(Q24685210)

2

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M Chiano

3

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A Dodge

4

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G Norbury

5

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E Rosser

6

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D Craufurd

Proceedings of the National Academy of Sciences of the United States of America

7

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language of work or name

English

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publication date

15 April 1997

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published in

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volume

94

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issue

8

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page(s)

3872-6

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cites work

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20534

Human GluR6 kainate receptor (GRIK2): molecular cloning, expression, polymorphism, and chromosomal assignment

7 April 2017

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Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20534

Trinucleotide repeat length instability and age of onset in Huntington's disease

28 September 2017

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The normal Huntington disease (HD) allele, or a closely linked gene, influences age at onset of HD

28 September 2017

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Structure and expression of the Huntington's disease gene: evidence against simple inactivation due to an expanded CAG repeat

28 September 2017

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Molecular analysis of late onset Huntington's disease

28 September 2017

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Molecular and clinical correlations in spinocerebellar ataxia type I: evidence for familial effects on the age at onset.

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1994 William Allan Award Address. Mitochondrial DNA variation in human evolution, degenerative disease, and aging

28 September 2017

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20534

Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease

28 September 2017

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Do defects in mitochondrial energy metabolism underlie the pathology of neurodegenerative diseases?

30 May 2018

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Apolipoprotein E in the genetics and epidemiology of Alzheimer's disease.

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Apolipoprotein E4 and Alzheimer's disease pathology in Lewy body disease and in other beta-amyloid-forming diseases.

21 January 2018

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Apolipoprotein E ε4 allele is associated with deposition of amyloid β-protein following head injury

21 January 2018

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Evidence for impairment of energy metabolism in vivo in Huntington's disease using localized 1H NMR spectroscopy

21 January 2018

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Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients.

21 January 2018

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Selective loss of [3H]kainic acid and [3H]AMPA binding in layer VI of frontal cortex in Huntington's disease

21 January 2018

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Complexity in a monogenic disease

21 January 2018

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Association of apolipoprotein E ∈4 allele with bulbar-onset motor neuron disease

21 January 2018

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Haplotype analysis of the delta 2642 and (CAG)n polymorphisms in the Huntington's disease (HD) gene provides an explanation for an apparent 'founder' HD haplotype

21 January 2018

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Restriction isotyping of human apolipoprotein E by gene amplification and cleavage with HhaI

28 November 2018

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inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Apolipoprotein E type ϵ4 allele frequency is increased in patients with schizophrenia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9108071

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Allelic variations in apolipoprotein E and prion protein genotype related to plaque formation and age of onset in sporadic Creutzfeldt-Jakob disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9108071