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Research 181–210 of 1000+
- Delayed Cutaneous Wound Healing and Aberrant Expression of Hair Follicle Stem Cell Markers in Mice Selectively Lacking Ctip2 in Epidermis
- Directed Expression of Keratin 16 to the Progenitor Basal Cells of Transgenic Mouse Skin Delays Skin Maturation
- Generalized atrophic benign epidermolysis bullosa.
- Histological and molecular restoration of type VII collagen in Recessive dystrophic epidermolysis bullosa mouse skin by topical injection of keratinocyte-like cells differentiated from human adipose-derived mesenchymal stromal cells
- PA11 A rare case of a severe papulopustular dermatosis secondary to a germline <i>EGFR</i> mutation
- 0873 Modeling junctional epidermolysis bullosa using tissue-engineered skin substitutes
- Local IL-17 orchestrates skin aging
- Effects of Skin Lightening Cream Agents – Hydroquinone and Kojic Acid, on the Skin of Adult Female Experimental Rats
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Alkaline ceramidase 1 is essential for mammalian skin homeostasis and regulating whole‐body energy expenditure
- Type I Keratin 17 Protein Is Phosphorylated on Serine 44 by p90 Ribosomal Protein S6 Kinase 1 (RSK1) in a Growth- and Stress-dependent Fashion
- Dietary lipids are largely deposited in skin and rapidly affect insulating properties
- Scanning electron microscopy of murine skin ultrathin sections and cultured keratinocytes
- The Utility of De-epithelialization in Subcutaneous Skin Flap Transposition.
- Selective photothermolysis to target sebaceous glands: Theoretical estimation of parameters and preliminary results using a free electron laser
- Skin Development and Disease: A Molecular Perspective
- The Scientific Legacy of Stephen Rothman
- Localization, Age- and Site-Dependent Expression, and Regulation of 11β-Hydroxysteroid Dehydrogenase Type 1 in Skin
- Keratins and disease at a glance
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Dermatoporosis: a further step to recognition
- Advances in Microengineered Platforms for Skin Research
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Transcriptome analysis reveals the genetic basis underlying the development of skin appendages and immunity in hedgehog (Atelerix albiventris)
- LEKTI: Netherton Syndrome and Atopic Dermatitis
- Anatomical and Dermatologic Manifestations of Estrogen Deficiency in Postmenopausal Women: A Systematic Review
- Expanding the Cutaneous Spectrum of Nicolaides‑Baraitser Syndrome: Eczema and Generalized Hair Loss