Search research articles
Contact Us
Filters
Showing results (91-100 of 183) with videos related to
Page
of 19
Sort By:
Virchows Archiv. A, Pathological Anatomy and Histopathology
|
January 1, 1988
Incidence and characterization of age related amyloid deposits in the human anterior pituitary gland
T Tashima, T Kitamoto, J Tateishi, et al.
Biochemical and Biophysical Research Communications
|
September 15, 1989
Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome
K Doh-ura, J Tateishi, H Sasaki, et al.
Journal of Virology
|
November 1, 1991
Abnormal isoform of prion protein accumulates in follicular dendritic cells in mice with Creutzfeldt-Jakob disease
T Kitamoto, T Muramoto, S Mohri, et al.
Acta Neuropathologica
|
January 1, 1988
Focal intracerebral accumulation of a novel type of amyloid protein. An early stage of cerebral amyloidoma?
A Hori, T Kitamoto, J Tateishi, et al.
Biochemical and Biophysical Research Communications
|
May 29, 1992
Cellular retinoic acid binding protein type II was preferentially localized in medium and posterior parts of the progress zone of the chick limb bud
S Miyagawa-Tomita, T Kitamoto, K Momma, et al.
Acta Neuropathologica
|
January 1, 1992
Creutzfeldt-Jakob disease with codon 129 polymorphism (valine): a comparative study of patients with codon 102 point mutation or without mutations
M Miyazono, T Kitamoto, K Doh-ura, et al.
Annals of Neurology
|
June 18, 1998
Codon 219 Lys allele of PRNP is not found in sporadic Creutzfeldt-Jakob disease
S Shibuya, J Higuchi, R W Shin, et al.
The American Journal of Pathology
|
April 1, 1992
Massive accumulation of modified tau and severe depletion of normal tau characterize the cerebral cortex and white matter of Alzheimer's disease. Demonstration using the hydrated autoclaving method
R W Shin, T Iwaki, T Kitamoto, et al.
Acta Neuropathologica
|
November 1, 1996
Mutation in the prion protein gene at codon 232 in Japanese patients with Creutzfeldt-Jakob disease: a clinicopathological, immunohistochemical and transmission study
M Z Hoque, T Kitamoto, H Furukawa, et al.
Journal of Virology
|
November 1, 1993
Species barrier prevents an abnormal isoform of prion protein from accumulating in follicular dendritic cells of mice with Creutzfeldt-Jakob disease
T Muramoto, T Kitamoto, M Z Hoque, et al.
Page
of 19
Search research articles
Search
Showing results (91-100 of 183) with videos related to
Sort By:
Page
of 19
Virchows Archiv. A, Pathological Anatomy and Histopathology
|
January 1, 1988
Incidence and characterization of age related amyloid deposits in the human anterior pituitary gland
T Tashima, T Kitamoto, J Tateishi, et al.
Biochemical and Biophysical Research Communications
|
September 15, 1989
Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome
K Doh-ura, J Tateishi, H Sasaki, et al.
Journal of Virology
|
November 1, 1991
Abnormal isoform of prion protein accumulates in follicular dendritic cells in mice with Creutzfeldt-Jakob disease
T Kitamoto, T Muramoto, S Mohri, et al.
Acta Neuropathologica
|
January 1, 1988
Focal intracerebral accumulation of a novel type of amyloid protein. An early stage of cerebral amyloidoma?
A Hori, T Kitamoto, J Tateishi, et al.
Biochemical and Biophysical Research Communications
|
May 29, 1992
Cellular retinoic acid binding protein type II was preferentially localized in medium and posterior parts of the progress zone of the chick limb bud
S Miyagawa-Tomita, T Kitamoto, K Momma, et al.
Acta Neuropathologica
|
January 1, 1992
Creutzfeldt-Jakob disease with codon 129 polymorphism (valine): a comparative study of patients with codon 102 point mutation or without mutations
M Miyazono, T Kitamoto, K Doh-ura, et al.
Annals of Neurology
|
June 18, 1998
Codon 219 Lys allele of PRNP is not found in sporadic Creutzfeldt-Jakob disease
S Shibuya, J Higuchi, R W Shin, et al.
The American Journal of Pathology
|
April 1, 1992
Massive accumulation of modified tau and severe depletion of normal tau characterize the cerebral cortex and white matter of Alzheimer's disease. Demonstration using the hydrated autoclaving method
R W Shin, T Iwaki, T Kitamoto, et al.
Acta Neuropathologica
|
November 1, 1996
Mutation in the prion protein gene at codon 232 in Japanese patients with Creutzfeldt-Jakob disease: a clinicopathological, immunohistochemical and transmission study
M Z Hoque, T Kitamoto, H Furukawa, et al.
Journal of Virology
|
November 1, 1993
Species barrier prevents an abnormal isoform of prion protein from accumulating in follicular dendritic cells of mice with Creutzfeldt-Jakob disease
T Muramoto, T Kitamoto, M Z Hoque, et al.
Page
of 19