Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16. (Q30445013)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15029481%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

title

Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16 (English)

1 reference

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25 December 2019

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25 December 2019

L. Adrienne Cupples

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Richard H Myers

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25 December 2019

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James F Gusella

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Christopher A Ross

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Marcy E MacDonald

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Alexandra Durr

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Luc Djoussé

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Beth Knowlton

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25 December 2019

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Marina Frontali

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Estrella Gómez-Tortosa

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Catherine Dode

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publication date

17 March 2004

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25 December 2019

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25 December 2019

volume

5

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25 December 2019

issue

2

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25 December 2019

page(s)

109-114

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https://scigraph.springernature.com/pub.10.1007/s10048-004-0175-2

25 December 2019

exact match

0 references

cites work

A genome scan for modifiers of age at onset in Huntington disease: The HD MAPS study.

1 reference

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The role of MSX1 in human tooth agenesis

20 June 2018

1 reference

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A nonsense mutation in MSX1 causes Witkop syndrome

20 June 2018

1 reference

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The likelihood of being affected with Huntington disease by a particular age, for a specific CAG size

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1866166

Genotypes at the GluR6 kainate receptor locus are associated with variation in the age of onset of Huntington disease

20 June 2018

1 reference

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A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

20 June 2018

1 reference

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

20 June 2018

1 reference

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

20 June 2018

1 reference

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

20 June 2018

1 reference

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A study of the Huntington's disease associated trinucleotide repeat in the Scottish population.

20 June 2018

1 reference

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Anticipation and instability of IT-15 (CAG)n repeats in parent-offspring pairs with Huntington disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1866166

Huntington's chorea on the island of Mauritius.

20 June 2018

1 reference

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A polymorphic DNA marker genetically linked to Huntington's disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1866166

Huntington disease: genetics and epidemiology

20 June 2018

1 reference

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20 June 2018

1 reference

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Homoeotic transformations in man: implications for the mechanism of embryonic development and for the organization of epithelia

20 June 2018

1 reference

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Predictability of phenotype in Huntington's disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1866166

The molecular genetics of embryonic pattern formation in Drosophila

20 June 2018

1 reference

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Homeo boxes in the study of development

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1866166

The human homeobox gene HOX7 maps to chromosome 4p16.1 and may be implicated in Wolf-Hirschhorn syndrome.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1866166

Structure and sequence of the human homeobox gene HOX7.

20 June 2018

1 reference

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A dinucleotide repeat polymorphism at the D4S127 locus

20 June 2018

1 reference

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The Huntington's disease candidate region exhibits many different haplotypes

20 June 2018

1 reference

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Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1866166

Evidence for the GluR6 gene associated with younger onset age of Huntington's disease

26 November 2018

1 reference

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Relationships of the 2642 deletion polymorphism (delta 2642) in the huntingtin gene with the CAG repeat expansion length and age at onset of the disease.

26 November 2018

1 reference

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Expansion of the (CAG)n repeat causing Huntington's disease in 352 patients of German origin

26 November 2018

1 reference

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Polymorphism analysis of the huntingtin gene in Italian families affected with Huntington disease.

26 November 2018

1 reference

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Ancestral differences in the distribution of the delta 2642 glutamic acid polymorphism is associated with varying CAG repeat lengths on normal chromosomes: insights into the genetic evolution of Huntington disease

26 November 2018

1 reference

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

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15029481

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S10048-004-0175-2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15029481%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15029481%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

1 reference