ER Dynamics and Derangement in Neurological Diseases.

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ER Dynamics and Derangement in Neurological 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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ER Dynamics and Derangement in Neurological Diseases.

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ER Dynamics and Derangement in Neurological Diseases.

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ER Dynamics and Derangement in Neurological Diseases.

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ER Dynamics and Derangement in Neurological Diseases.

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ER Dynamics and Derangement in Neurological Diseases.

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ER Dynamics and Derangement in Neurological Diseases.

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P1476

ER Dynamics and Derangement in Neurological Diseases.

@en

P2093

Nobuyuki Nukina

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Tomoyuki Yamanaka

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P2860

Interaction of two hereditary spastic paraplegia gene products, spastin and atlastin, suggests a common pathway for axonal maintenance

Rab18 and a Rab18 GEF complex are required for normal ER structure.

Hereditary spastic paraplegia proteins REEP1, spastin, and atlastin-1 coordinate microtubule interactions with the tubular ER network

A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis.

Rab10 GTPase regulates ER dynamics and morphology.

Role of syntaxin 18 in the organization of endoplasmic reticulum subdomains

A class of dynamin-like GTPases involved in the generation of the tubular ER network

Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy

Regulation of endoplasmic reticulum turnover by selective autophagy

There's Something Wrong with my MAM; the ER-Mitochondria Axis and Neurodegenerative Diseases

P304

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P31

scholarly article

P356

10.3389/FNINS.2018.00091

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P478

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P577

2018-02-20T00:00:00Z

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P698

29515361

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P932

5826232

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