学术探索
学术期刊
新闻热点
数据分析
智能评审

DJ-1 -: The second gene for early onset Parkinson disease

被引：6
作者：
Bandmann, O [1 ]
机构：
[1] Univ Sheffield, Sch Med, Acad Neurol Unit, Sheffield S10 2RX, S Yorkshire, England
来源：
NEUROLOGY | 2004年 / 62卷 / 03期
关键词：
D O I：
10.1212/WNL.62.3.357
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：357 / 358
页数：2
相关论文
共 10 条
  • [1] The role of pathogenic DJ-1 mutations in Parkinson's disease
    Abou-Sleiman, PM
    Healy, DG
    Quinn, N
    Lees, AJ
    Wood, NW
    [J]. ANNALS OF NEUROLOGY, 2003, 54 (03) : 283 - 286
  • [2] Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism
    Bonifati, V
    Rizzu, P
    van Baren, MJ
    Schaap, O
    Breedveld, GJ
    Krieger, E
    Dekker, MCJ
    Squitieri, F
    Ibanez, P
    Joosse, M
    van Dongen, JW
    Vanacore, N
    van Swieten, JC
    Brice, A
    Meco, G
    van Duijn, CM
    Oostra, BA
    Heutink, P
    [J]. SCIENCE, 2003, 299 (5604) : 256 - 259
  • [3] Assessment of a DJ-1 (PARK7) polymorphism in Finnish PD
    Eerola, J
    Hernandez, D
    Launes, J
    Hellström, O
    Hague, S
    Gulick, C
    Johnson, J
    Peuralinna, T
    Hardy, J
    Tienari, PJ
    Singleton, AB
    [J]. NEUROLOGY, 2003, 61 (07) : 1000 - 1002
  • [4] Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation
    Hague, S
    Rogaeva, E
    Hernandez, D
    Gulick, C
    Singleton, A
    Hanson, M
    Johnson, J
    Weiser, R
    Gallardo, M
    Ravina, B
    Gwinn-Hardy, K
    Crawley, A
    St George-Hyslop, PH
    Lang, AE
    Heutink, P
    Bonifati, V
    Hardy, J
    Singleton, A
    [J]. ANNALS OF NEUROLOGY, 2003, 54 (02) : 271 - 274
  • [5] DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease
    Hedrich, K
    Djarmati, A
    Schäfer, N
    Hering, R
    Wellenbrock, C
    Weiss, PH
    Hilker, R
    Vieregge, P
    Ozelius, LJ
    Heutink, P
    Bonifati, V
    Schwinger, E
    Lang, AE
    Noth, J
    Bressman, SB
    Pramstaller, PP
    Riess, O
    Klein, C
    [J]. NEUROLOGY, 2004, 62 (03) : 389 - 394
  • [6] Screening for DJ-1 mutations in early onset autosomal recessive parkinsonism
    Ibáñez, P
    De Michele, G
    Bonifati, V
    Lohmann, E
    Thobois, S
    Pollak, P
    Agid, Y
    Heutink, P
    Dürr, A
    Brice, A
    [J]. NEUROLOGY, 2003, 61 (10) : 1429 - 1431
  • [7] Association between early-onset Parkinson's disease and mutations in the parkin gene
    Lücking, CB
    Dürr, A
    Bonifati, V
    Vaughan, J
    De Michele, G
    Gasser, T
    Harhangi, BS
    Meco, G
    Denèfle, P
    Wood, NW
    Agid, Y
    Brice, A
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (21) : 1560 - 1567
  • [8] The DJ-1L166P mutant protein associated with early onset Parkinson's disease is unstable and forms higher-order protein complexes
    Macedo, MG
    Anar, B
    Bronner, IF
    Cannella, M
    Squitieri, F
    Bonifati, V
    Hoogeveen, A
    Heutink, P
    Rizzu, P
    [J]. HUMAN MOLECULAR GENETICS, 2003, 12 (21) : 2807 - 2816
  • [9] L166P mutant DJ-1, causative for recessive Parkinson's disease, is degraded through the ubiquitin-proteasome system
    Miller, DW
    Ahmad, R
    Hague, S
    Baptista, MJ
    Canet-Aviles, R
    McLendon, C
    Carter, DM
    Zhu, PP
    Stadler, J
    Chandran, J
    Klinefelter, GR
    Blackstone, C
    Cookson, MR
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (38) : 36588 - 36595
  • [10] Parkinson disease in twins - An etiologic study
    Tanner, CM
    Ottman, R
    Goldman, SM
    Ellenberg, J
    Chan, P
    Mayeux, R
    Langston, JW
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 281 (04): : 341 - 346
1