D.K.B. Armstrong

Epithelialization in Wound Healing: A Comprehensive Review

Basal cell carcinomas: attack of the hedgehog

Control of somatic tissue differentiation by the long non-coding RNA TINCR

Melanocortin 1 receptor variants and skin cancer risk

Structural and Functional Diversity of Connexin Genes in the Mouse and Human Genome

Digitoxin medication and cancer; case control and internal dose-response studies

Deregulation of keratinocyte differentiation and activation: a hallmark of venous ulcers

The human keratins: biology and pathology

Mutations of the gene encoding the protein kinase A type I-α regulatory subunit in patients with the Carney complex

Porphyrias

Cardiac Glycosides as Novel Cancer Therapeutic Agents

Diseases of epidermal keratins and their linker proteins

Comparisons of Estimated Economic Burdens due to Insufficient Solar Ultraviolet Irradiance and Vitamin D and Excess Solar UV Irradiance for the United States

The cornified envelope: a model of cell death in the skin

Identification and characterization of novel uroporphyrinogen decarboxylase gene mutations in a large series of porphyria cutanea tarda patients and relatives

The skin: an indispensable barrier

A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families

Vitamin D Deficiency in Children and Its Management: Review of Current Knowledge and Recommendations

The desmosome and pemphigus

A recurrent mutation in the loricrin gene underlies the ichthyotic variant of Vohwinkel syndrome

Wound repair and regeneration: Mechanisms, signaling, and translation

Digoxin and other cardiac glycosides inhibit HIF-1α synthesis and block tumor growth

Lessons from Loricrin-Deficient Mice

Nuclear entry and export of FIH are mediated by HIF1α and exportin1, respectively

microRNA-31/factor-inhibiting hypoxia-inducible factor 1 nexus regulates keratinocyte differentiation

Life cycle of connexins in health and disease

Transgenic Mice Expressing a Mutant Form of Loricrin Reveal the Molecular Basis of the Skin Diseases, Vohwinkel Syndrome and Progressive Symmetric Erythrokeratoderma

Identification of a Novel Genetic Locus for Familial Cardiac Myxomas and Carney Complex

Striate palmoplantar keratoderma arising from desmoplakin and desmoglein 1 mutations is associated with contrasting perturbations of desmosomes and the keratin filament network

A Novel Insertional Mutation in Loricrin in Vohwinkel’s Keratoderma

Naevus lipomatosus cutaneous superficialis

Hepatoerythropoietic porphyria: a missense mutation in the UROD gene is associated with mild disease and an unusual porphyrin excretion pattern

Carney complex: report of a kindred with predominantly cutaneous manifestations

Carney complex: report of a kindred with predominantly cutaneous manifestations