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Hereditary skin diseases of hemidesmosomes
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
10379703
retrieved
28 July 2017
review article
1 reference
stated in
Europe PubMed Central
title
Hereditary skin diseases of hemidesmosomes
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
10379703
retrieved
28 July 2017
main subject
skin disease
1 reference
based on heuristic
inferred from title
author name string
Jonkman MF
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
10379703
retrieved
28 July 2017
publication date
1 June 1999
1 reference
stated in
Europe PubMed Central
PubMed ID
10379703
retrieved
28 July 2017
published in
Journal of Dermatological Science
1 reference
stated in
Europe PubMed Central
PubMed ID
10379703
retrieved
28 July 2017
volume
20
1 reference
stated in
Europe PubMed Central
PubMed ID
10379703
retrieved
28 July 2017
page(s)
103-121
1 reference
stated in
Europe PubMed Central
PubMed ID
10379703
retrieved
28 July 2017
issue
2
1 reference
stated in
Europe PubMed Central
PubMed ID
10379703
retrieved
28 July 2017
cites work
Hemidesmosomes: roles in adhesion, signaling and human diseases
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Acquired skin disease of hemidesmosomes
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Crossref
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7 January 2021
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Molecular complexity of the cutaneous basement membrane zone. Revelations from the paradigms of epidermolysis bullosa
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Crossref
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7 January 2021
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Hemidesmosomal variants of epidermolysis bullosa. Mutations in the alpha6beta4 integrin and the 180-kD bullous pemphigoid antigen/type XVII collagen genes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary skin diseases of anchoring fibrils
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mutation in human keratin K6b produces a phenocopy of the K17 disorder pachyonychia congenita type 2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2.
1 reference
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Crossref
reference URL
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7 January 2021
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Point mutations in human keratin 14 genes of epidermolysis bullosa simplex patients: Genetic and functional analyses
1 reference
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Crossref
reference URL
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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
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A structural scaffolding of intermediate filaments in health and disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
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%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The cytoskeleton and disease: genetic disorders of intermediate filaments
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Severe palmo-plantar hyperkeratosis in Dowling-Meara epidermolysis bullosa simplex caused by a mutation in the keratin 14 gene (KRT14)
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
The genetic basis of epidermolysis bullosa simplex with mottled pigmentation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
A mutation in the V1 domain of keratin 5 causes epidermolysis bullosa simplex with mottled pigmentation.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Epidermolysis Bullosa Simplex (Dowling-Meara Type) Is a Genetic Disease Characterized by an Abnormal Keratin-Filament Network Involving Keratins K5 and K14
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Epidermolysis bullosa simplex, Dowling-Meara type. A report of two cases with different types of tonofilament clumping
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ultrastructural identification of basic abnormalities as clues to genetic disorders of the epidermis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Partial dominance of a keratin 14 mutation in epidermolysis bullosa simplex--increased severity of disease in a homozygote
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A human keratin 14 "knockout": the absence of K14 leads to severe epidermolysis bullosa simplex and a function for an intermediate filament protein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A functional "knockout" of human keratin 14.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Effects of keratin 14 ablation on the clinical and cellular phenotype in a kindred with recessive epidermolysis bullosa simplex
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homozygous nonsense mutation in helix 2 of K14 causes severe recessive epidermolysis bullosa simplex
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Three neonatal cases of epidermolysis bullosa herpetiformis (Dowling-Meara type) with severe erosive skin lesions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lethal Dowling-Meara-type epidermolysis bullosa simplex in a young infant
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Monoclonal antibody mapping of structural and functional plectin epitopes
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Isolation of complementary DNA for bullous pemphigoid antigen by use of patients' autoantibodies
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
IFAP 300 is common to desmosomes and hemidesmosomes and is a possible linker of intermediate filaments to these junctions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel hemidesmosomal plaque component: tissue distribution and incorporation into assembling hemidesmosomes in an in vitro model
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Laminin-5 and modulation of keratin cytoskeleton arrangement in FG pancreatic carcinoma cells: involvement of IFAP300 and evidence that laminin-5/cell interactions correlate with a dephosphorylation of alpha 6A integrin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
The plakin family: versatile organizers of cytoskeletal architecture
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cloning and sequencing of rat plectin indicates a 466-kD polypeptide chain with a three-domain structure based on a central alpha-helical coiled coil.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Targeted inactivation of plectin reveals essential function in maintaining the integrity of skin, muscle, and heart cytoarchitecture
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Intermediate filament-associated proteins
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Linking integrin alpha6beta4-based cell adhesion to the intermediate filament cytoskeleton: direct interaction between the beta4 subunit and plectin at multiple molecular sites.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a new hemidesmosomal protein, HD1: a major, high molecular mass component of isolated hemidesmosomes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organization
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Defective expression of plectin/HD1 in epidermolysis bullosa simplex with muscular dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Plectin deficiency results in muscular dystrophy with epidermolysis bullosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homozygous deletion mutations in the plectin gene (PLEC1) in patients with epidermolysis bullosa simplex associated with late-onset muscular dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A homozygous nonsense mutation in the PLEC1 gene in patients with epidermolysis bullosa simplex with muscular dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hemidesmosomes show abnormal association with the keratin filament network in junctional forms of epidermolysis bullosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Plectin and human genetic disorders of the skin and muscle. The paradigm of epidermolysis bullosa with muscular dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A panel of monoclonal antibodies to rat plectin: distinction by epitope mapping and immunoreactivity with different tissues and cell lines.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Plectin abnormality in epidermolysis bullosa simplex Ogna: non-responsiveness of basal keratinocytes to some anti-rat plectin antibodies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
GPT--epidermolysis bullosa simplex (EBS Ogna) linkage in man
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human plectin: organization of the gene, sequence analysis, and chromosome localization (8q24)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comparative structural analysis of desmoplakin, bullous pemphigoid antigen and plectin: members of a new gene family involved in organization of intermediate filaments
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gene targeting of BPAG1: abnormalities in mechanical strength and cell migration in stratified epithelia and neurologic degeneration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An essential cytoskeletal linker protein connecting actin microfilaments to intermediate filaments.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Integrin alpha 6/beta 4 complex is located in hemidesmosomes, suggesting a major role in epidermal cell-basement membrane adhesion
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
HD4, a 180 kDa bullous pemphigoid antigen, is a major transmembrane glycoprotein of the hemidesmosome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The alpha 6 beta 4 integrin is a receptor for both laminin and kalinin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Signal transduction by the alpha 6 beta 4 integrin: distinct beta 4 subunit sites mediate recruitment of Shc/Grb2 and association with the cytoskeleton of hemidesmosomes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hemidesmosome formation is initiated by the beta4 integrin subunit, requires complex formation of beta4 and HD1/plectin, and involves a direct interaction between beta4 and the bullous pemphigoid antigen 180
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Integrin alpha 6 beta 4 forms a complex with the cytoskeletal protein HD1 and induces its redistribution in transfected COS-7 cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Direct interaction between the intracellular domains of bullous pemphigoid antigen 2 (BP180) and beta 4 integrin, hemidesmosomal components of basal keratinocytes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The localization of bullous pemphigoid antigen 180 (BP180) in hemidesmosomes is mediated by its cytoplasmic domain and seems to be regulated by the beta4 integrin subunit
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Junctional epidermolysis bullosis: defects in expression of epiligrin/nicein/kalinin and integrin beta 4 that inhibit hemidesmosome formation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Integrin beta 4 mutations associated with junctional epidermolysis bullosa with pyloric atresia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel ITGB4 mutations in a patient with junctional epidermolysis bullosa-pyloric atresia syndrome and altered basement membrane zone immunofluorescence for the alpha6beta4 integrin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel ITGB4 mutations in lethal and nonlethal variants of epidermolysis bullosa with pyloric atresia: missense versus nonsense
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A homozygous mutation in the integrin alpha6 gene in junctional epidermolysis bullosa with pyloric atresia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homozygous alpha6 integrin mutation in junctional epidermolysis bullosa with congenital duodenal atresia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital pyloric atresia and junctional epidermolysis bullosa: A report of long-term survival and a review of the literature
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The pyloric atresia-junctional epidermolysis bullosa syndrome. Report of a case and review of the literature
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Junctional epidermolysis bullosa, pyloric atresia, and genitourinary disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Severe congenital skin defects in a newborn. Case report and relevance of several obstetrical parameters
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Absence of integrin alpha 6 leads to epidermolysis bullosa and neonatal death in mice.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Epithelial detachment due to absence of hemidesmosomes in integrin beta 4 null mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Beta4 integrin is required for hemidesmosome formation, cell adhesion and cell survival
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cell cycle and adhesion defects in mice carrying a targeted deletion of the integrin beta4 cytoplasmic domain.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A requirement for caveolin-1 and associated kinase Fyn in integrin signaling and anchorage-dependent cell growth
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The coupling of alpha6beta4 integrin to Ras-MAP kinase pathways mediated by Shc controls keratinocyte proliferation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The adaptor protein Shc couples a class of integrins to the control of cell cycle progression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Activation of phosphoinositide 3-OH kinase by the alpha6beta4 integrin promotes carcinoma invasion
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
α3β1 Integrin Is Required for Normal Development of the Epidermal Basement Membrane
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Distinct functions for integrins alpha 3 beta 1 in focal adhesions and alpha 6 beta 4/bullous pemphigoid antigen in a new stable anchoring contact (SAC) of keratinocytes: relation to hemidesmosomes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isolation and characterization of laminin-10/11 secreted by human lung carcinoma cells. laminin-10/11 mediates cell adhesion through integrin alpha3 beta1.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Generalized atrophic benign epidermolysis bullosa. Either 180-kd bullous pemphigoid antigen or laminin-5 deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cloning and primary structural analysis of the bullous pemphigoid autoantigen BP180
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Bullous pemphigoid and linear IgA dermatosis sera recognize a similar 120-kDa keratinocyte collagenous glycoprotein with antigenic cross-reactivity to BP180
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Demonstration of the molecular shape of BP180, a 180-kDa bullous pemphigoid antigen and its potential for trimer formation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A recombinant form of the human BP180 ectodomain forms a collagen-like homotrimeric complex
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Type XVII collagen (BP180) and LAD-1 are present as separate trimeric complexes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Two forms of collagen XVII in keratinocytes. A full-length transmembrane protein and a soluble ectodomain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Bullous pemphigoid and cicatricial pemphigoid autoantibodies react with ultrastructurally separable epitopes on the BP180 ectodomain: evidence that BP180 spans the lamina lucida
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The extracellular domain of BPAG2 localizes to anchoring filaments and its carboxyl terminus extends to the lamina densa of normal human epidermal basement membrane
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The hemidesmosomal plaque
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expression of type XVII collagen alpha 1 chain mRNA in the mouse heart.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular genetic studies of a human epidermal autoantigen (the 180-kD bullous pemphigoid antigen/BP180): identification of functionally important sequences within the BP180 molecule and evidence for an interaction between BP180 and alpha 6 integrin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Role of the bullous pemphigoid antigen 180 (BP180) in the assembly of hemidesmosomes and cell adhesion--reexpression of BP180 in generalized atrophic benign epidermolysis bullosa keratinocytes.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
180-kD bullous pemphigoid antigen (BP180) is deficient in generalized atrophic benign epidermolysis bullosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Diminished expression of the extracellular domain of bullous pemphigoid antigen 2 (BPAG2) in the epidermal basement membrane of patients with generalized atrophic benign epidermolysis bullosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the 180-kD bullous pemphigoid antigen (BPAG2), a hemidesmosomal transmembrane collagen (COL17A1), in generalized atrophic benign epidermolysis bullosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A homozygous deletion mutation in the gene encoding the 180-kDa bullous pemphigoid antigen (BPAG2) in a family with generalized atrophic benign epidermolysis bullosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Revertant mosaicism in epidermolysis bullosa caused by mitotic gene conversion
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Implications of intragenic marker homozygosity and haplotype sharing in a rare autosomal recessive disorder: the example of the collagen type XVII (COL17A1) locus in generalised atrophic benign epidermolysis bullosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Three novel homozygous point mutations and a new polymorphism in the COL17A1 gene: relation to biological and clinical phenotypes of junctional epidermolysis bullosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A homozygous in-frame deletion in the collagenous domain of bullous pemphigoid antigen BP180 (type XVII collagen) causes generalized atrophic benign epidermolysis bullosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Premature termination codons are present on both alleles of the bullous pemphigoid antigen 2/type XVII collagen gene in five Austrian families with generalized atrophic benign epidermolysis bullosa.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prognostic implications of determining 180 kDa bullous pemphigoid antigen (BPAG2) gene/protein pathology in neonatal junctional epidermolysis bullosa.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A deletion mutation in COL17A1 in five Austrian families with generalized atrophic benign epidermolysis bullosa represents propagation of an ancestral allele
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cycloheximide facilitates the identification of aberrant transcripts resulting from a novel splice-site mutation in COL17A1 in a patient with generalized atrophic benign epidermolysis bullosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel homozygous and compound heterozygous COL17A1 mutations associated with junctional epidermolysis bullosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The 97 kDa linear IgA bullous dermatosis antigen is not expressed in a patient with generalized atrophic benign epidermolysis bullosa with a novel homozygous G258X mutation in COL17A1.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Generalized atrophic benign epidermolysis bullosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Collagen metabolism in two rare forms of epidermolysis bullosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Benign junctional epidermolysis bullosa in three related Moroccan families
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Generalized atrophic benign form of junctional epidermolysis bullosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Junctional epidermolysis bullosa with urethral stricture
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Epidermolysis bullosa atrophicans generalisata mitis--report of a case with renal dysfunction
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
180-kDa bullous pemphigoid antigen defective generalized atrophic benign epidermolysis bullosa: report of four cases with an unusually mild phenotype.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ultrastructural morphometry of normal human dermal-epidermal junction. The influence of age, sex, and body region on laminar and nonlaminar components
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The basement membrane. Interface between the epithelium and the dermis: structural features
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hemidesmosome heterogeneity in junctional epidermolysis bullosa revealed by morphometric analysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Kalinin: an epithelium-specific basement membrane adhesion molecule that is a component of anchoring filaments
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
19-DEJ-1, a hemidesmosome-anchoring filament complex-associated monoclonal antibody. Definition of a new skin basement membrane antigenic defect in junctional and dystrophic epidermolysis bullosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
LAD-1, the linear IgA bullous dermatosis autoantigen, is a novel 120-kDa anchoring filament protein synthesized by epidermal cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
97-kDa linear IgA bullous dermatosis (LAD) antigen localizes to the lamina lucida of the epidermal basement membrane
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cloning and chromosomal mapping of mouse ladinin, a novel basement membrane zone component
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Localization of laminin-5 in the epidermal basement membrane
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Basement Membrane Proteins: Structure, Assembly, and Cellular Interactions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
19-DEJ-1, a monoclonal antibody to the hemidesmosome-anchoring filament complex, is the only reliable immunohistochemical probe for all major forms of junctional epidermolysis bullosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Type VII collagen and 19-DEJ-1 antigen. Comparison of expression in inversa and generalized variants of recessive dystrophic epidermolysis bullosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mosaic expression of uncein, linear IgA bullous dermatosis antigen and 180-kDa bullous pemphigoid antigen in generalized atrophic benign epidermolysis bullosa.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification and partial characterization of a novel 105-kDalton lower lamina lucida autoantigen associated with a novel immune-mediated subepidermal blistering disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Defective in vivo expression and apparently normal in vitro expression of a newly identified 105-kDa lower lamina lucida protein in dystrophic epidermolysis bullosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel subepidermal blistering disease with autoantibodies to a 200-kDa antigen of the basement membrane zone
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The 97 kDa linear IgA bullous disease antigen is identical to a portion of the extracellular domain of the 180 kDa bullous pemphigoid antigen, BPAg2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cleavage of BP180, a 180-kDa bullous pemphigoid antigen, yields a 120-kDa collagenous extracellular polypeptide
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
LAD-1 is absent in a subset of junctional epidermolysis bullosa patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new nomenclature for the laminins
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The dermal-epidermal junction
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The functions of laminins: lessons from in vivo studies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Laminin 5 binds the NC-1 domain of type VII collagen
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The assembly of laminin-5 subunits
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Self-assembly of laminin isoforms
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human amnion contains a novel laminin variant, laminin 7, which like laminin 6, covalently associates with laminin 5 to promote stable epithelial-stromal attachment
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The laminin alpha chains: expression, developmental transitions, and chromosomal locations of alpha1-5, identification of heterotrimeric laminins 8-11, and cloning of a novel alpha3 isoform
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
GB3 monoclonal antibody for diagnosis of junctional epidermolysis bullosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Herlitz junctional epidermolysis bullosa keratinocytes display heterogeneous defects of nicein/kalinin gene expression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cloning of the laminin alpha 3 chain gene (LAMA3) and identification of a homozygous deletion in a patient with Herlitz junctional epidermolysis bullosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A homozygous nonsense mutation in the beta 3 chain gene of laminin 5 (LAMB3) in Herlitz junctional epidermolysis bullosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the gamma 2 subunit of nicein/kalinin (LAMININ-5)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Extent of laminin-5 assembly and secretion effect junctional epidermolysis bullosa phenotype.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Immunohistochemical analysis of the skin in junctional epidermolysis bullosa using laminin 5 chain specific antibodies is of limited value in predicting the underlying gene mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Compound heterozygosity for nonsense ans missense mutations in the LAMB3 gene in nonlethal junctional epidermolysis bullosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular basis of non-lethal junctional epidermolysis bullosa: identification of a 38 basepair insertion and a splice site mutation in exon 14 of the LAMB3 gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expression of laminin alpha3, alpha4, and alpha5 chains by alveolar epithelial cells and fibroblasts
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
IAP insertion in the murine LamB3 gene results in junctional epidermolysis bullosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0923-1811%2899%2900017-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0923-1811(99)00017-1
1 reference
stated in
Europe PubMed Central
PubMed ID
10379703
retrieved
28 July 2017
PubMed ID
10379703
1 reference
stated in
Europe PubMed Central
PubMed ID
10379703
retrieved
28 July 2017
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