(Q36982924)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18931668%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

title

Linking SNPs to CAG repeat length in Huntington's disease patients (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18931668%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

0 references

6

1 reference

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24 December 2019

4

Steven Hersch

1 reference

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24 December 2019

author name string

Wanzhao Liu

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18931668%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

Lori A Kennington

2

1 reference

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24 December 2019

H Diana Rosas

3

1 reference

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24 December 2019

Jang-Ho Cha

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18931668%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

Neil Aronin

7

1 reference

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24 December 2019

publication date

19 October 2008

1 reference

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24 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18931668%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

volume

5

1 reference

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24 December 2019

issue

11

1 reference

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24 December 2019

page(s)

951-953

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18931668%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/nmeth.1261

24 December 2019

exact match

0 references

cites work

Therapeutic silencing of mutant huntingtin with siRNA attenuates striatal and cortical neuropathology and behavioral deficits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587014

Designing siRNA that distinguish between genes that differ by a single nucleotide

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587014

Selective silencing by RNAi of a dominant allele that causes amyotrophic lateral sclerosis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587014

Allele-specific silencing of dominant disease genes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587014

Rescue of polyglutamine-mediated cytotoxicity by double-stranded RNA-mediated RNA interference

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587014

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587014

Inactivation of the mouse Huntington's disease gene homolog Hdh

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587014

Increased apoptosis and early embryonic lethality in mice nullizygous for the Huntington's disease gene homologue

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587014

Genetic applications of an inverse polymerase chain reaction

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587014

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587014

Huntington's disease gene: regional and cellular expression in brain of normal and affected individuals

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587014

Identification and allele-specific silencing of the mutant huntingtin allele in Huntington's disease patient-derived fibroblasts.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587014

Mouse Huntington's disease homolog mRNA levels: variation and allele effects

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587014

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

4 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNMETH.1261

Fear of health insurance loss among individuals at risk for Huntington disease

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18931668

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NMETH.1261

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18931668%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18931668%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

1 reference