(Q44852329)

English

Intracellular ferritin accumulation in neural and extraneural tissue characterizes a neurodegenerative disease associated with a mutation in the ferritin light polypeptide gene

scientific article published in April 2004

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scholarly article

1 reference

Europe PubMed Central

6 December 2017

Intracellular ferritin accumulation in neural and extraneural tissue characterizes a neurodegenerative disease associated with a mutation in the ferritin light polypeptide gene (English)

1 reference

Europe PubMed Central

6 December 2017

neurodegeneration

1 reference

based on heuristic

inferred from title

author name string

Vidal R

1

1 reference

Europe PubMed Central

6 December 2017

Ghetti B

2

1 reference

Europe PubMed Central

6 December 2017

Takao M

3

1 reference

Europe PubMed Central

6 December 2017

Brefel-Courbon C

4

1 reference

Europe PubMed Central

6 December 2017

Uro-Coste E

5

1 reference

Europe PubMed Central

6 December 2017

Glazier BS

6

1 reference

Europe PubMed Central

6 December 2017

Siani V

7

1 reference

Europe PubMed Central

6 December 2017

Benson MD

8

1 reference

Europe PubMed Central

6 December 2017

Calvas P

9

1 reference

Europe PubMed Central

6 December 2017

Miravalle L

10

1 reference

Europe PubMed Central

6 December 2017

Rascol O

11

1 reference

Europe PubMed Central

6 December 2017

Delisle MB

12

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Europe PubMed Central

6 December 2017

publication date

1 April 2004

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Europe PubMed Central

6 December 2017

Journal of Neuropathology & Experimental Neurology

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Europe PubMed Central

6 December 2017

63

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Europe PubMed Central

6 December 2017

4

1 reference

Europe PubMed Central

6 December 2017

363-380

1 reference

Europe PubMed Central

6 December 2017

The ferritins: molecular properties, iron storage function and cellular regulation

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.4.363

21 January 2018

A mutation, in the iron-responsive element of H ferritin mRNA, causing autosomal dominant iron overload

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.4.363

21 January 2018

Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.4.363

21 January 2018

Hereditary ferritinopathy

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.4.363

21 January 2018

A decamer duplication in the 3' region of the BRI gene originates an amyloid peptide that is associated with dementia in a Danish kindred

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.4.363

21 January 2018

Neuroserpin, a brain-associated inhibitor of tissue plasminogen activator is localized primarily in neurons. Implications for the regulation of motor learning and neuronal survival

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.4.363

21 January 2018

ProFound: an expert system for protein identification using mass spectrometric peptide mapping information

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.4.363

21 January 2018

Application of multiple sequence alignment profiles to improve protein secondary structure prediction

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.4.363

21 January 2018

Ferritin and hemosiderin in pathological tissues

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.4.363

21 January 2018

Comparison of the three-dimensional structures of recombinant human H and horse L ferritins at high resolution

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.4.363

21 January 2018

Cooperativity of mutational effects within a six amino acid residues substitution that induces a major conformational change in human H ferritin

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.4.363

21 January 2018

Ferritin is a developmentally regulated nuclear protein of avian corneal epithelial cells.

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.4.363

21 January 2018

Intranuclear iron deposition in hepatocytes and renal tubular cells in mice treated with ferric nitrilotriacetate

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.4.363

21 January 2018

Characterization and accumulation of ferritin in hepatocyte nuclei of mice with iron overload

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.4.363

21 January 2018

Iron overload of the liver in the baboon. An ultrastructural study.

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.4.363

21 January 2018

Ferritoid, a Tissue-specific Nuclear Transport Protein for Ferritin in Corneal Epithelial Cells

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.4.363

21 January 2018

Neuroferritinopathy: a window on the role of iron in neurodegeneration.

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.4.363

21 January 2018

Neuroferritinopathy in a French family with late onset dominant dystonia

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.4.363

21 January 2018

Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.4.363

21 January 2018

Anemia and iron overload due to compound heterozygosity for novel ceruloplasmin mutations.

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.4.363

21 January 2018

Targeted deletion of the gene encoding iron regulatory protein-2 causes misregulation of iron metabolism and neurodegenerative disease in mice

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.4.363

21 January 2018

Identifiers

10.1093/JNEN/63.4.363

1 reference

Europe PubMed Central

6 December 2017

1 reference

Europe PubMed Central

6 December 2017

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