(Q35172288)

6 August 2017

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title

Disruption of cellular transport: a common cause of neurodegeneration? (English)

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6 August 2017

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Andrew H Crosby

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6 August 2017

publication date

1 May 2003

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6 August 2017

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6 August 2017

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6 August 2017

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6 August 2017

page(s)

311-316

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Molecular basis of inherited spastic paraplegias

6 August 2017

cites work

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7 January 2021

Is the transportation highway the right road for hereditary spastic paraplegia?

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7 January 2021

Progressive spastic paraparesis: hereditary spastic paraplegia and its relation to primary and amyotrophic lateral sclerosis

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7 January 2021

Hereditary (familial) spastic paraplegia; further clinical and pathologic observations.

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7 January 2021

Familial amyotrophic lateral sclerosis

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7 January 2021

Mitochondria and degenerative disorders

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7 January 2021

Endocytic traffic in polarized epithelial cells: role of the actin and microtubule cytoskeleton

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7 January 2021

Cruising along microtubule highways: how membranes move through the secretory pathway

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7 January 2021

Motor-cargo interactions: the key to transport specificity.

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7 January 2021

Mechanisms of trafficking in axons and dendrites: implications for development and neurodegeneration

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7 January 2021

Disruption of dynein/dynactin inhibits axonal transport in motor neurons causing late-onset progressive degeneration.

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7 January 2021

Cloning by insertional mutagenesis of a cDNA encoding Caenorhabditis elegans kinesin heavy chain

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7 January 2021

A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10)

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7 January 2021

Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta

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7 January 2021

Defective kinesin heavy chain behavior in mouse kinesin light chain mutants

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7 January 2021

SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia.

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7 January 2021

The Vps4p AAA ATPase regulates membrane association of a Vps protein complex required for normal endosome function

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7 January 2021

Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

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7 January 2021

Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics

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7 January 2021

The product of the ATM gene is a 370-kDa nuclear phosphoprotein

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7 January 2021

ATM immunolocalization in mouse neuronal endosomes: implications for ataxia-telangiectasia.

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7 January 2021

Further evidence that SPG3A gene mutations cause autosomal dominant hereditary spastic paraplegia

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7 January 2021

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

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7 January 2021

The dynamin family of mechanoenzymes: pinching in new places

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7 January 2021

The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis

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7 January 2021

A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2

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7 January 2021

Infantile-onset ascending hereditary spastic paralysis is associated with mutations in the alsin gene

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7 January 2021

Progress in the pathogenesis of amyotrophic lateral sclerosis

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7 January 2021

Differential expression of inflammation- and apoptosis-related genes in spinal cords of a mutant SOD1 transgenic mouse model of familial amyotrophic lateral sclerosis

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7 January 2021

Slowing of axonal transport is a very early event in the toxicity of ALS-linked SOD1 mutants to motor neurons

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7 January 2021

Going new places using an old MAP: tau, microtubules and human neurodegenerative disease.

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7 January 2021

Tau blocks traffic of organelles, neurofilaments, and APP vesicles in neurons and enhances oxidative stress

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7 January 2021

Tau proteins with frontotemporal dementia-17 mutations have both altered expression levels and phosphorylation profiles in differentiated neuroblastoma cells.

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7 January 2021

An R5L tau mutation in a subject with a progressive supranuclear palsy phenotype

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7 January 2021

Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

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7 January 2021

Mis-sense mutation Val&rarr;Ile in exon 17 of amyloid precursor protein gene in Japanese familial Alzheimer's disease

1 reference

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7 January 2021

Kinesin-mediated axonal transport of a membrane compartment containing beta-secretase and presenilin-1 requires APP

1 reference

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7 January 2021

https://api.crossref.org/works/10.1016%2FS1474-4422%2803%2900383-1

1 reference

7 January 2021

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

1 reference

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7 January 2021

Identification and localization of huntingtin in brain and human lymphoblastoid cell lines with anti-fusion protein antibodies

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7 January 2021

Huntingtin-associated protein 1 interacts with hepatocyte growth factor-regulated tyrosine kinase substrate and functions in endosomal trafficking

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2803%2900383-1

7 January 2021

HIP14, a novel ankyrin domain-containing protein, links huntingtin to intracellular trafficking and endocytosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2803%2900383-1

7 January 2021

Huntingtin-associated protein 1 (HAP1) interacts with the p150Glued subunit of dynactin

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2803%2900383-1

7 January 2021

Function of Hrs in endocytic trafficking and signalling

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https://api.crossref.org/works/10.1016%2FS1474-4422%2803%2900383-1

7 January 2021

Hrs interacts with sorting nexin 1 and regulates degradation of epidermal growth factor receptor

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7 January 2021

Hrs and hbp: possible regulators of endocytosis and exocytosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2803%2900383-1

7 January 2021

Wild-type and mutant huntingtins function in vesicle trafficking in the secretory and endocytic pathways

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2803%2900383-1

7 January 2021

Toxic proteins in neurodegenerative disease

1 reference

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7 January 2021

10.1016/S1474-4422(03)00383-1

Identifiers

DOI

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6 August 2017

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