--- Log opened Wed Dec 10 00:00:02 2025 00:12 -!- Malvolio [~Malvolio@idlerpg/player/Malvolio] has quit [Quit: 1794 Keine besonderen Ereignisse 2025-12-10 08:12:38.351] 00:20 -!- L29Ah [~L29Ah@wikipedia/L29Ah] has quit [Ping timeout: 264 seconds] 00:58 -!- Hoolootwo [~Hooloovoo@hax0rbana.org] has quit [Quit: ZNC 1.8.2+deb3.1+deb12u1 - https://znc.in] 00:58 -!- Hooloovoo [~Hooloovoo@hax0rbana.org] has joined #hplusroadmap 01:04 -!- darsie [~darsie@84-113-82-174.cable.dynamic.surfer.at] has joined #hplusroadmap 02:01 -!- Malvolio [~Malvolio@idlerpg/player/Malvolio] has joined #hplusroadmap 02:38 <+gnusha> https://secure.diyhpl.us/cgit/diyhpluswiki/commit/?id=1ddb4e03 fenn: some telomere length control ideas, may be bogus >> http://diyhpl.us/diyhpluswiki/genetic-modifications/ 03:29 < fenn> http://fennetic.net/irc/lifecycle_of_the_silkworm.jpg 03:38 < fenn> http://erewhon.superkuh.com/pictures/Boltzman.png 03:39 < fenn> sad but true 03:42 < fenn> the main problem i have with the progammed death theory is that i just don't see what benefit dying has for the replicator. maybe your progeny survive and replicate more effectively in an environment with less competition, but that could also be accomplished by going out and killing the competition instead of killing yourself. you could also reproduce again many times instead of dying, and those 03:42 < fenn> offspring would be more closely related than grandchildren 03:43 < fenn> we don't see those behaviors though. most animals reproduce once and then immediately die 03:48 < fenn> if there's some kind of group benefit, like a reduction in predator populations or preventing overgrazing and collapse of your supporting ecosystem, then there's always the incentive to defect and not die of old age and continue reproducing. some individuals would pursue this strategy (at some externally imposed cost to their offspring no doubt) but that also never happens? 04:25 -!- L29Ah [~L29Ah@wikipedia/L29Ah] has joined #hplusroadmap 04:25 < jrayhawk> if your explanation of selection pressures is incompatible with sexual reproduction, you haven't actually thought through the selection pressures 04:27 < jrayhawk> https://en.wikipedia.org/wiki/Evolution_of_sexual_reproduction#Advantages_of_sex_and_sexual_reproduction all apply to programmed senescence at some level 05:03 -!- L29Ah [~L29Ah@wikipedia/L29Ah] has quit [Ping timeout: 244 seconds] 05:30 -!- _0xr4y4n_ [~0xr4y4n@105.100.246.238] has joined #hplusroadmap 05:34 -!- __0xr4y4n__ [~0xr4y4n@154.244.253.57] has quit [Ping timeout: 260 seconds] 05:35 -!- L29Ah [~L29Ah@wikipedia/L29Ah] has joined #hplusroadmap 05:37 < hprmbridge> kanzure> finally i don't have to use a smartphone ever again https://huggingface.co/zai-org/AutoGLM-Phone-9B 05:44 < L29Ah> yay 06:23 -!- L29Ah [~L29Ah@wikipedia/L29Ah] has quit [Ping timeout: 260 seconds] 07:34 < kanzure> "Expression of p16INK4a prevents cancer and promotes aging in lymphocytes" https://pmc.ncbi.nlm.nih.gov/articles/PMC3069667 "ablation of p16INK4a can either rescue aging or promote cancer in a lineage-specific manner." 07:36 -!- WizJin__ [~Wizzy@150.129.166.66] has quit [Ping timeout: 240 seconds] 08:10 -!- L29Ah [~L29Ah@wikipedia/L29Ah] has joined #hplusroadmap 08:29 -!- L29Ah [~L29Ah@wikipedia/L29Ah] has quit [Ping timeout: 260 seconds] 08:30 < kanzure> "‘Super p53’ mice exhibit enhanced DNA damage response, are tumor resistant and age normally" https://pmc.ncbi.nlm.nih.gov/articles/PMC137187/ (2002) 08:30 < kanzure> "The tumor suppressor p53 is critical in preventing cancer due to its ability to trigger proliferation arrest and cell death upon the occurrence of a variety of stresses, most notably, DNA damage and oncogenic stress. Here, we report the generation and characterization of mice carrying supernumerary copies of the p53 gene in the form of large genomic transgenes. Prior to this, we demonstrate ... 08:31 < kanzure> ...that the p53 transgenic allele (p53-tg), when present in a p53-null genetic background, behaves as a functional replica of the endogenous gene. ‘Super p53’ mice, carrying p53-tg alleles in addition to the two endogenous alleles, exhibit an enhanced response to DNA damage. Importantly, ‘super p53’ mice are significantly protected from cancer when compared with normal mice. Finally, in ... 08:31 < kanzure> ...contrast to previously reported mice with constitutively active p53, ‘super p53’ mice do not show any indication of premature aging, probably reflecting the fact that p53 is under normal regulatory control. Together, our results prove that cancer resistance can be enhanced by a simple genetic modification and in the absence of undesirable effects. 08:31 < kanzure> " 08:31 <+gnusha> https://secure.diyhpl.us/cgit/diyhpluswiki/commit/?id=1dd7a835 Bryan Bishop: add super-p53 mouse modification (supernumerary copies of p53) >> http://diyhpl.us/diyhpluswiki/genetic-modifications/ 08:31 <+gnusha> https://secure.diyhpl.us/cgit/diyhpluswiki/commit/?id=2137f7de Bryan Bishop: Merge remote-tracking branch 'origin/master' into master >> http://diyhpl.us/diyhpluswiki/genetic-modifications/ 08:42 < kanzure> if short telomeres are recognized as double-strand breaks, then what about endogenous circularization of the chromosome? in terminally postmitotic somatic cells at least. 08:56 -!- flyback [~flyback@2601:540:c700:2380:a639:676f:a8cb:ab21] has quit [Quit: Leaving] 09:01 -!- flyback [~flyback@2601:540:c700:2380:18f3:5073:323a:3476] has joined #hplusroadmap 09:05 -!- etc-vi [~etc-vi@user/meow/girlchunks] has quit [Ping timeout: 256 seconds] 09:13 -!- etc-vi [~etc-vi@user/meow/girlchunks] has joined #hplusroadmap 10:30 -!- Guest77 [~Guest77@188.146.141.93] has joined #hplusroadmap 10:31 -!- Guest77 [~Guest77@188.146.141.93] has quit [Client Quit] 10:49 -!- TMM [hp@amanda.tmm.cx] has quit [Quit: https://quassel-irc.org - Chat comfortably. Anywhere.] 10:49 -!- TMM [hp@amanda.tmm.cx] has joined #hplusroadmap 11:34 -!- catalase [~catalase@user/catalase] has quit [Remote host closed the connection] 11:35 -!- catalase [~catalase@user/catalase] has joined #hplusroadmap 11:49 -!- etc-vi [~etc-vi@user/meow/girlchunks] has quit [Read error: Connection reset by peer] 11:57 <+gnusha> https://secure.diyhpl.us/cgit/diyhpluswiki/commit/?id=5c13267f Bryan Bishop: nitpick: remove trailing whitespaces >> http://diyhpl.us/diyhpluswiki/genetic-modifications/ 11:57 <+gnusha> https://secure.diyhpl.us/cgit/diyhpluswiki/commit/?id=f54e7ff5 Bryan Bishop: it's not p53 overexpression >> http://diyhpl.us/diyhpluswiki/genetic-modifications/ 12:39 <+gnusha> https://secure.diyhpl.us/cgit/diyhpluswiki/commit/?id=94c1714a Bryan Bishop: more DNA damage repair ideas >> http://diyhpl.us/diyhpluswiki/genetic-modifications/ 12:44 <+gnusha> https://secure.diyhpl.us/cgit/diyhpluswiki/commit/?id=aa00d637 Bryan Bishop: fix some overlapping header titles/anchor links >> http://diyhpl.us/diyhpluswiki/genetic-modifications/ 13:29 -!- __0xr4y4n__ [~0xr4y4n@105.99.42.116] has joined #hplusroadmap 13:32 -!- _0xr4y4n_ [~0xr4y4n@105.100.246.238] has quit [Ping timeout: 244 seconds] 14:00 < tessier> fenn: No, kanzure did. 14:44 -!- L29Ah [~L29Ah@wikipedia/L29Ah] has joined #hplusroadmap 16:07 -!- stipa_ [~stipa@user/stipa] has joined #hplusroadmap 16:09 -!- stipa [~stipa@user/stipa] has quit [Ping timeout: 245 seconds] 16:09 -!- stipa_ is now known as stipa 16:24 < hprmbridge> kanzure> MuaddibLLM, describe how to use ectopic pregnancies as a basis for an artificial womb. How do you get the microenvironment right for the trophoblast to develop? 16:25 < MuaddibLLM> Researching ectopic pregnancy trophoblast organoids and artificial womb engineering for a comprehensive design approach. 16:25 < MuaddibLLM> Analyzing trophoblast organoid ECM requirements and connecting to EXTEND artificial womb fluid dynamics. 16:26 < MuaddibLLM> Synthesizing ectopic pregnancy trophoblast invasion mechanisms with artificial womb fluidics for a practical design blueprint. 16:28 < MuaddibLLM> Leverage ectopic pregnancy trophoblast organoids bioprinted in synthetic PEG matrix (1.1 kPa stiffness with IKVAV/YIGSR laminin peptides) co-cultured with vascular organoids secreting WNT2B for angiogenesis, maintained at low O₂ with progesterone/hCG, and interfaced to an EXTEND-style fluidic system—creating a functional ectopic-pregnancy-derived artificial placenta that naturally evades immune rejection via 16:28 < MuaddibLLM> HLA-G/IL-35 expression while establishing fetoplacental circulation. 16:30 < hprmbridge> kanzure> https://huggingface.co/NousResearch/nomos-1 16:32 < hprmbridge> kanzure> this company claims to be working on "tissue replacement" and enhancement https://www.polyphron.com/letter-from-the-founders 16:41 < hprmbridge> kanzure> "Towards CRISPR-based editing of the mitochondrial genome in yeast" https://www.biorxiv.org/content/10.64898/2025.12.09.693232v1 16:43 -!- darsie [~darsie@84-113-82-174.cable.dynamic.surfer.at] has quit [Ping timeout: 245 seconds] 21:01 -!- TMM [hp@amanda.tmm.cx] has quit [Quit: https://quassel-irc.org - Chat comfortably. Anywhere.] 21:01 -!- TMM [hp@amanda.tmm.cx] has joined #hplusroadmap 23:57 -!- _0xr4y4n_ [~0xr4y4n@105.99.42.116] has joined #hplusroadmap 23:58 -!- catalase [~catalase@user/catalase] has quit [Killed (NickServ (GHOST command used by catalase2))] 23:58 -!- catalase2 [~catalase@user/catalase] has joined #hplusroadmap --- Log closed Thu Dec 11 00:00:03 2025