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MOUSE:SYUA

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Contents

Species (Taxon ID) Mus musculus (Mouse). (taxon:10090)
Gene Name(s) Snca ( synonyms: Syn )
Protein Name(s)
  • Alpha-synuclein
  • Non-A beta component of AD amyloid
  • Non-A4 component of amyloid precursor
  • NACP
External Links
UniProt Identifier SYUA_MOUSE
UniProt Accessions O55042, Q3U130, Q9CXF8, Q9EQC3, Q9QUR3,
EMBL AF044672, AF033261, AF179273, AF179272, AF179268, AF179269, AF179270, AF179271, AF163865, AK014472, AK156316, BC046764, AF277451,
RefSeq NP_001035916.1, NP_033247.1,
Ensembl ENSMUST00000114268, ENSMUST00000163779,
Pfam PF01387,

Annotations

Qualifier GO ID GO term name Reference Evidence Code with/from Aspect Notes Status
GO:0005829

cytosol

IDA: Inferred from Direct Assay

C

Source: UniProtKB

GO:0005634

nucleus

IDA: Inferred from Direct Assay

C

Source: UniProtKB

GO:0005886

plasma membrane

IDA: Inferred from Direct Assay

C

Source: MGI

GO:0019717

synaptosome

IDA: Inferred from Direct Assay

C

Source: MGI

GO:0050544

arachidonic acid binding

IDA: Inferred from Direct Assay

F

Source: MGI

GO:0042393

histone binding

IDA: Inferred from Direct Assay

F

Source: UniProtKB

GO:0042802

identical protein binding

IDA: Inferred from Direct Assay

F

Source: MGI

GO:0008344

adult locomotory behavior

IGI: Inferred from Genetic Interaction

P

Source: MGI

GO:0034599

cellular response to oxidative stress

IMP: Inferred from Mutant Phenotype

P

Source: MGI

GO:0042416

dopamine biosynthetic process

IMP: Inferred from Mutant Phenotype

P

Source: MGI

GO:0006631

fatty acid metabolic process

IMP: Inferred from Mutant Phenotype

P

Source: MGI

GO:0060291

long-term synaptic potentiation

IMP: Inferred from Mutant Phenotype

P

Source: MGI

GO:0001774

microglial cell activation

IMP: Inferred from Mutant Phenotype

P

Source: MGI

GO:0042775

mitochondrial ATP synthesis coupled electro...

IMP: Inferred from Mutant Phenotype

P

Source: MGI

GO:0007006

mitochondrial membrane organization

IMP: Inferred from Mutant Phenotype

P

Source: MGI

GO:0043524

negative regulation of neuron apoptosis

IGI: Inferred from Genetic Interaction

P

Source: MGI

GO:0006638

neutral lipid metabolic process

IMP: Inferred from Mutant Phenotype

P

Source: MGI

GO:0006644

phospholipid metabolic process

IMP: Inferred from Mutant Phenotype

P

Source: MGI

GO:0001956

positive regulation of neurotransmitter sec...

IDA: Inferred from Direct Assay

P

Source: MGI

GO:0050812

regulation of acyl-CoA biosynthetic process

IDA: Inferred from Direct Assay

P

Source: MGI

GO:0014059

regulation of dopamine secretion

IGI: Inferred from Genetic Interaction

P

Source: MGI

GO:0060079

regulation of excitatory postsynaptic membr...

IMP: Inferred from Mutant Phenotype

P

Source: MGI

GO:0014048

regulation of glutamate secretion

IMP: Inferred from Mutant Phenotype

P

Source: MGI

GO:0040012

regulation of locomotion

IMP: Inferred from Mutant Phenotype

P

Source: MGI

GO:0048169

regulation of long-term neuronal synaptic p...

IMP: Inferred from Mutant Phenotype

P

Source: MGI

GO:0043030

regulation of macrophage activation

IMP: Inferred from Mutant Phenotype

P

Source: MGI

GO:0042493

response to drug

IMP: Inferred from Mutant Phenotype

P

Source: MGI

GO:0001963

synaptic transmission, dopaminergic

IMP: Inferred from Mutant Phenotype

P

Source: MGI

GO:0048488

synaptic vesicle endocytosis

IMP: Inferred from Mutant Phenotype

P

Source: UniProtKB

GO:0000287

magnesium ion binding

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

F

GO:0001774

microglial cell activation

PMID:17035541[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2389489

P

GO:0001921

positive regulation of receptor recycling

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

P

GO:0001956

positive regulation of neurotransmitter secretion

PMID:15510220[2]

IDA: Inferred from Direct Assay

P

GO:0001963

synaptic transmission, dopaminergic

PMID:10707987[3]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1888382

P

GO:0001963

synaptic transmission, dopaminergic

PMID:12388586[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2389489

P

GO:0005509

calcium ion binding

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

F

GO:0005634

nucleus

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

C

GO:0005634

nucleus

PMID:16959795[5]

IDA: Inferred from Direct Assay

C

GO:0005737

cytoplasm

GO_REF:0000002

IEA: Inferred from Electronic Annotation

InterPro:IPR002460

C

GO:0005737

cytoplasm

GO_REF:0000004

IEA: Inferred from Electronic Annotation

SP_KW:KW-0963

C

GO:0005737

cytoplasm

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

C

GO:0005737

cytoplasm

GO_REF:0000023

IEA: Inferred from Electronic Annotation

SP_SL:SL-0086

C

GO:0005737

cytoplasm

PMID:17475220[6]

IDA: Inferred from Direct Assay

C

GO:0005737

cytoplasm

PMID:20457918[7]

IDA: Inferred from Direct Assay

C

GO:0005739

mitochondrion

PMID:16260631[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2389489

C

GO:0005829

cytosol

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

C

GO:0005829

cytosol

PMID:18980610[9]

IDA: Inferred from Direct Assay

C

GO:0005856

cytoskeleton

PMID:17077307[10]

IDA: Inferred from Direct Assay

C

GO:0005886

plasma membrane

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

C

GO:0005886

plasma membrane

PMID:17475220[6]

IDA: Inferred from Direct Assay

C

GO:0005938

cell cortex

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

C

GO:0006631

fatty acid metabolic process

PMID:14507911[11]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1888382

P

GO:0006631

fatty acid metabolic process

PMID:17250686[12]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2389489

P

GO:0006638

neutral lipid metabolic process

PMID:17250686[12]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2389489

P

GO:0006644

phospholipid metabolic process

PMID:15938614[13]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2389489

P

GO:0006644

phospholipid metabolic process

PMID:16260631[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2389489

P

GO:0006644

phospholipid metabolic process

PMID:16734431[14]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2389489

P

GO:0006916

anti-apoptosis

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

P

GO:0006919

activation of caspase activity

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

P

GO:0007006

mitochondrial membrane organization

PMID:16260631[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2389489

P

GO:0008198

ferrous iron binding

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

F

GO:0008270

zinc ion binding

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

F

GO:0008344

adult locomotory behavior

PMID:18333965[15]

IGI: Inferred from Genetic Interaction

MGI:MGI:1298397

P

GO:0010040

response to iron(II) ion

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

P

GO:0010517

regulation of phospholipase activity

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

P

GO:0010642

negative regulation of platelet-derived growth factor receptor signaling pathway

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

P

GO:0014048

regulation of glutamate secretion

PMID:17689254[16]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2154692

P

GO:0014059

regulation of dopamine secretion

GO_REF:0000002

IEA: Inferred from Electronic Annotation

InterPro:IPR002460

P

GO:0014059

regulation of dopamine secretion

PMID:18333965[15]

IGI: Inferred from Genetic Interaction

MGI:MGI:1298397

P

GO:0015629

actin cytoskeleton

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

C

GO:0016044

cellular membrane organization

PMID:14507911[11]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1888382

P

GO:0019717

synaptosome

PMID:10964942[17]

IDA: Inferred from Direct Assay

C

GO:0019894

kinesin binding

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

F

GO:0030424

axon

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

C

GO:0030426

growth cone

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

C

GO:0030544

Hsp70 protein binding

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

F

GO:0031092

platelet alpha granule membrane

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

C

GO:0031115

negative regulation of microtubule polymerization

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

P

GO:0031623

receptor internalization

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

P

GO:0032026

response to magnesium ion

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

P

GO:0032410

negative regulation of transporter activity

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

P

GO:0032496

response to lipopolysaccharide

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

P

GO:0032769

negative regulation of monooxygenase activity

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

P

GO:0033138

positive regulation of peptidyl-serine phosphorylation

PMID:21127069[18]

IMP: Inferred from Mutant Phenotype

P

GO:0034341

response to interferon-gamma

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

P

GO:0034599

cellular response to oxidative stress

PMID:16298531[19]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1888382

P

GO:0035067

negative regulation of histone acetylation

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

P

GO:0040012

regulation of locomotion

PMID:10707987[3]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1888382

P

GO:0042393

histone binding

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

F

GO:0042393

histone binding

PMID:16959795[5]

IDA: Inferred from Direct Assay

F

GO:0042416

dopamine biosynthetic process

PMID:10707987[3]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1888382

P

GO:0042417

dopamine metabolic process

PMID:15465911[20]

IGI: Inferred from Genetic Interaction

MGI:MGI:1889011

P

GO:0042493

response to drug

PMID:10707987[3]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1888382

P

GO:0042775

mitochondrial ATP synthesis coupled electron transport

PMID:16260631[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2389489

P

GO:0042802

identical protein binding

PMID:10978144[21]

IDA: Inferred from Direct Assay

F

GO:0043014

alpha-tubulin binding

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

F

GO:0043027

caspase inhibitor activity

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

F

GO:0043030

regulation of macrophage activation

PMID:17035541[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2389489

P

GO:0043154

negative regulation of caspase activity

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

P

GO:0043205

fibril

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

C

GO:0043524

negative regulation of neuron apoptosis

PMID:16269331[22]

IGI: Inferred from Genetic Interaction

MGI:MGI:892995

P

GO:0045502

dynein binding

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

F

GO:0045807

positive regulation of endocytosis

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

P

GO:0045920

negative regulation of exocytosis

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

P

GO:0046928

regulation of neurotransmitter secretion

PMID:10707987[3]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1888382

P

GO:0046928

regulation of neurotransmitter secretion

PMID:12388586[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2389489

P

GO:0046928

regulation of neurotransmitter secretion

PMID:15510220[2]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2429773

P

GO:0046928

regulation of neurotransmitter secretion

PMID:18333965[15]

IGI: Inferred from Genetic Interaction

MGI:MGI:1298397

P

GO:0048156

tau protein binding

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

F

GO:0048168

regulation of neuronal synaptic plasticity

PMID:17610578[23]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2429773

P

GO:0048169

regulation of long-term neuronal synaptic plasticity

PMID:15510220[2]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2429773

P

GO:0048488

synaptic vesicle endocytosis

PMID:18980610[9]

IMP: Inferred from Mutant Phenotype

P

GO:0048489

synaptic vesicle transport

PMID:12388586[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2389489

P

GO:0050544

arachidonic acid binding

PMID:16734431[14]

IDA: Inferred from Direct Assay

F

GO:0050806

positive regulation of synaptic transmission

PMID:15579163[24]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1888382

P

GO:0050812

regulation of acyl-CoA biosynthetic process

PMID:16636270[25]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2389489

P

GO:0050812

regulation of acyl-CoA biosynthetic process

PMID:16734431[14]

IDA: Inferred from Direct Assay

P

GO:0051219

phosphoprotein binding

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

F

GO:0051281

positive regulation of release of sequestered calcium ion into cytosol

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

P

GO:0051585

negative regulation of dopamine uptake

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

P

GO:0051612

negative regulation of serotonin uptake

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

P

GO:0051622

negative regulation of norepinephrine uptake

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

P

GO:0060079

regulation of excitatory postsynaptic membrane potential

PMID:17610578[23]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2429773

P

GO:0060291

long-term synaptic potentiation

PMID:17689254[16]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2154692

P

GO:0060732

positive regulation of inositol phosphate biosynthetic process

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

P

GO:0070495

negative regulation of thrombin receptor signaling pathway

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

P

GO:0070555

response to interleukin-1

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

P

GO:0071902

positive regulation of protein serine/threonine kinase activity

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSP00000378437

P

NOT

GO:0043523

regulation of neuron apoptosis

PMID:15380020[26]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2429773

P


Notes

References

See Help:References for how to manage references in GONUTS.

  1. ↑ 1.0 1.1 Austin SA et al. (2006) Alpha-synuclein expression modulates microglial activation phenotype. J Neurosci 26: 10558-63 PubMed GONUTS page
  2. ↑ 2.0 2.1 2.2 Liu S et al. (2004) alpha-Synuclein produces a long-lasting increase in neurotransmitter release. EMBO J 23: 4506-16 PubMed GONUTS page
  3. ↑ 3.0 3.1 3.2 3.3 3.4 Abeliovich A et al. (2000) Mice lacking alpha-synuclein display functional deficits in the nigrostriatal dopamine system. Neuron 25: 239-52 PubMed GONUTS page
  4. ↑ 4.0 4.1 4.2 Cabin DE et al. (2002) Synaptic vesicle depletion correlates with attenuated synaptic responses to prolonged repetitive stimulation in mice lacking alpha-synuclein. J Neurosci 22: 8797-807 PubMed GONUTS page
  5. ↑ 5.0 5.1 Kontopoulos E et al. (2006) Alpha-synuclein acts in the nucleus to inhibit histone acetylation and promote neurotoxicity. Hum Mol Genet 15: 3012-23 PubMed GONUTS page
  6. ↑ 6.0 6.1 Nakai M et al. (2007) Expression of alpha-synuclein, a presynaptic protein implicated in Parkinson's disease, in erythropoietic lineage. Biochem Biophys Res Commun 358: 104-10 PubMed GONUTS page
  7. ↑ Tong Y et al. (2010) Loss of leucine-rich repeat kinase 2 causes impairment of protein degradation pathways, accumulation of alpha-synuclein, and apoptotic cell death in aged mice. Proc Natl Acad Sci U S A 107: 9879-84 PubMed GONUTS page
  8. ↑ 8.0 8.1 8.2 8.3 Ellis CE et al. (2005) Mitochondrial lipid abnormality and electron transport chain impairment in mice lacking alpha-synuclein. Mol Cell Biol 25: 10190-201 PubMed GONUTS page
  9. ↑ 9.0 9.1 Ben Gedalya T et al. (2009) Alpha-synuclein and polyunsaturated fatty acids promote clathrin-mediated endocytosis and synaptic vesicle recycling. Traffic 10: 218-34 PubMed GONUTS page
  10. ↑ Duka T et al. (2006) Alpha-synuclein induces hyperphosphorylation of Tau in the MPTP model of parkinsonism. FASEB J 20: 2302-12 PubMed GONUTS page
  11. ↑ 11.0 11.1 Sharon R et al. (2003) Altered fatty acid composition of dopaminergic neurons expressing alpha-synuclein and human brains with alpha-synucleinopathies. J Biol Chem 278: 49874-81 PubMed GONUTS page
  12. ↑ 12.0 12.1 Barceló-Coblijn G et al. (2007) Brain neutral lipids mass is increased in alpha-synuclein gene-ablated mice. J Neurochem 101: 132-41 PubMed GONUTS page
  13. ↑ Golovko MY et al. (2005) Alpha-synuclein gene deletion decreases brain palmitate uptake and alters the palmitate metabolism in the absence of alpha-synuclein palmitate binding. Biochemistry 44: 8251-9 PubMed GONUTS page
  14. ↑ 14.0 14.1 14.2 Golovko MY et al. (2006) Acyl-CoA synthetase activity links wild-type but not mutant alpha-synuclein to brain arachidonate metabolism. Biochemistry 45: 6956-66 PubMed GONUTS page
  15. ↑ 15.0 15.1 15.2 Senior SL et al. (2008) Increased striatal dopamine release and hyperdopaminergic-like behaviour in mice lacking both alpha-synuclein and gamma-synuclein. Eur J Neurosci 27: 947-57 PubMed GONUTS page
  16. ↑ 16.0 16.1 Gureviciene I et al. (2007) Role of alpha-synuclein in synaptic glutamate release. Neurobiol Dis 28: 83-9 PubMed GONUTS page
  17. ↑ Kahle PJ et al. (2000) Subcellular localization of wild-type and Parkinson's disease-associated mutant alpha -synuclein in human and transgenic mouse brain. J Neurosci 20: 6365-73 PubMed GONUTS page
  18. ↑ Qureshi HY & Paudel HK (2011) Parkinsonian neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) and alpha-synuclein mutations promote Tau protein phosphorylation at Ser262 and destabilize microtubule cytoskeleton in vitro. J Biol Chem 286: 5055-68 PubMed GONUTS page
  19. ↑ Klivenyi P et al. (2006) Mice lacking alpha-synuclein are resistant to mitochondrial toxins. Neurobiol Dis 21: 541-8 PubMed GONUTS page
  20. ↑ Chandra S et al. (2004) Double-knockout mice for alpha- and beta-synucleins: effect on synaptic functions. Proc Natl Acad Sci U S A 101: 14966-71 PubMed GONUTS page
  21. ↑ Rochet JC et al. (2000) Inhibition of fibrillization and accumulation of prefibrillar oligomers in mixtures of human and mouse alpha-synuclein. Biochemistry 39: 10619-26 PubMed GONUTS page
  22. ↑ Chandra S et al. (2005) Alpha-synuclein cooperates with CSPalpha in preventing neurodegeneration. Cell 123: 383-96 PubMed GONUTS page
  23. ↑ 23.0 23.1 Liu S et al. (2007) Alpha-synuclein involvement in hippocampal synaptic plasticity: role of NO, cGMP, cGK and CaMKII. Eur J Neurosci 25: 3583-96 PubMed GONUTS page
  24. ↑ Martín ED et al. (2004) Stressor-related impairment of synaptic transmission in hippocampal slices from alpha-synuclein knockout mice. Eur J Neurosci 20: 3085-91 PubMed GONUTS page
  25. ↑ Stanic AK et al. (2006) Immune dysregulation accelerates atherosclerosis and modulates plaque composition in systemic lupus erythematosus. Proc Natl Acad Sci U S A 103: 7018-23 PubMed GONUTS page
  26. ↑ Stefanis L et al. (2004) Lack of alpha-synuclein does not alter apoptosis of neonatal catecholaminergic neurons. Eur J Neurosci 20: 1969-72 PubMed GONUTS page
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