Dr. Huber obtained her Ph.D. in Neurobiology in 1995 from The University of Texas Graduate School of Biomedical Sciences in Houston where she worked with Drs. Paul Kelly and Michael Mauk on the neurobiological mechanisms of learning and memory, specifically long-term changes in neuronal connections, termed synaptic plasticity. Dr. Huber performed her postdoctoral training with Dr. Mark Bear at the Howard Hughes Medical Institute and Brown University where she discovered novel mechanisms and forms of synaptic plasticity as well as demonstrated specific alterations in synaptic plasticity in a mouse model of Fragile X Syndrome, the most common genetic cause of human mental retardation and autism. Dr. Huber joined the faculty at UT Southwestern in 2001 where she is she is currently a Professor in the Department of Neuroscience and Southwestern Medical Foundation Endowed Scholar.
Research in the Huber lab is focused on understanding the cellular and molecular mechanisms of synapse and neural circuit development and plasticity as well as the role of genes implicated in human autism and intellectual disability in these processes. To address these questions her lab utilizes state-of-the-art neurophysiology, imaging, biochemistry and molecular biology techniques in mice. Her lab has discovered novel molecular mechanisms of synaptic plasticity as well as new functions and mechanisms for the Fragile X Mental Retardation gene 1 (Fmr1) in cortical synapse development and plasticity. Her work has led to a better understanding of the neurobiology of Fragile X Syndrome and autism as well as identified novel therapeutic strategies.
Work is the Huber laboratory is supported by grants from the NIH, FRAXA Research Foundation, The Simons Foundation for Autism Research Initiative and The Hartwell Foundation.
- Stephen F Austin State Uni (1987), Biology
- Graduate School
- Univ of Tx Health Science Ctr (1995), Neuroscience
- Cortical Synapse Development and Plasticity
- Dendritic Translational Control
- Metabotropic Glutamate Receptors
- Neurobiological Basis of Fragile X Syndrome/Autism/Intellectual disability
- Imbalance of neocortical excitation and inhibition and altered UP states reflect network hyperexcitability in the mouse model of fragile X syndrome.
- Gibson JR, Bartley AF, Hays SA, Huber KM J. Neurophysiol. 2008 Nov 100 5 2615-26
- Rapid translation of Arc/Arg3.1 selectively mediates mGluR dependent LTD through persistent increases in AMPAR endocytosis rate
- Waung, M.W., Pfeiffer, B.E., Nosyreva, E.D., Ronesi, J.A. and Huber, K.M. Neuron July 2008 59(1): 84-97
- Rapid translation of Arc/Arg3.1 selectively mediates mGluR-dependent LTD through persistent increases in AMPAR endocytosis rate.
- Waung MW, Pfeiffer BE, Nosyreva ED, Ronesi JA, Huber KM Neuron 2008 Jul 59 1 84-97
Honors & Awards
- Simons Foundation Autism Research Initiative - Individual Investigator Award
Simons Foundation (2012)
- William and Enid Rosen Research Award for Outstanding Contributions to Fragile X Syndrome
National Fragile X Foundation (2012)
- Simons Foundation Autism Research Initiative -Pilot Award
Simons Foundation (2009)
- McKnight Foundation Brain Disorder Award
- Endowed Scholars Award in Biomedical Research