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Differing tumor-suppressor functions of Arf and p53 in murine basal cell carcinoma initiation and progression

Oncogene, 2017-06, Vol.36 (26), p.3772-3780

2017

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Mutations in ATP2C1 , encoding a calcium pump, cause Hailey-Hailey disease

Nature genetics, 2000-01, Vol.24 (1), p.61-65

2000

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Activating Smoothened mutations in sporadic basal-cell carcinoma

Nature (London), 1998-01, Vol.391 (6662), p.90-92

1998

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Ultraviolet and ionizing radiation enhance the growth of BCCs and trichoblastomas in patched heterozygous knockout mice

Nature medicine, 1999-11, Vol.5 (11), p.1285-1291

1999

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Basal Cell Carcinomas in Mice Overexpressing Sonic Hedgehog

Science (American Association for the Advancement of Science), 1997-05, Vol.276 (5313), p.817-821

1997

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Epidermolysis Bullosa Simplex: Evidence in Two Families for Keratin Gene Abnormalities

Science (American Association for the Advancement of Science), 1991-11, Vol.254 (5035), p.1202-1205

1991

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Human Homolog of patched, a Candidate Gene for the Basal Cell Nevus Syndrome

Science (American Association for the Advancement of Science), 1996-06, Vol.272 (5268), p.1668-1671

1996

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Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis

Nature genetics, 1998-12, Vol.20 (4), p.366-369

1998

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Novel keratin 16 mutations and protein expression studies in pachyonychia congenita type 1 and focal palmoplantar keratoderma

Experimental dermatology, 2000-06, Vol.9 (3), p.170-177

2000

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Dupilumab improved atypical fibrotic skin plaques in atopic dermatitis

British journal of dermatology (1951), 2020-02, Vol.182 (2), p.487-488

2020

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Cloning of a cDNA for Steroid Sulfatase: Frequent Occurrence of Gene Deletions in Patients with Recessive X Chromosome-Linked Ichthyosis

Proceedings of the National Academy of Sciences - PNAS, 1987-12, Vol.84 (24), p.9248-9251

1987

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Molecular Genetics of Epidermolysis Bullosa

Science (American Association for the Advancement of Science), 1992-05, Vol.256 (5058), p.799-804

Epstein, Ervin H.

1992

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Identification of Mutations in the Human PATCHED Gene in Sporadic Basal Cell Carcinomas and in Patients with the Basal Cell Nevus Syndrome

Journal of investigative dermatology, 1998-06, Vol.110 (6), p.885-888

1998

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Mutations of the PATCHED gene in several types of sporadic extracutaneous tumors

Cancer research (Chicago, Ill.), 1997-06, Vol.57 (12), p.2369-2372

1997

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Activation of Expression of Hedgehog Target Genes in Basal Cell Carcinomas

Journal of investigative dermatology, 2001-05, Vol.116 (5), p.739-742

2001

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Identification of a novel mutation in keratin 1 in a family with epidermolytic hyperkeratosis

Experimental dermatology, 2000-02, Vol.9 (1), p.16-19

2000

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Ultraviolet B (UVB)-Induced COX-2 Expression in Murine Skin: An Immunohistochemical Study

Biochemical and biophysical research communications, 2001-02, Vol.280 (4), p.1042-1047

2001

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The genetics of human skin diseases

Current opinion in genetics & development, 1996-06, Vol.6 (3), p.295-300

Epstein, Ervin H

1996

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Lamellar Body-Enriched Fractions from Neonatal Mice: Preparative Techniques and Partial Characterization

Journal of investigative dermatology, 1985-10, Vol.85 (4), p.289-294

1985

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Stratum corneum lipids in disorders of cornification: steroid sulfatase and cholesterol sulfate in normal desquamation and the pathogenesis or recessive X-linked ichthyosis

The Journal of clinical investigation, 1984-10, Vol.74 (4), p.1414-1421

1984

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Localization of the gene whose mutations underlie Hailey—Hailey disease to chromosome 3q

Human molecular genetics, 1994-07, Vol.3 (7), p.1147-1150

1994

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Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the gamma 2 subunit of nicein/kalinin (LAMININ-5)

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

1994

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Loss of heterozygosity at chromosome 1q22 in basal cell carcinomas and exclusion of the basal cell nevus syndrome gene from this site

Cancer research (Chicago, Ill.), 1992-03, Vol.52 (6), p.1494-1498

1992

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Ultraviolet Radiation Mutagenesis of Hedgehog Pathway Genes in Basal Cell Carcinomas

The Journal of investigative dermatology symposium proceedings, 1999-09, Vol.4 (1), p.41-45

1999

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Immunoprevention of basal cell carcinomas with recombinant hedgehog-interacting protein

The Journal of experimental medicine, 2004-03, Vol.199 (6), p.753-761

2004

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Differing tumor-suppressor functions of Arf and p53 in murine basal cell carcinoma initiation and progression

Mutations in ATP2C1 , encoding a calcium pump, cause Hailey-Hailey disease

Activating Smoothened mutations in sporadic basal-cell carcinoma

Ultraviolet and ionizing radiation enhance the growth of BCCs and trichoblastomas in patched heterozygous knockout mice

Basal Cell Carcinomas in Mice Overexpressing Sonic Hedgehog

Epidermolysis Bullosa Simplex: Evidence in Two Families for Keratin Gene Abnormalities

Human Homolog of patched, a Candidate Gene for the Basal Cell Nevus Syndrome

Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis

Novel keratin 16 mutations and protein expression studies in pachyonychia congenita type 1 and focal palmoplantar keratoderma

Dupilumab improved atypical fibrotic skin plaques in atopic dermatitis

Cloning of a cDNA for Steroid Sulfatase: Frequent Occurrence of Gene Deletions in Patients with Recessive X Chromosome-Linked Ichthyosis

Molecular Genetics of Epidermolysis Bullosa

Identification of Mutations in the Human PATCHED Gene in Sporadic Basal Cell Carcinomas and in Patients with the Basal Cell Nevus Syndrome

Mutations of the PATCHED gene in several types of sporadic extracutaneous tumors

Activation of Expression of Hedgehog Target Genes in Basal Cell Carcinomas

Identification of a novel mutation in keratin 1 in a family with epidermolytic hyperkeratosis

Ultraviolet B (UVB)-Induced COX-2 Expression in Murine Skin: An Immunohistochemical Study

The genetics of human skin diseases

Lamellar Body-Enriched Fractions from Neonatal Mice: Preparative Techniques and Partial Characterization

Stratum corneum lipids in disorders of cornification: steroid sulfatase and cholesterol sulfate in normal desquamation and the pathogenesis or recessive X-linked ichthyosis

Localization of the gene whose mutations underlie Hailey—Hailey disease to chromosome 3q

Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the gamma 2 subunit of nicein/kalinin (LAMININ-5)

Loss of heterozygosity at chromosome 1q22 in basal cell carcinomas and exclusion of the basal cell nevus syndrome gene from this site

Ultraviolet Radiation Mutagenesis of Hedgehog Pathway Genes in Basal Cell Carcinomas

Immunoprevention of basal cell carcinomas with recombinant hedgehog-interacting protein

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