AFNN - Hoque,M.Z.; Kitamoto,T.; Furukawa,H.; Muramoto,T.; Tateishi,J. - Mutation in the prion protein gene at codon 232 in Japanese patients with Creutzfeldt-Jakob disease: a clinicopathological, immunohistochemical and transmission study. - Acta Neuropathologica 1996 Nov; 92(5): 441-6
AGNC - Kitamoto,T.; Mohri,S.; Ironside,J.W.; Miyoshi,I.; Tanaka,T.; Kitamoto,N.; Itohara,S.; Kasai,N.; Katsuki,M.; Higuchi,J.; Muramoto,T.; Shin,R.W. - Follicular dendritic cell of the knock-in mouse provides a new bioassay for human prions - Biochemical and Biophysical Research Communications 2002 Jun 7; 294(2): 280-6
AGNO - Kitamoto,T.; Doh-ura,K.; Muramoto,T.; Miyazono,M.; Tateishi,J. - The primary structure of the prion protein influences the distribution of abnormal prion protein in the central nervous system - American Journal of Pathology 1992 Aug; 141(2): 271-7
AGNP - Kitamoto,T.; Shin,R.W.; Doh-ura,K.; Tomokane,N.; Miyazono,M.; Muramoto,T.; Tateishi,J. - Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease - American Journal of Pathology 1992 Jun; 140(6): 1285-94
AGNQ - Kitamoto,T.; Muramoto,T.; Mohri,S.; Doh-ura,K.; Tateishi,J. - Abnormal isoform of prion protein accumulates in follicular dendritic cells in mice with Creutzfeldt-Jakob disease - Journal of Virology 1991 Nov; 65(11): 6292-5
AGNR - Kitamoto,T.; Muramoto,T.; Hilbich,C.; Beyreuther,K.; Tateishi,J. - N-terminal sequence of prion protein is also integrated into kuru plaques in patients with Gerstmann-Sträussler syndrome - Brain Research 1991 Apr 5; 545(1-2): 319-21
AQNA - Muramoto,T. - [Prion protein structure and its relationships with pathogenesis] - Rinsho Shinkeigaku. Clinical Neurology 2003 Nov; 43(11): 813-6
AIQY - Muramoto,T.; Tanaka,T.; Kitamoto,N.; Sano,C.; Hayashi,Y.; Kutomi,T.; Yutani,C.; Kitamoto,T. - Analyses of Gerstmann-Sträussler syndrome with 102Leu219Lys using monoclonal antibodies that specifically detect human prion protein with 219Glu - Neuroscience Letters 2000 Jul 21; 288(3): 179-82
AIQZ - Muramoto,T.; DeArmond,S.J.; Scott,M.R.D.; Telling,G.C.; Cohen,F.E.; Prusiner,S.B. - Heritable disorder resembling neuronal storage disease in mice expressing prion protein with deletion of an alpha-helix - Nature Medicine 1997 Jul; 3(7): 750-5
ASHG - Muramoto,T.; DeArmond,S.J.; Scott,M.; Cohen,F.E.; Prusiner,S.B. - Heritable neuronal storage disease in mice expressing prion protein with deletion of an alpha-helix - Neurology 1997; 48(3): 3044
AIRA - Muramoto,T.; Scott,M.R.D.; Cohen,F.E.; Prusiner,S.B. - Recombinant scrapie-like prion protein of 106 amino acids is soluble - Proceedings of the National Academy of Sciences of the United States of America 1996 Dec 24; 93(26): 15457-62
AIRB - Muramoto,T.; Kitamoto,T.; Tateishi,J.; Goto,I. - Accumulation of abnormal prion protein in mice infected with Creutzfeldt-Jakob disease via intraperitoneal route: a sequential study. - American Journal of Pathology 1993 Nov; 143(5): 1470-9
AIRC - Muramoto,T.; Kitamoto,T.; Hoque,M.Z.; Tateishi,J.; Goto,I. - Species barrier prevents an abnormal isoform of prion protein from accumulating in follicular dendritic cells of mice with Creutzfeldt-Jakob disease - Journal of Virology 1993 Nov; 67(11): 6808-10
AIRD - Muramoto,T.; Kitamoto,T.; Tateishi,J.; Goto,I. - Successful transmission of Creutzfeldt-Jakob disease from human to mouse verified by prion protein accumulation in mouse brains - Brain Research 1992 Dec 25; 599(2): 309-16
AIRE - Muramoto,T.; Kitamoto,T.; Tateishi,J.; Goto,I. - The sequential development of abnormal prion protein accumulation in mice with Creutzfeldt-Jakob disease - American Journal of Pathology 1992 Jun; 140(6): 1411-20
AIRF - Muramoto,T.; Kitamoto,T.; Koga,H.; Tateishi,J. - The coexistence of Alzheimer's disease and Creutzfeldt-Jakob disease in a patient with dementia of long duration - Acta Neuropathologica 1992; 84(6): 686-9
AJVJ - Raeber,A.J.; Muramoto,T.; Kornberg,T.B.; Prusiner,S.B. - Expression and targeting of Syrian hamster prion protein induced by heat shock in transgenic Drosophila melanogaster - Mechanisms of Development 1995 Jun; 51(2-3): 317-27
AQON - Satoh,K.; Shirabe,S.; Katamine,S.; Muramoto,T.; Kitamoto,T. - [Iatrogenic Creutzfeldt-Jakob disease] - Nippon Rinsho. Japanese Journal of Clinical Medicine 2004 Jan; 62 Suppl: 248-51
AOPG - Satoh,K.; Muramoto,T.; Tanaka,T.; Kitamoto,N.; Ironside,J.W.; Nagashima,K.; Yamada,M.; Sato,T.; Mohri,S.; Kitamoto,T. - Association of an 11-12 kDa protease-resistant prion protein fragment with subtypes of dura graft-associated Creutzfeldt-Jakob disease and other prion diseases - Journal of General Virology 2003 Oct; 84(10): 2885-93
AKUB - Shimizu,S.; Hoshi,K.; Muramoto,T.; Homma,M.; Ironside,J.W.; Kuzuhara,S.; Sato,T.; Yamamoto,T.; Kitamoto,T. - Creutzfeldt-Jakob disease with florid-type plaques after cadaveric dura mater grafting - Archives of Neurology 1999 Mar; 56(3): 357-62
ALGT - Supattapone,S.; Muramoto,T.; Legname,G.; Mehlhorn,I.; Cohen,F.E.; DeArmond,S.J.; Prusiner,S.B.; Scott,M.R.D. - Identification of two prion protein regions that modify scrapie incubation time - Journal of Virology 2001 Feb; 75(3): 1408-13
ALGU - Supattapone,S.; Nguyen,H.O.B.; Muramoto,T.; Cohen,F.E.; DeArmond,S.J.; Prusiner,S.B.; Scott,M.R.D. - Affinity-tagged miniprion derivatives spontaneously adopt protease-resistant conformations - Journal of Virology 2000 Dec; 74(24): 11928-34
ALGW - Supattapone,S.; Bosque,P.J.; Muramoto,T.; Wille,H.; Aagaard,C.; Peretz,D.; Nguyen,H.O.B.; Heinrich,C.; Torchia,M.; Safar,J.G.; Cohen,F.E.; DeArmond,S.J.; Prusiner,S.B.; Scott,M.R.D. - Prion protein of 106 residues creates an artifical transmission barrier for prion replication in transgenic mice - Cell 1999 Mar 19; 96(6): 869-78
APMM - Taguchi,Y.; Mohri,S.; Ironside,J.W.; Muramoto,T.; Kitamoto,T. - Humanized knock-in mice expressing chimeric prion protein showed varied susceptibility to different human prions - American Journal of Pathology 2003 Dec; 163(6): 2585-93