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Research 601–630 of 1000+
- Transcriptomic Analysis Reveals Candidate Ligand-Receptor Pairs and Signaling Networks Mediating Intercellular Communication between Hair Matrix Cells and Dermal Papilla Cells from Cashmere Goats
- Nanotechnology-Based Strategies for Hair Follicle Regeneration in Androgenetic Alopecia
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- The Case | Bilateral kidney tumors and lung cysts
- The Roles of Smad2 and Smad3 in Mouse Skin Development
- This Month in the Journal
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- Disruption of tubular Flcn expression as a mouse model for renal tumor induction
- Molecular Mechanisms Regulating Hair Follicle Development
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
- The inheritance of common baldness: Two B or not two B ?
- Genetic Disorders and Defects in Vitamin D Action
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- Hair-Cycle-Associated Remodeling of the Peptidergic Innervation of Murine Skin, and Hair Growth Modulation by Neuropeptides
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Role of FGFR2-signaling in the pathogenesis of acne
- Delayed epidermal permeability barrier formation and hair follicle aberrations in Inv-Cldn6 mice
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Lysophospholipid Mediators in Health and Disease
- Trichoscopy in Hair Shaft Disorders
- Pathophysiology of the Behçet's Disease
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color