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Genomics|November 26, 1998
Exon organization, coding sequence, physical mapping, and polymorphic intragenic markers for the human neuronal sodium channel gene SCN8AN W Plummer, J Galt, J M Jones, et al.Genetics|January 1, 1994
Insertional mutation on mouse chromosome 18 with vestibular and craniofacial abnormalitiesC N Ting, D Kohrman, D L Burgess, et al.Genomics|March 20, 1995
Insertional mutation of the motor endplate disease (med) locus on mouse chromosome 15D C Kohrman, N W Plummer, T Schuster, et al.Molecular and Cellular Neurosciences|May 18, 1999
beta subunit reshuffling modifies N- and P/Q-type Ca2+ channel subunit compositions in lethargic mouse brainD L Burgess, G H Biddlecome, S I McDonough, et al.Genomics|June 15, 1996
Localization of the homolog of a mouse craniofacial mutant to human chromosome 18q11 and evaluation of linkage to human CLP and CPOA J Griffith, D L Burgess, D C Kohrman, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 1, 1996
Location of the 9257 and ataxia mutations on mouse chromosome 18A J Griffith, G L Radice, D L Burgess, et al.Cell Death and Differentiation|August 3, 2004
Expression of apoptosis inhibitor protein Mcl1 linked to neuroprotection in CNS neuronsM Mori, D L Burgess, L A Gefrides, et al.Epilepsia|October 3, 2001
Loss of the potassium channel beta-subunit gene, KCNAB2, is associated with epilepsy in patients with 1p36 deletion syndromeH A Heilstedt, D L Burgess, A E Anderson, et al.Nature Genetics|October 4, 2000
Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10T Matsuura, T Yamagata, D L Burgess, et al.Pageof 2