Nuclear and mitochondrial genetics in Parkinson's disease.

作者: A H Schapira

DOI: 10.1136/JMG.32.6.411

关键词: Parkinson's diseaseGeneticsDegenerative diseaseCentral nervous system diseaseBiologyMPTPMitochondrial DNAMitochondrionHuman mitochondrial geneticsCell nucleus

摘要:

参考文章(46)
A.H.V. Schapira, J.M. Cooper, Biochemical and molecular features of deficiencies of Complexes I, II and III Mitochondrial Disorders in Neurology#R##N#Butterworth-Heinemann International Medical Reviews. pp. 75- 90 ,(1994) , 10.1016/B978-0-7506-0585-4.50009-5
K. Marder, G. Maestre, L. Cote, H. Mejia, B. Alfaro, A. Halim, M. Tang, B. Tycko, R. Mayeux, The apolipoprotein ϵ4 allele in Parkinson's disease with and without dementia Neurology. ,vol. 44, pp. 1330- 1330 ,(1994) , 10.1212/WNL.44.7.1330
P. Lestienne, I. Nelson, P. Riederer, H. Reichmann, K. Jellinger, Mitochondrial DNA in postmortem brain from patients with Parkinson's disease. Journal of Neurochemistry. ,vol. 56, pp. 1819- 1819 ,(1991) , 10.1111/J.1471-4159.1991.TB02087.X
P. Lestienne, J. Nelson, P. Riederer, K. Jellinger, H. Reichmann, Normal Mitochondrial Genome in Brain from Patients with Parkinson's Disease and Complex I Defect Journal of Neurochemistry. ,vol. 55, pp. 1810- 1812 ,(1990) , 10.1111/J.1471-4159.1990.TB04973.X
H. Bernheimer, W. Birkmayer, O. Hornykiewicz, K. Jellinger, F. Seitelberger, Brain dopamine and the syndromes of Parkinson and Huntington Clinical, morphological and neurochemical correlations Journal of the Neurological Sciences. ,vol. 20, pp. 415- 455 ,(1973) , 10.1016/0022-510X(73)90175-5
John M. Shoffner, Michael D. Brown, Antonio Torroni, Marie T. Lott, Margaret F. Cabell, Suzanne S. Mirra, M.Flint Beal, Chi-Chuan Yang, Marla Gearing, Rino Salvo, Ray L. Watts, Jorge L. Juncos, Lawrence A. Hansen, Barbara J. Crain, Michel Fayad, Calvin L. Reckord, Douglas C. Wallace, Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients Genomics. ,vol. 17, pp. 171- 184 ,(1993) , 10.1006/GENO.1993.1299
Ron Rempfer, Richard Crook, Henry Houlden, Karen Duff, Mike Hutton, GarethW. Roberts, Ravi Raghavan, Robert Perry, John Hardy, Parkinson's disease, but not Alzheimer's disease, Lewy body variant associated with mutant alleles at cytochrome P450 gene. The Lancet. ,vol. 344, pp. 815- 815 ,(1994) , 10.1016/S0140-6736(94)92370-1
Bernd Janetzky, Sabine Hauck, Moussa B.H. Youdim, Peter Riederer, Kurt Jellinger, Felix Pantucek, Robert Zo¨chling, Kurt W. Boissl, Heinz Reichmann, Unaltered aconitase activity, but decreased complex I activity in substantia nigra pars compacta of patients with Parkinson's disease Neuroscience Letters. ,vol. 169, pp. 126- 128 ,(1994) , 10.1016/0304-3940(94)90372-7
A. H. V. Schapira, V. M. Mann, J. M. Cooper, D. Dexter, S. E. Daniel, P. Jenner, J. B. Clark, C. D. Marsden, Anatomic and Disease Specificity of NADH CoQ1 Reductase (Complex I) Deficiency in Parkinson's Disease Journal of Neurochemistry. ,vol. 55, pp. 2142- 2145 ,(1990) , 10.1111/J.1471-4159.1990.TB05809.X
William G. Johnson, Susan E. Hodge, Roger Duvoisin, Twin studies and the genetics of Parkinson's disease--a reappraisal. Movement Disorders. ,vol. 5, pp. 187- 194 ,(1990) , 10.1002/MDS.870050302