(Q33347971)

26 July 2017

Positional cloning of the autosomal recessive juvenile parkinsonism (AR-JP) gene and its diversity in deletion mutations (English)

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26 July 2017

1 reference

parkinsonian syndrome

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Kitada T

1

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26 July 2017

Asakawa S

2

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26 July 2017

Matsumine H

3

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26 July 2017

Hattori N

4

1 reference

26 July 2017

Minoshima S

5

1 reference

26 July 2017

Shimizu N

6

1 reference

26 July 2017

Mizuno Y

7

1 reference

26 July 2017

1 December 1999

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26 July 2017

6

1 reference

Parkinsonism and Related Disorders

inferred from page(s)

published in

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26 July 2017

5

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26 July 2017

4

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26 July 2017

163-168

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Familial juvenile parkinsonism: clinical and pathologic study in a family.

26 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900032-2

7 January 2021

Paralysis agitans of early onset with marked diurnal fluctuation of symptoms

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900032-2

7 January 2021

Clinical analysis of 17 patients in 12 Japanese families with autosomal-recessive type juvenile parkinsonism.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900032-2

7 January 2021

New insights into the cause of Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900032-2

7 January 2021

Mitochondrial complex I deficiency in Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900032-2

7 January 2021

Biosynthesis and regulation of superoxide dismutases

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900032-2

7 January 2021

Structural dimorphism in the mitochondrial targeting sequence in the human manganese superoxide dismutase gene. A predictive evidence for conformational change to influence mitochondrial transport and a study of allelic association in Parkinson's di

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900032-2

7 January 2021

Early onset parkinsonism with diurnal fluctuation maps to a locus for juvenile parkinsonism.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900032-2

7 January 2021

A microdeletion of D6S305 in a family of autosomal recessive juvenile parkinsonism (PARK2).

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900032-2

7 January 2021

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900032-2

7 January 2021

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900032-2

1 reference

7 January 2021

The ubiquitin-proteasome proteolytic pathway

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900032-2

7 January 2021

Ubiquitin, proteasomes, and the regulation of intracellular protein degradation

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900032-2

7 January 2021

Identification and preliminary characterization of a protein motif related to the zinc finger

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900032-2

7 January 2021

Does this have a familiar RING?

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900032-2

7 January 2021

The PHD finger: implications for chromatin-mediated transcriptional regulation

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900032-2

7 January 2021

Molecular genetic analysis of a novelParkin gene in Japanese families with autosomal recessive juvenile parkinsonism: Evidence for variable homozygous deletions in theParkin gene in affected individuals

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900032-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900032-2

7 January 2021

Autosomal recessive juvenile parkinsonism maps to 6q25.2-q27 in four ethnic groups: detailed genetic mapping of the linked region

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900032-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900032-2

7 January 2021

Alz-50, ubiquitin and tau immunoreactivity of neurofibrillary tangles, Pick bodies and Lewy bodies.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900032-2

7 January 2021

The ubiquitin pathway in Parkinson's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900032-2

7 January 2021

Substrate specificity of deubiquitinating enzymes: ubiquitin C-terminal hydrolases

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900032-2

7 January 2021

Ubiquitin carboxyl-terminal hydrolase (PGP 9.5) is selectively present in ubiquitinated inclusion bodies characteristic of human neurodegenerative diseases.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900032-2

7 January 2021

The tails of ubiquitin precursors are ribosomal proteins whose fusion to ubiquitin facilitates ribosome biogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900032-2

7 January 2021

10.1016/S1353-8020(99)00032-2

Identifiers

DOI

1 reference

26 July 2017

1 reference