(Q50277786)

28 February 2018

title

In cis autosomal dominant mutation of Senataxin associated with tremor/ataxia syndrome. (English)

1 reference

28 February 2018

author name string

A G Bassuk

1

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28 February 2018

Y Z Chen

2

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28 February 2018

S D Batish

3

1 reference

28 February 2018

N Nagan

4

1 reference

28 February 2018

P Opal

5

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28 February 2018

P F Chance

6

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28 February 2018

C L Bennett

7

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28 February 2018

publication date

10 November 2006

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28 February 2018

published in

Neurogenetics

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28 February 2018

volume

8

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28 February 2018

issue

1

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28 February 2018

page(s)

45-49

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28 February 2018

https://scigraph.springernature.com/pub.10.1007/s10048-006-0067-8

exact match

0 references

cites work

SEN1, a positive effector of tRNA-splicing endonuclease in Saccharomyces cerevisiae

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10048-006-0067-8

The putative nucleic acid helicase Sen1p is required for formation and stability of termini and for maximal rates of synthesis and levels of accumulation of small nucleolar RNAs in Saccharomyces cerevisiae

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10048-006-0067-8

The yeast SEN3 gene encodes a regulatory subunit of the 26S proteasome complex required for ubiquitin-dependent protein degradation in vivo

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10048-006-0067-8

Autosomal dominant juvenile amyotrophic lateral sclerosis.

21 January 2018

1 reference

12 December 2020

The yeast SEN1 gene is required for the processing of diverse RNA classes

1 reference

12 December 2020

Autosomal recessive ataxia with peripheral neuropathy and elevated AFP: novel mutations in SETX.

1 reference

12 December 2020

Inactivation of the yeast Sen1 protein affects the localization of nucleolar proteins

1 reference

12 December 2020

Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2.

1 reference

12 December 2020

Frequency and phenotypic spectrum of ataxia with oculomotor apraxia 2: a clinical and genetic study in 18 patients.

1 reference

12 December 2020

Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study.

1 reference

12 December 2020

DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4)

1 reference

12 December 2020

Screening for connexin 32 mutations in Charcot-Marie-Tooth disease families with possible X-linked inheritance

1 reference

12 December 2020

Mutations affecting the tRNA-splicing endonuclease activity of Saccharomyces cerevisiae

1 reference

12 December 2020

Multiple protein/protein and protein/RNA interactions suggest roles for yeast DNA/RNA helicase Sen1p in transcription, transcription-coupled DNA repair and RNA processing

1 reference

12 December 2020

Mutations in senataxin responsible for Quebec cluster of ataxia with neuropathy

1 reference

12 December 2020

Senataxin, the yeast Sen1p orthologue: characterization of a unique protein in which recessive mutations cause ataxia and dominant mutations cause motor neuron disease

1 reference

12 December 2020

Inverse thinking about double mutants of enzymes

1 reference

12 December 2020

The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin

1 reference

12 December 2020

10.1007/S10048-006-0067-8

Identifiers

DOI

1 reference

28 February 2018

PubMed ID

17096168

1 reference

28 February 2018