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A 500-kb region on chromosome 16p13.1 contains the pseudoxanthoma elasticum locus : high-resolution mapping and genomic structure

Journal of molecular medicine (Berlin, Germany), 2000, Vol.78 (1), p.36-46

2000

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Biochemical Composition of the Connective Tissue in Keloids and Analysis of Collagen Metabolism in Keloid Fibroblast Cultures

Journal of investigative dermatology, 1985-05, Vol.84 (5), p.384-390

1985

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Breaking the Connection: Caspase 6 Disconnects Intermediate Filament-Binding Domain of Periplakin from its Actin-Binding N-Terminal Region

Journal of investigative dermatology, 2005-01, Vol.124 (1), p.46-55

2005

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Characterization of elastase-like enzymes in various blistering diseases

Acta dermato-venereologica, 1986, Vol.66 (1), p.1-5

1986

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Classification of pseudoxanthoma elasticum: Report of a consensus conference

Journal of the American Academy of Dermatology, 1994, Vol.30 (1), p.103-107

1994

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Cloning of Partial cDNA for Mouse 180-kDa Bullous Pemphigoid Antigen (BPAG2), a Highly Conserved Collagenous Protein of the Cutaneous Basement Membrane Zone

Journal of investigative dermatology, 1992-09, Vol.99 (3), p.258-263

1992

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A Combination of a Common Splice Site Mutation and Frameshift Mutation in the COL7A1 Gene: Absence of Functional Collagen VII in Keratinocytes and Skin

Journal of investigative dermatology, 1997-09, Vol.109 (3), p.384-389

1997

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Complete Paternal Uniparental Isodisomy of Chromosome 1: A Novel Mechanism for Herlitz Junctional Epidermolysis Bullosa

Journal of investigative dermatology, 2000-08, Vol.115 (2), p.307-311

2000

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Compound Heterozygosity for Non-Sense and Mis-Sense Mutations in Desmoplakin Underlies Skin Fragility/Woolly Hair Syndrome

Journal of investigative dermatology, 2002-02, Vol.118 (2), p.232-238

2002

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Compound Heterozygosity for Novel Splice Site Mutations in the BPAG2/COL17A1 Gene Underlies Generalized Atrophic Benign Epidermolysis Bullosa

Journal of investigative dermatology, 1999-12, Vol.113 (6), p.1114-1118

1999

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Connective tissue alterations in systemic sclerosis

Clinics in dermatology, 1994-07, Vol.12 (3), p.387-396

1994

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Demonstration of Collagenase and Elastase Activities in the Blister Fluids from Bullous Skin Diseases. Comparison Between Dermatitis Herpetiformis and Bullous Pemphigoid

Journal of investigative dermatology, 1983-09, Vol.81 (3), p.261-266

1983

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Dominant Dystrophic Epidermolysis Bullosa (Pasini) Caused by a Novel Glycine Substitution Mutation in the Type VII Collagen Gene (COL7A1)

Journal of investigative dermatology, 1999-05, Vol.112 (5), p.815-817

1999

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Effect of therapeutic radiation on wound healing

Clinics in dermatology, 1994-01, Vol.12 (1), p.57-70

1994

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Enhanced Elastin and Fibrillin Gene Expression in Chronically Photodamaged Skin

Journal of investigative dermatology, 1994-08, Vol.103 (2), p.182-186

1994

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Epidermolysis Bullosa Carrier Frequencies in the US Population

Journal of investigative dermatology, 2001-03, Vol.116 (3), p.483-484

2001

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Epidermolysis Bullosa Simplex Associated with Severe Mucous Membrane Involvement and Novel Mutations in the Plectin Gene

Journal of investigative dermatology, 2000-02, Vol.114 (2), p.376-380

2000

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Epidermolysis Bullosa Simplex: Recurrent and De Novo Mutations in the KRT5 and KRT14 Genes, Phenotype/Genotype Correlations, and Implications for Genetic Counseling and Prenatal Diagnosis

Journal of general internal medicine : JGIM, 2005-08, Vol.125 (2), p.239-243

2005

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Epidermolytic Hyperkeratosis and Epidermolysis Bullosa Simplex Caused by Frameshift Mutations Altering the V2 Tail Domains of Keratin 1 and Keratin 5

Journal of investigative dermatology, 2003-04, Vol.120 (4), p.623-626

2003

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Exacerbation of pemphigus foliaceus after tetanus vaccination accompanied by synthesis of auto-antibodies against paraneoplastic pemphigus antigens

Acta dermato-venereologica, 2002-11, Vol.82 (6), p.482-483

2002

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Expression of p53 in normal sun-exposed and protected skin (type IV-V) in different decades of age

Acta dermato-venereologica, 2003, Vol.83 (2), p.98-104

2003

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Fibronectin Gene Expression by Epithelial Tumor Cells in Basal Cell Carcinoma: An Immunocytochemical and In Situ Hybridization Study

Journal of investigative dermatology, 1988-10, Vol.91 (4), p.289-293

1988

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Four Novel Plectin Gene Mutations in Japanese Patients with Epidermolysis Bullosa with Muscular Dystrophy Disclosed by Heteroduplex Scanning and Protein Truncation Tests

Journal of investigative dermatology, 1999-01, Vol.112 (1), p.109-112

1999

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Genetic Basis of Dominantly Inherited Transient Bullous Dermolysis of the Newborn: A Splice Site Mutation in the Type VII Collagen Gene

Journal of investigative dermatology, 1997-12, Vol.109 (6), p.811-814

1997

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Genetic Linkage Between the Collagen VII (COL7A1) Gene and the Autosomal Dominant Form of Dystrophic Epidermolysis Bullosa in Two Dutch Kindreds

Journal of investigative dermatology, 1992-11, Vol.99 (5), p.528-530

1992

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A 500-kb region on chromosome 16p13.1 contains the pseudoxanthoma elasticum locus : high-resolution mapping and genomic structure

Biochemical Composition of the Connective Tissue in Keloids and Analysis of Collagen Metabolism in Keloid Fibroblast Cultures

Breaking the Connection: Caspase 6 Disconnects Intermediate Filament-Binding Domain of Periplakin from its Actin-Binding N-Terminal Region

Characterization of elastase-like enzymes in various blistering diseases

Classification of pseudoxanthoma elasticum: Report of a consensus conference

Cloning of Partial cDNA for Mouse 180-kDa Bullous Pemphigoid Antigen (BPAG2), a Highly Conserved Collagenous Protein of the Cutaneous Basement Membrane Zone

A Combination of a Common Splice Site Mutation and Frameshift Mutation in the COL7A1 Gene: Absence of Functional Collagen VII in Keratinocytes and Skin

Complete Paternal Uniparental Isodisomy of Chromosome 1: A Novel Mechanism for Herlitz Junctional Epidermolysis Bullosa

Compound Heterozygosity for Non-Sense and Mis-Sense Mutations in Desmoplakin Underlies Skin Fragility/Woolly Hair Syndrome

Compound Heterozygosity for Novel Splice Site Mutations in the BPAG2/COL17A1 Gene Underlies Generalized Atrophic Benign Epidermolysis Bullosa

Connective tissue alterations in systemic sclerosis

Demonstration of Collagenase and Elastase Activities in the Blister Fluids from Bullous Skin Diseases. Comparison Between Dermatitis Herpetiformis and Bullous Pemphigoid

Dominant Dystrophic Epidermolysis Bullosa (Pasini) Caused by a Novel Glycine Substitution Mutation in the Type VII Collagen Gene (COL7A1)

Effect of therapeutic radiation on wound healing

Enhanced Elastin and Fibrillin Gene Expression in Chronically Photodamaged Skin

Epidermolysis Bullosa Carrier Frequencies in the US Population

Epidermolysis Bullosa Simplex Associated with Severe Mucous Membrane Involvement and Novel Mutations in the Plectin Gene

Epidermolysis Bullosa Simplex: Recurrent and De Novo Mutations in the KRT5 and KRT14 Genes, Phenotype/Genotype Correlations, and Implications for Genetic Counseling and Prenatal Diagnosis

Epidermolytic Hyperkeratosis and Epidermolysis Bullosa Simplex Caused by Frameshift Mutations Altering the V2 Tail Domains of Keratin 1 and Keratin 5

Exacerbation of pemphigus foliaceus after tetanus vaccination accompanied by synthesis of auto-antibodies against paraneoplastic pemphigus antigens

Expression of p53 in normal sun-exposed and protected skin (type IV-V) in different decades of age

Fibronectin Gene Expression by Epithelial Tumor Cells in Basal Cell Carcinoma: An Immunocytochemical and In Situ Hybridization Study

Four Novel Plectin Gene Mutations in Japanese Patients with Epidermolysis Bullosa with Muscular Dystrophy Disclosed by Heteroduplex Scanning and Protein Truncation Tests

Genetic Basis of Dominantly Inherited Transient Bullous Dermolysis of the Newborn: A Splice Site Mutation in the Type VII Collagen Gene

Genetic Linkage Between the Collagen VII (COL7A1) Gene and the Autosomal Dominant Form of Dystrophic Epidermolysis Bullosa in Two Dutch Kindreds

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