Mouse models for neurological disease (Q35172443)

6 August 2017

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title

Mouse models for neurological disease (English)

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6 August 2017

4

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6 August 2017

Majid Hafezparast

1

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Nicholas W. Wood

object named as

Nicholas W Wood

series ordinal

3

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Elizabeth M. C. Fisher

series ordinal

5

object named as

Elizabeth M C Fisher

1 reference

6 August 2017

Azlina Ahmad-Annuar

2

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6 August 2017

publication date

1 August 2002

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6 August 2017

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6 August 2017

volume

1

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6 August 2017

issue

4

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6 August 2017

page(s)

215-224

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

6 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

AlaSOPro mutation in the gene encoding α-synuclein in Parkinson's disease

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7 January 2021

α-Synuclein in Lewy bodies

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7 January 2021

alpha-synuclein gene haplotypes are associated with Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Alpha-synuclein and neurodegenerative diseases

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

The alpha-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: a study of 230 European cases. European Consortium on Genetic Susceptibility in Parkinson's Disease

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Friedreich's ataxia: a clinical and genetic study of 90 families with an analysis of early diagnostic criteria and intrafamilial clustering of clinical features

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

A worldwide assessment of the frequency of suicide, suicide attempts, or psychiatric hospitalization after predictive testing for Huntington disease.

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Transgenic mouse models of Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Transgenic mouse models of Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Genes, models and Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Transgenic mouse models of Alzheimer's disease: phenotype and mechanisms of pathogenesis

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Alzheimer disease: mouse models pave the way for therapeutic opportunities

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Transgenic mouse models of Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

The value of transgenic models for the study of neurodegenerative diseases

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Mouse models of Alzheimer's disease: a quest for plaques and tangles

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Single and multiple transgenic mice as models for Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Mice, the motor system, and human motor neuron pathology

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Of mice, men and motor neurons

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Transgenic mouse models and human neurodegenerative disorders.

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Animal models of amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Auditory and vestibular mouse mutants: models for human deafness

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Inherited hearing defects in mice

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Murine models for Down syndrome

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Too much of a good thing: mechanisms of gene action in Down syndrome.

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Mouse models of Huntington's disease

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Modeling Huntington's disease in cells, flies, and mice

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Of mice and men: solving the molecular mysteries of Huntington's disease

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Insights from mouse models into the molecular basis of neurodegeneration

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Mouse models of alpha-synucleinopathy and Lewy pathology. Alpha-synuclein expression in transgenic mice.

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Molecular pathogenesis of hereditary motor, sensory and autonomic neuropathies

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Trembler as a mouse model of CMT1A?

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Genetic abnormalities in Prader-Willi syndrome and lessons from mouse models.

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Neuroinvasion of prions: insights from mouse models

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Prion protein genes and prion diseases: studies in transgenic mice

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Mitochondrial disorders: genetics, counseling, prenatal diagnosis and reproductive options.

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Molecular mechanisms in spinal muscular atrophy: models and perspectives

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Regulation of the helix-loop-helix proteins, E2A and Id3, by the Ras-ERK MAPK cascade

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Early onset of severe familial amyotrophic lateral sclerosis with a SOD-1 mutation: potential impact of CNTF as a candidate modifier gene

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Trinucleotide repeats: mechanisms and pathophysiology

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Polyglutamine expansion neurodegenerative disease

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

The myotonic dystrophies

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Parents of children with spinal muscular atrophy are not obligate carriers: Carrier testing is important for reproductive decision-making

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

DNA methylation in genomic imprinting, development, and disease

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Imprinted genes and mental dysfunction

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy.

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

The role of tissue-specific imprinting as a source of phenotypic heterogeneity in human disease.

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

The role of genomic imprinting in human developmental disorders: lessons from Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Mouse autosomal trisomy: two's company, three's a crowd.

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Genome architecture, rearrangements and genomic disorders

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Clinical and molecular genetics of ADHD and Tourette syndrome. Two related polygenic disorders

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Advances in the genetics of cerebrovascular disease and stroke

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Molecular genetics of schizophrenia: past, present and future

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

The other human genome

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Diseases of oxidative phosphorylation due to mtDNA mutations

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Mitochondria and degenerative disorders

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Human mitochondrial DNA diseases

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

The mitochondrial genome and mitochondrial muscle disorders.

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Mitochondrial disorders

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Murine mucopolysaccharidosis VIL: impact of therapies on the phenotype, clinical course, and pathology in a model of a lysosomal storage disease

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

A mouse model of TSC1 reveals sex-dependent lethality from liver hemangiomas, and up-regulation of p70S6 kinase activity in Tsc1 null cells

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Of replications and refutations: the status of Alzheimer's disease genetic research

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Genealogies of mouse inbred strains

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

1 reference

7 January 2021

The mousetrap: what we can learn when the mouse model does not mimic the human disease

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Disruption of murine Hexa gene leads to enzymatic deficiency and to neuronal lysosomal storage, similar to that observed in Tay-Sachs disease

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Dramatically different phenotypes in mouse models of human Tay-Sachs and Sandhoff diseases

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Mouse models of Tay-Sachs and Sandhoff diseases differ in neurologic phenotype and ganglioside metabolism

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

A Proposed Test Battery and Constellations of Specific Behavioral Paradigms to Investigate the Behavioral Phenotypes of Transgenic and Knockout Mice

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

The use of behavioral test batteries: effects of training history

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Mouse molecular genetic technologies: promise for psychiatric research

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Quantitative genetics and mouse behavior

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Episodic-like memory in animals: psychological criteria, neural mechanisms and the value of episodic-like tasks to investigate animal models of neurodegenerative disease

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Testing of SHIRPA, a mouse phenotypic assessment protocol, on Dmd(mdx) and Dmd(mdx3cv) dystrophin-deficient mice

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Behavioral and functional analysis of mouse phenotype: SHIRPA, a proposed protocol for comprehensive phenotype assessment

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

SHIRPA, a protocol for behavioral assessment: validation for longitudinal study of neurological dysfunction in mice.

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

ALS-linked SOD1 mutant G85R mediates damage to astrocytes and promotes rapidly progressive disease with SOD1-containing inclusions.

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Transgenic mice expressing an altered murine superoxide dismutase gene provide an animal model of amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

A transgene insertion creating a heritable chromosome deletion mouse model of Prader-Willi and angelman syndromes

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Animal model of Gaucher's disease from targeted disruption of the mouse glucocerebrosidase gene

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Transgenic mouse model for the fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Frataxin knockin mouse

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Ablation of NF1 function in neurons induces abnormal development of cerebral cortex and reactive gliosis in the brain

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Reversal of neuropathology and motor dysfunction in a conditional model of Huntington's disease

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Post-natal knockout of prion protein alters hippocampal CA1 properties, but does not result in neurodegeneration

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Transchromosomal mouse embryonic stem cell lines and chimeric mice that contain freely segregating segments of human chromosome 21.

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Mice containing a human chromosome 21 model behavioral impairment and cardiac anomalies of Down's syndrome

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Functional expression and germline transmission of a human chromosome fragment in chimaeric mice

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Animal models for respiratory chain disease

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Mito-mice: animal models for mitochondrial DNA-based diseases

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Mouse models for mitochondrial disease

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Making mitochondrial mutants

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

A type VII myosin encoded by the mouse deafness gene shaker-1

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Mutations in the myosin VIIA gene cause non-syndromic recessive deafness

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Neuromuscular degeneration (nmd): a mutation on mouse chromosome 19 that causes motor neuron degeneration

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Identification of the mouse neuromuscular degeneration gene and mapping of a second site suppressor allele

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Genotype-based screen for ENU-induced mutations in mouse embryonic stem cells

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Systematic approaches to mouse mutagenesis

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Establishing an ENU mutagenesis screen for the piebald region of mouse Chromosome 14.

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Genome-wide, large-scale production of mutant mice by ENU mutagenesis.

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Efficient generation and mapping of recessive developmental mutations using ENU mutagenesis

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Genome-wide ENU mutagenesis to reveal immune regulators

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Generating mouse models of retinal disease using ENU mutagenesis.

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Novel ENU-induced eye mutations in the mouse: models for human eye disease

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

ENU mutagenesis and the search for deafness genes

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Sensitized polygenic trait analysis

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Finding the molecular basis of quantitative traits: successes and pitfalls.

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Complex trait analysis in the mouse: The strengths, the limitations and the promise yet to come

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

QTL analysis and genomewide mutagenesis in mice: complementary genetic approaches to the dissection of complex traits

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Modulation of disease severity in cystic fibrosis transmembrane conductance regulator deficient mice by a secondary genetic factor

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13.

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Suppression of polyglutamine-mediated neurodegeneration in Drosophila by the molecular chaperone HSP70.

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Over-expression of inducible HSP70 chaperone suppresses neuropathology and improves motor function in SCA1 mice

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Towards new models of disease and physiology in the neurosciences: the role of induced and naturally occurring mutations

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

The mouse: genetics meets behaviour

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

Welfare issues of genetically modified animals

1 reference

https://api.crossref.org/works/10.1016/S1474-4422(02)00100-X

7 January 2021

10.1016/S1474-4422(02)00100-X

Identifiers

DOI

1 reference

6 August 2017

1 reference