Zebrafish atlastin controls motility and spinal motor axon architecture via inhibition of the BMP pathway. - Wikidata - wikimedia - TriplyDB

Zebrafish atlastin controls motility and spinal motor axon architecture via inhibition of the BMP pathway.

Zebrafish atlastin controls motility and spinal motor axon architecture via inhibition of the BMP pathway.

http://www.wikidata.org/entity/Q34142763

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CLP1 founder mutation links tRNA splicing and maturation to cerebellar development and neurodegeneration Identification and functional analysis of a SLC33A1: c.339T>G (p.Ser113Arg) variant in the original SPG42 family Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegia Function Over Form: Modeling Groups of Inherited Neurological Conditions in Zebrafish The Crossroads of Synaptic Growth Signaling, Membrane Traffic and Neurological Disease: Insights from Drosophila BMP signaling in axon regeneration The Wnt and BMP families of signaling morphogens at the vertebrate neuromuscular junction Adaptor protein complexes AP-4 and AP-5: new players in endosomal trafficking and progressive spastic paraplegia Growth differentiation factor 6 as a putative risk factor in neuromuscular degeneration Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders An ESCRT-spastin interaction promotes fission of recycling tubules from the endosome.Spastin, atlastin, and ER relocalization are involved in axon but not dendrite regeneration.Emerging aspects of ER organization in root hair tip growth: lessons from RHD3 and Atlastin.Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms.Souffle/Spastizin controls secretory vesicle maturation during zebrafish oogenesis.Targeted high-throughput sequencing identifies mutations in atlastin-1 as a cause of hereditary sensory neuropathy type I.Mechanisms of disease in hereditary sensory and autonomic neuropathies.Pharmacologic rescue of axon growth defects in a human iPSC model of hereditary spastic paraplegia SPG3A.Axonal Transport Defects in a Mitofusin 2 Loss of Function Model of Charcot-Marie-Tooth Disease in Zebrafish.Comparison of human and Drosophila atlastin GTPases Fusing a lasting relationship between ER tubules.Membrane fusion by the GTPase atlastin requires a conserved C-terminal cytoplasmic tail and dimerization through the middle domain.ER network formation and membrane fusion by atlastin1/SPG3A disease variants.Weaving the web of ER tubules Hereditary spastic paraplegia-causing mutations in atlastin-1 interfere with BMPRII trafficking.Knockdown of Pnpla6 protein results in motor neuron defects in zebrafish.The effects of ER morphology on synaptic structure and function in Drosophila melanogaster.A newly discovered member of the Atlastin family, BmAtlastin-n, has an antiviral effect against BmNPV in Bombyx mori Spartin regulates synaptic growth and neuronal survival by inhibiting BMP-mediated microtubule stabilization.S113R mutation in SLC33A1 leads to neurodegeneration and augmented BMP signaling in a mouse model.Quantitative proteomics reveal proteins enriched in tubular endoplasmic reticulum of Saccharomyces cerevisiae Hereditary spastic paraplegias: membrane traffic and the motor pathway.Cellular pathways of hereditary spastic paraplegia.Fishing for causes and cures of motor neuron disorders.Bone morphogenetic protein signaling in vertebrate motor neurons and neuromuscular communication.Modeling Axonal Defects in Hereditary Spastic Paraplegia with Human Pluripotent Stem Cells.The hereditary spastic paraplegia protein strumpellin: characterisation in neurons and of the effect of disease mutations on WASH complex assembly and function.Reticulon-like-1, the Drosophila orthologue of the hereditary spastic paraplegia gene reticulon 2, is required for organization of endoplasmic reticulum and of distal motor axons.Planar polarity pathway and Nance-Horan syndrome-like 1b have essential cell-autonomous functions in neuronal migration.Pathogenesis of autosomal dominant hereditary spastic paraplegia (SPG6) revealed by a rat model.

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P2860

Zebrafish atlastin controls motility and spinal motor axon architecture via inhibition of the BMP pathway.

http://www.wikidata.org/entity/Q34142763

description

2010 nî lūn-bûn

@nan

2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

Zebrafish atlastin controls mo ...... inhibition of the BMP pathway.

@ast

Zebrafish atlastin controls mo ...... inhibition of the BMP pathway.

@en

Zebrafish atlastin controls mo ...... inhibition of the BMP pathway.

@nl

type

label

Zebrafish atlastin controls mo ...... inhibition of the BMP pathway.

@ast

Zebrafish atlastin controls mo ...... inhibition of the BMP pathway.

@en

Zebrafish atlastin controls mo ...... inhibition of the BMP pathway.

@nl

prefLabel

Zebrafish atlastin controls mo ...... inhibition of the BMP pathway.

@ast

Zebrafish atlastin controls mo ...... inhibition of the BMP pathway.

@en

Zebrafish atlastin controls mo ...... inhibition of the BMP pathway.

@nl

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Nature Neuroscience

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Zebrafish atlastin controls mo ...... inhibition of the BMP pathway.

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P2093

Andrew Lumsden

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

Fatiha Nothias

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James A Hutt

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

Jamilé Hazan

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P2860

The reticulons: a family of proteins with diverse functions

Modeling spinal muscular atrophy in Drosophila

Cellular localization, oligomerization, and membrane association of the hereditary spastic paraplegia 3A (SPG3A) protein atlastin

Atlastin GTPases are required for Golgi apparatus and ER morphogenesis.

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

A Drosophila model of ALS: human ALS-associated mutation in VAP33A suggests a dominant negative mechanism

Stages of embryonic development of the zebrafish

Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia

SPG3A protein atlastin-1 is enriched in growth cones and promotes axon elongation during neuronal development

Dorsomorphin inhibits BMP signals required for embryogenesis and iron metabolism

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1380-1387

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scholarly article

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10.1038/NN.2662

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11

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13

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Steffen Scholpp

Sylvie Schneider-Maunoury

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2010-10-10T00:00:00Z

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47384803

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1007048076

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20935645

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