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A D Roses

Showing results (191-200 of 347) with videos related to

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Biochemical and Biophysical Research Communications|March 15, 1994
A new human slow skeletal troponin T (TnTs) mRNA isoform derived from alternative splicing of a single geneF Samson, L Mesnard, M Mihovilovic, et al.
Journal of Cellular Physiology|May 1, 1981
Patients with myotonic dystrophy, a possible segmental progeroid syndrome, and Duchenne muscular dystrophy have fibroblasts with normal limits for in vitro lifespan and growth characteristicsR L Wertz, G B Hartwig, A P Frost, et al.
The American Journal of Pathology|February 1, 1997
Beta-amyloid protein-containing inclusions in skeletal muscle of apolipoprotein-E-deficient miceT A Robertson, N S Dutton, R N Martins, et al.
Annals of Neurology|April 1, 1994
Novel amyloid precursor protein gene mutation (codon 665Asp) in a patient with late-onset Alzheimer's diseaseM L Peacock, D L Murman, A A Sima, et al.
Lancet (London, England)|January 7, 1995
Apolipoprotein E in Creutzfeldt-Jacob diseaseA D Roses, A M Saunders, W J Strittmatter, et al.
Archives of Neurology|August 1, 1991
Diagnostic criteria for multiple sclerosis research involving multiply affected familiesD E Goodkin, T H Doolittle, S S Hauser, et al.
Journal of Neuroscience Research|December 1, 1990
Isolation and localization of a slow troponin (TnT) gene on chromosome 19 by subtraction hybridization of a cDNA muscle library using myotonic dystrophy muscle cDNAF Samson, J E Lee, W Y Hung, et al.
Neuroscience|December 13, 2000
Susceptibility of transgenic mice expressing human apolipoprotein E to closed head injury: the allele E3 is neuroprotective whereas E4 increases fatalitiesT Sabo, L Lomnitski, A Nyska, et al.
The Journal of Clinical Investigation|May 1, 1995
Modulation of skeletal muscle sodium channels by human myotonin protein kinaseJ P Mounsey, P Xu, J E John, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1993
Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer diseaseW J Strittmatter, A M Saunders, D Schmechel, et al.
Pageof 35

Showing results (191-200 of 347) with videos related to

Sort By:
Pageof 35
Biochemical and Biophysical Research Communications|March 15, 1994
A new human slow skeletal troponin T (TnTs) mRNA isoform derived from alternative splicing of a single geneF Samson, L Mesnard, M Mihovilovic, et al.
Journal of Cellular Physiology|May 1, 1981
Patients with myotonic dystrophy, a possible segmental progeroid syndrome, and Duchenne muscular dystrophy have fibroblasts with normal limits for in vitro lifespan and growth characteristicsR L Wertz, G B Hartwig, A P Frost, et al.
The American Journal of Pathology|February 1, 1997
Beta-amyloid protein-containing inclusions in skeletal muscle of apolipoprotein-E-deficient miceT A Robertson, N S Dutton, R N Martins, et al.
Annals of Neurology|April 1, 1994
Novel amyloid precursor protein gene mutation (codon 665Asp) in a patient with late-onset Alzheimer's diseaseM L Peacock, D L Murman, A A Sima, et al.
Lancet (London, England)|January 7, 1995
Apolipoprotein E in Creutzfeldt-Jacob diseaseA D Roses, A M Saunders, W J Strittmatter, et al.
Archives of Neurology|August 1, 1991
Diagnostic criteria for multiple sclerosis research involving multiply affected familiesD E Goodkin, T H Doolittle, S S Hauser, et al.
Journal of Neuroscience Research|December 1, 1990
Isolation and localization of a slow troponin (TnT) gene on chromosome 19 by subtraction hybridization of a cDNA muscle library using myotonic dystrophy muscle cDNAF Samson, J E Lee, W Y Hung, et al.
Neuroscience|December 13, 2000
Susceptibility of transgenic mice expressing human apolipoprotein E to closed head injury: the allele E3 is neuroprotective whereas E4 increases fatalitiesT Sabo, L Lomnitski, A Nyska, et al.
The Journal of Clinical Investigation|May 1, 1995
Modulation of skeletal muscle sodium channels by human myotonin protein kinaseJ P Mounsey, P Xu, J E John, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1993
Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer diseaseW J Strittmatter, A M Saunders, D Schmechel, et al.
Pageof 35