PRKN, DJ-1, and PINK1 screening identifies novel splice site mutation in PRKN and two novel DJ-1 mutations.

about

Mutation in ADORA1 identified as likely cause of early-onset parkinsonism and cognitive dysfunction.Genetic insights into sporadic Parkinson's disease pathogenesis.Free radicals impair the anti-oxidative stress activity of DJ-1 through the formation of SDS-resistant dimer.

P2860

Q29347530-A2C21E13-0114-4517-BCDA-9BAFF7665421 Q37583402-E1539828-F268-48F7-A804-649F1452F82E Q51033505-710FD454-C2A4-4E87-8B9C-C2F9ED40B02A

P2860

PRKN, DJ-1, and PINK1 screening identifies novel splice site mutation in PRKN and two novel DJ-1 mutations.

Item

http://www.wikidata.org/entity/Q54612834

description

2010 nî lūn-bûn

@nan

2010年の論文

@ja

2010年学术文章

@wuu

2010年学术文章

@zh-cn

2010年学术文章

@zh-hans

2010年学术文章

@zh-my

2010年学术文章

@zh-sg

2010年學術文章

@yue

2010年學術文章

@zh

2010年學術文章

@zh-hant

name

PRKN, DJ-1, and PINK1 screenin ...... and two novel DJ-1 mutations.

@en

PRKN, DJ-1, and PINK1 screenin ...... and two novel DJ-1 mutations.

@nl

type

Item

label

PRKN, DJ-1, and PINK1 screenin ...... and two novel DJ-1 mutations.

@en

PRKN, DJ-1, and PINK1 screenin ...... and two novel DJ-1 mutations.

@nl

prefLabel

PRKN, DJ-1, and PINK1 screenin ...... and two novel DJ-1 mutations.

@en

PRKN, DJ-1, and PINK1 screenin ...... and two novel DJ-1 mutations.

@nl

P1476

PRKN, DJ-1, and PINK1 screenin ...... N and two novel DJ-1 mutations

@en

P2093

Elahe Elahi

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

Farzad Sina

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

Farzaneh Ghazavi

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

Gholam-Ali Shahidi

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

Homa Sadeghi

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

Khosro Parsa

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

Mohammad Hossein Kazemi

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

Mohammad Rohani

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

Mostafa Ronaghi

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

Nasser Ghaemi

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

P2860

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

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

The expression of DJ-1 (PARK7) in normal human CNS and idiopathic Parkinson's disease

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

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

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

The 1.6-A crystal structure of the class of chaperones represented by Escherichia coli Hsp31 reveals a putative catalytic triad

Crystal structure of human DJ-1, a protein associated with early onset Parkinson's disease

The 1.1-A resolution crystal structure of DJ-1, the protein mutated in autosomal recessive early onset Parkinson's disease

P304

80-89

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P31

scholarly article

P356

10.1002/MDS.23417

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

P407

English

P433

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

P478

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

P50

Sayed-Rzgar Hosseini

P577

2010-11-08T00:00:00Z

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

P5875

49836935

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

P698

21322020

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

PRKN, DJ-1, and PINK1 screening identifies novel splice site mutation in PRKN and two novel DJ-1 mutations.

about

P2860

P2860

PRKN, DJ-1, and PINK1 screening identifies novel splice site mutation in PRKN and two novel DJ-1 mutations.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P5875

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P5875

P698