(Q28306319)

2

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Simone M Sauter

3

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Anne Rauber

4

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Paula C Byrne

5

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Juergen Neesen

6

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Wolfgang Engel

https://scigraph.springernature.com/pub.10.1007/s10048-006-0034-4

7

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language of work or name

English

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publication date

May 2006

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published in

Neurogenetics

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volume

7

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issue

2

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page(s)

93-103

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exact match

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cites work

Novel mutations in spastin gene and absence of correlation with age at onset of symptoms

1 reference

https://api.crossref.org/works/10.1007%2FS10048-006-0034-4

The mouse SKD1, a homologue of yeast Vps4p, is required for normal endosomal trafficking and morphology in mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-006-0034-4

The cellular and molecular pathology of the motor system in hereditary spastic paraparesis due to mutation of the spastin gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-006-0034-4

SPG15, a new locus for autosomal recessive complicated HSP on chromosome 14q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-006-0034-4

Neuronal differentiation is accompanied by NSP-C expression

21 January 2018

1 reference

12 December 2020

The hereditary spastic paraplegia protein spastin interacts with the ESCRT-III complex-associated endosomal protein CHMP1B.

1 reference

12 December 2020

Cloning of a novel member of the reticulon gene family (RTN3): gene structure and chromosomal localization to 11q13

1 reference

12 December 2020

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

1 reference

12 December 2020

The hereditary spastic paraplegias: nine genes and counting

1 reference

12 December 2020

Improved method for high efficiency transformation of intact yeast cells

1 reference

12 December 2020

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

1 reference

12 December 2020

Strümpell's familial spastic paraplegia: genetics and neuropathology

1 reference

12 December 2020

Classification of the hereditary ataxias and paraplegias

1 reference

12 December 2020

Science in motion: common molecular pathological themes emerge in the hereditary spastic paraplegias

1 reference

12 December 2020

Identification of nuclear localisation sequences in spastin (SPG4) using a novel Tetra-GFP reporter system

1 reference

12 December 2020

Hereditary spastic paraplegia caused by mutations in the SPG4 gene

1 reference

12 December 2020

Neuroendocrine-specific protein C (NSP-C): subcellular localization and differential expression in relation to NSP-A

1 reference

12 December 2020

The hereditary spastic paraplegia gene, spastin, regulates microtubule stability to modulate synaptic structure and function.

1 reference

12 December 2020

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

1 reference

12 December 2020

Reticulon3 expression in rat optic and olfactory systems.

1 reference

12 December 2020

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

1 reference

12 December 2020

NIPA1 Gene Mutations Cause Autosomal Dominant Hereditary Spastic Paraplegia (SPG6)

1 reference

12 December 2020

A reticular rhapsody: phylogenic evolution and nomenclature of the RTN/Nogo gene family

1 reference

12 December 2020

Nogo and its paRTNers

1 reference

12 December 2020

Phylogenetic analysis of AAA proteins

1 reference

12 December 2020

Hereditary spastic paraparesis: disrupted intracellular transport associated with spastin mutation

1 reference

12 December 2020

Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia

1 reference

12 December 2020

The AAA team: related ATPases with diverse functions

1 reference

12 December 2020

Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis

1 reference

12 December 2020

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

1 reference

12 December 2020

Reticulon 1-C/neuroendocrine-specific protein-C interacts with SNARE proteins.

1 reference

12 December 2020

Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia

1 reference

12 December 2020

Advances in hereditary spastic paraplegia.

1 reference

12 December 2020

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

1 reference

12 December 2020

Cellular Localization, Oligomerization, and Membrane Association of the Hereditary Spastic Paraplegia 3A (SPG3A) Protein Atlastin

1 reference

12 December 2020

Spastin interacts with the centrosomal protein NA14, and is enriched in the spindle pole, the midbody and the distal axon

1 reference

12 December 2020

Mutations of SPG4 are responsible for a loss of function of spastin, an abundant neuronal protein localized in the nucleus

1 reference

12 December 2020

Xenopus embryos regulate the nuclear localization of XMyoD

1 reference

12 December 2020

Spastin subcellular localization is regulated through usage of different translation start sites and active export from the nucleus

1 reference

12 December 2020

Maspardin is mutated in mast syndrome, a complicated form of hereditary spastic paraplegia associated with dementia

1 reference

12 December 2020

The identification of a conserved domain in both spartin and spastin, mutated in hereditary spastic paraplegia

1 reference

12 December 2020

Three novel spastin (SPG4) mutations in families with autosomal dominant hereditary spastic paraplegia

1 reference

12 December 2020

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

1 reference

12 December 2020

Human reticulon 1-A and 1-B interact with a medium chain of the AP-2 adaptor complex

1 reference

12 December 2020

Linking axonal degeneration to microtubule remodeling by Spastin-mediated microtubule severing

1 reference

12 December 2020

Spastin gene mutation in Japanese with hereditary spastic paraplegia

1 reference

12 December 2020

Cloning and expression of alternative transcripts of a novel neuroendocrine-specific gene and identification of its 135-kDa translational product

1 reference

12 December 2020

Escrt-III: an endosome-associated heterooligomeric protein complex required for mvb sorting

1 reference

12 December 2020

NSP-encoded reticulons, neuroendocrine proteins of a novel gene family associated with membranes of the endoplasmic reticulum

1 reference

12 December 2020

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

1 reference

12 December 2020

Sequence analysis of the AAA protein family

1 reference

12 December 2020

SNAREpins: minimal machinery for membrane fusion

1 reference

12 December 2020

Mutation analysis of the spastin gene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia

1 reference

12 December 2020

Identification of katanin, an ATPase that severs and disassembles stable microtubules

1 reference

12 December 2020

A 200-amino acid ATPase module in search of a basic function

1 reference

12 December 2020