(Q35770559)

10 August 2017

1 reference

title

Genetics of neurological disorders (English)

1 reference

10 August 2017

2

Salim Mottagui-Tabar

1 reference

10 August 2017

Mohammad Ali Faghihi

1

1 reference

PubMed ID

15137899

10 August 2017

Claes Wahlestedt

series ordinal

3

1 reference

10 August 2017

1 May 2004

1 reference

Expert Review of Molecular Diagnostics: new diagnostic technologies are set to revolutionise healthcare

10 August 2017

1 reference

10 August 2017

4

1 reference

10 August 2017

317-332

1 reference

10 August 2017

3

1 reference

Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum

10 August 2017

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Alzheimer's disease and Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Visualization of A beta 42(43) and A beta 40 in senile plaques with end-specific A beta monoclonals: evidence that an initially deposited species is A beta 42(43).

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Intramembrane proteolysis by presenilins

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Molecular basis of the neurodegenerative disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Genetic and host factors for dementia in Down's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Two transmembrane aspartates in presenilin-1 required for presenilin endoproteolysis and gamma-secretase activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

A novel mutation (G217D) in the Presenilin 1 gene ( PSEN1) in a Japanese family: presenile dementia and parkinsonism are associated with cotton wool plaques in the cortex and striatum

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

The amyloid hypothesis of Alzheimer's disease: progress and problems on the road to therapeutics

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Variability and validity of polymorphism association studies in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Alpha-2 macroglobulin is genetically associated with Alzheimer disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

A polymorphism in the cystatin C gene is a novel risk factor for late-onset Alzheimer's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

A novel polymorphism of the brain-derived neurotrophic factor (BDNF) gene associated with late-onset Alzheimer's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Genetic variation in a haplotype block spanningIDE influences Alzheimer disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Genetic association between Alzheimer disease and the alpha-synuclein gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Neuroinflammatory signaling upregulation in Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Genes, models and Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Antibody therapy for Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Set back to Alzheimer vaccine studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Apolipoprotein E gene in diffuse Lewy body disease with or without co-existing Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Parkinson disease in twins: an etiologic study

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

The genetics of disorders with synuclein pathology and parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Alpha-synuclein in Lewy bodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Mapping of a gene for Parkinson's disease to chromosome 4q21-q23

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Glial cytoplasmic inclusions in white matter oligodendrocytes of multiple system atrophy brains contain insoluble alpha-synuclein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Alpha synuclein promoter and risk of Parkinson's disease: microsatellite and allelic size variability

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

alpha-Synuclein locus triplication causes Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Parkin-deficient mice exhibit nigrostriatal deficits but not loss of dopaminergic neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Lack of nigral pathology in transgenic mice expressing human alpha-synuclein driven by the tyrosine hydroxylase promoter

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Mitochondrial pathology and apoptotic muscle degeneration in Drosophila parkin mutants

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

A Drosophila model of Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Dopaminergic neuronal loss and motor deficits in Caenorhabditis elegans overexpressing human alpha-synuclein

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Chaperones increase association of tau protein with microtubules

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

TorsinA and heat shock proteins act as molecular chaperones: suppression of alpha-synuclein aggregation

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Lewy bodies and parkinsonism in families with parkin mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Parkin's substrates and the pathways leading to neuronal damage

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

The ubiquitin pathway in Parkinson's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Effects of the mutations Ala30 to Pro and Ala53 to Thr on the physical and morphological properties of alpha-synuclein protein implicated in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

A susceptibility locus for Parkinson's disease maps to chromosome 2p13.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

21 January 2018

Genes and parkinsonism

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Parkin ubiquitinates the alpha-synuclein-interacting protein, synphilin-1: implications for Lewy-body formation in Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Inducible expression of mutant alpha-synuclein decreases proteasome activity and increases sensitivity to mitochondria-dependent apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

21 January 2018

Genetics of parkinsonism

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Chronic Parkinsonism in humans due to a product of meperidine-analog synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Alcohol consumption and the incidence of Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

The application of functional genomics to Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Pharmacogenomics for the treatment of dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Pharmacogenomics of psychiatric drug treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Pharmacogenomics in schizophrenia: the quest for individualized therapy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Candidate gene for the chromosome 1 familial Alzheimer's disease locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

A novel tau mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

A distinct familial presenile dementia with a novel missense mutation in the tau gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Cloning and characterization of three novel genes, ALS2CR1, ALS2CR2, and ALS2CR3, in the juvenile amyotrophic lateral sclerosis (ALS2) critical region at chromosome 2q33-q34: candidate genes for ALS2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Identification of two novel loci for dominantly inherited familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

Familial Aggregation of Parkinson's Disease in Iceland

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

A susceptibility gene for late-onset idiopathic Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.4.3.317

21 January 2018

Identifiers

DOI

10.1586/14737159.4.3.317

1 reference

10 August 2017

1 reference

PubMed ID

15137899