(Q28243587)

https://api.crossref.org/works/10.1111/J.0906-6705.2005.00324.X

Analysis of the interactions between BP180, BP230, plectin and the integrin alpha6beta4 important for hemidesmosome assembly

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.0906-6705.2005.00324.X

Plakins: a family of versatile cytolinker proteins

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.0906-6705.2005.00324.X

Human plectin: organization of the gene, sequence analysis, and chromosome localization (8q24)

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.0906-6705.2005.00324.X

Plectin deficiency results in muscular dystrophy with epidermolysis bullosa

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.0906-6705.2005.00324.X

Homozygous deletion mutations in the plectin gene (PLEC1) in patients with epidermolysis bullosa simplex associated with late-onset muscular dystrophy

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.0906-6705.2005.00324.X

Plectin sidearms mediate interaction of intermediate filaments with microtubules and other components of the cytoskeleton

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.0906-6705.2005.00324.X

A site-specific plectin mutation causes dominant epidermolysis bullosa simplex Ogna: two identical de novo mutations

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.0906-6705.2005.00324.X

Progress in epidermolysis bullosa: genetic classification and clinical implications

21 April 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.0906-6705.2005.00324.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0906-6705.2005.00324.X

Laminin 5 mutations in junctional epidermolysis bullosa: molecular basis of Herlitz vs. non-Herlitz phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0906-6705.2005.00324.X

Mutation analysis and molecular genetics of epidermolysis bullosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0906-6705.2005.00324.X

Occurrence and immunolocalization of plectin in tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0906-6705.2005.00324.X

Unusual 5' transcript complexity of plectin isoforms: novel tissue-specific exons modulate actin binding activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0906-6705.2005.00324.X

A missense mutation in the rod domain of keratin 14 associated with recessive epidermolysis bullosa simplex.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0906-6705.2005.00324.X

Under the Tucson sun: a meeting in the desert on mRNA decay

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0906-6705.2005.00324.X

Plectin transcript diversity: identification and tissue distribution of variants with distinct first coding exons and rodless isoforms

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0906-6705.2005.00324.X

Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0906-6705.2005.00324.X

Novel ITGB4 mutations in lethal and nonlethal variants of epidermolysis bullosa with pyloric atresia: missense versus nonsense

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0906-6705.2005.00324.X

Epidermolysis bullosa simplex associated with pyloric atresia is a novel clinical subtype caused by mutations in the plectin gene (PLEC1)

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0906-6705.2005.00324.X

Identification of a lethal form of epidermolysis bullosa simplex associated with a homozygous genetic mutation in plectin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0906-6705.2005.00324.X

Linking integrin alpha6beta4-based cell adhesion to the intermediate filament cytoskeleton: direct interaction between the beta4 subunit and plectin at multiple molecular sites.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0906-6705.2005.00324.X

Prenatal diagnosis for epidermolysis bullosa: a study of 144 consecutive pregnancies at risk.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0906-6705.2005.00324.X

Recessive epidermolysis bullosa simplex associated with plectin mutations: infantile respiratory complications in two unrelated cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0906-6705.2005.00324.X

Mutation reports: epidermolysis bullosa simplex associated with severe mucous membrane involvement and novel mutations in the plectin gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0906-6705.2005.00324.X

A compound heterozygous one amino-acid insertion/nonsense mutation in the plectin gene causes epidermolysis bullosa simplex with plectin deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0906-6705.2005.00324.X

Disorganization of the desmin cytoskeleton and mitochondrial dysfunction in plectin-related epidermolysis bullosa simplex with muscular dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0906-6705.2005.00324.X

Severe mucous membrane involvement in epidermolysis bullosa simplex with muscular dystrophy due to a novel plectin gene mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0906-6705.2005.00324.X

10.1111/J.0906-6705.2005.00324.X

21 January 2018

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

release_rtpxd6fqubdklntade7ywwah3e

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/rtpxd6fqubdklntade7ywwah3e

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

15810881

1 reference

Consolidated OpenCitations Corpus – April 2017