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Research 451–480 of 1000+
- Bone morphogenetic protein-2 (BMP-2) transactivates Dlx3 through Smad1 and Smad4: alternative mode for Dlx3 induction in mouse keratinocytes
- Folliculin, the Product of the Birt-Hogg-Dube Tumor Suppressor Gene, Interacts with the Adherens Junction Protein p0071 to Regulate Cell-Cell Adhesion
- Generalized atrophic benign epidermolysis bullosa.
- The color of skin: white diseases of the skin, nails, and mucosa
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Aberrant Activation of the Hedgehog Signaling Pathway in Malignant Hematological Neoplasms
- Swiss Practice Recommendations for the Management of Hidradenitis Suppurativa/Acne Inversa
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Update on hidradenitis suppurativa: connecting the tracts
- Disruption of tubular Flcn expression as a mouse model for renal tumor induction
- Analogs of human genetic skin disease in domesticated animals
- Co-occurrence of monilethrix and Type 1 diabetes mellitus
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- Differential Expression and Analysis of TBX3 Gene in Skin Tissues of Dun Mongolian Horses with and Without Bider Markings
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Polycystic ovary syndrome
- PTEN Mediates Activation of Core Clock Protein BMAL1 and Accumulation of Epidermal Stem Cells
- Junctional Epidermolysis Bullosa, Generalized Intermediate Type
- Frizzled Receptors in Development and Disease
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Vitamin D and skin diseases: A review
- Keratins 6, 16, and 17 in Health and Disease: A Summary of Recent Findings
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- Pleiotropic Role of Notch Signaling in Human Skin Diseases
- An N-Ethyl-N-Nitrosourea Induced Corticotropin-Releasing Hormone Promoter Mutation Provides a Mouse Model for Endogenous Glucocorticoid Excess