(Q35871644)

10 August 2017

1 reference

title

Neurodegeneration caused by proteins with an aberrant carboxyl-terminus (English)

1 reference

10 August 2017

Marie Bernadette Delisle

object named as

Marie Bernadette Delisle

0 references

Bernardino F. Ghetti

series ordinal

3

object named as

Bernardino Ghetti

1 reference

10 August 2017

Ruben Vidal

1

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10 August 2017

1 August 2004

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Journal of Neuropathology & Experimental Neurology

10 August 2017

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10 August 2017

63

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10 August 2017

787-800

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10 August 2017

8

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10 August 2017

Conformational disease

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Protein aggregation: folding aggregates, inclusion bodies and amyloid

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

The cerebral proteopathies: neurodegenerative disorders of protein conformation and assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Protein folding and misfolding

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Unfolding the role of protein misfolding in neurodegenerative diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Familial conformational diseases and dementias

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Disordered proteins in dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

New familial forms of cerebral amyloid and dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Familial Presenile Dementia with Spastic Paralysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Familial cerebral amyloid angiopathy with nonneuritic amyloid plaque formation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Familial British dementia with amyloid angiopathy: early clinical, neuropsychological and imaging findings

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Cytoskeletal pathology in familial cerebral amyloid angiopathy (British type) with non-neuritic amyloid plaque formation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Regional distribution of amyloid-Bri deposition and its association with neurofibrillary degeneration in familial British dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Familial Danish dementia: a novel form of cerebral amyloidosis associated with deposition of both amyloid-Dan and amyloid-beta

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Ocular changes in heredo-oto-ophthalmo-encephalopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

A stop-codon mutation in the BRI gene associated with familial British dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Isolation of markers for chondro-osteogenic differentiation using cDNA library subtraction. Molecular cloning and characterization of a gene belonging to a novel multigene family of integral membrane proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

ITM2A is induced during thymocyte selection and T cell activation and causes downregulation of CD8 when overexpressed in CD4(+)CD8(+) double positive thymocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Furin mediates enhanced production of fibrillogenic ABri peptides in familial British dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Sequence, genomic structure and tissue expression of Human BRI3, a member of the BRI gene family

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Genomic organization and chromosomal localization of the Itm2a gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

cDNA sequence analysis, chromosomal assignment and expression pattern of the gene coding for integral membrane protein 2B.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Collagenase-3 (MMP-13) and integral membrane protein 2a (Itm2a) are marker genes of chondrogenic/osteoblastic cells in bone formation: sequential temporal, and spatial expression of Itm2a, alkaline phosphatase, MMP-13, and osteocalcin in the mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Identification of genes expressed in human CD34(+) hematopoietic stem/progenitor cells by expressed sequence tags and efficient full-length cDNA cloning

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Expression of mBRI2 in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Familial British dementia: colocalization of furin and ABri amyloid.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Expression of BRI, the normal precursor of the amyloid protein of familial British dementia, in human brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Axonal transport of British and Danish amyloid peptides via secretory vesicles

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Extensive analysis of the 13q14 region in human prostate tumors: DNA analysis and quantitative expression of genes lying in the interval of deletion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Proapoptotic activity of ITM2B(s), a BH3-only protein induced upon IL-2-deprivation which interacts with Bcl-2

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Induction of p53-independent apoptosis by the BH3-only protein ITM2Bs

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Subtractive hybridization reveals the expression of immunoglobulin-like transcript 7, Eph-B1, granzyme B, and 3 novel transcripts in human plasmacytoid dendritic cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

BRICHOS: a conserved domain in proteins associated with dementia, respiratory distress and cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Furin: a mammalian subtilisin/Kex2p-like endoprotease involved in processing of a wide variety of precursor proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Proteolytic processing in the secretory pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Expression of BRI-amyloid beta peptide fusion proteins: a novel method for specific high-level expression of amyloid beta peptides

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Systemic amyloid deposits in familial British dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Evidence for tissue-specific forms of glutaminyl cyclase.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Amino- and carboxyl-terminal heterogeneity of beta-amyloid peptides deposited in human brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

N-terminal heterogeneity of parenchymal and cerebrovascular Abeta deposits.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

The A beta 3-pyroglutamyl and 11-pyroglutamyl peptides found in senile plaque have greater beta-sheet forming and aggregation propensities in vitro than full-length A beta.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Effect of the disulfide bridge and the C-terminal extension on the oligomerization of the amyloid peptide ABri implicated in familial British dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Non-fibrillar oligomeric species of the amyloid ABri peptide, implicated in familial British dementia, are more potent at inducing apoptotic cell death than protofibrils or mature fibrils

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

pH-Dependent Amyloid and Protofibril Formation by the ABri Peptide of Familial British Dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Complement activation in chromosome 13 dementias. Similarities with Alzheimer's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Neuroferritinopathy in a French family with late onset dominant dystonia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Palatal tremor and cognitive decline in neuroferritinopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Molecular control of vertebrate iron metabolism: mRNA-based regulatory circuits operated by iron, nitric oxide, and oxidative stress

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Iron-sulfur clusters as biosensors of oxidants and iron

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Ferritin and the response to oxidative stress

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Structural description of the active sites of mouse L-chain ferritin at 1.2 A resolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Intranuclear neuronal inclusions: a common pathogenic mechanism for glutamine-repeat neurodegenerative diseases?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

The Worster-Drought syndrome and other syndromes of dementia with spastic paraparesis: the paradox of molecular pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

Hereditary ferritinopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F63.8.787

21 January 2018

Identifiers

DOI

10.1093/JNEN/63.8.787

1 reference

10 August 2017

1 reference

PubMed ID

15330334