Development of allele-specific therapeutic siRNA for keratin 5 mutations in epidermolysis bullosa simplex (Q28242020)

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6 February 2020

title

Development of allele-specific therapeutic siRNA for keratin 5 mutations in epidermolysis bullosa simplex (English)

1 reference

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epidermolysis bullosa simplex

6 February 2020

main subject

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inferred from title

author

Victoria E McGilligan

2

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6 February 2020

Johnny Moore

6

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6 February 2020

Tara Moore

7

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6 February 2020

Irwin McLean

8

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6 February 2020

4

Ildiko Szeverenyi

1 reference

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6 February 2020

Haihui Liao

3

object named as

Haihui Liao

1 reference

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6 February 2020

author name string

Sarah D Atkinson

1

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6 February 2020

Frances J D Smith

5

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6 February 2020

language of work or name

English

0 references

publication date

30 June 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21716320%20AND%20SRC:MED&resulttype=core&format=json

Journal of Investigative Dermatology

6 February 2020

published in

1 reference

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6 February 2020

volume

131

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6 February 2020

issue

10

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6 February 2020

page(s)

2079-2086

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Epidermolysis Bullosa Simplex: Evidence in Two Families for Keratin Gene Abnormalities

6 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

RNAi therapeutics: a potential new class of pharmaceutical drugs

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

An inducible mouse model for epidermolysis bullosa simplex: implications for gene therapy

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

Specific inhibition of gene expression by small double-stranded RNAs in invertebrate and vertebrate systems

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

Point mutations in human keratin 14 genes of epidermolysis bullosa simplex patients: Genetic and functional analyses

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

Knocking down disease with siRNAs

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

Dominant-negative effects of COL7A1 mutations can be rescued by controlled overexpression of normal collagen VII.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

SiRNA-mediated selective inhibition of mutant keratin mRNAs responsible for the skin disorder pachyonychia congenita

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

Single-nucleotide-specific siRNA targeting in a dominant-negative skin model

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

The prevalence of epidermolysis bullosa in Scotland

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

Three keratin gene mutations account for the majority of dominant simplex epidermolysis bullosa cases within the population of Ireland

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

Human keratin diseases: the increasing spectrum of disease and subtlety of the phenotype-genotype correlation

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

Epidermolysis Bullosa Simplex (Dowling-Meara Type) Is a Genetic Disease Characterized by an Abnormal Keratin-Filament Network Involving Keratins K5 and K14

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

Ribozyme therapeutics

1 reference

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7 January 2021

Challenges in developing therapies for rare diseases including pachyonychia congenita

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

Achieving successful delivery of nucleic acids to skin: 6th Annual Meeting of the International Pachyonychia Congenita Consortium

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

Broken bricks and cracked mortar – epidermal diseases resulting from genetic abnormalities

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

A mutation in the conserved helix termination peptide of keratin 5 in hereditary skin blistering

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

Therapeutic siRNAs for dominant genetic skin disorders including pachyonychia congenita.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

First-in-human mutation-targeted siRNA phase Ib trial of an inherited skin disorder.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

Epidermolysis bullosa carrier frequencies in the US population

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

Epidermolysis bullosa simplex in Scotland caused by a spectrum of keratin mutations.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

Laryngeal involvement in the Dowling-Meara variant of epidermolysis bullosa simplex with keratin mutations of severely disruptive potential.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

Cloning of human, murine, and marsupial keratin 7 and a survey of K7 expression in the mouse

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

The Human Intermediate Filament Database: comprehensive information on a gene family involved in many human diseases.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

K14 mRNA reprogramming for dominant epidermolysis bullosa simplex.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

siRNA-based inhibition specific for mutant SOD1 with single nucleotide alternation in familial ALS, compared with ribozyme and DNA enzyme

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.169

7 January 2021

Identifiers

DOI

10.1038/JID.2011.169

2 references

Consolidated OpenCitations Corpus – April 2017

1506896

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21716320%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

6 February 2020

1040899609

0 references

1506896

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

1506896

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21716320%20AND%20SRC:MED&resulttype=core&format=json