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Tamaki Muramoto
Observed names:
T Muramoto,
T. Muramoto,
TAMAKI MURAMOTO,
Tamaki MURAMOTO
Institution:
Tohoku University
Observed institutions:
Kyushu University,
University of California, San Francisco,
Tohoku University,
Japan Science and Technology Agency,
Takatsuki Red Cross Hospital,
Institute for Neurodegenerative Diseases
show all 6
OpenAlex ID:
A5021323927
Abnormal isoform of prion protein accumulates in follicular dendritic cells in mice with Creutzfeldt-Jakob disease
1991
·
T Kitamoto
, T Muramoto
, et al.
·
Journal of Virology
·
294
PDF
Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease.
1992
·
T Kitamoto
, R W Shin
, et al.
·
PubMed
·
269
Prion Protein of 106 Residues Creates an Artificial Transmission Barrier for Prion Replication in Transgenic Mice
1999
·
Surachai Supattapone
, Patrick Bosque
, et al.
·
Cell
·
206
PDF
Recombinant scrapie-like prion protein of 106 amino acids is soluble
1996
·
Tamaki Muramoto
, Michael Scott
, et al.
·
Proceedings of the National Academy of Sciences
·
174
Heritable disorder resembling neuronal storage disease in mice expressing prion protein with deletion of an α-helix
1997
·
Tamaki Muramoto
, Stephen J. DeArmond
, et al.
·
Nature Medicine
·
120
Identification of Two Prion Protein Regions That Modify Scrapie Incubation Time
2001
·
Surachai Supattapone
, Tamaki Muramoto
, et al.
·
Journal of Virology
·
102
Creutzfeldt-Jakob Disease With Florid-Type Plaques After Cadaveric Dura Mater Grafting
1999
·
Saori Shimizu
, Ken-ichi Hoshi
, et al.
·
Archives of Neurology
·
86
The sequential development of abnormal prion protein accumulation in mice with Creutzfeldt-Jakob disease.
1992
·
T Muramoto
, T Kitamoto
, et al.
·
PubMed
·
80
The primary structure of the prion protein influences the distribution of abnormal prion protein in the central nervous system.
1992
·
T Kitamoto
, K Doh-ura
, et al.
·
PubMed
·
62
Interaction of Aluminum with PHFτ in Alzheimer's Disease Neurofibrillary Degeneration Evidenced by Desferrioxamine-Assisted Chelating Autoclave Method
1999
·
Harunobu Murayama
, Ryong-Woon Shin
, et al.
·
American Journal Of Pathology
·
59
PDF
Association of an 11–12 kDa protease-resistant prion protein fragment with subtypes of dura graft-associated Creutzfeldt–Jakob disease and other prion diseases
2003
·
Katsuya Satoh
, Tamaki Muramoto
, et al.
·
Journal of General Virology
·
58
A novel anti-prion protein monoclonal antibody and its single-chain fragment variable derivative with ability to inhibit abnormal prion protein accumulation in cultured cells
2009
·
Yoshihisa Shimizu
, Yuko Kaku-Ushiki
, et al.
·
Microbiology and Immunology
·
56
Humanized Knock-In Mice Expressing Chimeric Prion Protein Showed Varied Susceptibility to Different Human Prions
2003
·
Yuzuru Taguchi
, Shirou Mohri
, et al.
·
American Journal Of Pathology
·
56
PDF
N-terminal sequence of prion protein is also intergrated into kuru plaques in patients with Gerstmann-Stra¨ussler syndrome
1991
·
Tetsuyuki Kitamoto
, Tamaki Muramoto
, et al.
·
Brain Research
·
51
Mutation in the prion protein gene at codon 232 in Japanese patients with Creutzfeldt-Jakob disease: a clinicopathological, immunohistochemical and transmission study
1996
·
Mohammad Zahirul Hoque
, Tetsuyuki Kitamoto
, et al.
·
Acta Neuropathologica
·
49
Follicular dendritic cell of the knock-in mouse provides a new bioassay for human prions
2002
·
Tetsuyuki Kitamoto
, Shirou Mohri
, et al.
·
Biochemical and Biophysical Research Communications
·
47
Expression and targeting of Syrian hamster prion protein induced by heat shock in transgenic Drosophila melanogaster
1995
·
Alex J. Raeber
, Tamaki Muramoto
, et al.
·
Mechanisms of Development
·
45
PDF
Accumulation of abnormal prion protein in mice infected with Creutzfeldt-Jakob disease via intraperitoneal route: a sequential study.
1993
·
T Muramoto
, T Kitamoto
, et al.
·
PubMed
·
41
The coexistence of Alzheimer's disease and Creutzfeldt-Jakob disease in a patient with dementia of long duration
1992
·
T. Muramoto
, T. Kitamoto
, et al.
·
Acta Neuropathologica
·
41
A missense mutation in the proteolipid protein gene responsible for Pelizaeus—Merzbacher disease in a Japanese family
1993
·
Akiko Iwaki
, Tamaki Muramoto
, et al.
·
Human Molecular Genetics
·
27
Species Barrier Prevents an Abnormal Isoform of Prion Protein from Accumulating in Follicular Dendritic Cells of Mice with Creutzfeldt-Jakob Disease
1993
·
Tamaki Muramoto
, Tetsuyuki Kitamoto
, et al.
·
Journal of Virology
·
24
Analyses of Gerstmann–Straussler syndrome with 102Leu219Lys using monoclonal antibodies that specifically detect human prion protein with 219Glu
2000
·
Tamaki Muramoto
, Tomoyuki Tanaka
, et al.
·
Neuroscience Letters
·
22
Successful transmission of Creutzfeldt-Jakob disease from human to mouse verified by prion protein accumulation in mouse brains
1992
·
Tamaki Muramoto
, Tetsuyuki Kitamoto
, et al.
·
Brain Research
·
22
Affinity-Tagged Miniprion Derivatives Spontaneously Adopt Protease-Resistant Conformations
2000
·
Surachai Supattapone
, Hoang-Oanh B. Nguyen
, et al.
·
Journal of Virology
·
11
[Prion protein structure and its relationships with pathogenesis].
2003
·
Tamaki Muramoto
·
PubMed
·
1
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Works count:
30
Citation count:
2,005
H-index:
22
I10-index:
24
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