Exfoliation Syndrome: A Disease of Autophagy and LOXL1 Proteopathy.

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Exfoliation Syndrome: A Disease of Autophagy and LOXL1 Proteopathy.

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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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Exfoliation Syndrome: A Disease of Autophagy and LOXL1 Proteopathy.

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Exfoliation Syndrome: A Disease of Autophagy and LOXL1 Proteopathy.

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Item

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Exfoliation Syndrome: A Disease of Autophagy and LOXL1 Proteopathy.

@en

Exfoliation Syndrome: A Disease of Autophagy and LOXL1 Proteopathy.

@nl

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Exfoliation Syndrome

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Exfoliation Syndrome: A Disease of Autophagy and LOXL1 Proteopathy.

@en

Exfoliation Syndrome: A Disease of Autophagy and LOXL1 Proteopathy.

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P1476

Exfoliation Syndrome: A Disease of Autophagy and LOXL1 Proteopathy.

@en

P2093

Audrey M Bernstein

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J Mario Wolosin

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Robert Ritch

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P2860

Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update

Beclin1 controls the levels of p53 by regulating the deubiquitination activity of USP10 and USP13

Autophagy, mitochondria and oxidative stress: cross-talk and redox signalling

Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa

Shattuck lecture--neurodegenerative diseases and prions

Protein degradation by the ubiquitin-proteasome pathway in normal and disease states

Inducible proteopathies

Spectrum of ABCR gene mutations in autosomal recessive macular dystrophies

Intracellular clusterin causes juxtanuclear aggregate formation and mitochondrial alteration

Major review: Exfoliation syndrome; advances in disease genetics, molecular biology, and epidemiology.

P304

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P31

scholarly article

P356

10.1097/IJG.0000000000000919

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P577

2018-03-15T00:00:00Z

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P698

29547474

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P932

6028293

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