Marissa

@anothermarissa.bsky.social

#CDKL5 🧬 | Former school social worker turned stay-at-home medical mama | 🎙️Producer, content creator, & co-host of the CDKL5 in Color Podcast @cdkl5incolor.bsky.social www.CDKL5inColor.com

Almost all previous studies on CDKL5 have used a C-terminal tagging strategy (presumably to position the tag away from the kinase domain), but here we show that such modification of the C-term is disasterous as it abolishes CDKL5 synaptic localisation and function. www.biorxiv.org/content/10.1...

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Ben Goult@bengoult.bsky.social · last yr.

Excited to share our new preprint in @biorxiv-neursci.bsky.social "Cyclin-dependent kinase-like 5 (CDKL5) binds to talin and is anchored at the postsynaptic density via direct interaction with PDZ domains" Instead of a 🧵 the paper is summarised in this video. www.biorxiv.org/content/10.1...

✨🎙 New podcast episode is out! We reflect on how it’s been going for us at the CDKL5 in Color podcast and what people can expect in our upcoming (first!) newsletter! Sign up so you get all the info right to your inbox: www.cdkl5incolor.com/newsletter-s... 🎧 Listen on Spotify or Apple Podcasts

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This was a fun (fun? 🤔) episode to record because it was all still fresh in my mind after spending two weeks inpatient with my son for flu A! Never navigated a hospital stay with your child? Tune in to hear what it’s like. If you’ve been there, nod your head along with us as we share some stories.

CDKL5 in Color@cdkl5incolor.bsky.social · 2y ago

New podcast episode is out! We are talking #CDKL5 and hospitalizations. Have a listen on Spotify and Apple Podcasts! creators.spotify.com/pod/show/mar...

When you are primary caregiver to a medically complex child, being able to travel is an incredible challenge so I absolutely appreciate when there are virtual options available!

CDKL5 in Color@cdkl5incolor.bsky.social · 2y ago

🦓 Rare Disease Week on Capitol Hill is happening February 24-26, 2025. Hosted by the Rare Disease Legislative Advocates (RDLA), a program of @everylifeorg.bsky.social, this event empowers participants to learn key policies affecting the rare community & share their stories with Members of Congress.

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