Back

FMRP regulates adult human cortical neuron excitability via cyclic-AMP signalling

Knops, M. J.; Meftah, S.; Wilson, M. A.; Taylor, L. W.; Bonthron, C.; Bilal, A.; Liaquat, I.; Brennan, P. M.; Durrant, C. S.; Booker, S. A.

2025-11-14 neuroscience
10.1101/2025.10.14.682273 bioRxiv
Show abstract

Fragile X Syndrome (FXS) is a common inherited neurodevelopmental condition, resulting from loss of Fragile X Messenger Ribonuclear Protein (FMRP). Rodent models of FXS display cellular hyperexcitability, but it is not known to what extent this is the case in intact human neurons. Depleting FMRP in human brain slice cultures reveals cyclic-AMP-dependent cellular hyperexcitability which is corrected by phosphodiesterase 4D inhibition and may be independent of neurodevelopment.

Matching journals

The top 7 journals account for 50% of the predicted probability mass.

50% of probability mass above

"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.