Prions: food and drug safety
Presents a collection of work on prion research that was presented at the 2004 symposium. This volume includes topics ranging from basic research to clinical aspects of prion diseases. It is intended for researchers and clinicians, and aims to encourage developments by researchers in the field.
Gespeichert in:
| Format: | Buch |
|---|---|
| Sprache: | English |
| Veröffentlicht: |
Tokyo [u.a.]
Springer
2005
|
| Schlagworte: | |
| Online-Zugang: | Klappentext Inhaltsverzeichnis |
| Zusammenfassung: | Presents a collection of work on prion research that was presented at the 2004 symposium. This volume includes topics ranging from basic research to clinical aspects of prion diseases. It is intended for researchers and clinicians, and aims to encourage developments by researchers in the field. |
| Beschreibung: | Literaturangaben |
| Beschreibung: | XV, 271 S. Ill., graph. Darst. 24 cm |
| ISBN: | 4431255397 |
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| 520 | 3 | |a Presents a collection of work on prion research that was presented at the 2004 symposium. This volume includes topics ranging from basic research to clinical aspects of prion diseases. It is intended for researchers and clinicians, and aims to encourage developments by researchers in the field. | |
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Datensatz im Suchindex
| _version_ | 1804135031199760384 |
|---|---|
| adam_text | Contents
Preface
Organization of Symposium
Guest Speakers
Acknowledgment
Pathology of variant Creutzfeldt-Jakob disease
J.W. Ironside
Clinical aspects of variant CJD
R. Knight
Dura mater related Creutzfeldt-Jakob disease in Japan: Relationship
between sites of grafts and clinical features
T. Sato, M. Masuda, Y. Utsumi, Y. Enomoto, M. Yamada,
H. Mizusawa and T. Kitamoto
Treatment options in patients with prion disease
cerebroventricular infusion of pentosan polysulphate
N.G Rainov, I.R. Whittle and K. Doh-ura
Human prion diseases: novel diagnostic principles
M. Glatzel
History and state of the art of PrP-res typing in Creutzfeldt-Jakob
disease
P.
Chronic wasting disease in cervids in North America
E.S.Williams
Bovine spongiform encephalopathy (BSE) in Japan
T. Yokoyama,
The role of host PrP in control of incubation time
J.
The role of the immune system in TSE agent
N.A. Mabbott, J. Mohan and M.E. Bruce
IX
Prion protein
GS.
Semi-classical quantization of protein dynamics: Novel NMR
relaxation formalism and its application to prion
K. Kuwata
Surveillance of chronic wasting disease (CWD) in Japan
K. Shimada, Y. Iwamara, H. Hayashi, M.
Y.K. Ushiki,
M. Shinagawa and T. Yokoyama
Unexpected high incidence of visceral AA-amyloidosis in slaughtered
cattle in Japan
K.
andS.
A Novel BSE screening kit with simplified preparation method for
EIA
T.
H. Tsukagoshi-Nagai, T. Yokoyama, Y. Tagawa, T.
Y. Yamakawa,
Detection of
correlation spectroscopy
F.
and M. Kinjo
PrPSc distribution
encephalopathy
Y. Iwamaru, Y. Okubo, T. Ikeda, H. Hayashi, M.
T. Yokoyama and M. Shinagawa
Report
R. Irie, H. Okada, H. Hayashi, Y. Iwamaru, T. Yokoyama
andM. Shinagawa
The development of the intracerebral inoculation method and BSE
experimental transmissions to calves
S. Fukuda, S. Nikaido, Y. Matsui, S. Kageyama and S. Onoe
Comparative analyses of three mouse-adapted scrapie strains Gl,
Obihiro, and
ICR mice
M. Horiuchi, Y. Tamura and H. Furaoka
XI
Dose effect on detection of PrPSc in follicular dendritic cells of
knock-in mice for rapid bioassay
S. Mohri, M.
and
Cell surface retention of PrPc by anti-PrP antibody prevents
protease-resistant PrP formation
M. Horiuchi, C.-L. Kim, M. Ogino, H. Furuoka and M. Shinagawa
Prion-conformation-specifíc
display library
S. Hashiguchi, M. Yamamoto, S. Kitamoto, T. Nakashima,
H. Yamanaka, D. Ishibashi, S. Sakaguchi, S. Katamine, Y.
and
Partial characterization of monoclonal antibodies which bind to
disease-associated prion protein in immunoprecipitaion assay
Y.K. Ushiki, R. Endo,
S. Hattori, S. Irie and T. Yokoyama
Production and characterization of monoclonal antibodies specific
for prion protein
M. Morita, A. Ohmizu, H. Maeno, T. Matsuo, Y. Ogata, M. Naiki,
S. Suzuki and I.
In vitro selection of anti-mouse prion protein
S. Sekiya, K. Noda, P.K.R. Kumar, T. Yokoyama
and S. Nishikawa
Detection of the prion protein in a liquid phase capture assay using
magnetic beads coupled to protein A
W.-C. Yang, E.S. Yeung, M.J. Schmerr and W. Bodemer
New
prion protein
K. Sasaki, K. Doh-ura and T. Iwaki
Cellular prion protein suppresses the apoptosis in
established from type-1 prion protein gene-deficient mice
K. Saeki, T. Nishimura, A. Sakudo, Y. Matsumoto and T. Onodera
Cellular prion protein suppressess the apoptotic cell death by
mediating the intracellular H2Oi in primary culture and immortalized
neuronal
I. Nakamura, T. Nishimura, K. Saeki,
andT. Onodera
XII
Targeting
BCL-l pathway induces mitochondrial apoptosis
N.S. Hachiya, M. Yamada, K. Watanabe, A. Jozuka, Y. Kozuka,
Y. Sakasegawa and K. Kaneko
Microtubule-dependent intracellular trafficking of cellular prion protein
N.S. Hachiya, K. Watanabe, M. Yamada, Y. Sakasegawa
and K. Kaneko
Hsp90 modifies the conformation of
in vitro
Y. Sakasegawa, N.S. Hachiya and K. Kaneko
Purification and characterization of a novel ATP-dependent robust
protein-unfoldase, Unfoldin
N.S. Hachiya, M. Yamada, A. Jozuka, Y. Kozuka,
and K. Kaneko
Nucleic acid and prion protein interaction produces spherical
amyloids which in vivo can function as coats of spongiform
encephalopathy agent
P.K. Nandi and
Species barrier in yeast
H.
Molecular memory of [PSI+] prion strains in S. cerevisiae is dependent
on the primary structure of the Sup35 prion domain
C.G. Crist, T. Nakayashiki, H. Kurahashi and Y. Nakamura
Expression of a splice variant of prion protein during hypoxia in human
glioblastoma cell line T98G
Y. Kikuchi, T. Kakeya, A. Sakai, H. Matsuda, T. Yamazaki,
K. Tanamoto, K. Ikeda,
PRNP promoter region polymorphism in Creutzfeldt-Jakob disease
P.P.
and T.J.
Tubulovesicular structures are consistently found in prion diseases
including vCJD and FF1
P.P.
Autophagy is a common
prion diseases
B. Sikorska, P.P.
XIII
Type
methionine
Creutzfeldt-Jakob disease
A. Kobayashi, S. Satoh, J.W. Ironside, S. Mohri andT. Kitamoto
A pitfall in diagnosis of human prion diseases using detection of
protease-resistant prion protein in urine: contamination with bacterial
outer membrane proteins
H. Furukawa, K. Doh-ura, R. Okuwaki, S. Shirabe, K. Yamamoto,
H. Udono, T.
Comparative analysis of chronological data of total
serial studies of
features in patients with sporadic CJD
K. Satoh
Duration between initial manifestation of CJD and detection of PSD,
specific findings on
N.
and H. Mizusawa
Biochemical analysis of peripheral tissue involvement in transmissible
spongiform encephalopathies
V.A. Lawson, A.F. Hill, V. Lewis, R. Sharpies, S. Collins
and C.L. Masters
Involvement of the peripheral nervous system in human prion diseases
including
С
MM2 type sporadic Creutzfeldt-Jakob disease: clinicoradiologic
features and clinical diagnosis
T. Hamaguchi, T. Kitamoto, T. Sato, H. Mizusawa, Y. Nakamura,
M. Noguchi, Y. Furukawa,
S. Murayama, T.
T.
S. Kuroda,
and M. Yamada
Early clinical and radiological diagnosis of sporadic Creuzfeldt- Jakob s
disease (sCJD)
K. Ishihara, M. Sugie, J. Shiota, M. Kawamura, T. Kitamoto
and
XIV
Familial
codon
Y. Shiga, H. Mizuno, S. Watanabe, M. Tateyama, I. Nakashima,
K. Fujihara, T. Kitamoto and
Familial
Y.
Y. Komatzusaki, S.
M.
A
and codon
Y. Nishida,
and
Inhibition
mouse monoclonal antibodies against prion protein
K. Miyamoto,
H. Horiuchi, S. Furusawa and H. Matsuda
The inhibitory effect of the ScFv of an anti-prion protein antibody
secreted from N2a58 cells on abnormal prion protein accumulation in
scrapie-infected cells, ScN2a
Y. Shimizu, Y. Kaku-Ushiki, S. Fukuda, M. Shinagawa, T. Yokoyama
andY. Tagawa
Mucosal immunogenicity of prion protein fused with heat-labile
enterotoxin
H.
Identification of drugs that enhance the stimulatory effect of PrP on
the fibrinolytic system
G Epple, G
Screening study of prion binding agents and their inhibitory effect on
the conversion of prion protein
N.
and
Can forage grasses inhibit prion replication
T. Miyamoto, R. Sadatomi, H. Tanaka, R. Higuchi, S. Kawatake
andK. Doh-ura
Inhibition of abnormal PrP formation by amyloid-imaging probes
in vitro
K. Ishikawa, Y. Kudo andK. Doh-ura
XV
Treatment
Creutzfeldt-Jakob disease patients
Y. Tsuboi, F. Fujiki, A. Yamauchi, K. Doh-ura, Y. Kataoka and
T
Effect of oral administration of pentosan polysulfate for patients with
Creutzfeldt-Jakob disease (CJD) and new design for low
molecular-weight of pentosan polysulfate
S. Shirabe, K. Satoh, K. Eguchi, M.
A. Yamauchi, Y. Kataoka and S. Katamine
Key Word Index
PRIONS
Prion diseases recently have attracted
interest not only scientifically but also
socially because of the bovine spongiform
encephalopathy (BSE) epidemic and the
outbreak of variant Creutzfeldt-Jakob
disease (vCJD) in the United Kingdom. In
2004,
Prion Diseases for Food and Drug Safety
was held October 31-November
Sendai, Japan, where,
arguments were first heard on whether
the
spongiform encephalopathy was
scrapie-associated fibrils. This volume is a
collection of current work on prion
research that was presented at the
symposium. Topics included range from
basic research to clinical aspects of prion
diseases, making the book a valuable
resource for researchers and clinicians,
and encouraging further developments
by the next generation of researchers.
|
| adam_txt |
Contents
Preface
Organization of Symposium
Guest Speakers
Acknowledgment
Pathology of variant Creutzfeldt-Jakob disease
J.W. Ironside
Clinical aspects of variant CJD
R. Knight
Dura mater related Creutzfeldt-Jakob disease in Japan: Relationship
between sites of grafts and clinical features
T. Sato, M. Masuda, Y. Utsumi, Y. Enomoto, M. Yamada,
H. Mizusawa and T. Kitamoto
Treatment options in patients with prion disease
cerebroventricular infusion of pentosan polysulphate
N.G Rainov, I.R. Whittle and K. Doh-ura
Human prion diseases: novel diagnostic principles
M. Glatzel
History and state of the art of PrP-res "typing" in Creutzfeldt-Jakob
disease
P.
Chronic wasting disease in cervids in North America
E.S.Williams
Bovine spongiform encephalopathy (BSE) in Japan
T. Yokoyama,
The role of host PrP in control of incubation time
J.
The role of the immune system in TSE agent
N.A. Mabbott, J. Mohan and M.E. Bruce
IX
Prion protein
GS.
Semi-classical quantization of protein dynamics: Novel NMR
relaxation formalism and its application to prion
K. Kuwata
Surveillance of chronic wasting disease (CWD) in Japan
K. Shimada, Y. Iwamara, H. Hayashi, M.
Y.K. Ushiki,
M. Shinagawa and T. Yokoyama
Unexpected high incidence of visceral AA-amyloidosis in slaughtered
cattle in Japan
K.
andS.
A Novel BSE screening kit with simplified preparation method for
EIA
T.
H. Tsukagoshi-Nagai, T. Yokoyama, Y. Tagawa, T.
Y. Yamakawa,
Detection of
correlation spectroscopy
F.
and M. Kinjo
PrPSc distribution
encephalopathy
Y. Iwamaru, Y. Okubo, T. Ikeda, H. Hayashi, M.
T. Yokoyama and M. Shinagawa
Report
R. Irie, H. Okada, H. Hayashi, Y. Iwamaru, T. Yokoyama
andM. Shinagawa
The development of the intracerebral inoculation method and BSE
experimental transmissions to calves
S. Fukuda, S. Nikaido, Y. Matsui, S. Kageyama and S. Onoe
Comparative analyses of three mouse-adapted scrapie strains Gl,
Obihiro, and
ICR mice
M. Horiuchi, Y. Tamura and H. Furaoka
XI
Dose effect on detection of PrPSc in follicular dendritic cells of
knock-in mice for rapid bioassay
S. Mohri, M.
and
Cell surface retention of PrPc by anti-PrP antibody prevents
protease-resistant PrP formation
M. Horiuchi, C.-L. Kim, M. Ogino, H. Furuoka and M. Shinagawa
Prion-conformation-specifíc
display library
S. Hashiguchi, M. Yamamoto, S. Kitamoto, T. Nakashima,
H. Yamanaka, D. Ishibashi, S. Sakaguchi, S. Katamine, Y.
and
Partial characterization of monoclonal antibodies which bind to
disease-associated prion protein in immunoprecipitaion assay
Y.K. Ushiki, R. Endo,
S. Hattori, S. Irie and T. Yokoyama
Production and characterization of monoclonal antibodies specific
for prion protein
M. Morita, A. Ohmizu, H. Maeno, T. Matsuo, Y. Ogata, M. Naiki,
S. Suzuki and I.
In vitro selection of anti-mouse prion protein
S. Sekiya, K. Noda, P.K.R. Kumar, T. Yokoyama
and S. Nishikawa
Detection of the prion protein in a liquid phase capture assay using
magnetic beads coupled to protein A
W.-C. Yang, E.S. Yeung, M.J. Schmerr and W. Bodemer
New
prion protein
K. Sasaki, K. Doh-ura and T. Iwaki
Cellular prion protein suppresses the apoptosis in
established from type-1 prion protein gene-deficient mice
K. Saeki, T. Nishimura, A. Sakudo, Y. Matsumoto and T. Onodera
Cellular prion protein suppressess the apoptotic cell death by
mediating the intracellular H2Oi in primary culture and immortalized
neuronal
I. Nakamura, T. Nishimura, K. Saeki,
andT. Onodera
XII
Targeting
BCL-l pathway induces mitochondrial apoptosis
N.S. Hachiya, M. Yamada, K. Watanabe, A. Jozuka, Y. Kozuka,
Y. Sakasegawa and K. Kaneko
Microtubule-dependent intracellular trafficking of cellular prion protein
N.S. Hachiya, K. Watanabe, M. Yamada, Y. Sakasegawa
and K. Kaneko
Hsp90 modifies the conformation of
in vitro
Y. Sakasegawa, N.S. Hachiya and K. Kaneko
Purification and characterization of a novel ATP-dependent robust
protein-unfoldase, Unfoldin
N.S. Hachiya, M. Yamada, A. Jozuka, Y. Kozuka,
and K. Kaneko
Nucleic acid and prion protein interaction produces spherical
amyloids which in vivo can function as coats of spongiform
encephalopathy agent
P.K. Nandi and
Species barrier in yeast
H.
Molecular memory of [PSI+] prion strains in S. cerevisiae is dependent
on the primary structure of the Sup35 prion domain
C.G. Crist, T. Nakayashiki, H. Kurahashi and Y. Nakamura
Expression of a splice variant of prion protein during hypoxia in human
glioblastoma cell line T98G
Y. Kikuchi, T. Kakeya, A. Sakai, H. Matsuda, T. Yamazaki,
K. Tanamoto, K. Ikeda,
PRNP promoter region polymorphism in Creutzfeldt-Jakob disease
P.P.
and T.J.
Tubulovesicular structures are consistently found in prion diseases
including vCJD and FF1
P.P.
Autophagy is a common
prion diseases
B. Sikorska, P.P.
XIII
Type
methionine
Creutzfeldt-Jakob disease
A. Kobayashi, S. Satoh, J.W. Ironside, S. Mohri andT. Kitamoto
A pitfall in diagnosis of human prion diseases using detection of
protease-resistant prion protein in urine: contamination with bacterial
outer membrane proteins
H. Furukawa, K. Doh-ura, R. Okuwaki, S. Shirabe, K. Yamamoto,
H. Udono, T.
Comparative analysis of chronological data of total
serial studies of
features in patients with sporadic CJD
K. Satoh
Duration between initial manifestation of CJD and detection of PSD,
specific findings on
N.
and H. Mizusawa
Biochemical analysis of peripheral tissue involvement in transmissible
spongiform encephalopathies
V.A. Lawson, A.F. Hill, V. Lewis, R. Sharpies, S. Collins
and C.L. Masters
Involvement of the peripheral nervous system in human prion diseases
including
С
MM2 type sporadic Creutzfeldt-Jakob disease: clinicoradiologic
features and clinical diagnosis
T. Hamaguchi, T. Kitamoto, T. Sato, H. Mizusawa, Y. Nakamura,
M. Noguchi, Y. Furukawa,
S. Murayama, T.
T.
S. Kuroda,
and M. Yamada
Early clinical and radiological diagnosis of sporadic Creuzfeldt- Jakob's
disease (sCJD)
K. Ishihara, M. Sugie, J. Shiota, M. Kawamura, T. Kitamoto
and
XIV
Familial
codon
Y. Shiga, H. Mizuno, S. Watanabe, M. Tateyama, I. Nakashima,
K. Fujihara, T. Kitamoto and
Familial
Y.
Y. Komatzusaki, S.
M.
A
and codon
Y. Nishida,
and
Inhibition
mouse monoclonal antibodies against prion protein
K. Miyamoto,
H. Horiuchi, S. Furusawa and H. Matsuda
The inhibitory effect of the ScFv of an anti-prion protein antibody
secreted from N2a58 cells on abnormal prion protein accumulation in
scrapie-infected cells, ScN2a
Y. Shimizu, Y. Kaku-Ushiki, S. Fukuda, M. Shinagawa, T. Yokoyama
andY. Tagawa
Mucosal immunogenicity of prion protein fused with heat-labile
enterotoxin
H.
Identification of drugs that enhance the stimulatory effect of PrP on
the fibrinolytic system
G Epple, G
Screening study of prion binding agents and their inhibitory effect on
the conversion of prion protein
N.
and
Can forage grasses inhibit prion replication
T. Miyamoto, R. Sadatomi, H. Tanaka, R. Higuchi, S. Kawatake
andK. Doh-ura
Inhibition of abnormal PrP formation by amyloid-imaging probes
in vitro
K. Ishikawa, Y. Kudo andK. Doh-ura
XV
Treatment
Creutzfeldt-Jakob disease patients
Y. Tsuboi, F. Fujiki, A. Yamauchi, K. Doh-ura, Y. Kataoka and
T
Effect of oral administration of pentosan polysulfate for patients with
Creutzfeldt-Jakob disease (CJD) and new design for low
molecular-weight of pentosan polysulfate
S. Shirabe, K. Satoh, K. Eguchi, M.
A. Yamauchi, Y. Kataoka and S. Katamine
Key Word Index
PRIONS
Prion diseases recently have attracted
interest not only scientifically but also
socially because of the bovine spongiform
encephalopathy (BSE) epidemic and the
outbreak of variant Creutzfeldt-Jakob
disease (vCJD) in the United Kingdom. In
2004,
Prion Diseases for Food and Drug Safety
was held October 31-November
Sendai, Japan, where,
arguments were first heard on whether
the
spongiform encephalopathy was
scrapie-associated fibrils. This volume is a
collection of current work on prion
research that was presented at the
symposium. Topics included range from
basic research to clinical aspects of prion
diseases, making the book a valuable
resource for researchers and clinicians,
and encouraging further developments
by the next generation of researchers. |
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| genre | (DE-588)1071861417 Konferenzschrift 2004 Sendai gnd-content |
| genre_facet | Konferenzschrift 2004 Sendai |
| id | DE-604.BV021258067 |
| illustrated | Illustrated |
| index_date | 2024-07-02T13:41:09Z |
| indexdate | 2024-07-09T20:34:02Z |
| institution | BVB |
| isbn | 4431255397 |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-014579342 |
| oclc_num | 61714777 |
| open_access_boolean | |
| owner | DE-355 DE-BY-UBR DE-12 |
| owner_facet | DE-355 DE-BY-UBR DE-12 |
| physical | XV, 271 S. Ill., graph. Darst. 24 cm |
| publishDate | 2005 |
| publishDateSearch | 2005 |
| publishDateSort | 2005 |
| publisher | Springer |
| record_format | marc |
| spelling | Prions food and drug safety T. Kitamoto (ed.) Tokyo [u.a.] Springer 2005 XV, 271 S. Ill., graph. Darst. 24 cm txt rdacontent n rdamedia nc rdacarrier Literaturangaben Presents a collection of work on prion research that was presented at the 2004 symposium. This volume includes topics ranging from basic research to clinical aspects of prion diseases. It is intended for researchers and clinicians, and aims to encourage developments by researchers in the field. Prion Diseases Congresses Prion diseases Prions Prions Congresses Prionprotein (DE-588)4619314-5 gnd rswk-swf Prionkrankheit (DE-588)4711087-9 gnd rswk-swf (DE-588)1071861417 Konferenzschrift 2004 Sendai gnd-content Prionprotein (DE-588)4619314-5 s DE-604 Prionkrankheit (DE-588)4711087-9 s Kitamoto, Tetsuyuki Sonstige (DE-588)130508934 oth Digitalisierung UB Regensburg application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=014579342&sequence=000003&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Klappentext Digitalisierung UB Regensburg application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=014579342&sequence=000004&line_number=0002&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis |
| spellingShingle | Prions food and drug safety Prion Diseases Congresses Prion diseases Prions Prions Congresses Prionprotein (DE-588)4619314-5 gnd Prionkrankheit (DE-588)4711087-9 gnd |
| subject_GND | (DE-588)4619314-5 (DE-588)4711087-9 (DE-588)1071861417 |
| title | Prions food and drug safety |
| title_auth | Prions food and drug safety |
| title_exact_search | Prions food and drug safety |
| title_exact_search_txtP | Prions food and drug safety |
| title_full | Prions food and drug safety T. Kitamoto (ed.) |
| title_fullStr | Prions food and drug safety T. Kitamoto (ed.) |
| title_full_unstemmed | Prions food and drug safety T. Kitamoto (ed.) |
| title_short | Prions |
| title_sort | prions food and drug safety |
| title_sub | food and drug safety |
| topic | Prion Diseases Congresses Prion diseases Prions Prions Congresses Prionprotein (DE-588)4619314-5 gnd Prionkrankheit (DE-588)4711087-9 gnd |
| topic_facet | Prion Diseases Congresses Prion diseases Prions Prions Congresses Prionprotein Prionkrankheit Konferenzschrift 2004 Sendai |
| url | http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=014579342&sequence=000003&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=014579342&sequence=000004&line_number=0002&func_code=DB_RECORDS&service_type=MEDIA |
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