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Neuron|September 8, 2001
Listen carefully: positional cloning of an audiogenic seizure mutation may yield Frings benefitsD L BurgessAnnals of the New York Academy of Sciences|July 22, 1999
Voltage-dependent calcium channel mutations in neurological diseaseD L Burgess, J L NoebelsEpilepsy Research|October 9, 1999
Single gene defects in mice: the role of voltage-dependent calcium channels in absence modelsD L Burgess, J L NoebelsEpilepsia|January 22, 2000
Genetic localization of the Ca2+ channel gene CACNG2 near SCA10 on chromosome 22q13D L Burgess, T Matsuura, T Ashizawa, et al.Genome Research|December 30, 1999
Identification of three novel Ca(2+) channel gamma subunit genes reveals molecular diversification by tandem and chromosome duplicationD L Burgess, C F Davis, L A Gefrides, et al.Genomics|February 15, 2001
A cluster of three novel Ca2+ channel gamma subunit genes on chromosome 19q13.4: evolution and expression profile of the gamma subunit gene familyD L Burgess, L A Gefrides, P J Foreman, et al.Cell|February 7, 1997
Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouseD L Burgess, J M Jones, M H Meisler, et al.Genomics|November 1, 1992
Isolation of DNA markers from a region between incontinentia pigmenti 1 (IP1) X-chromosomal translocation breakpoints by a comparative PCR analysis of a radiation hybrid subclone mapping panelJ L Gorski, E N Burright, E L Reyner, et al.Genomics|June 1, 1993
Phosphoenolpyruvate carboxykinase (GTP): characterization of the human PCK1 gene and localization distal to MODY on chromosome 20C N Ting, D L Burgess, J S Chamberlain, et al.Nature Genetics|August 1, 1995
Mutation of a new sodium channel gene, Scn8a, in the mouse mutant 'motor endplate disease'D L Burgess, D C Kohrman, J Galt, et al.Pageof 2