| 1. |
Parkinson, J. (1817) An Essay on the Shaking Palsy. Sherwood, Neely, and Jones. London.
|
| |
| 2. |
Lewy, F. H. (1912) Paralysis agitans. I. Pathologische Anatomie, in Handbuch der Neurologie, vol. 3 (Lewandowsky, M. and Abelsdorff, G., eds.), Springer, Berlin, pp. 920–933.
|
| |
| 3. |
Trétiakoff, M. C. (1919) Thesis, University of Paris.
|
| |
| 4. |
Forno, L. S. (1996) Neuropathology of Parkinson’s disease. J. Neuropathol. Exp. Neurol.
55, 259–272.
|
| |
| 5. |
Duffy, P. E. and Tennyson, V. M. (1965) Phase and electron microscopic observations on Lewy bodies and melanin granules in
the substantia nigra and locus coeruleus in Parkinson’s disease. J. Neuropathol. Exp. Neurol.
24, 398–414.
|
| |
| 6. |
Okazaki, H., Lipkin, L. E., and Aronson, S. M. (1961) Diffuse intracytoplasmic ganglionic inclusions (Lewy type) associated
with progressive dementia and quadriparesis in flexion. J. Neuropathol. Exp. Neurol.
21, 442–449.
|
| |
| 7. |
Kosaka, K. (1978) Lewy bodies in cerebral cortex. Report of three cases. Acta Neuropathol.
42, 127–134.
|
| |
| 8. |
Hansen, L. A., Salmon, D., Galasko, D., Masliah, E., Katzman, R., DeTeresa, L., et al. (1990) The Lewy body variant of Alzheimer’s
disease: a clinical and pathological entity. Neurology
40, 1–8.
|
| |
| 9. |
Perry, R. H., Irving, D., Blessed, G., Fairbairn, A., and Perry, E. K. (1990) Senile dementia of the Lewy body type. A clinically
and neuropathologically distinct form of Lewy body dementia in the elderly. J. Neurol. Sci.
85, 119–139.
<Occurrence Type="DOI"><Handle>10.1016/0022-510X(90)90236-G</Handle></Occurrence>
|
| |
| 10. |
Polymeropoulos, M. H., Lavedan, C., Leroy, E., Ide, S. E., Dehejia, A., Dutra, A., et al. (1997) Mutation in the α-synuclein
gene identified in families with Parkinson’s disease. Science
276, 2045–2047.
|
| |
| 11. |
Spillantini, M. G., Schmidt, M. L., Lee, V. M.-Y., Trojanowski, J. Q., Jakes, R., and Goedert, M. (1997) α-Synuclein in Lewy
bodies. Nature
388, 839–840.
|
| |
| 12. |
Spillantini, M. G., Crowther, R. A., Jakes, R., Hasegawa, M. and Goedert M. (1998) α-Synuclein in filamentous inclusions of
Lewy bodies from Parkinson’s disease and dementia with Lewy bodies. Proc. Natl. Acad. Sci. USA
95, 6469–6473.
|
| |
| 13. |
Lippa, C. F., Fujiwara, H., Mann, D. M. A., Giasson, B., Baba, M., Schmidt, M. L., et al. (1998) Lewy bodies contain altered
α-synuclein in brains of many familial Alzheimer’s disease patients with mutations in presenilin and amyloid precursor protein
genes. Am. J. Pathol.
153, 1365–1370.
|
| |
| 14. |
Lippa, C. F., Schmidt, M. L., Lee, V. M.-Y., and Trojanowski, J. Q. (1999) Antibodies to α-synuclein detect Lewy bodies in
many Down’s syndrome brains with Alzheimer’s disease. Ann. Neurol.
45, 353–357.
<Occurrence Type="DOI"><Handle>10.1002/1531-8249(199903)45:3<353::AID-ANA11>3.0.CO;2-4</Handle></Occurrence>
|
| |
| 15. |
Spillantini, M. G., Tolnay, M., Love, S., and Goedert, M. (1999) Microtubule-associated protein tau, heparan sulphate and
α-synuclein in several neurodegenerative diseases with dementia. Acta Neuropathol.
97, 585–594.
|
| |
| 16. |
Tu, P.-H., Galvin, J. E., Baba, M., Giasson, B., Tomita, T., Leight, S., et al. (1998) Glial cytoplasmic inclusions in white
matter oligodendrocytes of multiple system atrophy brains contain insoluble α-synuclein. Ann. Neurol.
44, 415–422.
|
| |
| 17. |
Arawaka, S., Saito, Y., Murayama, S. and Mori, H. (1998) Lewy body in neurodegeneration with brain iron accumulation type
1 is immunoreactive for α-synuclein. Neurology
51, 887–889.
|
| |
| 18. |
Wakabayashi, K., Yoshimoto, M., Fukushima, T., Koide, R., Horikawa, Y., Morita, T., and Takahashi, G. H. (1999) Widespread
occurrence of α-synuclein/NACPimmunoreactive neuronal inclusions in juvenile and adult-onset Hallervorden-Spatz disease with
Lewy bodies. Neuropathol. Appl. Neurobiol.
25, 363–368.
|
| |
| 19. |
Wakabayashi, K., Yoshimoto, M., Tsuji, S., and Takahashi, H. (1998) α-Synuclein immunoreactivity in glial cytoplasmic inclusions
in multiple system atrophy. Neurosci. Lett.
249, 180–182.
<Occurrence Type="DOI"><Handle>10.1016/S0304-3940(98)00407-8</Handle></Occurrence>
|
| |
| 20. |
Mezey, E., Dehejia, A., Harta, G., Papp, M. I., Polymeropoulos, M. H., and Brownstein, M. J. (1998) Alpha synuclein in neurodegenerative
disorders: Murderer or accomplice? Nature Med.
4, 755–757.
|
| |
| 21. |
Spillantini, M. G., Crowther, R. A., Jakes, R., Cairns, N. J., Lantos, P. L., and Goedert, M. (1998) Filamentous α-synuclein
inclusions link multiple system atrophy with Parkinson’s disease and dementia with Lewy bodies. Neurosci. Lett.
251, 205–208.
<Occurrence Type="DOI"><Handle>10.1016/S0304-3940(98)00504-7</Handle></Occurrence>
|
| |
| 22. |
Gai, W. P., Power, J. H. T., Blumbergs, P. C., and Blessing, W. W. (1998) Multiple system atrophy: a new α-synuclein disease?
Lancet
352, 547–548.
<Occurrence Type="DOI"><Handle>10.1016/S0140-6736(05)79256-4</Handle></Occurrence>
|
| |
| 23. |
Maroteaux, L., Campanelli, J. T., and Scheller, R. H. (1988) Synuclein: A neuronspecific protein localized to the nucleus
and presynaptic nerve terminal. J. Neurosci.
8, 2804–2815.
|
| |
| 24. |
Maroteaux, L. and Scheller, R. H. (1991) The rat brain synucleins; family of proteins transiently associated with neuronal
membrane. Mol. Brain Res.
11, 335–343.
<Occurrence Type="DOI"><Handle>10.1016/0169-328X(91)90043-W</Handle></Occurrence>
|
| |
| 25. |
Tobe, T., Nakajo, S., Tanaka, A., Mitoya, A., Omata, K., Nakaya, K., et al. (1992) Cloning and characterization of the cDNA
encoding a novel specific 14-kDa protein. J. Neurochem.
59, 1624–1629.
|
| |
| 26. |
Uéda, K., Fukushima, H., Masliah, E., Xia, Y., Iwai, A., Yoshimoto, M., et al. (1993) Molecular cloning of cDNA encoding an
unrecognized component of amyloid in Alzheimer disease. Proc. Natl. Acad. Sci. USA
90, 11,282–11,286.
|
| |
| 27. |
Bayer, T. A., Jäkälä, P., Hartmann, T., Havas, L., McLean, C., Culvenor, J. G., et al. (1999) α-Synuclein accumulates in Lewy
bodies in Parkinson’s disease and dementia with Lewy bodies but not in Alzheimer’s disease β-amyloid cores. Neurosci. Lett.
266, 213–216.
<Occurrence Type="DOI"><Handle>10.1016/S0304-3940(99)00311-0</Handle></Occurrence>
|
| |
| 28. |
Culvenor, J. G., McLean, C. A., Cutt, S., Campbell, B. C. V., Maher, F., Jäkälä, P., et al. (1999) Non-Aβ component of Alzheimer’s
disease amyloid (NAC) revisited. NAC and α-synuclein are not associated with Aβ amyloid. Am. J. Pathol. 155, 1173–188
|
| |
| 29. |
Jakes, R., Spillantini, M. G., and Goedert, M. (1994) Identification of two distinct synucleins from human brain. FEBS Lett.
345, 27–32.
<Occurrence Type="DOI"><Handle>10.1016/0014-5793(94)00395-5</Handle></Occurrence>
|
| |
| 30. |
George, J. M., Jin, H., Woods, W. S., and Clayton, D. F. (1995) Characterization of a novel protein regulated during the critical
period for song learning in the zebra finch. Neuron
15, 361–372.
<Occurrence Type="DOI"><Handle>10.1016/0896-6273(95)90040-3</Handle></Occurrence>
|
| |
| 31. |
Campion, D., Martin, C., Heilig, R., Charbonnier, F., Moreau, V., Flaman, J. M., et al. (1995) The NACP/synuclein gene: Chromosomal
assignment and screening for alterations in Alzheimer disease. Genomics
26, 254–257.
<Occurrence Type="DOI"><Handle>10.1016/0888-7543(95)80208-4</Handle></Occurrence>
|
| |
| 32. |
Chen, X., de Silva, H. A. R., Pettenati, M. J., Rao, P. N., St. George-Hyslop, P., Roses, A. D., et al. (1995) The human NACP/α-synuclein
gene: chromosome assignment to 4q21. 3-q22 and TaqI RFLP analysis. Genomics
26, 425–427.
<Occurrence Type="DOI"><Handle>10.1016/0888-7543(95)80237-G</Handle></Occurrence>
|
| |
| 33. |
Spillantini, M. G., Divane, A., and Goedert, M. (1995) Assignment of human α-synuclein (SNCA) and β-synuclein (SNCB) genes
to chromosomes 4q21 and 5q35. Genomics
27, 379–381.
|
| |
| 34. |
Shibasaki, Y., Baillie, D. A. M., St. Clair, D., and Brookes, A. J. (1995) High-resolution mapping of SNCA encoding α-synuclein,
the non-Aβ component of Alzheimer’s disease precursor, to human chromosome 4q21.3-q22 by fluorescence in situ hybridization.
Cytogenet. Cell. Genet.
71, 54,55.
|
| |
| 35. |
Lavedan, C., Leroy, E., Torres, R., Dehejia, A., Dutra, A., Buchholtz, S., et al. (1998) Genomic organization and expression
of the human β-synuclein gene (SNCB). Genomics
54, 173–175.
|
| |
| 36. |
Uéda, K., Saitoh, T., and Mori, H. (1994) Tissue-dependent alternative splicing of mRNA for NACP, the precursor of non-Aβ
component of Alzheimer’s disease amyloid. Biochem. Biophys. Res. Commun.
205, 1366–1372.
|
| |
| 37. |
Weinreb, P. H., Zhen, W., Poon, A. W., Conway, K. A., and Lansbury, P. T. (1996) NACP, a protein implicated in Alzheimer’s
disease and learning, is natively unfolded. Biochemistry
35, 13,709–13,715.
|
| |
| 38. |
Davidson, W. S., Jonas, A., Clayton, D. F., and George, J. M. (1998) Stabilization of α-synuclein secondary structure upon
binding to synthetic membranes. J. Biol. Chem.
273, 9443–9449.
|
| |
| 39. |
Jensen, P. H., Nielsen, M. H., Jakes, R., Dotti, C. G., and Goedert, M. (1998) Binding of α-synuclein to rat brain vesicles
is abolished by familial Parkinson’s disease mutation. J. Biol. Chem.
273, 26,292–26,294.
|
| |
| 40. |
Jenco, J. M., Rawlingson, A., Daniels, B., and Morris, A. J. (1998) Regulation of phospholipase D2: Selective inhibition of
mammalian phospholipase D isoenzymes by α-and β-synucleins. Biochemistry
37, 4901–4909.
|
| |
| 41. |
Colley, W. C., Sung, T.-C., Roll, R., Jenco, J., Hammond, S. M., Altshuller, Y., et al. (1997) Phospholipase D2, a distinct
phospholipase D isoform with novel regulatory properties that provokes cytoskeletal reorganization. Curr. Biol.
7, 191–201.
<Occurrence Type="DOI"><Handle>10.1016/S0960-9822(97)70090-3</Handle></Occurrence>
|
| |
| 42. |
Okochi, M., Walter, J., Koyama, A., Nakajo, S., Baba, M., Iwatsubo, T., et al. (2000) Constitutive phosphorylation of the
Parkinson’s disease-associated α-synuclein. J. Biol. Chem.
275, 390–397.
|
| |
| 43. |
Ji, H., Liu, Y. E., Jia, T., Wang, M., Liu, J., Xiao, G., et al. (1997) Identification of a breast cancer-specific gene, BCSG1, by direct differential cDNA sequencing. Cancer Res.
57, 759–764.
|
| |
| 44. |
Goedert, M., Jakes, R., and Spillantini, M. G. (1998) Alpha-synuclein and the Lewy body. NeuroSci. News
1, 47–52.
|
| |
| 45. |
Buchman, V. L., Hunter, H. J. A., Pinon, L. G. P., Thompson, J., Privalova, E. M., Ninkina, N. N., et al. (1998) Persyn, a
member of the synuclein family, has a distinct pattern of expression in the developing nervous system. J. Neurosci.
18, 9335–9341.
|
| |
| 46. |
Lavedan, C., Leroy, E., Dehejia, A., Buchholtz, S., Dutra, A., Nussbaum, R. L., et al. (1998) Identification, localization
and characterization of the human γ-synuclein gene. Hum. Genet.
103, 106–112.
|
| |
| 47. |
Ninkina, N. N., Alimova-Kost, M. V., Paterson, J. W. E., Delaney, L., Cohen, B. B., Imreh, S., et al. (1998) Organization,
expression and polymorphism of the human persyn gene. Hum. Mol. Genet.
7, 1417–1424.
|
| |
| 48. |
Surguchov, A., Surgucheva, I., Solessio, E., and Baehr, W. (1999) Synoretin—a new protein belonging to the synuclein family.
Mol. Cell. Neurosci.
13, 95–103.
|
| |
| 49. |
Golbe, L. I., Di Iorio, G., Bonavita, V., Miller, D. C., and Duvoisin, R. C. (1990) A large kindred with autosomal dominant
Parkinson’s disease. Ann. Neurol.
27, 276–282.
|
| |
| 50. |
Polymeropoulos, M. H., Higgins, J. J., Golbe, L. I., Johnson, W. G., Ide, S. E., Di Iorio, G., et al. (1996) Mapping of a
gene for Parkinson’s disease to chromosome 4q21-q23. Science
274, 1197–1199.
|
| |
| 51. |
Athanassiadou, A., Voutsinas, G., Psiouri, L., Leroy, E., Polymeropoulos, M. H., Ilias, A., Maniatis, G. M., and Papapetropoulos,
T. (1999) Genetic analysis of families with Parkinson disease that carry the Ala53Thr mutation in the gene encoding α-synuclein.
Am. J. Hum. Genet.
65, 555–558.
|
| |
| 52. |
Lincoln, S., Gwinn-Hardy, K., Goudreau, J., Chartier-Harlin, M. C., Baker, M., Mouroux, V., et al. (1999) No pathogenic mutations
in the persyn gene in Parkinson’s disease. Neurosci. Lett.
259, 65,66.
<Occurrence Type="DOI"><Handle>10.1016/S0304-3940(98)00901-X</Handle></Occurrence>
|
| |
| 53. |
Lincoln, S., Crook, R., Chartier-Harlin, M. C., Gwinn-Hardy, K., Baker, M., Mouroux, V., et al. (1999) No pathogenic mutations
in the β-synuclein gene in Parkinson’s disease. Neurosci. Lett.
269, 107–109.
<Occurrence Type="DOI"><Handle>10.1016/S0304-3940(99)00420-6</Handle></Occurrence>
|
| |
| 54. |
Flowers, J. M., Leigh, P. N., Davies, A. M., Ninkina, N. N., Buchman, V. L., Vaughan, J., et al. (1999) Mutations in the gene
encoding human persyn are not associated with amyotrophic lateral sclerosis or familial Parkinson’s disease. Neurosci. Lett.
274, 21–24.
<Occurrence Type="DOI"><Handle>10.1016/S0304-3940(99)00673-4</Handle></Occurrence>
|
| |
| 55. |
Krüger, R., Kuhn, W., Müller, T., Woitalla, D., Graeber, M., Kösel, S., et al. (1998) Ala30Pro mutation in the gene encoding
α-synuclein in Parkinson’s disease. Nature Genet.
18, 106–108.
|
| |
| 56. |
Bennett, M. C., Bishop, J. F., Leng, Y., Chock, P. B., Chase, T. N., and Mouradian, M. M. (1999) Degradation of α-synuclein
by proteasome. J. Biol. Chem.
274, 33,855–33,858.
|
| |
| 57. |
Wakabayashi, K., Matsumoto, K., Takayama, K., Yoshimoto, M., and Takahashi, H. (1997) NACP, a presynaptic protein, immunoreactivity
in Lewy bodies in Parkinson’s disease. Neurosci. Lett.
239, 45–48.
<Occurrence Type="DOI"><Handle>10.1016/S0304-3940(97)00891-4</Handle></Occurrence>
|
| |
| 58. |
Takeda, A., Mallory, M., Sundsmo, M., Honer, W., Hansen, L., and Masliah, E. (1998) Abnormal accumulation of NACP/α-synuclein
in neurodegenerative disorders. Am. J. Pathol.
152, 367–372.
|
| |
| 59. |
Baba, M., Nakajo, S., Tu, P.-H., Tomita, T., Nakaya, K., Lee, V. M.-Y., et al. (1998) Aggregation of α-synuclein in Lewy bodies
of sporadic Parkinson’s disease and dementia with Lewy bodies. Am. J. Pathol.
152, 879–884.
|
| |
| 60. |
Irizarry, M. C., Growdon, W., Gomez-Isla, T., Newell, K., George, J. M., Clayton, D. F., et al. (1998) Nigral and cortical
Lewy bodies and dystrophic nigral neurites in Parkinson’s disease and cortical Lewy body disease contain α-synuclein immunoreactivity.
J. Neuropathol. Exp. Neurol.
57, 334–337.
|
| |
| 61. |
Mezey, E., Dehejia, A. M., Harta, G., Suchy, S. F., Nussbaum, R. L., Brownstein, M. J., et al. (1998) Alpha synuclein is present
in Lewy bodies in sporadic Parkinson’s disease. Mol. Psychiat.
3, 493–499.
|
| |
| 62. |
Arai, T., Uéda, K., Ikeda, K., Akiyama, H., Haga, C., Kondo, H., et al. (1999) Argyrophilic glial inclusions in the midbrain
of patients with Parkinson’s disease and diffuse Lewy body disease are immunopositive for NACP/α-synuclein. Neurosci. Lett.
259, 83–86.
<Occurrence Type="DOI"><Handle>10.1016/S0304-3940(98)00890-8</Handle></Occurrence>
|
| |
| 63. |
Braak, H., Sandmann-Keil, D., Gai, W. P., and Braak, E. (1999) Extensive axonal Lewy neurites in Parkinson’s disease: a novel
pathological feature revealed by α-synuclein immunocytochemistry. Neurosci. Lett.
265, 67–69.
<Occurrence Type="DOI"><Handle>10.1016/S0304-3940(99)00208-6</Handle></Occurrence>
|
| |
| 64. |
Jakes, R., Crowther, R. A., Lee, V. M.-Y., Trojanowski, J. Q., Iwatsubo, T., and Goedert, M. (1999) Epitope mapping of LB509,
a monoclonal antibody directed against human α-synuclein. Neurosci. Lett.
269, 13–16.
<Occurrence Type="DOI"><Handle>10.1016/S0304-3940(99)00411-5</Handle></Occurrence>
|
| |
| 65. |
Giasson, B. I., Jakes, R., Goedert, M., Duda, J. E., Leight, S., Trojanowski, J. Q., et al. (2000) A panel of epitope-specific
antibodies detects protein domains distributed throughout human α-synuclein in Lewy bodies of Parkinson’s disease. J. Neurosci. Res.
59, 528–533.
<Occurrence Type="DOI"><Handle>10.1002/(SICI)1097-4547(20000215)59:4<528::AID-JNR8>3.0.CO;2-0</Handle></Occurrence>
|
| |
| 66. |
Wakabayashi, K., Hayashi, S., Kakita, A., Yamada, M., Toyoshima, Y., Yoshimoto, M., et al. (1998) Accumulation of α-synuclein/NACP
is a cytopathological feature common to Lewy body disease and multiple system atrophy. Acta Neuropathol.
96, 445–452.
|
| |
| 67. |
Arima, K., Uéda, K., Sunohara, N., Hirai, S., Izumiyama, Y., Tonozuka-Uehara, H., et al. (1998) Immunoelectron-microscopic
demonstration of NACP/α-synuclein-epitopes on the filamentous component of Lewy bodies in Parkinson’s disease and in dementia
with Lewy bodies. Brain Res.
808, 93–100.
<Occurrence Type="DOI"><Handle>10.1016/S0006-8993(98)00734-3</Handle></Occurrence>
|
| |
| 68. |
Graham, J. C. and Oppenheimer, D. R. (1969) Orthostatic hypotension and nicotine sensitivity in a case of multiple system
atrophy. J. Neurol. Neurosurg. Psychiat.
32, 28–34.
|
| |
| 69. |
Papp, M. I., Kahn, J. E., and Lantos, P. L. (1989) Glial cytoplasmic inclusions in the CNS of patients with multiple system
atrophy. J. Neurol. Sci.
94, 79–100.
<Occurrence Type="DOI"><Handle>10.1016/0022-510X(89)90219-0</Handle></Occurrence>
|
| |
| 70. |
Kato, S. and Nakamura, H. (1990) Cytoplasmic argyrophilic inclusions in neurons of pontine nuclei in patients with olivopontocerebellar
atrophy: Immunohistochemical and ultrastructural studies. Acta Neuropathol.
79, 584–594.
|
| |
| 71. |
Arima, K., Uéda, K., Sunohara, N., Arakawa, K., Hirai, S., Nakamura, M., et al. (1998) NACP/α-synuclein immunoreactivity in
fibrillary components of neuronal and oligodendroglial cytoplasmic inclusions in the pontine nuclei in multiple system atrophy.
Acta Neuropathol.
96, 439–444.
|
| |
| 72. |
Gai, W. P., Power, J. H. T., Blumbergs, P. C., Culvenor, J. G., and Jensen, P. H. (1999) α-Synuclein immunoisolation of glial
inclusions from multiple system atrophy brain reveals multiprotein components. J. Neurochem.
73, 2093–2100.
|
| |
| 73. |
Dickson, D. W., Liu, W.-K., Hardy, J., Farrer, M., Mehta, N., Uitti, R., et al. (1999) Widespread alterations of α-synuclein
in multiple system atrophy. Am. J. Pathol.
155, 1241–1251.
|
| |
| 74. |
Ozawa, T., Takano, H., Onodera, O., Kobayashi, H., Ikeuchi, T., Koide, R., et al. (1999) No mutation in the entire coding
region of the α-synuclein gene in pathologically confirmed cases of multiple system atrophy. Neurosci. Lett.
270, 110–112.
<Occurrence Type="DOI"><Handle>10.1016/S0304-3940(99)00475-9</Handle></Occurrence>
|
| |
| 75. |
Crowther, R. A., Jakes, R., Spillantini, M. G., and Goedert, M. (1998) Synthetic filaments assembled from C-terminally truncated
α-synuclein. FEBS Lett.
436, 309–312.
<Occurrence Type="DOI"><Handle>10.1016/S0014-5793(98)01146-6</Handle></Occurrence>
|
| |
| 76. |
El-Agnaf, O. M. A., Jakes, R., Curran, M. D., and Wallace, A. (1998) Effects of the mutations Ala30 to Pro and Ala53 to Thr
on the physical and morphological properties of α-synuclein protein implicated in Parkinson’s disease. FEBS Lett.
440, 67–70.
<Occurrence Type="DOI"><Handle>10.1016/S0014-5793(98)01419-7</Handle></Occurrence>
|
| |
| 77. |
Conway, K. A., Harper, J. D., and Lansbury, P. T. (1998) Accelerated in vitro fibril formation by a mutant α-synuclein linked
to early-onset Parkinson disease. Nature Med.
4, 1318–1320.
|
| |
| 78. |
Giasson, B. I., Uryu, K., Trojanowski, J. Q., and Lee, V. M.-Y. (1999) Mutant and wild type human α-synucleins assemble into
elongated filaments with distinct morphologies in vitro. J. Biol. Chem.
274, 7619–7622.
|
| |
| 79. |
Narhi, L., Wood, S. J., Steavenson, S., Jiang, Y., Wu, G. M., Anafi, D., et al. (1999) Both familial Parkinson’s disease mutations
accelerate α-synuclein aggregation. J. Biol. Chem.
274, 9843–9846.
|
| |
| 80. |
Wood, S. J., Wypych, J., Steavenson, S., Louis, J.-C., Citron, M., and Biere, A. L. (1999) α-Synuclein fibrillogenesis is
nucleation-dependent. J. Biol. Chem.
274, 19,509–19,512.
|
| |
| 81. |
Serpell, L. S., Berriman, J., Jakes, R., Goedert, M., and Crowther, R. A. (2000) Fibre diffraction of synthetic α-synuclein
filaments shows amyloid-like cross-β conformation. Proc. Natl. Acad. Sci. USA
97, 4897–4902
|
| |
| 82. |
Han, H., Weinreb, P. H., and Lansbury, P. T. (1995) The core of Alzheimer’s peptide NAC forms amyloid fibrils which seed and
are seeded by β-amyloid: Is NAC a common trigger or target in neurodegenerative disease? Chem. Biol.
2, 163–169.
<Occurrence Type="DOI"><Handle>10.1016/1074-5521(95)90071-3</Handle></Occurrence>
|
| |
| 83. |
Greenberg, S. G. and Davies, P. (1990) A preparation of Alzheimer paired helical filaments that displays distinct tau proteins
by polyacrylamide gel electrophoresis. Proc. Natl. Acad. Sci. USA
87, 5827–5831.
|
| |
| 84. |
Goedert, M., Spillantini, M. G., Cairns, N. J., and Crowther, R. A. (1992) Tau proteins of Alzheimer paired helical filaments:
abnormal phosphorylation of all six brain isoforms. Neuron
8, 159–168.
<Occurrence Type="DOI"><Handle>10.1016/0896-6273(92)90117-V</Handle></Occurrence>
|
| |