Iron in neurodegenerative disorders of protein misfolding: a case of prion disorders and Parkinson's disease. - Wikidata - wikimedia - TriplyDB

Iron in neurodegenerative disorders of protein misfolding: a case of prion disorders and Parkinson's disease.

Iron in neurodegenerative disorders of protein misfolding: a case of prion disorders and Parkinson's disease.

http://www.wikidata.org/entity/Q38186783

about

The Chemistry of Neurodegeneration: Kinetic Data and Their Implications.Deficiency of prion protein induces impaired autophagic flux in neurons.Eryptosis as a marker of Parkinson's disease Viscoelastic and ultrastructural characteristics of whole blood and plasma in Alzheimer-type dementia, and the possible role of bacterial lipopolysaccharides (LPS)Coherent and Contradictory Facts, Feats and Fictions Associated with Metal Accumulation in Parkinson's Disease: Epicenter or Outcome, Yet a Demigod Question.Prion protein facilitates retinal iron uptake and is cleaved at the β-site: Implications for retinal iron homeostasis in prion disorders.Lipid rafts: linking prion protein to zinc transport and amyloid-β toxicity in Alzheimer's disease α-Synuclein impairs ferritinophagy in the retinal pigment epithelium: Implications for retinal iron dyshomeostasis in Parkinson's disease.Hemoglobin mRNA Changes in the Frontal Cortex of Patients with Neurodegenerative Diseases.Prion protein modulates glucose homeostasis by altering intracellular iron.Differential expression of miRNA 155 and miRNA 146a in Parkinson's disease patients

P2860

Q30973484-1F058579-2857-41D7-A7C8-EF58C3195B8C Q34081999-C581CC39-C84A-4AEA-A97D-C48077DACB70 Q34585744-BF9B732F-A7DF-46BE-9F14-E2939A95E96C Q36546334-9CA15E6A-073C-40B4-B287-A9A19F1A7BB8 Q38915163-9716D87C-C800-4502-859A-1A35CC0F4507 Q40075661-2EE0CC09-B2B6-46D5-8CEC-0CA2B7D30458 Q41957300-A047B438-D893-4DDB-A134-C460716F8C36 Q42373959-5216065A-C4FF-43EE-875E-CF49C34C9620 Q49388205-C4953258-F0EC-434E-A97B-2A942BDE834B Q55285231-3EAF3E84-30FD-4996-A214-26F6A18A42CE Q58740022-9F548F81-085C-456D-AE17-42137D0B751F

P2860

Iron in neurodegenerative disorders of protein misfolding: a case of prion disorders and Parkinson's disease.

http://www.wikidata.org/entity/Q38186783

description

article científic

@ca

article scientifique

@fr

articol științific

@ro

articolo scientifico

@it

artigo científico

@gl

artigo científico

@pt

artigo científico

@pt-br

artikel ilmiah

@id

artikull shkencor

@sq

artículo científico

@es

name

Iron in neurodegenerative diso ...... rders and Parkinson's disease.

@en

type

label

Iron in neurodegenerative diso ...... rders and Parkinson's disease.

@en

prefLabel

Iron in neurodegenerative diso ...... rders and Parkinson's disease.

@en

P1433

Q38186783-49AF4AB2-DD87-4FE8-84AC-379FCE985F41

P1476

Q38186783-49E97648-3A7C-469D-BAEC-219E08605894

P2093

Q38186783-40DDB71A-14BF-498D-AD10-B4F9C3AFD71A

Q38186783-48EB5A75-5B26-46A1-8EEA-9CE57C60C986

Q38186783-A36EA7B9-9186-4630-B338-29FF639BA76D

Q38186783-AD2C45E4-7027-48DF-8E71-7E35405146DE

Q38186783-CFC58AE6-6632-430C-9D88-4D61412CB674

P2860

Q38186783-01D56606-42EE-47CD-87E5-39CA21AE1DA3

Q38186783-02848453-BFE4-4DD1-87CE-5D86150F3B7C

Q38186783-038CA2A0-F6D7-4C33-83D7-903ACBB3136F

Q38186783-04A13B93-4EF1-4A13-AC95-4699E4BD387E

Q38186783-04F056DA-B9F9-437A-B582-002BC71301C6

Q38186783-06466A03-2F98-4DB9-AD9C-99DB72D5A879

Q38186783-087D232E-361B-4339-9114-EB79E3E0E320

Q38186783-0A886B3A-ADEB-4E3B-976D-78A4D9E446E6

Q38186783-0B174309-4AD6-4EB9-952A-E2FB30C64647

Q38186783-0C00ADDC-3D24-4A19-A56F-B5DD9879F05F

P304

Q38186783-73CC484F-417D-4200-9363-CDDD31D16CC5

P31

Q38186783-0DE8AFAA-A41D-44C5-8A8A-8251DA445523

P356

Q38186783-42BFBE2F-B841-4DBE-8876-89AF3339B398

P433

Q38186783-02718A4C-AE7D-445E-A0D4-08414B076949

P478

Q38186783-5BE2A222-0DE8-438C-A613-C65704B14819

P50

Q38186783-578DEAA6-DF33-4CE6-A3E9-DBC906003902

P577

Q38186783-1C0ADA1E-CCCE-4332-A26F-A97497B46D5A

P698

Q38186783-08C667BE-FDEE-47E7-A74D-B450D3458E8D

P921

Q38186783-06A466B1-8C58-4A8B-B994-F25CD30FC85E

Q38186783-9324AA8A-4FAA-44E2-8254-C3077B855913

P932

Q38186783-F04C390F-16FC-462E-A689-6624D33FD37C

P356

P1433

Antioxidants & Redox Signaling

P1476

Iron in neurodegenerative diso ...... orders and Parkinson's disease

@en

P2093

Amber Beserra

http://www.w3.org/2001/XMLSchema#string

Katharine Horback

http://www.w3.org/2001/XMLSchema#string

Matthew K McElwee

http://www.w3.org/2001/XMLSchema#string

Neena Singh

http://www.w3.org/2001/XMLSchema#string

Swati Haldar

http://www.w3.org/2001/XMLSchema#string

P2860

DJ-1 is a redox-dependent molecular chaperone that inhibits alpha-synuclein aggregate formation

Missing pieces in the Parkinson's disease puzzle

Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase

Parkin functions as an E2-dependent ubiquitin- protein ligase and promotes the degradation of the synaptic vesicle-associated protein, CDCrel-1

Leucine-rich repeat kinase 2 (LRRK2) interacts with parkin, and mutant LRRK2 induces neuronal degeneration.

Previously uncharacterized isoforms of divalent metal transporter (DMT)-1: implications for regulation and cellular function

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism

Leucine-Rich Repeat Kinase 2 interacts with Parkin, DJ-1 and PINK-1 in a Drosophila melanogaster model of Parkinson's disease

Hereditary early-onset Parkinson's disease caused by mutations in PINK1

P304

471-484

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1089/ARS.2014.5874

http://www.w3.org/2001/XMLSchema#string

P433

3

http://www.w3.org/2001/XMLSchema#string

P478

21

http://www.w3.org/2001/XMLSchema#string

P50

Ajai K. Tripathi

P577

2014-02-27T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

24512387

http://www.w3.org/2001/XMLSchema#string

P921

neurodegeneration

Prion protein family

P932

4076993

http://www.w3.org/2001/XMLSchema#string