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P J Brophy

Showing results (61-70 of 69) with videos related to

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Neuropathology and Applied Neurobiology|August 1, 1991
Rumpshaker: an X-linked mutation affecting CNS myelination. A study of the female heterozygoteM L Fanarraga, I R Griffiths, M C McCulloch, et al.
Brain : a Journal of Neurology|October 17, 2006
Disruption of neurofascin localization reveals early changes preceding demyelination and remyelination in multiple sclerosisO W Howell, A Palser, A Polito, et al.
The Journal of Cell Biology|August 10, 2000
An oligodendrocyte cell adhesion molecule at the site of assembly of the paranodal axo-glial junctionS Tait, F Gunn-Moore, J M Collinson, et al.
Annals of the New York Academy of Sciences|January 1, 1990
Physiologic properties of myelin proteins revealed by their expression in nonglial cellsD R Colman, S M Staugaitis, D D'Urso, et al.
The Journal of Cell Biology|September 21, 2001
Overlapping functions of the cell adhesion molecules Nr-CAM and L1 in cerebellar granule cell developmentT Sakurai, M Lustig, J Babiarz, et al.
Glia|October 1, 1993
Oligodendrocyte development and differentiation in the rumpshaker mutationM L Fanarraga, I U Sommer, I R Griffiths, et al.
Human Molecular Genetics|February 7, 2001
A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth diseaseA Guilbot, A Williams, N Ravisé, et al.
Journal of Neuroscience Research|October 1, 1992
Developmental expression of major myelin protein genes in the CNS of X-linked hypomyelinating mutant rumpshakerL S Mitchell, S C Gillespie, F McAllister, et al.
Neuron|June 6, 2000
Peripheral demyelination and neuropathic pain behavior in periaxin-deficient miceC S Gillespie, D L Sherman, S M Fleetwood-Walker, et al.
Pageof 7

Showing results (61-70 of 69) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 69 results.
Neuropathology and Applied Neurobiology|August 1, 1991
Rumpshaker: an X-linked mutation affecting CNS myelination. A study of the female heterozygoteM L Fanarraga, I R Griffiths, M C McCulloch, et al.
Brain : a Journal of Neurology|October 17, 2006
Disruption of neurofascin localization reveals early changes preceding demyelination and remyelination in multiple sclerosisO W Howell, A Palser, A Polito, et al.
The Journal of Cell Biology|August 10, 2000
An oligodendrocyte cell adhesion molecule at the site of assembly of the paranodal axo-glial junctionS Tait, F Gunn-Moore, J M Collinson, et al.
Annals of the New York Academy of Sciences|January 1, 1990
Physiologic properties of myelin proteins revealed by their expression in nonglial cellsD R Colman, S M Staugaitis, D D'Urso, et al.
The Journal of Cell Biology|September 21, 2001
Overlapping functions of the cell adhesion molecules Nr-CAM and L1 in cerebellar granule cell developmentT Sakurai, M Lustig, J Babiarz, et al.
Glia|October 1, 1993
Oligodendrocyte development and differentiation in the rumpshaker mutationM L Fanarraga, I U Sommer, I R Griffiths, et al.
Human Molecular Genetics|February 7, 2001
A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth diseaseA Guilbot, A Williams, N Ravisé, et al.
Journal of Neuroscience Research|October 1, 1992
Developmental expression of major myelin protein genes in the CNS of X-linked hypomyelinating mutant rumpshakerL S Mitchell, S C Gillespie, F McAllister, et al.
Neuron|June 6, 2000
Peripheral demyelination and neuropathic pain behavior in periaxin-deficient miceC S Gillespie, D L Sherman, S M Fleetwood-Walker, et al.
Pageof 7