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Research 721–750 of 1000+
- Parallels in signaling between development and regeneration in ectodermal organs
- 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
- 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
- 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
- Atrichia With Papular Lesions
- Platelet-rich plasma—an ‘Elixir’ for treatment of alopecia: personal experience on 117 patients with review of literature
- Ectodysplasin research—Where to next?
- 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.
- Ulerythema Ophryogenes
- Genetics of Structural Hair Disorders
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Epidermal stem cell fate: what can we learn from embryonic stem cells?
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Dermatopathology and molecular genetics
- A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by<i>DSP</i>mutations
- Clinical Case Notes. Propecia-associated bilateral cataract
- Hair loss among a group of Egyptian children