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Research 91–120 of 1000+
- A novel EDA variant that causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family
- Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome with Concomitant Lymphopenia: A Novel TP63 Mutation
- Trichothiodystrophy: Review of sulfur-deficient brittle hair syndromes and association with the ectodermal dysplasias
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- 1435 Dynamic morphogen-p63 chromatin interactions that guide epigenetic changes and p63 activity in surface ectoderm commitment
- Onset of Keratin 17 Expression Coincides with the Definition of Major Epithelial Lineages during Skin Development
- A Unique Case of Trichorrhexis Nodosa—"Bamboo Hairs"
- Altered skin development and impaired proliferative and inflammatory responses in transgenic mice overexpressing the glucocorticoid receptor
- Neural Potential of a Stem Cell Population in the Hair Follicle
- Myodegeneration in EDA-A2 Transgenic Mice Is Prevented by XEDAR Deficiency
- Hair structure anatomy and comparative anatomy1 1Dedicated to the memory of the late Dr. R. E. Rivett whose untimely death prevented his role in co-authorship.
- Familial Uncombable Hair Syndrome: Ultrastructural Hair Study and Response to Biotin
- Prenatal hair development: Implications for drug exposure determination
- Trichoscopy in Hair Shaft Disorders
- Ichthyosis with confetti: clinics, molecular genetics and management
- Expression of COUP-TF-interacting protein 2 (CTIP2) in mouse skin during development and in adulthood
- Multipotent Nestin-Positive Stem Cells Reside in the Stroma of Human Eccrine and Apocrine Sweat Glands and Can Be Propagated Robustly In Vitro
- Atrichia With Papular Lesions
- Platelet-rich plasma—an ‘Elixir’ for treatment of alopecia: personal experience on 117 patients with review of literature
- <i>WNT10A</i> , dermatology and dentistry
- Ectodysplasin research—Where to next?
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Genetic Hair Disorders: A Review
- Gastrointestinal polyposis with protein-losing enteropathy, abnormal skin pigmentation and loss of hair and nails (Cronkhite-Canada syndrome)
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Inherited disorders of the skin in human and mouse: from development to differentiation.
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Ulerythema Ophryogenes
- Hair and Nail Relationship
- HOXC8 initiates an ectopic mammary program by regulating Fgf10 and Tbx3 expression, and Wnt/β-catenin signaling