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Alpha-synuclein overexpression increases dopamine toxicity in BE2-M17 cells.

Bisaglia M, Greggio E, Maric D, Miller DW, Cookson MR, Bubacco L.

BMC Neurosci · 2010-03-25

DOI: 10.1186/1471-2202-11-41PMID: 20334701

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Non-classical exocytosis of alpha-synuclein is sensitive to folding states and promoted under stress conditions.

Jang A, Lee HJ, Suk JE, Jung JW, Kim KP, Lee SJ.

J Neurochem · 2010-03-24

DOI: 10.1111/j.1471-4159.2010.06695.xPMID: 20345754

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The structure of dopamine induced alpha-synuclein oligomers.

Rekas A, Knott RB, Sokolova A, Barnham KJ, Perez KA, Masters CL, Drew SC, Cappai R, Curtain CC, Pham CL.

Eur Biophys J · 2010-03-23

DOI: 10.1007/s00249-010-0595-xPMID: 20309679

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Multi-organ distribution of phosphorylated alpha-synuclein histopathology in subjects with Lewy body disorders.

Beach TG, Adler CH, Sue LI, Vedders L, Lue L, White Iii CL, Akiyama H, Caviness JN, Shill HA, Sabbagh MN, Walker DG, Arizona Parkinson's Disease Consortium.

Acta Neuropathol · 2010-03-21

DOI: 10.1007/s00401-010-0664-3PMID: 20306269

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Involvement of the cerebral cortex in Parkinson disease linked with G2019S LRRK2 mutation without cognitive impairment.

Gomez A, Ferrer I.

Acta Neuropathol · 2010-03-16

DOI: 10.1007/s00401-010-0669-yPMID: 20232069

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Filamentous phages reduce alpha-synuclein oligomerization in the membrane fraction of SH-SY5Y cells.

Dimant H, Solomon B.

Neurodegener Dis · 2010-03-12

DOI: 10.1159/000295664PMID: 20224286

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Dopamine quinones interact with alpha-synuclein to form unstructured adducts.

Bisaglia M, Tosatto L, Munari F, Tessari I, de Laureto PP, Mammi S, Bubacco L.

Biochem Biophys Res Commun · 2010-03-10

DOI: 10.1016/j.bbrc.2010.03.044PMID: 20226175

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Alpha-synuclein induced membrane depolarization and loss of phosphorylation capacity of isolated rat brain mitochondria: implications in Parkinson's disease.

Banerjee K, Sinha M, Pham Cle L, Jana S, Chanda D, Cappai R, Chakrabarti S.

FEBS Lett · 2010-03-10

DOI: 10.1016/j.febslet.2010.03.012PMID: 20226185

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The heritability of risk and age at onset of Parkinson's disease after accounting for known genetic risk factors.

Hamza TH, Payami H.

J Hum Genet · 2010-03-05

DOI: 10.1038/jhg.2010.13PMID: 20203693

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Lysosomal degradation of alpha-synuclein in vivo.

Mak SK, McCormack AL, Manning-Bog AB, Cuervo AM, Di Monte DA.

J Biol Chem · 2010-03-03

DOI: 10.1074/jbc.m109.074617PMID: 20200163

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Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans.

Lesage S, Patin E, Condroyer C, Leutenegger AL, Lohmann E, Giladi N, Bar-Shira A, Belarbi S, Hecham N, Pollak P, Ouvrard-Hernandez AM, Bardien S, Carr J, Benhassine T, Tomiyama H, Pirkevi C, Hamadouche T, Cazeneuve C, Basak AN, Hattori N, Dürr A, Tazir M, Orr-Urtreger A, Quintana-Murci L, Brice A, French Parkinson's Disease Genetics Study Group.

Hum Mol Genet · 2010-03-02

DOI: 10.1093/hmg/ddq081PMID: 20197411

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alpha-Synuclein abnormalities in mouse models of peroxisome biogenesis disorders.

Yakunin E, Moser A, Loeb V, Saada A, Faust P, Crane DI, Baes M, Sharon R.

J Neurosci Res · 2010-03-01

DOI: 10.1002/jnr.22246PMID: 19830841

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Records come from scientific sources. Bibliographic counts do not represent completed translations or editorial approvals.

15.097 articles found

Alpha-synuclein overexpression increases dopamine toxicity in BE2-M17 cells.

Non-classical exocytosis of alpha-synuclein is sensitive to folding states and promoted under stress conditions.

The structure of dopamine induced alpha-synuclein oligomers.

Multi-organ distribution of phosphorylated alpha-synuclein histopathology in subjects with Lewy body disorders.

Involvement of the cerebral cortex in Parkinson disease linked with G2019S LRRK2 mutation without cognitive impairment.

Filamentous phages reduce alpha-synuclein oligomerization in the membrane fraction of SH-SY5Y cells.

Dopamine quinones interact with alpha-synuclein to form unstructured adducts.

Alpha-synuclein induced membrane depolarization and loss of phosphorylation capacity of isolated rat brain mitochondria: implications in Parkinson's disease.

The heritability of risk and age at onset of Parkinson's disease after accounting for known genetic risk factors.

Lysosomal degradation of alpha-synuclein in vivo.

Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans.

alpha-Synuclein abnormalities in mouse models of peroxisome biogenesis disorders.

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