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Research 31–60 of 1000+
- [G-proteins, receptor signal transduction, and growth hormone secretion].
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- Conditional knock out of N-WASP in keratinocytes causes skin barrier defects and atopic dermatitis-like inflammation
- A comparative study of the effects of 4-META/MMA-TBB resin and cyanoacrylate on wound healing of skin defects
- A Congenital Hair Defect: Trichoschisis With Alternating Birefringence and Low Sulfur Content
- Management of congenital ichthyoses: European guidelines of care, part two
- Line-Field Optical Coherence Tomography: Usefulness in the Non-Invasive Differential Diagnosis of Congenital Alopecia of Infancy
- Stem cells and aberrant signaling of molecular systems in skin aging
- Genetic Defects of Female Sexual Differentiation
- Trichoscopy of aplasia cutis congenita of the scalp in skin of color
- Neuroimaging Findings in Congenital Biotinidase Deficiency: A Case Report
- Enhancing Lower Extremity Defect Coverage: High Viability Ultra-Thin Split-Thickness Skin Grafts Obtained from the Scalp
- Intraoperative Bioprinting of Human Adipose-derived Stem cells and Extra-cellular Matrix Induces Hair Follicle-Like Downgrowths and Adipose Tissue Formation during Full-thickness Craniomaxillofacial Skin Reconstruction
- Hairless is a nuclear receptor corepressor essential for skin function
- Skin, Genetic Defects, and Aging
- Acne in Dark Skin
- Activated Kras Alters Epidermal Homeostasis of Mouse Skin, Resulting in Redundant Skin and Defective Hair Cycling
- MENSTRUAL DISORDERS IN ADOLESCENTS
- Secondary cicatricial and other permanent alopecias
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- Low prevalence of twisted hair in anorexia nervosa
- Congenital triangular alopecia: Is it always confined to fronto-temporal region?
- Defining the identity of mouse embryonic dermal fibroblasts
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- Manual of chemical peels: Superficial and medium depth
- Cutaneous manifestations of systemic infection in children
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy
- Defects in Androgen Biosynthesis Causing 46,XY Disorders of Sexual Development
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1‐deficient Jack Russell Terriers and response to topical ceramide