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B Ghetti

Showing results (171-180 of 227) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|July 8, 1999
Structure of tau exon 10 splicing regulatory element RNA and destabilization by mutations of frontotemporal dementia and parkinsonism linked to chromosome 17L Varani, M Hasegawa, M G Spillantini, et al.
The American Journal of Pathology|December 24, 1997
Diverse cell death pathways result from a single missense mutation in weaver mouseA Migheli, R Piva, J Wei, et al.
Neuroendocrinology|January 5, 1999
Hypothalamic-pituitary-gonadal axis in the mutant weaver mouseN B Schwartz, M Szabo, T Verina, et al.
Neurochemical Research|November 1, 1994
Studies on the striatal dopamine uptake system of weaver mutant mice and effects of ventral mesencephalic graftsL C Triarhou, E H Stotz, W C Low, et al.
Acta Neuropathologica|July 21, 1999
A mutation at codon 279 (N279K) in exon 10 of the Tau gene causes a tauopathy with dementia and supranuclear palsyM B Delisle, J R Murrell, R Richardson, et al.
Experimental Brain Research|January 1, 1997
Atrophy and loss of dopaminergic mesencephalic neurons in heterozygous weaver miceT Verina, J A Norton, J J Sorbel, et al.
Brain Research|July 9, 1993
A68 is a component of paired helical filaments of Gerstmann-Sträussler-Scheinker disease, Indiana kindredF Tagliavini, G Giaccone, F Prelli, et al.
Brain Pathology (Zurich, Switzerland)|April 1, 1996
Prion protein amyloidosisB Ghetti, P Piccardo, B Frangione, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 29, 1994
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphismL Monari, S G Chen, P Brown, et al.
Journal of Neuropathology and Experimental Neurology|July 1, 1997
In situ hybridization analysis of Girk2 expression in the developing central nervous system in normal and weaver miceJ Wei, S R Dlouhy, S Bayer, et al.
Pageof 23

Showing results (171-180 of 227) with videos related to

Sort By:
Pageof 23
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1999
Structure of tau exon 10 splicing regulatory element RNA and destabilization by mutations of frontotemporal dementia and parkinsonism linked to chromosome 17L Varani, M Hasegawa, M G Spillantini, et al.
The American Journal of Pathology|December 24, 1997
Diverse cell death pathways result from a single missense mutation in weaver mouseA Migheli, R Piva, J Wei, et al.
Neuroendocrinology|January 5, 1999
Hypothalamic-pituitary-gonadal axis in the mutant weaver mouseN B Schwartz, M Szabo, T Verina, et al.
Neurochemical Research|November 1, 1994
Studies on the striatal dopamine uptake system of weaver mutant mice and effects of ventral mesencephalic graftsL C Triarhou, E H Stotz, W C Low, et al.
Acta Neuropathologica|July 21, 1999
A mutation at codon 279 (N279K) in exon 10 of the Tau gene causes a tauopathy with dementia and supranuclear palsyM B Delisle, J R Murrell, R Richardson, et al.
Experimental Brain Research|January 1, 1997
Atrophy and loss of dopaminergic mesencephalic neurons in heterozygous weaver miceT Verina, J A Norton, J J Sorbel, et al.
Brain Research|July 9, 1993
A68 is a component of paired helical filaments of Gerstmann-Sträussler-Scheinker disease, Indiana kindredF Tagliavini, G Giaccone, F Prelli, et al.
Brain Pathology (Zurich, Switzerland)|April 1, 1996
Prion protein amyloidosisB Ghetti, P Piccardo, B Frangione, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 29, 1994
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphismL Monari, S G Chen, P Brown, et al.
Journal of Neuropathology and Experimental Neurology|July 1, 1997
In situ hybridization analysis of Girk2 expression in the developing central nervous system in normal and weaver miceJ Wei, S R Dlouhy, S Bayer, et al.
Pageof 23