Pexophagy: Molecular Mechanisms and Implications for Health and Diseases.

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Overview of the Minireviews on Autophagy.

P2860

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Pexophagy: Molecular Mechanisms and Implications for Health and Diseases.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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name

Pexophagy: Molecular Mechanisms and Implications for Health and Diseases.

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Pexophagy: Molecular Mechanisms and Implications for Health and Diseases.

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type

Item

label

Pexophagy: Molecular Mechanisms and Implications for Health and Diseases.

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Pexophagy: Molecular Mechanisms and Implications for Health and Diseases.

@nl

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Pexophagy: Molecular Mechanisms and Implications for Health and Diseases.

@en

Pexophagy: Molecular Mechanisms and Implications for Health and Diseases.

@nl

P1476

Pexophagy: Molecular Mechanisms and Implications for Health and Diseases.

@en

P2093

Dong-Hyung Cho

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Doo Sin Jo

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

Eun-Kyeong Jo

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

Seong-Kyu Choe

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

Yi Sak Kim

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P2860

Comparative analysis of gene regulation by the transcription factor PPARalpha between mouse and human

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

Defective PEX gene products correlate with the protein import, biochemical abnormalities, and phenotypic heterogeneity in peroxisome biogenesis disorders

Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G

Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction

Homeostatic levels of p62 control cytoplasmic inclusion body formation in autophagy-deficient mice

p62/SQSTM1 is a target gene for transcription factor NRF2 and creates a positive feedback loop by inducing antioxidant response element-driven gene transcription

Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata

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55-64

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scholarly article

review article

P356

10.14348/MOLCELLS.2018.2245

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

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

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2018-01-23T00:00:00Z

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2018-01-31T00:00:00Z

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P698

29370694

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P921

Zellweger syndrome

membrane proteins

Achyolli

P932

5792714

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Pexophagy: Molecular Mechanisms and Implications for Health and Diseases.

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P2860

Pexophagy: Molecular Mechanisms and Implications for Health and Diseases.

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