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cherrylab.bsky.social

@cherrylab.bsky.social

cherrylab.bsky.social @cherrylab.bsky.social · 08/09/2025

Join us for the Seattle Walk to End Hydrocephalus, 9am Sept. 20 at Magnuson Park. Organized by the Hydrocephalus Association, that has supported our research into genetic causes of hydrocephalus and potential therapeutic targets. You can also donate at support.hydroassoc.org/goto/Team_Re...

support.hydroassoc.org

2025 Seattle WALK To End Hydrocephalus: Tim Cherry's Personal Fundraising Page

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cherrylab.bsky.social @cherrylab.bsky.social · 02/08/2025

1/5: How does a presumably redundant microRNA contribute to mammalian brain development and neurodevelopmental disease? Check out our new work led by Dr. Santiago Fregoso now on bioRxiv! www.biorxiv.org/content/10.1... #Neurodev #miRNA #hydrocephalus #Genetics #bioRxiv.

biorxiv.org

Loss of miR-9-2 Causes Cerebral Hemorrhage and Hydrocephalus by Widespread Disruption of Cell-Type-Specific Neurodevelopmental Gene Networks.

MIR-9-2 is a broadly and highly expressed microRNA in the developing brain and is frequently deleted in 5q14.3 Microdeletion Syndrome, a rare but severe neurodevelopmental disorder. Despite this, litt...

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cherrylab.bsky.social @cherrylab.bsky.social · 26/02/2025

Saying goodbye is hard! So is interpreting non-coding variants in visual disorders! Luckily, that is the gift that Dr. Leah VandenBosch left us with after a very successful postdoc in the Cherry Lab. Check your own favorite retinal regulatory variants here: genome.ucsc.edu/s/CherryLab/...

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