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Neurology
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November 12, 2003
Creutzfeldt-Jakob disease with a novel extra-repeat insertional mutation in the PRNP gene
V Pietrini, G Puoti, L Limido, et al.
Neuropathology and Applied Neurobiology
|
January 23, 2008
Atypical tauopathy with massive involvement of the white matter
G Giaccone, G Marcon, M Mangieri, et al.
Biochimica Et Biophysica Acta
|
June 8, 2014
Defective collagen VI α6 chain expression in the skeletal muscle of patients with collagen VI-related myopathies
F Tagliavini, C Pellegrini, F Sardone, et al.
Journal of Neuropathology and Experimental Neurology
|
January 5, 2002
Ectopic white matter neurons, a developmental abnormality that may be caused by the PSEN1 S169L mutation in a case of familial AD with myoclonus and seizures
M Takao, B Ghetti, J R Murrell, et al.
Journal of Molecular Biology
|
July 25, 2000
Tetracycline affects abnormal properties of synthetic PrP peptides and PrP(Sc) in vitro
F Tagliavini, G Forloni, L Colombo, et al.
The Biochemical Journal
|
August 5, 1999
Molecular determinants of the physicochemical properties of a critical prion protein region comprising residues 106-126
M Salmona, P Malesani, L De Gioia, et al.
The American Journal of Pathology
|
June 17, 1998
An antibody raised against a conserved sequence of the prion protein recognizes pathological isoforms in human and animal prion diseases, including Creutzfeldt-Jakob disease and bovine spongiform encephalopathy
P Piccardo, J P Langeveld, A F Hill, et al.
Neurochemistry International
|
March 29, 2002
Expression in E. coli and purification of recombinant fragments of wild type and mutant human prion protein
A Corsaro, S Thellung, C Russo, et al.
Neurology
|
April 23, 2008
A novel PSEN2 mutation associated with a peculiar phenotype
P Piscopo, G Marcon, M R Piras, et al.
Lancet (London, England)
|
February 16, 2000
Reversion of prion protein conformational changes by synthetic beta-sheet breaker peptides
C Soto, R J Kascsak, G P Saborío, et al.
Page
of 14
Search research articles
Search
Showing results (111-120 of 133) with videos related to
Sort By:
Page
of 14
Neurology
|
November 12, 2003
Creutzfeldt-Jakob disease with a novel extra-repeat insertional mutation in the PRNP gene
V Pietrini, G Puoti, L Limido, et al.
Neuropathology and Applied Neurobiology
|
January 23, 2008
Atypical tauopathy with massive involvement of the white matter
G Giaccone, G Marcon, M Mangieri, et al.
Biochimica Et Biophysica Acta
|
June 8, 2014
Defective collagen VI α6 chain expression in the skeletal muscle of patients with collagen VI-related myopathies
F Tagliavini, C Pellegrini, F Sardone, et al.
Journal of Neuropathology and Experimental Neurology
|
January 5, 2002
Ectopic white matter neurons, a developmental abnormality that may be caused by the PSEN1 S169L mutation in a case of familial AD with myoclonus and seizures
M Takao, B Ghetti, J R Murrell, et al.
Journal of Molecular Biology
|
July 25, 2000
Tetracycline affects abnormal properties of synthetic PrP peptides and PrP(Sc) in vitro
F Tagliavini, G Forloni, L Colombo, et al.
The Biochemical Journal
|
August 5, 1999
Molecular determinants of the physicochemical properties of a critical prion protein region comprising residues 106-126
M Salmona, P Malesani, L De Gioia, et al.
The American Journal of Pathology
|
June 17, 1998
An antibody raised against a conserved sequence of the prion protein recognizes pathological isoforms in human and animal prion diseases, including Creutzfeldt-Jakob disease and bovine spongiform encephalopathy
P Piccardo, J P Langeveld, A F Hill, et al.
Neurochemistry International
|
March 29, 2002
Expression in E. coli and purification of recombinant fragments of wild type and mutant human prion protein
A Corsaro, S Thellung, C Russo, et al.
Neurology
|
April 23, 2008
A novel PSEN2 mutation associated with a peculiar phenotype
P Piscopo, G Marcon, M R Piras, et al.
Lancet (London, England)
|
February 16, 2000
Reversion of prion protein conformational changes by synthetic beta-sheet breaker peptides
C Soto, R J Kascsak, G P Saborío, et al.
Page
of 14