In the News
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"That’s how you go from treating a few hundred patients to treating thousands.” –Matt Simon, project director at JAX's Rare Disease Translational Center
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Lucy has a rare genetic disorder. Two doctors are leading the desperate hunt for a cure: her parents, Nov. 3, 2022
Erin Allday, San Francisco Chronicle Feature Story,
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Moonshots for Unicorns seeks to treat ultra-rare conditions, September 21, 2022
Nonprofit founded by Danville physicians to find cure for daughter's disorder
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Decentralized yeast lab for drug repurposing, September 8, 2022
Newsletter: Our pop-up yeast lab went live last month, and the first project out of the gate is PGAP3-CDG.
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Pharmaphorum: How these parents of a child with a rare disease are making precision medicine, September 8, 2022
A focus on precision medicine
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Effie Parks: Once Upon a Gene Podcast, August 26, 2022
An Ambitious and Innovative Project with Geri and Zach Landman
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San Francisco Business Times (Cover Story), August 19, 2022
‘Our unicorn baby': Lucy has a rare genetic disorder. Can a S.F. startup help?
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PatientWorthy: Rare Disease News, August 17, 2022
Moonshots for Unicorns: The Quest to Cure PGAP3 – and Other Single-Gene Disorers (Pt. 2)
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PatientWorthy: Rare Disease News, August 16, 2022
Moonshots for Unicorns: The Quest to Cure PGAP3 – and Other Single-Gene Disorders (Pt. 1)
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Incremental Healthcare: Podcast July 11 2022
Personalized Medicine for Everyone
