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Protective prion protein polymorphisms against sporadic Creutzfeldt-Jakob disease
被引:72
作者
:
Shibuya, S
论文数:
0
引用数:
0
h-index:
0
机构:
Tohoku Univ, Sch Med, Dept Neurol Sci, Sendai, Miyagi 980, Japan
Tohoku Univ, Sch Med, Dept Neurol Sci, Sendai, Miyagi 980, Japan
Shibuya, S
[
1
]
Higuchi, J
论文数:
0
引用数:
0
h-index:
0
机构:
Tohoku Univ, Sch Med, Dept Neurol Sci, Sendai, Miyagi 980, Japan
Tohoku Univ, Sch Med, Dept Neurol Sci, Sendai, Miyagi 980, Japan
Higuchi, J
[
1
]
Shin, RW
论文数:
0
引用数:
0
h-index:
0
机构:
Tohoku Univ, Sch Med, Dept Neurol Sci, Sendai, Miyagi 980, Japan
Tohoku Univ, Sch Med, Dept Neurol Sci, Sendai, Miyagi 980, Japan
Shin, RW
[
1
]
Tateishi, J
论文数:
0
引用数:
0
h-index:
0
机构:
Tohoku Univ, Sch Med, Dept Neurol Sci, Sendai, Miyagi 980, Japan
Tohoku Univ, Sch Med, Dept Neurol Sci, Sendai, Miyagi 980, Japan
Tateishi, J
[
1
]
Kitamoto, T
论文数:
0
引用数:
0
h-index:
0
机构:
Tohoku Univ, Sch Med, Dept Neurol Sci, Sendai, Miyagi 980, Japan
Tohoku Univ, Sch Med, Dept Neurol Sci, Sendai, Miyagi 980, Japan
Kitamoto, T
[
1
]
机构
:
[1]
Tohoku Univ, Sch Med, Dept Neurol Sci, Sendai, Miyagi 980, Japan
来源
:
LANCET
|
1998年
/ 351卷
/ 9100期
关键词
:
D O I
:
10.1016/S0140-6736(05)78358-6
中图分类号
:
R5 [内科学];
学科分类号
:
1002 ;
100201 ;
摘要
:
引用
收藏
页码:419 / 419
页数:1
相关论文
共 4 条
[1]
NEW VARIANT PRION PROTEIN IN A JAPANESE FAMILY WITH GERSTMANN-STRAUSSLER SYNDROME
FURUKAWA, H
论文数:
0
引用数:
0
h-index:
0
机构:
KYUSHU UNIV, FAC MED, NEUROL INST, DEPT NEUROPATHOL, FUKUOKA, JAPAN
FURUKAWA, H
KITAMOTO, T
论文数:
0
引用数:
0
h-index:
0
机构:
KYUSHU UNIV, FAC MED, NEUROL INST, DEPT NEUROPATHOL, FUKUOKA, JAPAN
KITAMOTO, T
TANAKA, Y
论文数:
0
引用数:
0
h-index:
0
机构:
KYUSHU UNIV, FAC MED, NEUROL INST, DEPT NEUROPATHOL, FUKUOKA, JAPAN
TANAKA, Y
TATEISHI, J
论文数:
0
引用数:
0
h-index:
0
机构:
KYUSHU UNIV, FAC MED, NEUROL INST, DEPT NEUROPATHOL, FUKUOKA, JAPAN
TATEISHI, J
[J].
MOLECULAR BRAIN RESEARCH,
1995,
30
(02):
: 385
-
388
[2]
HUMAN PRION DISEASES WITH VARIANT PRION PROTEIN
KITAMOTO, T
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Neuropathology, Kyushu University, Fukuoka
KITAMOTO, T
TATEISHI, J
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Neuropathology, Kyushu University, Fukuoka
TATEISHI, J
[J].
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES,
1994,
343
(1306)
: 391
-
398
[3]
HOMOZYGOUS PRION PROTEIN GENOTYPE PREDISPOSES TO SPORADIC CREUTZFELDT-JAKOB DISEASE
PALMER, MS
论文数:
0
引用数:
0
h-index:
0
机构:
ST MARYS HOSP,SCH MED,DEPT BIOCHEM & MOLEC GENET,PRION DIS GRP,NORFOLK PL,LONDON W2 1PG,ENGLAND
PALMER, MS
DRYDEN, AJ
论文数:
0
引用数:
0
h-index:
0
机构:
ST MARYS HOSP,SCH MED,DEPT BIOCHEM & MOLEC GENET,PRION DIS GRP,NORFOLK PL,LONDON W2 1PG,ENGLAND
DRYDEN, AJ
HUGHES, JT
论文数:
0
引用数:
0
h-index:
0
机构:
ST MARYS HOSP,SCH MED,DEPT BIOCHEM & MOLEC GENET,PRION DIS GRP,NORFOLK PL,LONDON W2 1PG,ENGLAND
HUGHES, JT
COLLINGE, J
论文数:
0
引用数:
0
h-index:
0
机构:
ST MARYS HOSP,SCH MED,DEPT BIOCHEM & MOLEC GENET,PRION DIS GRP,NORFOLK PL,LONDON W2 1PG,ENGLAND
COLLINGE, J
[J].
NATURE,
1991,
352
(6333)
: 340
-
342
[4]
Petraroli R, 1996, AM J HUM GENET, V58, P888
←
1
→
共 4 条
[1]
NEW VARIANT PRION PROTEIN IN A JAPANESE FAMILY WITH GERSTMANN-STRAUSSLER SYNDROME
FURUKAWA, H
论文数:
0
引用数:
0
h-index:
0
机构:
KYUSHU UNIV, FAC MED, NEUROL INST, DEPT NEUROPATHOL, FUKUOKA, JAPAN
FURUKAWA, H
KITAMOTO, T
论文数:
0
引用数:
0
h-index:
0
机构:
KYUSHU UNIV, FAC MED, NEUROL INST, DEPT NEUROPATHOL, FUKUOKA, JAPAN
KITAMOTO, T
TANAKA, Y
论文数:
0
引用数:
0
h-index:
0
机构:
KYUSHU UNIV, FAC MED, NEUROL INST, DEPT NEUROPATHOL, FUKUOKA, JAPAN
TANAKA, Y
TATEISHI, J
论文数:
0
引用数:
0
h-index:
0
机构:
KYUSHU UNIV, FAC MED, NEUROL INST, DEPT NEUROPATHOL, FUKUOKA, JAPAN
TATEISHI, J
[J].
MOLECULAR BRAIN RESEARCH,
1995,
30
(02):
: 385
-
388
[2]
HUMAN PRION DISEASES WITH VARIANT PRION PROTEIN
KITAMOTO, T
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Neuropathology, Kyushu University, Fukuoka
KITAMOTO, T
TATEISHI, J
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Neuropathology, Kyushu University, Fukuoka
TATEISHI, J
[J].
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES,
1994,
343
(1306)
: 391
-
398
[3]
HOMOZYGOUS PRION PROTEIN GENOTYPE PREDISPOSES TO SPORADIC CREUTZFELDT-JAKOB DISEASE
PALMER, MS
论文数:
0
引用数:
0
h-index:
0
机构:
ST MARYS HOSP,SCH MED,DEPT BIOCHEM & MOLEC GENET,PRION DIS GRP,NORFOLK PL,LONDON W2 1PG,ENGLAND
PALMER, MS
DRYDEN, AJ
论文数:
0
引用数:
0
h-index:
0
机构:
ST MARYS HOSP,SCH MED,DEPT BIOCHEM & MOLEC GENET,PRION DIS GRP,NORFOLK PL,LONDON W2 1PG,ENGLAND
DRYDEN, AJ
HUGHES, JT
论文数:
0
引用数:
0
h-index:
0
机构:
ST MARYS HOSP,SCH MED,DEPT BIOCHEM & MOLEC GENET,PRION DIS GRP,NORFOLK PL,LONDON W2 1PG,ENGLAND
HUGHES, JT
COLLINGE, J
论文数:
0
引用数:
0
h-index:
0
机构:
ST MARYS HOSP,SCH MED,DEPT BIOCHEM & MOLEC GENET,PRION DIS GRP,NORFOLK PL,LONDON W2 1PG,ENGLAND
COLLINGE, J
[J].
NATURE,
1991,
352
(6333)
: 340
-
342
[4]
Petraroli R, 1996, AM J HUM GENET, V58, P888
←
1
→