Skin deep

Disease modeling in 8p brain organoids led to the discovery of Reelin as a novel potential driver gene. Will skin cells from 8p heroes teach us about the disease and lead to treatments? We think so.

Project 8p is the world’s first nonprofit biotech whose mission is to lead the charge toward treatments and cures for complex chromosome diseases caused by megabase rearrangements. Pick your flavor combo: deletion, duplication, and even inversion. 8p heroes can have all three, including heroes who just have an 8p deletion or an 8p duplication.

For some perspective on scale, and as another reminder why 8p is particularly challenging: you can fit an entire copy of human chromosome 21, which encodes several hundred genes, inside a single typical 8p duplicated segment.

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The Project 8p Foundation (Project 8p) was created in 2018 to:

  • Accelerate future treatments, not only for 8p, but potentially for other chromosome-wide diseases as well.
  • Lead with knowledge from patients. Currently, there is no cure for 8p disorders, nor is there a standard course of treatment.

The Project 8p Foundation (Project 8p) was created in 2018 to:

  • Raise transformative funding for pioneering scientific research into treatments for a complex, rare disease involving 250+ affected genes on the short arm of the 8 th chromosome (8p). Rearrangements of these genes causes significant abnormalities to the entire neurological system, thus all organs and functions of the body– with variance in cognitive functions, gross motor skills, social development and other challenges during infancy, and throughout life;
  • Empower a unified community of 8p patients and their families so they can have meaningful lives today; and
  • Accelerate future treatments, not only for 8p, but potentially for other chromosome-wide diseases as well.