(Q34332541)

1 August 2017

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title

TorsinA: movement at many levels (English)

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1 August 2017

author

Xandra O. Breakefield

series ordinal

object named as

Breakefield XO

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1 August 2017

Kamm C

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1 August 2017

Hanson PI

series ordinal

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1 August 2017

language of work or name

English

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publication date

1 July 2001

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1 August 2017

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1 August 2017

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1 August 2017

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1 August 2017

page(s)

9-12

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Traffic jam: a compendium of human diseases that affect intracellular transport processes

1 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900350-6

7 January 2021

The dynein heavy chain: structure, mechanics and evolution

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https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900350-6

7 January 2021

Mutations in ooc-5 and ooc-3 disrupt oocyte formation and the reestablishment of asymmetric PAR protein localization in two-cell Caenorhabditis elegans embryos

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900350-6

7 January 2021

The DYT1 phenotype and guidelines for diagnostic testing

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900350-6

7 January 2021

Structure and conformational changes in NSF and its membrane receptor complexes visualized by quick-freeze/deep-etch electron microscopy

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900350-6

7 January 2021

Mutant torsinA, responsible for early-onset torsion dystonia, forms membrane inclusions in cultured neural cells

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900350-6

7 January 2021

A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia

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https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900350-6

7 January 2021

Human deafness dystonia syndrome is a mitochondrial disease

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https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900350-6

7 January 2021

Stimulation of erythropoiesis by inhibiting a new hematopoietic death receptor in transgenic zebrafish

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https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900350-6

7 January 2021

Up-regulation of nuclear and mitochondrial genes in the skeletal muscle of mice lacking the heart/muscle isoform of the adenine nucleotide translocator

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900350-6

7 January 2021

The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900350-6

7 January 2021

The TOR1A (DYT1) gene family and its role in early onset torsion dystonia

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900350-6

7 January 2021

Hereditary progressive dystonia with marked diurnal fluctuation

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900350-6

7 January 2021

Cellular defenses against unfolded proteins: a cell biologist thinks about neurodegenerative diseases

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https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900350-6

7 January 2021

AAA proteins. Lords of the ring

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https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900350-6

7 January 2021

Posttranslational quality control: folding, refolding, and degrading proteins.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900350-6

7 January 2021

10.1016/S0896-6273(01)00350-6

Identifiers

DOI

1 reference

1 August 2017

1 reference