(Q33594145)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10203734%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

review article

1 reference

title

The palmoplantar keratodermas: much more than palms and soles (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10203734%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10203734%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

author name string

H P Stevens

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10203734%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

publication date

1 March 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10203734%20AND%20SRC:MED&resulttype=core&format=json

Trends in Molecular Medicine

4 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10203734%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

volume

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10203734%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10203734%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

page(s)

107-113

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10203734%20AND%20SRC:MED&resulttype=core&format=json

Structure, function, and dynamics of keratin intermediate filaments

4 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Human keratin diseases: hereditary fragility of specific epithelial tissues

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Keratin 9 gene mutations in epidermolytic palmoplantar keratoderma (EPPK).

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Novel mutations in keratin 16 gene underly focal non-epidermolytic palmoplantar keratoderma (NEPPK) in two families

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Keratin 16 and keratin 17 mutations cause pachyonychia congenita

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Mutation of a type II keratin gene (K6a) in pachyonychia congenita

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

The gene for diffuse palmoplantar keratoderma of the type found in northern Sweden is localized to chromosome 12q11-q13

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Genetic linkage studies in non-epidermolytic palmoplantar keratoderma: evidence for heterogeneity

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

A mutation in the V1 end domain of keratin 1 in non-epidermolytic palmar-plantar keratoderma

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Mutations in the rod domains of keratins 1 and 10 in epidermolytic hyperkeratosis

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

A highly conserved lysine residue on the head domain of type II keratins is essential for the attachment of keratin intermediate filaments to the cornified cell envelope through isopeptide crosslinking by transglutaminases

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Desmosomes and hemidesmosomes: structure and function of molecular components.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Cytoskeleton-membrane interactions

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Making a connection: direct binding between keratin intermediate filaments and desmosomal proteins

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Plectin deficiency results in muscular dystrophy with epidermolysis bullosa

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Localization of a locus for the striated form of palmoplantar keratoderma to chromosome 18q near the desmosomal cadherin gene cluster.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

A YAC contig joining the desmocollin and desmoglein loci on human chromosome 18 and ordering of the desmocollin genes

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

The desmocollins of human foreskin epidermis: identification and chromosomal assignment of a third gene and expression patterns of the three isoforms

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Linkage of the gene for the triple A syndrome to chromosome 12q13 near the type II keratin gene cluster

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Hereditary epidermolytic palmoplantar keratoderma associated with breast and ovarian cancer in a large kindred

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Epidermolytic palmoplantar keratoderma cosegregates with a keratin 9 mutation in a pedigree with breast and ovarian cancer

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Tylosis associated with carcinoma of the oesophagus and oral leukoplakia in a large Liverpool family--a review of six generations

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Close mapping of the focal non-epidermolytic palmoplantar keratoderma (PPK) locus associated with oesophageal cancer (TOC)

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Tylosis oesophageal cancer mapped

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Palmoplantar keratoderma in association with carcinoma of the esophagus maps to chromosome 17q distal to the keratin gene cluster.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Tylosis esophageal cancer locus on chromosome 17q25.1 is commonly deleted in sporadic human esophageal cancer

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Keratoderma hereditarium mutilans (Vohwinkel's syndrome) associated with congenital deaf-mutism

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Loricrin mutation in Vohwinkel's keratoderma is unique to the variant with ichthyosis

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

The molecular pathology of progressive symmetric erythrokeratoderma: a frameshift mutation in the loricrin gene and perturbations in the cornified cell envelope

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

The gene responsible for Clouston hidrotic ectodermal dysplasia maps to the pericentromeric region of chromosome 13q

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Confirmation of Linkage of Clouston Syndrome (Hidrotic Ectodermal Dysplasia) to 13q11-q12.1 with Evidence for Multiple Independent Mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Expression of gap junction proteins Cx26, Cx31.1, Cx37, and Cx43 in developing and mature rat epidermis

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Gene for arrhythmogenic right ventricular cardiomyopathy with diffuse nonepidermolytic palmoplantar keratoderma and woolly hair (Naxos disease) maps to 17q21

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Localisation of a gene for Papillon-Lefèvre syndrome to chromosome 11q14-q21 by homozygosity mapping

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Localization of the gene causing keratolytic winter erythema to chromosome 8p22-p23, and evidence for a founder effect in South African Afrikaans-speakers

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

Point mutations in the tyrosine aminotransferase gene in tyrosinemia type II

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901428-2

7 January 2021

10.1016/S1357-4310(98)01428-2

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10203734%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

1 reference