村本環 (Tamaki Muramoto) - マイポータル - researchmap

基本情報

所属: 旧所属東北大学大学院医学系研究科附属創生応用医学研究センター助手

学位: 博士(医学)(九州大学)

J-GLOBAL ID: 200901091054735476
researchmap会員ID: 1000282973

外部リンク: http://www.med.tohoku.ac.jp/study-room/49/index.html

研究分野

1

ライフサイエンス / 実験病理学 /

MISC

36

Identification of two prion protein regions that modify scrapie incubation time

SUPATTAPONE S, MURAMOTO T, LEGNAME G, MEHLHORN I, COHEN F E, DEARMOND S J, PRUSINER S B, SCOTT M R

J. Virol. 75(3) 1408-1413 2001年
Identification of two prion protein regions that modify scrapie incubation time

J. Virol. 75(3) 1408-1413 2001年
Analyses of Gerstmann-Straussler syndrome with 102Leu219Lys using monoclonal antibodies that specifically detect human prion protein with 219Glu

T Muramoto, T Tanaka, N Kitamoto, C Sano, Y Hayashi, T Kutomi, C Yutani, T Kitamoto

NEUROSCIENCE LETTERS 288(3) 179-182 2000年7月
Analyses of Gerstmann-Straussler syndrome with 102Leu219Lys using monoclonal antibodies that specifically detect human prion protein with 219Glu

T Muramoto, T Tanaka, N Kitamoto, C Sano, Y Hayashi, T Kutomi, C Yutani, T Kitamoto

NEUROSCIENCE LETTERS 288(3) 179-182 2000年7月
Affinity-tagged miniprion derivatives spontaneously adopt protease-resistant conformations

SUPATTAPONE S, NGUYEN H‐O B, MURAMOTO T, COHEN F E, DEARMOND S J, PRUSINER S B, SCOTT M

J. Virol. 74(24) 11928-11934 2000年
Affinity-tagged miniprion derivatives spontaneously adopt protease-resistant conformations

J. Virol. 74(24) 11928-11934 2000年
Creutzfeldt-Jakob disease with florid-type plaques after cadaveric dura mater grafting

S Shimizu, K Hoshi, T Muramoto, M Homma, JW Ironside, S Kuzuhara, T Sato, T Yamamoto, T Kitamoto

ARCHIVES OF NEUROLOGY 56(3) 357-362 1999年3月
Prion protein of 106 residues creates an artificial transmission barrier for prion replication in transgenic mice

S Supattapone, P Bosque, T Muramoto, H Wille, C Aagaard, D Peretz, HOB Nguyen, C Heinrich, M Torchia, J Safar …

CELL 96(6) 869-878 1999年3月
Creutzfeldt-Jakob disease with florid-type plaques after cadaveric dura mater grafting

S Shimizu, K Hoshi, T Muramoto, M Homma, JW Ironside, S Kuzuhara, T Sato, T Yamamoto, T Kitamoto

ARCHIVES OF NEUROLOGY 56(3) 357-362 1999年3月
Prion protein of 106 residues creates an artificial transmission barrier for prion replication in transgenic mice

S Supattapone, P Bosque, T Muramoto, H Wille, C Aagaard, D Peretz, HOB Nguyen, C Heinrich, M Torchia, J Safar …

CELL 96(6) 869-878 1999年3月
Heritable disorder resembling neuronal storage disease in mice expressing prion protein with deletion of an α-helix.

MURAMOTO T, DEARMOND S J, SCOTT M, TELLING G C, COHEN F E, PRUSINER S B

Nature Medicine 3(7) 750-755 1997年7月
Heritable disorder resembling neuronal storage disease in mice expressing prion protein with deletion of an alpha-helix

T Muramoto, SJ DeArmond, M Scott, GC Telling, FE Cohen, SB Prusiner

NATURE MEDICINE 3(7) 750-755 1997年7月
Mutation in the prion protein gene at codon 232 in Japanese patients with Creutzfeldt-Jakob disease: A clinicopathological, immunohistochemical and transmission study

MZ Hoque, T Kitamoto, H Furukawa, T Muramoto, J Tateishi

ACTA NEUROPATHOLOGICA 92(5) 441-446 1996年11月
Mutation in the prion protein gene at codon 232 in Japanese patients with Creutzfeldt-Jakob disease: A clinicopathological, immunohistochemical and transmission study

MZ Hoque, T Kitamoto, H Furukawa, T Muramoto, J Tateishi

ACTA NEUROPATHOLOGICA 92(5) 441-446 1996年11月
Recombinant scrapie-like prion protein of 106 amino acids is soluble.

MURAMOTO T, SCOTT M, COHEN F E, PRUSINER S B

Proc. Natl. Acad. Sci. USA 93(26) 15457-15462 1996年
Recombinant scrapie-like prion protein of 106 amino acids is soluble.

Proc. Natl. Acad. Sci. USA 93(26) 15457-15462 1996年
Expression and targeting of Syrian hamster prion protein in transgenic Drosophila melanogaster

RAEBER A J, MURAMOTO T, KORNBERG T B, PRUSINER S B

Mech. Dev. 51(2/3) 317-327 1995年
Expression and targeting of Syrian hamster prion protein in transgenic Drosophila melanogaster

Mech. Dev. 51(2/3) 317-327 1995年
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, MZ HOQUE, J TATEISHI, GOTO, I

JOURNAL OF VIROLOGY 67(11) 6808-6810 1993年11月
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, MZ HOQUE, J TATEISHI, GOTO, I

JOURNAL OF VIROLOGY 67(11) 6808-6810 1993年11月

もっとみる

所属学協会

3

Works(作品等)

12

共同研究・競争的資金等の研究課題

2