Riboflavin Responsive Mitochondrial Dysfunction in Neurodegenerative Diseases.

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Update on riboflavin and multiple sclerosis: a systematic review.FAD influx enhances neuronal differentiation of human neural stem cells by facilitating nuclear localization of LSD1.

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Riboflavin Responsive Mitochondrial Dysfunction in Neurodegenerative Diseases.

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http://www.wikidata.org/entity/Q39285651

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

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2017年論文

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2017年論文

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2017年論文

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2017年論文

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2017年论文

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2017年论文

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2017年论文

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name

Riboflavin Responsive Mitochondrial Dysfunction in Neurodegenerative Diseases.

@en

Riboflavin Responsive Mitochondrial Dysfunction in Neurodegenerative Diseases.

@nl

type

Item

label

Riboflavin Responsive Mitochondrial Dysfunction in Neurodegenerative Diseases.

@en

Riboflavin Responsive Mitochondrial Dysfunction in Neurodegenerative Diseases.

@nl

prefLabel

Riboflavin Responsive Mitochondrial Dysfunction in Neurodegenerative Diseases.

@en

Riboflavin Responsive Mitochondrial Dysfunction in Neurodegenerative Diseases.

@nl

P1476

Riboflavin Responsive Mitochondrial Dysfunction in Neurodegenerative Diseases

@en

P2093

Henry Houlden

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

Mohan Rajeshwari

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

Perumal Varalakshmi

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

Tamilarasan Udhayabanu

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

P2860

Brown-Vialetto-Van Laere syndrome

Cytochrome c oxidase and mitochondrial F1F0-ATPase (ATP synthase) activities in platelets and brain from patients with Alzheimer's disease

Brown-Vialetto-Van Laere syndrome, a ponto-bulbar palsy with deafness, is caused by mutations in c20orf54

Brown-Vialetto-Van Laere and Fazio Londe syndrome is associated with a riboflavin transporter defect mimicking mild MADD: a new inborn error of metabolism with potential treatment

INTRAMITOCHONDRIAL FIBERS WITH DNA CHARACTERISTICS. I. FIXATION AND ELECTRON STAINING REACTIONS

The structure and properties of methylenetetrahydrofolate reductase from Escherichia coli suggest how folate ameliorates human hyperhomocysteinemia

Riboflavin uptake and FAD synthesis in Saccharomyces cerevisiae mitochondria: involvement of the Flx1p carrier in FAD export.

SLC52A2 [p.P141T] and SLC52A3 [p.N21S] causing Brown-Vialetto-Van Laere Syndrome in an Indian patient: First genetically proven case with mutations in two riboflavin transporters

The chemical and biological versatility of riboflavin

Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria

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scholarly article

P356

10.3390/JCM6050052

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Andreea Manole

Balasubramaniem Ashokkumar

P577

2017-05-05T00:00:00Z

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28475111

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P921

neurodegeneration

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5447943

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Riboflavin Responsive Mitochondrial Dysfunction in Neurodegenerative Diseases.

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P2860

P2860

Riboflavin Responsive Mitochondrial Dysfunction in Neurodegenerative Diseases.

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P1433

P1476

P2093

P2860

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P1476

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P31

P356

P433

P478

P50

P577

P698

P921

P932