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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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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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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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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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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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Glycine Substitution Mutations in the Type VII Collagen Gene (COL7A1) in Dystrophic Epidermolysis Bullosa: Implications for Genetic Counseling

Journal of investigative dermatology, 1997-02, Vol.108 (2), p.224-228

1997

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A Glycine-to-Arginine Substitution in the Triple-Helical Domain of Type VII Collagen in a Family with Dominant Dystrophic Epidermolysis Bullosa Pruriginosa

Journal of investigative dermatology, 1997-06, Vol.108 (6), p.947-949

1997

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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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A Homozygous In-Frame Deletion in the Collagenous Domain of Bullous Pemphigoid Antigen BP180 (Type XVII Collagen) Causes Generalized Atrophic Benign Epidermolysis Bullosa

Journal of investigative dermatology, 1997-07, Vol.109 (1), p.74-78

1997

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The human breast cell DNA synthesome: its purification from tumor tissue and cell culture

Oncology research, 1996, Vol.8 (10-11), p.435

1996

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KRT14 Haploinsufficiency Results in Increased Susceptibility of Keratinocytes to TNF-α-Induced Apoptosis and Causes Naegeli–Franceschetti–Jadassohn Syndrome

Journal of investigative dermatology, 2008-06, Vol.128 (6), p.1517-1524

2008

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Laser treatment of keloids: A clinical trial and an in vitro study with Nd:YAG laser

Lasers in surgery and medicine, 1984, Vol.4 (3), p.291-295

1984

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Mapping of epidermolysis bullosa simplex mutation to chromosome 12

American journal of human genetics, 1991-11, Vol.49 (5), p.978-984

1991

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Mapping specific protein-protein interactions within the core component of the breast cell DNA synthesome

Oncology research, 1997, Vol.9 (11-12), p.629

1997

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Maternal Uniparental Disomy of Chromosome 1 with Reduction to Homozygosity of the LAMB3 Locus in a Patient with Herlitz Junctional Epidermolysis Bullosa

American journal of human genetics, 1997-09, Vol.61 (3), p.611-619

1997

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Maternal Uniparental Meroisodisomy in the LAMB3 Region of Chromosome 1 Results in Lethal Junctional Epidermolysis Bullosa

Journal of investigative dermatology, 1998-05, Vol.110 (5), p.828-831

1998

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

Nature genetics, 1996-05, Vol.13 (1), p.70-77

1996

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A mutation detection strategy for the human keratin 6A gene and novel missense mutations in two cases of pachyonychia congenita type 1

Experimental dermatology, 1999-04, Vol.8 (2), p.109-114

1999

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Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy

Nature genetics, 1997-06, Vol.16 (2), p.184-187

1997

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Novel COL7A1 Mutations in Dystrophic Forms of Epidermolysis Bullosa

Journal of investigative dermatology, 1998-09, Vol.111 (3), p.534-537

1998

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Novel Glycine Substitution Mutations in COL7A1 Reveal that the Pasini and Cockayne–Touraine Variants of Dominant Dystrophic Epidermolysis Bullosa Are Allelic

Journal of investigative dermatology, 1997-11, Vol.109 (5), p.684-687

1997

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Papillon–Lefèvre Syndrome: Mutations and Polymorphisms in the Cathepsin C Gene

Journal of investigative dermatology, 2001-02, Vol.116 (2), p.339-343

2001

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

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

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)

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

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

Glycine Substitution Mutations in the Type VII Collagen Gene (COL7A1) in Dystrophic Epidermolysis Bullosa: Implications for Genetic Counseling

A Glycine-to-Arginine Substitution in the Triple-Helical Domain of Type VII Collagen in a Family with Dominant Dystrophic Epidermolysis Bullosa Pruriginosa

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

A Homozygous In-Frame Deletion in the Collagenous Domain of Bullous Pemphigoid Antigen BP180 (Type XVII Collagen) Causes Generalized Atrophic Benign Epidermolysis Bullosa

The human breast cell DNA synthesome: its purification from tumor tissue and cell culture

KRT14 Haploinsufficiency Results in Increased Susceptibility of Keratinocytes to TNF-α-Induced Apoptosis and Causes Naegeli–Franceschetti–Jadassohn Syndrome

Laser treatment of keloids: A clinical trial and an in vitro study with Nd:YAG laser

Mapping of epidermolysis bullosa simplex mutation to chromosome 12

Mapping specific protein-protein interactions within the core component of the breast cell DNA synthesome

Maternal Uniparental Disomy of Chromosome 1 with Reduction to Homozygosity of the LAMB3 Locus in a Patient with Herlitz Junctional Epidermolysis Bullosa

Maternal Uniparental Meroisodisomy in the LAMB3 Region of Chromosome 1 Results in Lethal Junctional Epidermolysis Bullosa

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

A mutation detection strategy for the human keratin 6A gene and novel missense mutations in two cases of pachyonychia congenita type 1

Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy

Novel COL7A1 Mutations in Dystrophic Forms of Epidermolysis Bullosa

Novel Glycine Substitution Mutations in COL7A1 Reveal that the Pasini and Cockayne–Touraine Variants of Dominant Dystrophic Epidermolysis Bullosa Are Allelic

Papillon–Lefèvre Syndrome: Mutations and Polymorphisms in the Cathepsin C Gene

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