Another batch of character sheet comms! Once again, a huge thank you to folks for trusting me with your beloved characters ❤️🙏
Safe - Anna Calleja , 2020.
Maltese , b. 1997 -
Oil on panel , 30 x 40 in.
[ID: A painting centered on a brown tabby cat held securely in the arms of a person in a thick, gray cable-knit sweater. They’re seated together with soft sunlight coming in from the right, and the cat’s tail curls relaxedly over the person’s arm. Its eyes are squinted, as if slowly closing to sleep /End ID]
(via smouldered)
gold foil print of Themis 💕 my contribution to the Themis zine 星に願いを
I’m so excited to receive it ! The whole zone package is super awesome 🤩
oh no….my balls,,,
(via messydiabolical)
vertical gardens by Patrick Blanc
Fingal’s Cave is a geological formation located on the uninhabited island of Staffa, in the Inner Hebrides of Scotland.
It is known for its extraordinary structure of hexagonal basalt columns, which were formed from rapidly cooled volcanic lava millions of years ago. The cave is approximately 72 meters long and is notable for its natural acoustics, giving it a cathedral-like quality.
“A patient with type 1 diabetes has become the first in the world to produce his own insulin via transplanted cells edited with CRISPR.
The edits halted his own immune system from attacking the cells, leading to production of insulin in the pancreas as if he never had the disease in the first place.
Unlike the rampant type 2 diabetes, type 1 manifests as an autoimmune disorder whereby the patient’s immune system attacks and destroys a type of cell created in the pancreas to produce insulin, known as islet cells. 9.5 million people worldwide suffer from type 1 diabetes and there is no cure.
The standard of care beyond daily insulin injections involves using donated islet cells to allow a patient’s metabolism to function normally, followed by medications used to prevent the immune system from attacking those cells. These medications have harmful side effects.
A team of biomedical researchers primarily from Uppsala University, Sweden, in collaboration with UC San Francisco, successfully used the CRISPR gene-editing method to take a donor’s islet cells and modify them so as to evade prosecution by the patient’s immune system.
Three changes in total to the genetic code were needed to ensure the transplanted donor cells didn’t trigger an immune response, including changes to cell membrane signal proteins used as a sign of attack by white blood cells.
CRISPR TO THE RESCUE:
- Infant With Incurable Disease is First to Successfully Receive Personalized Gene Therapy Treatment
- Aggressive Leukemia Disappears in 13-Year-old Girl Who was First to Receive New CRISPR Treatment
- First Patient to Receive Gene Therapy ‘Cure’ for Beta-Thalassemia Living Pain-Free
As a preliminary study, the man received only a small amount of the donated, modified cells, meaning he still requires daily insulin injections. However the results show that the cells produced their own insulin and remained unperturbed by the immune system.
After 12 weeks, the cells were still producing endogenous insulin, setting the stage for longer-term and more robust experiments in the future.
The study was published in the New England Journal of Medicine.”
-via Good News Network, August 25, 2025
(via shinjis9)
No transphobes allowed, only transborbs.
Check out my stuff!
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(via catboygirling)
Grim Reaper Part 1
Grim Reaper Part 2
It’s the Hound Knight again, AT LAST!
Check out my Patreon for the 2 bonus panels.
My stuff :
✧Read Namesake✧ ✧Read Crow Time✧ ✧Store✧ ✧Patreon✧
(via shinjis9)

























































