Kimberly M Huber

Publication Activity (10 Years)

Years Active: 2017-2021
Publications (10 Years): 5

Top Topics

Depressive Symptoms

Cerebral Blood Flow

Top Venues

Science advances

Science translational medicine

Molecular autism

This page only lists publications with an associated author ORCID identifier.

Publications

Patrick K McCamphill, Laura J Stoppel, Rebecca K Senter, Michael C Lewis, Arnold J Heynen, David C Stoppel, Vinay Sridhar, Katie A Collins, Xi Shi, Jen Q Pan, Jon Madison, Jeffrey R Cottrell, Kimberly M Huber, Edward M Scolnick, Edward B Holson, Florence F Wagner, Mark F Bear
Selective inhibition of glycogen synthase kinase 3α corrects pathophysiology in a mouse model of fragile X syndrome. Science translational medicine 12 (544) (2021)
Zhe Zhang, Jay R Gibson, Kimberly M Huber
Experience-dependent weakening of callosal synaptic connections in the absence of postsynaptic FMRP. eLife 10 (2021)
Seung-Kyoon Kim, Xihui Liu, Jongmin Park, Dahun Um, Gokhul Kilaru, Cheng-Ming Chiang, Mingon Kang, Kimberly M Huber, Keunsoo Kang, Tae-Kyung Kim
Functional coordination of BET family proteins underlies altered transcription associated with memory impairment in fragile X syndrome. Science advances 7 (21) (2021)
Annie Hien, Gemma Molinaro, Botao Liu, Kimberly M Huber, Joel D Richter
Ribosome profiling in mouse hippocampus: plasticity-induced regulation and bidirectional control by TSC2 and FMRP. Molecular autism 11 (1) (2020)
Chia-Wei Chang, Julia R Wilkerson, Carly F Hale, Jay R Gibson, Kimberly M Huber
Distinct stages of synapse elimination are induced by burst firing of CA1 neurons and differentially require MEF2A/D. eLife 6 (2017)