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Research 721–750 of 1000+
- WRIST PAIN IN A GYMNAST WITH PRIMARY AMENORRHEA
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- 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.
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Causes and Management of Hypertrichosis
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- The Link Between Obesity and the Skin
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Wnt/β-Catenin Signaling Stabilizes Hemidesmosomes in Keratinocytes
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- Acne-Associated Syndromes
- Solitary Nodular Lesion Over Face
- Characterization of distinct microbiota associated with androgenetic alopecia patients treated and untreated with platelet‐rich plasma (PRP)
- Bioengineered skin organoids: from development to applications
- Hair in the Wrong Place
- Molecular mechanisms of asymmetric divisions in mammary stem cells
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting
- Sustained Exosome‐Guided Macrophage Polarization Using Hydrolytically Degradable PEG Hydrogels for Cutaneous Wound Healing: Identification of Key Proteins and MiRNAs, and Sustained Release Formulation
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Central centrifugal cicatricial alopecia: challenges and solutions
- Characterization of the epidermal-dermal junction in hiPSC-derived skin organoids
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- A recently characterized, underdiagnosed cause of female androgenetic alopecia and polycystic ovarian syndrome: non-classical 21 hydroxylase deficiency
- Targeting Superficial or Nodular Basal Cell Carcinoma with Topically Formulated Small Molecule Inhibitor of Smoothened
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor
- Differential sensitivity of epidermal cell subpopulations to β-catenin-induced ectopic hair follicle formation
- Overexpression of hepatoma-derived growth factor in melanocytes does not lead to oncogenic transformation
- Comparative advantage and efficacy of natural products for polycystic ovary syndrome