Peroxisome biogenesis disorders.

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Peroxisome biogenesis disorders.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年學術文章

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2016年學術文章

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name

Peroxisome biogenesis disorders.

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Peroxisome biogenesis disorders.

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Item

label

Peroxisome biogenesis disorders.

@en

Peroxisome biogenesis disorders.

@nl

prefLabel

Peroxisome biogenesis disorders.

@en

Peroxisome biogenesis disorders.

@nl

P1476

Peroxisome biogenesis disorders.

@en

P2093

Catherine Argyriou

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

Maria Daniela D'Agostino

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Nancy Braverman

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P2860

Expression of PEX11beta mediates peroxisome proliferation in the absence of extracellular stimuli

Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.

3-Hydroxy-3-methylglutaryl coenzyme A lyase: targeting and processing in peroxisomes and mitochondria

Peroxisome synthesis in the absence of preexisting peroxisomes

Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly

Purification, molecular cloning, and expression of 2-hydroxyphytanoyl-CoA lyase, a peroxisomal thiamine pyrophosphate-dependent enzyme that catalyzes the carbon-carbon bond cleavage during alpha-oxidation of 3-methyl-branched fatty acids

Mutations in the gene encoding peroxisomal alpha-methylacyl-CoA racemase cause adult-onset sensory motor neuropathy

PEX19 binds multiple peroxisomal membrane proteins, is predominantly cytoplasmic, and is required for peroxisome membrane synthesis

The human peroxisomal targeting signal receptor, Pex5p, is translocated into the peroxisomal matrix and recycled to the cytosol

Structure-function analysis of phytanoyl-CoA 2-hydroxylase mutations causing Refsum's disease

P304

111-144

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P31

scholarly article

P356

10.3233/TRD-160003

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P433

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P478

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P577

2016-11-07T00:00:00Z

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P698

29152457

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P932

5678237

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