(Q40836565)

24 September 2017

Parkin expression in the adult mouse brain (English)

1 reference

24 September 2017

C C Stichel

1

1 reference

24 September 2017

M Augustin

2

1 reference

24 September 2017

K Kühn

3

1 reference

24 September 2017

X R Zhu

4

1 reference

24 September 2017

P Engels

5

1 reference

24 September 2017

C Ullmer

6

1 reference

24 September 2017

H Lübbert

7

1 reference

24 September 2017

language of work or name

English

0 references

publication date

1 December 2000

1 reference

European Journal of Neuroscience

24 September 2017

1 reference

24 September 2017

12

1 reference

24 September 2017

4181-4194

1 reference

24 September 2017

12

1 reference

A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease

24 September 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2000.01314.X

Protein synthesis in axons and terminals: significance for maintenance, plasticity and regulation of phenotype. With a critique of slow transport theory

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2000.01314.X

Estrogen receptors in dendrites and axon terminals in the guinea pig hypothalamus

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2000.01314.X

Fast transport and retrograde movement of huntingtin and HAP 1 in axons.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2000.01314.X

Cloning and distribution of the rat parkin mRNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2000.01314.X

Analysis of the subcellular localization of huntingtin with a set of rabbit polyclonal antibodies in cultured mammalian cells of neuronal origin: comparison with the distribution of huntingtin in Huntington's disease autopsy brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2000.01314.X

Point mutations (Thr240Arg and Gln311Stop) [correction of Thr240Arg and Ala311Stop] in the Parkin gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2000.01314.X

Identification and distribution of Parkin in rat brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2000.01314.X

Pathology of Parkinson's disease. Changes other than the nigrostriatal pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2000.01314.X

alpha-Synuclein is expressed in a variety of brain tumors showing neuronal differentiation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2000.01314.X

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2000.01314.X

Molecular cloning, gene expression, and identification of a splicing variant of the mouse parkin gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2000.01314.X

The ubiquitin pathway in Parkinson's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2000.01314.X

Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. The European Consortium on Genetic Susceptibility in Parkinson's Disease and the French Parkinson's Disease Genetics Study Gro

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2000.01314.X

Dopaminergic loss and inclusion body formation in alpha-synuclein mice: implications for neurodegenerative disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2000.01314.X

Autosomal-recessive juvenile parkinsonism in a Jewish Yemenite kindred: mutation of Parkin gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2000.01314.X

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2000.01314.X

Immunohistochemical and subcellular localization of Parkin protein: absence of protein in autosomal recessive juvenile parkinsonism patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2000.01314.X

Ultrastructure of PkC(II/III)-immunopositive structures in rat primary visual cortex

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2000.01314.X

Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson's Disease Genetics Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2000.01314.X

10.1111/J.1460-9568.2000.01314.X

21 January 2018

Identifiers

DOI

1 reference

24 September 2017

1 reference