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Research 91–120 of 1000+
- Skin Graft
- Westwood Carolina Conference on Clinical Dermatology
- Skin Development and Disease: A Molecular Perspective
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- Platelet-rich Plasma Injection and Lipofilling-assisted Hair Transplantation on Residual Scalp Alopecia Post Aplasia Cutis Congenita Verticis (ACCV)
- Immunological control of skin development: from homeostasis to developmental pathologies
- Scalp Reconstruction
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- [Nevus comedonicus. A rare skin disease of the hair follicles].
- Forkhead/winged-helix transcription factor whn regulates hair keratin gene expression: Molecular analysis of theNude skin phenotype
- Keratin disorders: from gene to therapy
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- Aplasia cutis congenita on lumbosacral area
- Hair loss in children.
- What does acne genetics teach us about disease pathogenesis?
- Clinical Experience With Tissue Expansion
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Acne-Associated Syndromes
- The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
- Role of Stearoyl-CoA Desaturase-1 in Skin Integrity and Whole Body Energy Balance
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Hair follicle stem cell progeny heal blisters while pausing skin development