Transfer of genetic therapy across human populations: molecular targets for increasing patient coverage in repeat expansion diseases. (Q43082851)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25990798%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

title

Transfer of genetic therapy across human populations: molecular targets for increasing patient coverage in repeat expansion diseases (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25990798%20AND%20SRC:MED&resulttype=core&format=json

human population genetics

8 March 2020

main subject

1 reference

3

1 reference

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8 March 2020

Suzan M Hammond

4

1 reference

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8 March 2020

Janine Scholefield

7

1 reference

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8 March 2020

Matthew J. Wood

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25990798%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

author name string

Miguel A Varela

1

1 reference

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8 March 2020

Helen J Curtis

2

1 reference

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8 March 2020

Aisling J O'Loughlin

5

1 reference

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8 March 2020

Maria J Sobrido

6

1 reference

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8 March 2020

publication date

20 May 2015

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25990798%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Human Genetics

8 March 2020

published in

1 reference

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8 March 2020

volume

24

1 reference

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8 March 2020

issue

2

1 reference

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8 March 2020

page(s)

271-276

1 reference

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https://scigraph.springernature.com/pub.10.1038/ejhg.2015.94

8 March 2020

exact match

0 references

cites work

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Rational design of antisense oligonucleotides targeting single nucleotide polymorphisms for potent and allele selective suppression of mutant Huntingtin in the CNS.

25 May 2018

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25 May 2018

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Towards an Ecology of Collective Innovation: Human Variome Project (HVP), Rare Disease Consortium for Autosomal Loci (RaDiCAL) and Data-Enabled Life Sciences Alliance (DELSA)

25 May 2018

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'Costa da Morte' ataxia is spinocerebellar ataxia 36: clinical and genetic characterization

25 May 2018

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25 May 2018

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25 May 2018

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A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

25 May 2018

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Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

25 May 2018

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Expansion of intronic GGCCTG hexanucleotide repeat in NOP56 causes SCA36, a type of spinocerebellar ataxia accompanied by motor neuron involvement

25 May 2018

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RNAi: a potential new class of therapeutic for human genetic disease

25 May 2018

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25 May 2018

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Heterogeneous distribution of SNPs in the human genome: microsatellites as predictors of nucleotide diversity and divergence

25 May 2018

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Five siRNAs targeting three SNPs may provide therapy for three-quarters of Huntington's disease patients

25 May 2018

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CAG expansion in the Huntington disease gene is associated with a specific and targetable predisposing haplogroup

25 May 2018

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Design of LNA probes that improve mismatch discrimination

25 May 2018

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Determinants of specific RNA interference-mediated silencing of human beta-globin alleles differing by a single nucleotide polymorphism

25 May 2018

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25 May 2018

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Recovering the geographic origin of early modern humans by realistic and spatially explicit simulations

25 May 2018

1 reference

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A systematic analysis of the silencing effects of an active siRNA at all single-nucleotide mismatched target sites

25 May 2018

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Geography predicts neutral genetic diversity of human populations

25 May 2018

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Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset

25 May 2018

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The International HapMap Project

25 May 2018

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Genetic structure of human populations

25 May 2018

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High incidence rate and absent family histories in one quarter of patients newly diagnosed with Huntington disease in British Columbia

25 May 2018

1 reference

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Measurement of mutational flow implies both a high new-mutation rate for Huntington disease and substantial underascertainment of late-onset cases.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4717213

Heterogeneous nature and distribution of interruptions in dinucleotides may indicate the existence of biased substitutions underlying microsatellite evolution.

25 May 2018

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Origin of the SCA7 gene mutation in South Africa: implications for molecular diagnostics

15 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25990798

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/EJHG.2015.94

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25990798%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

8 March 2020

1033146515

0 references

Fatcat ID

release_gruh2yzzfbdl5jtbpvk62gmc2i

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/gruh2yzzfbdl5jtbpvk62gmc2i

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25990798%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25990798%20AND%20SRC:MED&resulttype=core&format=json