NGLY1Niemann-Pick Type APMM2-CDGMultiple Sulfatase DeficiencyGNAOICoffin-Lowry SyndromePancreatitisCori DiseaseMPSIIIAMSIIIBLeigh SyndromeAPOL1 kidney disease

We identified tool compounds,
repurposable drugs as well as
novel chemotypes that rescue
worm and fly disease models.

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We identified overlapping hits
between worm and patient fibroblast
drug repurposing screens.

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Type A
Niemann-Pick Type A Perlquest

We identified natural products
and repurposable drugs that rescue
yeast and worm disease models.

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MSD mutant flies are in the lab
and phenotyping has begun!

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Sulfatase
Deficiency

"Perlara’s work will help put
children with a GNAO1-related
neurodevelopmental disorder
further on the radar of researchers
and pharmaceutical companies.”

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Coffin-Lowry Syndrome PerlQuest1200x600px

"The collaborative drug
discovery effort gives hope
for new insights about CLS
and better lives for our children.”

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Syndrome

We’re excited to break new ground
scientifically with a yeast-to-organoid
drug screening pipeline for pancreatitis
and cystic fibrosis.

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Perlara’s expertise will accelerate
the identification of small molecules
as potential treatments for GSD patients.

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With children losing ground to this
disease every day we have to we are
hopeful that our PerlQuests will bring
us ever closer to help for patients
with Sanfilippo syndrome.

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We are developing nematode and fly
disease models and screening
compounds for promising leads.
Stay tuned.

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"A new treatment for Leigh syndrome
could have broader implications for
aging, sports medicine, traumatic
brain injury, neurodegeneration
and other indications."

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Syndrome
Mitochondria 2000x1000px

"Genetic risk for APOL1 kidney
disease affects ~100 million
people worldwide"

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kidney disease
APOL1 Kidney Disease hero 2400x1200px

Welcome to the archival website of Perlara 1.

Take a look around at the foundations of Perlara’s exciting new Guided Cures™ Journey.

Perlara scientists are working with highly motivated families, patient organizations and researchers to develop cures for rare diseases and learn how genes work across diseases to map connections to common ailments. We call these exciting journeys of discovery PerlQuests™

Organic Intelligence (OI): more cures for more individuals and diseases

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