Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q77725541)
Watch
English
Inherited disorders of epidermal keratinization
scientific article published on 01 December 1998
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9865446
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9865446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
review article
1 reference
stated in
Europe PubMed Central
title
Inherited disorders of epidermal keratinization
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9865446
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9865446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
author name string
A Ishida-Yamamoto
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9865446
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9865446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
H Tanaka
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9865446
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9865446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
H Nakane
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9865446
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9865446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
H Takahashi
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9865446
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9865446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
H Iizuka
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9865446
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9865446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
publication date
1 December 1998
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9865446
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9865446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
published in
Journal of Dermatological Science
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9865446
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9865446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
volume
18
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9865446
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9865446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9865446
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9865446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
page(s)
139-154
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9865446
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9865446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
cites work
Localization and Composition of Lipids in Neonatal Mouse Stratum Granulosum and Stratum Corneum
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Structural organization of cornified cell envelopes and alterations in inherited skin disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Epidermal differentiation: the bare essentials
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Epidermal structural proteins in skin disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
JSID Tanioku Memorial Lecture 1996. Genetic disorders of keratins and their associated proteins.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Keratin biochemistry
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human keratin diseases: hereditary fragility of specific epithelial tissues
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence for specific proteolytic cleavage of the N-terminal domain of human profilaggrin during epidermal differentiation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The proteins elafin, filaggrin, keratin intermediate filaments, loricrin, and small proline-rich proteins 1 and 2 are isodipeptide cross-linked components of the human epidermal cornified cell envelope
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Highly active soluble processed forms of the transglutaminase 1 enzyme in epidermal keratinocytes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inactive zymogen and highly active proteolytically processed membrane-bound forms of the transglutaminase 1 enzyme in human epidermal keratinocytes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Biochemical evidence that small proline-rich proteins and trichohyalin function in epithelia by modulation of the biomechanical properties of their cornified cell envelopes.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Covalently bound lipids of human stratum corneum
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Defects in the barrier
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ichthyosiform dermatoses. Classification based on anatomic and biometric observations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Reduced stability and bi-allelic, coequal expression of profilaggrin mRNA in keratinocytes cultured from subjects with ichthyosis vulgaris
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ichthyosis vulgaris: identification of a defect in synthesis of filaggrin correlated with an absence of keratohyaline granules
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization of point mutations in patients with X-linked ichthyosis. Effects on the structure and function of the steroid sulfatase protein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel point mutation in the steroid sulfatase gene in X-linked ichthyosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lipids in the pathogenesis of ichthyosis: topical cholesterol sulfate-induced scaling in hairless mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Stratum corneum lipids in disorders of cornification. Steroid sulfatase and cholesterol sulfate in normal desquamation and the pathogenesis of recessive X-linked ichthyosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Calorimetric and electron spin resonance examination of lipid phase transitions in human stratum corneum: molecular basis for normal cohesion and abnormal desquamation in recessive X-linked ichthyosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal dominant lamellar ichthyosis: a new skin disorder
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the gene for transglutaminase 1 in autosomal recessive lamellar ichthyosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations of keratinocyte transglutaminase in lamellar ichthyosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genotype/phenotype correlation in autosomal recessive lamellar ichthyosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transglutaminase 1 mutations in autosomal recessive congenital ichthyosis: private and recurrent mutations in an isolated population
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lamellar Ichthyosis Is Genetically Heterogeneous–Cases with Normal Keratinocyte Transglutaminase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital recessive ichthyosis unlinked to loci for epidermal transglutaminases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mapping of a second locus for lamellar ichthyosis to chromosome 2q33-35.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Consequences of seven novel mutations on the expression and structure of keratinocyte transglutaminase.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transglutaminase 1 Mutations in Lamellar Ichthyosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Barrier function regulates epidermal DNA synthesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel dinucleotide mutation in keratin 10 in the annular epidermolytic ichthyosis variant of bullous congenital ichthyosiform erythroderma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A transgenic mouse model that recapitulates the clinical features of both neonatal and adult forms of the skin disease epidermolytic hyperkeratosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The relationship between hyperproliferation and epidermal thickening in a mouse model for BCIE.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Selective involvement of keratins K1 and K10 in the cytoskeletal abnormality of epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Filaggrin expression in epidermolytic ichthyosis (epidermolytic hyperkeratosis)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The mitotic rate and duration in lesions of psoriasis and ichthyosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence against keratin gene mutations in a family with ichthyosis hystrix Curth-Macklin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Harlequin ichthyosis. Variability in expression and hypothesis for disease mechanism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Protein phosphatase activity in human keratinocytes cultured from normal epidermis and epidermis from patients with harlequin ichthyosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The molecular pathology of progressive symmetric erythrokeratoderma: a frameshift mutation in the loricrin gene and perturbations in the cornified cell envelope
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Loricrin mutation in Vohwinkel's keratoderma is unique to the variant with ichthyosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Linkage studies in erythrokeratodermias: fine mapping, genetic heterogeneity and analysis of candidate genes.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sjögren-Larsson syndrome is caused by mutations in the fatty aldehyde dehydrogenase gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of PAHX, a Refsum disease gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Refsum disease is caused by mutations in the phytanoyl-CoA hydroxylase gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rhizomelic chondrodysplasia punctata is a peroxisomal protein targeting disease caused by a non-functional PTS2 receptor
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked dominant Conradi-Hünermann syndrome presenting as congenital erythroderma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Peroxisomal enzyme deficiency in the Conradi-Hunerman form of chondrodysplasia punctata
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked dominant ichthyosis with peroxisomal deficiency. An ultrastructural and ultracytochemical study of the Conradi-Hünermann syndrome and its murine homologue, the bare patches mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked dominant chondrodysplasia punctata/ichthyosis/cataract syndrome in males
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Systematized inflammatory epidermal nevus with symmetrical involvement: an unusual case of CHILD syndrome?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Peroxisomal abnormality in fibroblasts from involved skin of CHILD syndrome. Case study and review of peroxisomal disorders in relation to skin disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Acylglycerol recycling from triacylglycerol to phospholipid, not lipase activity, is defective in neutral lipid storage disease fibroblasts
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neutral lipid storage disease with ichthyosis. Defective lamellar body contents and intracellular dispersion.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel amino acid modification in sulfatases that is defective in multiple sulfatase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Trichothiodystrophy: review of sulfur-deficient brittle hair syndromes and association with the ectodermal dysplasias
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A 3' --> 5' XPB helicase defect in repair/transcription factor TFIIH of xeroderma pigmentosum group B affects both DNA repair and transcription
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Consequences of beta-glucocerebrosidase deficiency in epidermis. Ultrastructure and permeability barrier alterations in Gaucher disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital ichthyosis preceding neurologic symptoms in two sibs with type 2 Gaucher disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gaucher disease in the neonate: a distinct Gaucher phenotype is analogous to a mouse model created by targeted disruption of the glucocerebrosidase gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Glucosylceramides stimulate murine epidermal hyperproliferation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Stratum corneum lipids serve as a bound-water modulator
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mutation in the V1 end domain of keratin 1 in non-epidermolytic palmar-plantar keratoderma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Keratin 9 point mutation in the pedigree of epidermolytic hereditary palmoplantar keratoderma perturbs keratin intermediate filament network formation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel mutations in keratin 16 gene underly focal non-epidermolytic palmoplantar keratoderma (NEPPK) in two families
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Keratoma hereditarium mutilans
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Keratoma hereditaria mutilans (Vohwinkel). Differentiating features of conditions with constriction of digits
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tylosis oesophageal cancer mapped
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Linkage of an American pedigree with palmoplantar keratoderma and malignancy (palmoplantar ectodermal dysplasia type III) to 17q24. Literature survey and proposed updated classification of the keratodermas
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Richner-Hanhart syndrome: importance of early diagnosis and early intervention
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Localisation of a gene for Papillon-Lefèvre syndrome to chromosome 11q14-q21 by homozygosity mapping
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2898%2900041-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0923-1811(98)00041-3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9865446
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9865446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
PubMed publication ID
9865446
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9865446
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9865446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit