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English
Epidermal disease: faulty keratin filaments take their toll
scientific article published on 01 January 1994
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7511022
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7511022%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
title
Epidermal disease: faulty keratin filaments take their toll
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7511022
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7511022%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
main subject
epidermal disease
1 reference
based on heuristic
inferred from title
author name string
Compton JG
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7511022
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7511022%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
publication date
1 January 1994
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7511022
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7511022%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7511022
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7511022%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
volume
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7511022
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7511022%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7511022
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7511022%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
page(s)
6-7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7511022
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7511022%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
exact match
https://scigraph.springernature.com/pub.10.1038/ng0194-6
0 references
cites work
The molecular biology of intermediate filament proteins
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Intermediate filaments: not so tough after all.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Epidermolysis Bullosa Simplex: Evidence in Two Families for Keratin Gene Abnormalities
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Point mutations in human keratin 14 genes of epidermolysis bullosa simplex patients: Genetic and functional analyses
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mutation in the conserved helix termination peptide of keratin 5 in hereditary skin blistering
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Linkage of epidermolytic hyperkeratosis to the type II keratin gene cluster on chromosome 12q
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the rod domains of keratins 1 and 10 in epidermolytic hyperkeratosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A leucine----proline mutation in the H1 subdomain of keratin 1 causes epidermolytic hyperkeratosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The genetic basis of epidermolytic hyperkeratosis: a disorder of differentiation-specific epidermal keratin genes.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Distribution of a special subset of keratinocytes characterized by the expression of cytokeratin 9 in adult and fetal human epidermis of various body sites
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization of human cytokeratin 2, an epidermal cytoskeletal protein synthesized late during differentiation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Suprabasal marker proteins distinguishing keratinizing squamous epithelia: cytokeratin 2 polypeptides of oral masticatory epithelium and epidermis are different
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mapping of a gene for epidermolytic palmoplantar keratoderma to the region of the acidic keratin gene cluster at 17q12-q21.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of the genetic locus for keratosis palmaris et plantaris on chromosome 17 near the RARA and keratin type I genes.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Epidermolytic palmoplantar keratoderma cosegregates with a keratin 9 mutation in a pedigree with breast and ovarian cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Keratin intermediate filament structure. Crosslinking studies yield quantitative information on molecular dimensions and mechanism of assembly
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Conservation of the structure of keratin intermediate filaments: molecular mechanism by which different keratin molecules integrate into preexisting keratin intermediate filaments during differentiation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A synthetic peptide representing the consensus sequence motif at the carboxy-terminal end of the rod domain inhibits intermediate filament assembly and disassembles preformed filaments
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A function for keratins and a common thread among different types of epidermolysis bullosa simplex diseases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A keratin 14 mutational hot spot for epidermolysis bullosa simplex, Dowling-Meara: implications for diagnosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Interferon gamma regulation of de novo protein synthesis in human dermal fibroblasts in culture is anatomic site dependent
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A missense mutation in the rod domain of keratin 14 associated with recessive epidermolysis bullosa simplex.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mutation (Met-->Arg) in the type I keratin (K14) gene responsible for autosomal dominant epidermolysis bullosa simplex.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel three-nucleotide deletion in the helix 2B region of keratin 14 in epidermolysis bullosa simplex: delta E375.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a leucine-to-proline mutation in the keratin 5 gene in a family with the generalized Köbner type of epidermolysis bullosa simplex
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0194-6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7511022
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7511022%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
PubMed publication ID
7511022
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7511022
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7511022%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
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