Marianne R. Smith

Functional Analysis of the Mouse Scn8a Sodium Channel

Nicholas W. Plummer, A. L. Goldin, Alan L. Goldin, 1998, The Journal of Neuroscience.

A potent and selective Sirtuin 1 inhibitor alleviates pathology in multiple animal and cell models of Huntington's disease.

J. Purcell, A. Syed, J. Marsh, 2014, Human molecular genetics.

A Missense Mutation in the Sodium Channel Scn8a Is Responsible for Cerebellar Ataxia in the Mouse Mutant jolting

A. L. Goldin, M. Meisler, Marianne R. Smith, 1996, The Journal of Neuroscience.

Morphometric analysis of Huntington's disease neurodegeneration in Drosophila.

J. Purcell, A. Syed, J. Marsh, 2013, Methods in molecular biology.

Nonmammalian Models of Huntington's Disease.

A. Syed, J. Marsh, Marianne R. Smith, 2018, Methods in molecular biology.

A gain-of-function mutation in the sodium channel gene Scn2a results in seizures and behavioral abnormalities

A. L. Goldin, S. Waxman, J. Kapur, 2001, Neuroscience.

Interaction between the sodium channel inactivation linker and domain III S4-S5.

A. L. Goldin, M. Smith, Marianne R. Smith, 1997, Biophysical journal.

A mutation that causes ataxia shifts the voltage-dependence of the Scn8a sodium channel.

A. L. Goldin, M. Smith, Marianne R. Smith, 1999, Neuroreport.