn't all high p-value. Somebody must have actually looked at telomere lengthening / telomerase activation. If no one had looked at it, why would these guys have (as someone said) licensed the patent from Geron? IMHO, one of the key experiments in humans will be to look not just at telomere lengthening, but tissue distribution of the effects. It sure sucks that something with such seeming promise would wind up in the hands of people who at least give the appearance of acting like clueless shysters. Is this appearance problem simply a function of them trying to make tons of money off of a genuinely revolutionary therapy? Or are they just crooks? At this point my hopeful nature leans toward the former, but the cynic in me doesn't yet rule out the latter. |
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May 2 2007, 12:54 AM
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#11
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Group: Registered User Joined: 29-April 07 Posts: 45 |
Can anyone answer my following questions on telomerase:
1. By activating the telomerase in the senesecent cells which has undergone damage in Mitochondria, has lipofuscin, etc...the new cell formed by multiplication has all the damages reversed or removed to form young cells? 2. I have seen literature of Prof.Shay and Wright on extending the telomerase in animals..Do they live longer? Link to Shay and Wright lab is given below: http://www4.utsouthwestern.edu/cellbio/sha...ight/index.html |
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May 2 2007, 12:58 AM
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#12
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Group: Registered User Joined: 29-April 07 Posts: 45 |
Links to the patents of Astragalus activation on Telomerase (thanks to the link presented in google groups on life extension by jc101)
http://tinyurl.com/2yypov http://tinyurl.com/3db889 |
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Jun 12 2007, 11:22 AM
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#13
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Group: Registered User Joined: 30-October 04 Posts: 31 |
QUOTE Links to the patents of Astragalus activation on Telomerase (thanks to the link presented in google groups on life extension by jc101) http://tinyurl.com/2yypov http://tinyurl.com/3db889 Those links produce PDF files that appear to have only the title page. Here is a link to the first document on the WIPO site. The second seems to have been withdrawn: http://www.wipo.int/pctdb/en/wo.jsp?wo=2005000245 |
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Jun 24 2007, 01:45 AM
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#14
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Group: Registered User Joined: 28-March 07 Posts: 177 |
QUOTE Can anyone answer my following questions on telomerase: 1. By activating the telomerase in the senesecent cells which has undergone damage in Mitochondria, has lipofuscin, etc...the new cell formed by multiplication has all the damages reversed or removed to form young cells? 2. I have seen literature of Prof.Shay and Wright on extending the telomerase in animals..Do they live longer? Link to Shay and Wright lab is given below: http://www4.utsouthwestern.edu/cellbio/sha...ight/index.html The answer to question one is absolutely not. They will pass on their accumulated genetic damage to their daughter cells. Damaged materials not encoding information, ie proteins and lipids, will be diluted or replaced, depending on their turnover rate in mitotic cells. |
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Jun 24 2007, 05:40 AM
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#15
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Group: Member Threadstarter Joined: 15-February 07 Posts: 1,077 From: Atlanta, Ga |
QUOTE The answer to question one is absolutely not. That is not absolutely true. While all of the complicated functions of telomerase are not fully understood. There are studies showing that telomerase induces apoptosis, additionally, (I don't have a study to back this claim up, it is more of an observation) the body normally cleanses it's soma by destroying damaged cells and replacing them with healthy cells. When cells become senescent and lose their reproductive capacity, that is also when the soma stops cleansing and will leave behind damaged cells. It is possible that by reintroducing telomerase, lots of the damaged cells could die off leaving more healthy cells behind. |
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Jun 24 2007, 07:04 AM
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#16
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Group: Registered User Joined: 28-March 07 Posts: 177 |
No, my answer is correct. Go back and re-read his question. You missed his point. He asked specifically, if a cell with damaged DNA is taken out of senescence and begins replicating, will the DNA be restored to its original state. The answer still is no.
To address your other points, terminally differentiated tissues are not as a rule destroyed when they become damaged, unless that damage is quite severe. This is because the threshold for their becoming cancerous is much higher than that of actively mitotic cells. Horeover, most of these cells are irreplaceable or not efficiently replaceable, and destroying them will cause serious deleterious effects, like brain damage or heart failure. If all the damaged, senescent cells in your brain suddenly underwent apoptosis, you'd be seriously screwed, and they would not be replaced. QUOTE That is not absolutely true. While all of the complicated functions of telomerase are not fully understood. There are studies showing that telomerase induces apoptosis, additionally, (I don't have a study to back this claim up, it is more of an observation) the body normally cleanses it's soma by destroying damaged cells and replacing them with healthy cells. When cells become senescent and lose their reproductive capacity, that is also when the soma stops cleansing and will leave behind damaged cells. It is possible that by reintroducing telomerase, lots of the damaged cells could die off leaving more healthy cells behind.
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Jul 19 2007, 04:27 AM
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#17
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Group: Registered User Joined: 29-April 07 Posts: 45 |
The use of resveratrol to activate NOS to produce more mitochondrial biogenesis even in old mice (David sinclair's work) thus leading to life span extension prove the possibility of generating more functional mitochondrias even in old mice. If just activating telomerase does not lead to more functional mitochondrias, does the combo with compounds like resveratrol would reverse the damage and improve the longevity of the cell?
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Aug 20 2007, 03:45 PM
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#18
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Group: Registered User Joined: 16-August 07 Posts: 4 |
What astonishes me is that this research was announced 4 months ago and has not yet reached the mainstream media. I have followed longevity research for 25 years and this is waaay bigger news than Growth Hormone or Glycation Bond Breakers (ALT-711), Resveratrol/sir2P gene activation, or farnesyl transferase inhibitors or anything else that has been discovered in the past quarter century. If you read the patents and realize what is actually being claimed... well it boggles the mind. This could really be it. A naturally occuring, non-patentable substance that kicks the Hayflick Limit into the next century. Will I take this stuff? Absofuckinglutely. Already do as a matter of fact. 1500 mg a day of standardized Astragalus exract standardized to 0.4% (20mg) of 4hydroxy 3 methoxyisoflavone. Cost is about 50 cents a day...LOL Now does this extract contain the proper astrogaloside or whatever TA-65 is? No way of knowing without obtaining a sample of TA-65 and running a comparison to the readily available Astragalus extracts. I am willing to bet it does however based on my read of the patent. It's just a simple ethanolic extraction and hey if I get other compounds so much the better. There is NOTHING in the literature to indicate any untoward effects from Astragalus extract. Been used for several THOUSAND years by the Chinese.
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Aug 20 2007, 04:05 PM
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#19
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Group: Registered User Joined: 16-August 07 Posts: 4 |
The principle compound, astragaloside IV, is typically found at 0.15 mg/g in astragalus root. A typical dose of TA-65 is 5 mg, equivilant to 5mg/0.15mg/g = 33.33 grams of Astragalus root if it is astragaloside IV, while the typical maximum dose of Astragalus root used in treatment is 30 grams. However, since Geron prescribes astragaloside IV at 50 mg to 100 mg and cycloastragenol at 5 mg, it is far more likely that TA-65 is cycloastragenol. [See Links/Astragaloside IV, Source Chengdu Cogon Biotech, Chinese sources, Books/Astragaloside IV.] A Geron patent cites astragaloside IV as one embodiment of a formula for a telomerase activator. Geron's European patent describes other telomerase activators from astragalus root extract including cycloastragenol, astragenol, and astragaloside IV 16-one.
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Aug 29 2007, 03:44 PM
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#20
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Group: Registered User Joined: 29-April 07 Posts: 45 |
Another basic question, I have, what makes a cell to divide? Does it require enough mitochondrial mutation, lipofuscin to happen or even younger cells which has less or negligible mutations or lipofuscin also divide (i would assume, that is the case, since, during the initial stages of growth of a baby, the cells divide pretty fast). If my hypothesis is correct, then increasing telomerase should definitely minimize the lipofuscin since, it is now getting distributed to higher number of cells (due to replication), so that senescence can be delayed? Any counter explanations is welcome?
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