电邮这篇文章 NOSITEL'STVO MUTATsII V GENE DJ-1 (PARK7) PRI BOLEZNI PARKINSONA
- 作者: Yakovenko EV1, Fedotova EY.1, Abramycheva NY.1, Illarioshkin SN1
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隶属关系:
- Научный центр неврологии
- 期: 卷 38, 编号 3 (Прил) (2019)
- 页面: 176-177
- 栏目: Articles
- URL: https://medbiosci.ru/RMMArep/article/view/26176
- DOI: https://doi.org/10.17816/rmmar26176
- ID: 26176
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作者简介
E Yakovenko
Научный центр неврологииМосква
E Fedotova
Научный центр неврологииМосква
N Abramycheva
Научный центр неврологииМосква
S Illarioshkin
Научный центр неврологииМосква
参考
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- Bonifati, V. Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism / V. Bonifati, P. Rizzu, M.J. van Baren, O. Schaap, G.J. Breedveld, E. Krieger, M.C. Dekker, F. Squitieri, P. Ibanez, M. Joosse, J.W. van Dongen, N. Vanacore, J.C. van Swieten, A. Brice, G. Meco, C.M. van Duijn, B.A. Oostra, P. Heutink // Science - 2003. - Vol. 299, № 5604. - P. 256-259.
- Repici, M. DJ-1 in Parkinson’s Disease: Clinical Insights and Therapeutic Perspectives / M. Repici, F. Giorgini // J Clin Med. - 2019. - Vol. 8, №9.
- Dolgacheva, L.P. Role of DJ-1 in the mechanism of pathogenesis of Parkinson’s disease / L.P. Dolgacheva, A.V. Berezhnov, E.I. Fedotova, V.P. Zinchenko, A.Y. Abramov // J Bioenerg Biomembr. - 2019. - Vol. 51, № 3. - P. 175-188.
- Taipa, R. DJ-1 linked parkinsonism (PARK7) is associated with Lewy body pathology / R. Taipa, C. Pereira, I. Reis, I. Alonso, A. Bastos-Lima, M. Melo-Pires, M. Magalhгes // Brain - 2016. - Vol. 139, № 6. - P. 1680-1687.
- Djarmati, A. Detection of Parkin (PARK2) and DJ1 (PARK7) mutations in early-onset Parkinson disease: Parkin mutation frequency depends on ethnic origin of patients / A. Djarmati, K. Hedrich, M. Svetel, N. Schдfer, V. Juric, S. Vukosavic, R. Hering, O. Riess, S. Romac, C. Klein, V. Kostic // Hum Mutat. - 2004. - Vol. 23, № 5:525.
- Hedrich, K. DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease / K. Hedrich, A. Djarmati, N. Schдfer, R. Hering, C. Wellenbrock, P.H. Weiss, R. Hilker, P. Vieregge, L.J. Ozelius, P. Heutink, V. Bonifati, E. Schwinger, A.E. Lang, J. Noth, S.B. Bressman, P.P. Pramstaller, O. Riess, C. Klein // Neurology - 2004. - Vol. 62, № 3. - P. 389-394.
- Hedrich, K. The importance of gene dosage studies: mutational analysis of the parkin gene in early-onset parkinsonism / K. Hedrich, M. Kann, A.J. Lanthaler, A. Dalski, C. Eskelson, O. Landt, E. Schwinger, P. Vieregge, A.E. Lang, X.O. Breakefield, L.J. Ozelius, P.P. Pramstaller, C. Klein // Hum. Mol. Genet. - 2001. - Vol. 10, №16. - P. 1649-1656.
- West, A. Complex relationship between Parkin mutations and Parkinson disease / A. West, M. Periquet, S. Lincoln, C.B. Lьcking, D. Nicholl, V. Bonifati, N. Rawal, T. Gasser, E. Lohmann, J.F. Deleuze, D. Maraganore, A. Levey, N. Wood, A. Dьrr, J. Hardy, A. Brice, M. Farrer // Am. J. Med. Genet. - 2002. Vol. 114, №5. - P. 584 -591.
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