(Q34291351)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11422179%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

review article

1 reference

title

Keratinocyte adhesion and the missing link: from Dowling-Meara to Hay-Wells. St John's Hospital Dermatological Society Annual Oration 2000 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11422179%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11422179%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

author name string

McGrath JA

series ordinal

1

1 reference

1 August 2017

publication date

1 May 2001

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11422179%20AND%20SRC:MED&resulttype=core&format=json

Clinical and Experimental Dermatology

8 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11422179%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

volume

26

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11422179%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11422179%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

page(s)

296-304

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11422179%20AND%20SRC:MED&resulttype=core&format=json

Ultrastructural morphometry of normal human dermal-epidermal junction. The influence of age, sex, and body region on laminar and nonlaminar components

8 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

Structure and function of hemidesmosomes: more than simple adhesion complexes

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

Are desmosomes more than tethers for intermediate filaments?

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

Epidermolysis bullosa resembling juvenile dermatitis herpetiformis

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.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/10.1046%2FJ.1365-2230.2001.00819.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa. A consensus report by the Subcommittee on Diagnosis and Classification of the National Epidermolysis Bullosa Registry

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

Revised classification system for inherited epidermolysis bullosa: Report of the Second International Consensus Meeting on diagnosis and classification of epidermolysis bullosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

Mutations in the plakophilin 1 gene result in ectodermal dysplasia/skin fragility syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

Genomic amplification of the human plakophilin 1 gene and detection of a new mutation in ectodermal dysplasia/skin fragility syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

Haploinsufficiency of desmoplakin causes a striate subtype of palmoplantar keratoderma

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

Striate palmoplantar keratoderma resulting from desmoplakin haploinsufficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratoderma

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

Desmoplakin is required early in development for assembly of desmosomes and cytoskeletal linkage

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease).

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

Targeted mutation of plakoglobin in mice reveals essential functions of desmosomes in the embryonic heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

The syndrome of ankyloblepharon, ectodermal defects and cleft lip and palate: an autosomal dominant condition

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

p53, the cellular gatekeeper for growth and division

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

p63, a p53 homolog at 3q27-29, encodes multiple products with transactivating, death-inducing, and dominant-negative activities

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

P63 and P73: P53 mimics, menaces and more

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

p63 is essential for regenerative proliferation in limb, craniofacial and epithelial development

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

p63 is a p53 homologue required for limb and epidermal morphogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

OMIM passes the 1,000-disease-gene mark

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2001.00819.X

10.1046/J.1365-2230.2001.00819.X

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11422179%20AND%20SRC:MED&resulttype=core&format=json

release_2b4ludkusjhl3i4ldo36iep2si

8 November 2019

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/2b4ludkusjhl3i4ldo36iep2si

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference