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Beginning to understand hereditary spastic paraplegia atlastin
被引:1
作者
:
Elliott, JL
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Texas, SW Med Ctr, Dept Neurol, Dallas, TX 75290 USA
Univ Texas, SW Med Ctr, Dept Neurol, Dallas, TX 75290 USA
Elliott, JL
[
1
]
机构
:
[1]
Univ Texas, SW Med Ctr, Dept Neurol, Dallas, TX 75290 USA
来源
:
ARCHIVES OF NEUROLOGY
|
2004年
/ 61卷
/ 12期
关键词
:
D O I
:
10.1001/archneur.61.12.1842
中图分类号
:
R74 [神经病学与精神病学];
学科分类号
:
摘要
:
引用
收藏
页码:1842 / 1843
页数:2
相关论文
共 8 条
[1]
Atlastin1 mutations are frequent in young-onset autosomal dominant spastic paraplegia
[J].
Dürr, A
论文数:
0
引用数:
0
h-index:
0
机构:
Hop La Pitie Salpetriere, Dept Genet Cytogente & Embryol, INSERM U289, F-75013 Paris, France
Dürr, A
;
Camuzat, AS
论文数:
0
引用数:
0
h-index:
0
机构:
Hop La Pitie Salpetriere, Dept Genet Cytogente & Embryol, INSERM U289, F-75013 Paris, France
Camuzat, AS
;
Colin, E
论文数:
0
引用数:
0
h-index:
0
机构:
Hop La Pitie Salpetriere, Dept Genet Cytogente & Embryol, INSERM U289, F-75013 Paris, France
Colin, E
;
Tallaksen, C
论文数:
0
引用数:
0
h-index:
0
机构:
Hop La Pitie Salpetriere, Dept Genet Cytogente & Embryol, INSERM U289, F-75013 Paris, France
Tallaksen, C
;
Hannequin, D
论文数:
0
引用数:
0
h-index:
0
机构:
Hop La Pitie Salpetriere, Dept Genet Cytogente & Embryol, INSERM U289, F-75013 Paris, France
Hannequin, D
;
Coutinho, P
论文数:
0
引用数:
0
h-index:
0
机构:
Hop La Pitie Salpetriere, Dept Genet Cytogente & Embryol, INSERM U289, F-75013 Paris, France
Coutinho, P
;
Fontaine, B
论文数:
0
引用数:
0
h-index:
0
机构:
Hop La Pitie Salpetriere, Dept Genet Cytogente & Embryol, INSERM U289, F-75013 Paris, France
Fontaine, B
;
Rossi, A
论文数:
0
引用数:
0
h-index:
0
机构:
Hop La Pitie Salpetriere, Dept Genet Cytogente & Embryol, INSERM U289, F-75013 Paris, France
Rossi, A
;
Gil, R
论文数:
0
引用数:
0
h-index:
0
机构:
Hop La Pitie Salpetriere, Dept Genet Cytogente & Embryol, INSERM U289, F-75013 Paris, France
Gil, R
;
Rousselle, C
论文数:
0
引用数:
0
h-index:
0
机构:
Hop La Pitie Salpetriere, Dept Genet Cytogente & Embryol, INSERM U289, F-75013 Paris, France
Rousselle, C
;
Ruberg, M
论文数:
0
引用数:
0
h-index:
0
机构:
Hop La Pitie Salpetriere, Dept Genet Cytogente & Embryol, INSERM U289, F-75013 Paris, France
Ruberg, M
;
Stevanin, G
论文数:
0
引用数:
0
h-index:
0
机构:
Hop La Pitie Salpetriere, Dept Genet Cytogente & Embryol, INSERM U289, F-75013 Paris, France
Stevanin, G
;
Brice, A
论文数:
0
引用数:
0
h-index:
0
机构:
Hop La Pitie Salpetriere, Dept Genet Cytogente & Embryol, INSERM U289, F-75013 Paris, France
Brice, A
.
ARCHIVES OF NEUROLOGY,
2004,
61
(12)
:1867
-1872
[2]
The hereditary spastic paraplegias - Nine genes and counting
[J].
Fink, JK
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Michigan, Dept Neurol, Ann Arbor, MI 48109 USA
Fink, JK
.
ARCHIVES OF NEUROLOGY,
2003,
60
(08)
:1045
-1049
[3]
Science in motion: common molecular pathological themes emerge in the hereditary spastic paraplegias
[J].
论文数:
引用数:
h-index:
机构:
Reid, E
.
JOURNAL OF MEDICAL GENETICS,
2003,
40
(02)
:81
-86
[4]
Sauter S M, 2004, Hum Mutat, V23, P98, DOI 10.1002/humu.9205
[5]
Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome
[J].
Windpassinger, C
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Windpassinger, C
;
Auer-Grumbach, M
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Auer-Grumbach, M
;
Irobi, J
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Irobi, J
;
Patel, H
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Patel, H
;
Petek, E
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Petek, E
;
Hörl, G
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Hörl, G
;
Malli, R
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Malli, R
;
Reed, JA
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Reed, JA
;
Dierick, I
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Dierick, I
;
Verpoorten, N
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Verpoorten, N
;
Warner, TT
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Warner, TT
;
Proukakis, C
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Proukakis, C
;
Van den Bergh, P
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Van den Bergh, P
;
Verellen, C
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Verellen, C
;
Van Maldergem, L
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Van Maldergem, L
;
Merlini, L
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Merlini, L
;
De Jonghe, P
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
De Jonghe, P
;
Timmerman, V
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Timmerman, V
;
Crosby, AH
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Crosby, AH
;
Wagner, K
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Wagner, K
.
NATURE GENETICS,
2004,
36
(03)
:271
-276
[6]
Abnormal neurofilament transport caused by targeted disruption of neuronal kinesin heavy chain KIF5A
[J].
Xia, CH
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Calif San Diego, HHMI CMM, La Jolla, CA 92093 USA
Xia, CH
;
Roberts, EA
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Calif San Diego, HHMI CMM, La Jolla, CA 92093 USA
Roberts, EA
;
Her, LS
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Calif San Diego, HHMI CMM, La Jolla, CA 92093 USA
Her, LS
;
Liu, XR
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Calif San Diego, HHMI CMM, La Jolla, CA 92093 USA
Liu, XR
;
Williams, DS
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Calif San Diego, HHMI CMM, La Jolla, CA 92093 USA
Williams, DS
;
Cleveland, DW
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Calif San Diego, HHMI CMM, La Jolla, CA 92093 USA
Cleveland, DW
;
Goldstein, LSB
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Calif San Diego, HHMI CMM, La Jolla, CA 92093 USA
Goldstein, LSB
.
JOURNAL OF CELL BIOLOGY,
2003,
161
(01)
:55
-66
[7]
Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia
[J].
Zhao, XP
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Michigan, Dept Neurol, Ann Arbor, MI 48109 USA
Zhao, XP
;
Alvarado, D
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Michigan, Dept Neurol, Ann Arbor, MI 48109 USA
Alvarado, D
;
Rainier, S
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Michigan, Dept Neurol, Ann Arbor, MI 48109 USA
Rainier, S
;
Lemons, R
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Michigan, Dept Neurol, Ann Arbor, MI 48109 USA
Lemons, R
;
论文数:
引用数:
h-index:
机构:
Hedera, P
;
Weber, CH
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Michigan, Dept Neurol, Ann Arbor, MI 48109 USA
Weber, CH
;
Tukel, T
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Michigan, Dept Neurol, Ann Arbor, MI 48109 USA
Tukel, T
;
Apak, M
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Michigan, Dept Neurol, Ann Arbor, MI 48109 USA
Apak, M
;
Heiman-Patterson, T
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Michigan, Dept Neurol, Ann Arbor, MI 48109 USA
Heiman-Patterson, T
;
Ming, L
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Michigan, Dept Neurol, Ann Arbor, MI 48109 USA
Ming, L
;
Bui, M
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Michigan, Dept Neurol, Ann Arbor, MI 48109 USA
Bui, M
;
Fink, JK
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Michigan, Dept Neurol, Ann Arbor, MI 48109 USA
Univ Michigan, Dept Neurol, Ann Arbor, MI 48109 USA
Fink, JK
.
NATURE GENETICS,
2001,
29
(03)
:326
-331
[8]
Cellular localization, oligomerization, and membrane association of the hereditary spastic paraplegia 3A (SPG3A) protein atlastin
[J].
Zhu, PP
论文数:
0
引用数:
0
h-index:
0
机构:
NINDS, Cellular Neurol Unit, NIH, Bethesda, MD 20892 USA
Zhu, PP
;
Patterson, A
论文数:
0
引用数:
0
h-index:
0
机构:
NINDS, Cellular Neurol Unit, NIH, Bethesda, MD 20892 USA
Patterson, A
;
Lavoie, B
论文数:
0
引用数:
0
h-index:
0
机构:
NINDS, Cellular Neurol Unit, NIH, Bethesda, MD 20892 USA
Lavoie, B
;
Stadler, J
论文数:
0
引用数:
0
h-index:
0
机构:
NINDS, Cellular Neurol Unit, NIH, Bethesda, MD 20892 USA
Stadler, J
;
Shoeb, M
论文数:
0
引用数:
0
h-index:
0
机构:
NINDS, Cellular Neurol Unit, NIH, Bethesda, MD 20892 USA
Shoeb, M
;
Patel, R
论文数:
0
引用数:
0
h-index:
0
机构:
NINDS, Cellular Neurol Unit, NIH, Bethesda, MD 20892 USA
Patel, R
;
Blackstone, C
论文数:
0
引用数:
0
h-index:
0
机构:
NINDS, Cellular Neurol Unit, NIH, Bethesda, MD 20892 USA
Blackstone, C
.
JOURNAL OF BIOLOGICAL CHEMISTRY,
2003,
278
(49)
:49063
-49071
←
1
→
共 8 条
[1]
Atlastin1 mutations are frequent in young-onset autosomal dominant spastic paraplegia
[J].
Dürr, A
论文数:
0
引用数:
0
h-index:
0
机构:
Hop La Pitie Salpetriere, Dept Genet Cytogente & Embryol, INSERM U289, F-75013 Paris, France
Dürr, A
;
Camuzat, AS
论文数:
0
引用数:
0
h-index:
0
机构:
Hop La Pitie Salpetriere, Dept Genet Cytogente & Embryol, INSERM U289, F-75013 Paris, France
Camuzat, AS
;
Colin, E
论文数:
0
引用数:
0
h-index:
0
机构:
Hop La Pitie Salpetriere, Dept Genet Cytogente & Embryol, INSERM U289, F-75013 Paris, France
Colin, E
;
Tallaksen, C
论文数:
0
引用数:
0
h-index:
0
机构:
Hop La Pitie Salpetriere, Dept Genet Cytogente & Embryol, INSERM U289, F-75013 Paris, France
Tallaksen, C
;
Hannequin, D
论文数:
0
引用数:
0
h-index:
0
机构:
Hop La Pitie Salpetriere, Dept Genet Cytogente & Embryol, INSERM U289, F-75013 Paris, France
Hannequin, D
;
Coutinho, P
论文数:
0
引用数:
0
h-index:
0
机构:
Hop La Pitie Salpetriere, Dept Genet Cytogente & Embryol, INSERM U289, F-75013 Paris, France
Coutinho, P
;
Fontaine, B
论文数:
0
引用数:
0
h-index:
0
机构:
Hop La Pitie Salpetriere, Dept Genet Cytogente & Embryol, INSERM U289, F-75013 Paris, France
Fontaine, B
;
Rossi, A
论文数:
0
引用数:
0
h-index:
0
机构:
Hop La Pitie Salpetriere, Dept Genet Cytogente & Embryol, INSERM U289, F-75013 Paris, France
Rossi, A
;
Gil, R
论文数:
0
引用数:
0
h-index:
0
机构:
Hop La Pitie Salpetriere, Dept Genet Cytogente & Embryol, INSERM U289, F-75013 Paris, France
Gil, R
;
Rousselle, C
论文数:
0
引用数:
0
h-index:
0
机构:
Hop La Pitie Salpetriere, Dept Genet Cytogente & Embryol, INSERM U289, F-75013 Paris, France
Rousselle, C
;
Ruberg, M
论文数:
0
引用数:
0
h-index:
0
机构:
Hop La Pitie Salpetriere, Dept Genet Cytogente & Embryol, INSERM U289, F-75013 Paris, France
Ruberg, M
;
Stevanin, G
论文数:
0
引用数:
0
h-index:
0
机构:
Hop La Pitie Salpetriere, Dept Genet Cytogente & Embryol, INSERM U289, F-75013 Paris, France
Stevanin, G
;
Brice, A
论文数:
0
引用数:
0
h-index:
0
机构:
Hop La Pitie Salpetriere, Dept Genet Cytogente & Embryol, INSERM U289, F-75013 Paris, France
Brice, A
.
ARCHIVES OF NEUROLOGY,
2004,
61
(12)
:1867
-1872
[2]
The hereditary spastic paraplegias - Nine genes and counting
[J].
Fink, JK
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Michigan, Dept Neurol, Ann Arbor, MI 48109 USA
Fink, JK
.
ARCHIVES OF NEUROLOGY,
2003,
60
(08)
:1045
-1049
[3]
Science in motion: common molecular pathological themes emerge in the hereditary spastic paraplegias
[J].
论文数:
引用数:
h-index:
机构:
Reid, E
.
JOURNAL OF MEDICAL GENETICS,
2003,
40
(02)
:81
-86
[4]
Sauter S M, 2004, Hum Mutat, V23, P98, DOI 10.1002/humu.9205
[5]
Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome
[J].
Windpassinger, C
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Windpassinger, C
;
Auer-Grumbach, M
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Auer-Grumbach, M
;
Irobi, J
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Irobi, J
;
Patel, H
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Patel, H
;
Petek, E
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Petek, E
;
Hörl, G
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Hörl, G
;
Malli, R
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Malli, R
;
Reed, JA
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Reed, JA
;
Dierick, I
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Dierick, I
;
Verpoorten, N
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Verpoorten, N
;
Warner, TT
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Warner, TT
;
Proukakis, C
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Proukakis, C
;
Van den Bergh, P
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Van den Bergh, P
;
Verellen, C
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Verellen, C
;
Van Maldergem, L
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Van Maldergem, L
;
Merlini, L
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
Merlini, L
;
De Jonghe, P
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Graz, Inst Med Biol & Human Genet, A-8010 Graz, Austria
De Jonghe, P
;
Timmerman, V
论文数:
0
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