REEPing the benefits of an animal model of hereditary spastic paraplegia

about

Membrane-shaping disorders: a common pathway in axon degeneration Hereditary spastic paraplegia-linked REEP1 modulates endoplasmic reticulum/mitochondria contacts.

P2860

Q26852808-5BB032A4-A77D-4DAB-AF62-612043CFAA14 Q40707464-DABB3171-A770-4AEC-8287-DA0E1B50FB40

P2860

REEPing the benefits of an animal model of hereditary spastic paraplegia

Item

http://www.wikidata.org/entity/Q42020684

description

2013 nî lūn-bûn

@nan

2013年の論文

@ja

2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

2013年论文

@zh

2013年论文

@zh-cn

name

REEPing the benefits of an animal model of hereditary spastic paraplegia

@en

REEPing the benefits of an animal model of hereditary spastic paraplegia

@nl

type

Item

label

REEPing the benefits of an animal model of hereditary spastic paraplegia

@en

REEPing the benefits of an animal model of hereditary spastic paraplegia

@nl

prefLabel

REEPing the benefits of an animal model of hereditary spastic paraplegia

@en

REEPing the benefits of an animal model of hereditary spastic paraplegia

@nl

P1476

REEPing the benefits of an animal model of hereditary spastic paraplegia

@en

P2093

Ariel Y Deutch

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

Peter Hedera

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

P2860

Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12

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

Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31

Spastic paraplegia mutation N256S in the neuronal microtubule motor KIF5A disrupts axonal transport in a Drosophila HSP model

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

ER tubules mark sites of mitochondrial division

Hereditary spastic paraplegia-associated mutations in the NIPA1 gene and its Caenorhabditis elegans homolog trigger neural degeneration in vitro and in vivo through a gain-of-function mechanism

A spastic paraplegia mouse model reveals REEP1-dependent ER shaping.

REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31.

Sir Charles Sherrington's the integrative action of the nervous system: a centenary appreciation.

P304

4134-4136

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

P31

scholarly article

P356

10.1172/JCI72324

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

P407

English

P433

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

P478

123

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

P50

Roger J. Colbran

P577

2013-09-24T00:00:00Z

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

P698

24051371

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

P932

3784552

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

REEPing the benefits of an animal model of hereditary spastic paraplegia

about

P2860

P2860

REEPing the benefits of an animal model of hereditary spastic paraplegia

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932