Sialic acid deficiency is associated with oxidative stress leading to muscle atrophy and weakness in GNE myopathy.

about

GNE myopathy: from clinics and genetics to pathology and research strategies.Fighting the Cause of Alzheimer's and GNE Myopathy

P2860

Q55268638-170464E4-2E0E-4E73-B6AF-0719D7AB065D Q58122164-433BCB8C-2F07-447A-AA26-F302D0D7AAF3

P2860

Sialic acid deficiency is associated with oxidative stress leading to muscle atrophy and weakness in GNE myopathy.

Item

http://www.wikidata.org/entity/Q38785817

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

@zh-cn

name

Sialic acid deficiency is asso ...... and weakness in GNE myopathy.

@en

type

Item

label

Sialic acid deficiency is asso ...... and weakness in GNE myopathy.

@en

prefLabel

Sialic acid deficiency is asso ...... and weakness in GNE myopathy.

@en

P1476

Sialic acid deficiency is asso ...... and weakness in GNE myopathy.

@en

P2093

Anna Cho

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

Ichizo Nishino

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

Ikuya Nonaka

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

May Christine

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

Miho Miyakawa

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

Satoru Noguchi

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

V Malicdan

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

P2860

UDP-GlcNAc 2-epimerase: a regulator of cell surface sialylation

Mutations in the human UDP-N-acetylglucosamine 2-epimerase gene define the disease sialuria and the allosteric site of the enzyme

Atrogin-1, a muscle-specific F-box protein highly expressed during muscle atrophy

Siglecs and immune regulation

Sialic acids in the brain: gangliosides and polysialic acid in nervous system development, stability, disease, and regeneration

ATP-dependent reduction of cysteine-sulphinic acid by S. cerevisiae sulphiredoxin.

VCP/p97 is essential for maturation of ubiquitin-containing autophagosomes and this function is impaired by mutations that cause IBMPFD

The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy

Relationship between human aging muscle and oxidative system pathway

Identification of ubiquitin ligases required for skeletal muscle atrophy

P304

3081-3093

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

P31

scholarly article

P356

10.1093/HMG/DDX192

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

P433

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

P478

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

P577

2017-05-13T00:00:00Z

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

P698

28505249

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

P932

6075185

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

Sialic acid deficiency is associated with oxidative stress leading to muscle atrophy and weakness in GNE myopathy.

about

P2860

P2860

Sialic acid deficiency is associated with oxidative stress leading to muscle atrophy and weakness in GNE myopathy.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P932