Parkinson Disease and Melanoma: A Common Genetic Pathway Linked to PARKIN Inactivation

被引:0
|
作者
Hu, H-H [1 ]
Lesage, S. [2 ]
Michel, L. [3 ]
Descamps, V [3 ]
Mourah, S. [3 ]
Lebbe, C. [3 ]
Basset-Seguin, N. [3 ]
Bagot, M. [3 ]
Bensussan, A. [3 ]
Deschamps, L. [4 ]
Leccia, M. T. [5 ]
Sivaramakrishna, R. P. [6 ]
Klebe, S. [2 ]
Kumar, R. [6 ]
Kannengiesser, C. [7 ]
Couvelard, A. [4 ]
Thomas, L. [8 ]
Brice, A. [2 ]
Dumaz, N. [3 ]
Grandchamp, B. [7 ]
Nadem, S. [1 ]
机构
[1] Univ Paris 07, Bichat Hosp, APHP, INSERM,Genet Dept,U976, Paris, France
[2] Univ Paris 06, INSERM, Hop La Pitie Salpetriere, AP HP,UMR S975,Ctr Rech,Inst Cerveau & Moelle Epi, Paris, France
[3] Univ Paris 07, INSERM, U976, Skin Res Ctr, Paris, France
[4] Univ Paris 07, Dept Pathol, Bichat Hosp, APHP, Paris, France
[5] CHU Grenoble, Dept Dermatol, F-38043 Grenoble, France
[6] German Canc Res Ctr, Div Mol Genet Epidemiol, Heidelberg, Germany
[7] Univ Paris 07, Dept Genet, Bichat Hosp, APHP, Paris, France
[8] Univ Lyon 1, Dept Dermatol, Ctr Hosp Lyon Sud, F-69365 Lyon, France
关键词
D O I
暂无
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
引用
收藏
页码:47 / 47
页数:1
相关论文
共 50 条
  • [31] Parkinson's disease-linked Parkin mutations impair glutamatergic signaling in hippocampal neurons
    Zhu, Mei
    Cortese, Giuseppe P.
    Waites, Clarissa L.
    BMC BIOLOGY, 2018, 16 : 100
  • [32] Genetic causes of Parkinson's disease:: extending the pathway
    Riess, O.
    Krueger, R.
    Hochstrasser, H.
    Soehn, A. S.
    Nuber, S.
    Franck, T.
    Berg, D.
    JOURNAL OF NEURAL TRANSMISSION-SUPPLEMENT, 2006, (70): : 181 - 189
  • [33] Parkinson's disease in Ireland: Clinical presentation and genetic heterogeneity in patients with parkin mutations
    Wiley, J
    Lynch, T
    Lincoln, S
    Skipper, L
    Hulihan, M
    Gosal, D
    Bisceglio, G
    Kachergus, J
    Hardy, J
    Farrer, MJ
    MOVEMENT DISORDERS, 2004, 19 (06) : 677 - 681
  • [34] Correction to: Overlapping genetic architecture between Parkinson disease and melanoma
    Umber Dube
    Laura Ibanez
    John P. Budde
    Bruno A. Benitez
    Albert A. Davis
    Oscar Harari
    Mark M. Iles
    Matthew H. Law
    Kevin M. Brown
    Carlos Cruchaga
    Acta Neuropathologica, 2020, 139 : 963 - 963
  • [35] Rhomboid-7 and HtrA2/Omi act in a common pathway with the Parkinson's disease factors Pink1 and Parkin
    Whitworth, Alexander J.
    Lee, Jeffrey R.
    Ho, Venus M-W.
    Flick, Robert
    Chowdhury, Ruhena
    McQuibban, G. Angus
    DISEASE MODELS & MECHANISMS, 2008, 1 (2-3) : 168 - 174
  • [36] Parkin and the molecular pathways of Parkinson's disease
    Giasson, BI
    Lee, VMY
    NEURON, 2001, 31 (06) : 885 - 888
  • [37] Parkin-associated Parkinson's disease
    von Coelln, R
    Dawson, VL
    Dawson, TM
    CELL AND TISSUE RESEARCH, 2004, 318 (01) : 175 - 184
  • [38] Familial Parkinson's disease α-synuclein and parkin
    Mizuno, Y
    Hattori, N
    Kitada, T
    Matsumine, H
    Mori, H
    Shimura, H
    Kubo, S
    Kobayashi, H
    Asakawa, S
    Minoshima, S
    Shimizu, N
    PARKINSON'S DISEASE, 2001, 86 : 13 - 21
  • [39] Parkin mutations and idiopathic Parkinson disease (PD).
    Scott, WK
    Rogala, AR
    Rampersaud, E
    Stajich, JM
    Nance, MA
    Watts, RL
    Hubble, JP
    Scott, BL
    Haines, JL
    Koller, WC
    Stern, MB
    Hiner, BC
    Jankovic, J
    Allen, FH
    Goetz, CG
    Small, GW
    Laing, NG
    Perlcak-Vance, MA
    Vance, JM
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) : 19 - 19
  • [40] Parkin, ubiquitination and the syns of Parkinson's disease
    Dawson, TM
    MOVEMENT DISORDERS, 2002, 17 : S3 - S3