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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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Collagenase activity in gingival crevicular fluid of patients with juvenile periodontitis

Oral microbiology and immunology, 1991-02, Vol.6 (1), p.24-29

1991

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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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Connective tissue alterations in systemic sclerosis

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

1994

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Cutaneous gene therapy : Principles and prospects: New and Emerging Therapies

Dermatologic clinics, 2000, Vol.18 (1)

2000

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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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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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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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Genomic Organization and Fine Mapping of the Keratin 2e Gene (KRT2E): K2e V1 Domain Polymorphism and Novel Mutations in Ichthyosis Bullosa of Siemens

Journal of investigative dermatology, 1998-11, Vol.111 (5), p.817-821

1998

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Glucocorticoid receptors in cultured human skin fibroblsts: evidence for down-regulation of receptor by glucocorticoid hormone

Acta dermato-venereologica, 1987, Vol.67 (6), p.461-468

1987

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Herlitz Junctional Epidermolysis Bullosa: Novel and Recurrent Mutations in the LAMB3 Gene and the Population Carrier Frequency

Journal of investigative dermatology, 2000-09, Vol.115 (3), p.493-498

2000

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Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the γ2 subunit of nicein/kalinin (LAMININ-5)

Nature genetics, 1994-03, Vol.6 (3), p.299-304

1994

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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

Collagenase activity in gingival crevicular fluid of patients with juvenile periodontitis

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

Connective tissue alterations in systemic sclerosis

Cutaneous gene therapy : Principles and prospects: New and Emerging Therapies

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

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

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

Genomic Organization and Fine Mapping of the Keratin 2e Gene (KRT2E): K2e V1 Domain Polymorphism and Novel Mutations in Ichthyosis Bullosa of Siemens

Glucocorticoid receptors in cultured human skin fibroblsts: evidence for down-regulation of receptor by glucocorticoid hormone

Herlitz Junctional Epidermolysis Bullosa: Novel and Recurrent Mutations in the LAMB3 Gene and the Population Carrier Frequency

Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the γ2 subunit of nicein/kalinin (LAMININ-5)

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