(Q46011246)

18 December 2017

title

Identification and characterization of novel PDYN mutations in dominant cerebellar ataxia cases. (English)

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18 December 2017

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18 December 2017

Georgy Bakalkin

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18 December 2017

Alexandra Durr

object named as

Alexandra Durr

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18 December 2017

Alexis Brice

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18 December 2017

Michiel R Fokkens

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18 December 2017

Dineke S Verbeek

object named as

Dineke S Verbeek

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18 December 2017

author name string

Justyna Jezierska

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18 December 2017

Hiroyuki Watanabe

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18 December 2017

Fabien Zagnoli

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18 December 2017

Jérôme Kok

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18 December 2017

Jean-Yves Goas

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18 December 2017

Pierre Bertrand

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18 December 2017

Christophe Robin

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18 December 2017

publication date

8 March 2013

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18 December 2017

published in

Journal of Neurology

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18 December 2017

volume

260

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18 December 2017

issue

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18 December 2017

page(s)

1807-1812

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18 December 2017

Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS00415-013-6882-6

Prodynorphin mutations cause the neurodegenerative disorder spinocerebellar ataxia type 23.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-013-6882-6

Expansion of Intronic GGCCTG Hexanucleotide Repeat in NOP56 Causes SCA36, a Type of Spinocerebellar Ataxia Accompanied by Motor Neuron Involvement

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-013-6882-6

TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-013-6882-6

A conserved eEF2 coding variant in SCA26 leads to loss of translational fidelity and increased susceptibility to proteostatic insult

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-013-6882-6

Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-013-6882-6

Mutations in KCND3 cause spinocerebellar ataxia type 22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-013-6882-6

Endogenous Opioids: Biology and Function

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-013-6882-6

Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-013-6882-6

Prodynorphin storage and processing in axon terminals and dendrites

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-013-6882-6

The posttranslational processing of prodynorphin in the rat anterior pituitary.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-013-6882-6

Big dynorphin, a prodynorphin-derived peptide produces NMDA receptor-mediated effects on memory, anxiolytic-like and locomotor behavior in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-013-6882-6

Translocation of dynorphin neuropeptides across the plasma membrane. A putative mechanism of signal transmission

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-013-6882-6

Pronociceptive role of dynorphins in uninjured animals: N-ethylmaleimide-induced nociceptive behavior mediated through inhibition of dynorphin degradation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-013-6882-6

The frequency of spinocerebellar ataxia type 23 in a UK population.

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23471613

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Prodynorphin transcripts and proteins differentially expressed and regulated in the adult human brain.

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23471613

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Mutations in the PDYN gene (SCA23) are not a frequent cause of dominant ataxia in Central Europe

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23471613

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S00415-013-6882-6

1 reference

18 December 2017

1 reference

18 December 2017