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Research 391–420 of 1000+
- Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up
- Familial and Sporadic Porphyria Cutanea Tarda
- Morphological Approach to Hair Disorders
- Platelet-derived growth factor signaling modulates adult hair follicle dermal stem cell maintenance and self-renewal
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Trichoscopy in Hair Shaft Disorders
- Vitamin D receptor polymorphisms and the polycystic ovary syndrome: A systematic review
- Aromatase deficiency in a male patient - Case report and review of the literature.
- Epigenetic control of skin and hair regeneration after wounding
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Planar cell polarity-dependent and independent functions in the emergence of tissue-scale hair follicle patterns
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Afamin serum concentrations are associated with insulin resistance and metabolic syndrome in polycystic ovary syndrome
- Oncogenic senescence: a multi-functional perspective
- Fate of Prominin-1 Expressing Dermal Papilla Cells during Homeostasis, Wound Healing and Wnt Activation
- Loss of Keratin K2 Expression Causes Aberrant Aggregation of K10, Hyperkeratosis, and Inflammation
- Disrupted Ectodermal Organ Morphogenesis in Mice with a Conditional Histone Deacetylase 1, 2 Deletion in the Epidermis
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- Variation in the caprine keratin-associated protein 15-1 (KAP15-1) gene affects cashmere fibre diameter
- An Ovol2‐Zeb1 transcriptional circuit regulates epithelial directional migration and proliferation
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Removing all obstacles: A critical role for p53 in promoting tissue renewal
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Enzyme Replacement Therapy Ameliorates Multiple Symptoms of Murine Homocystinuria
- CAG Repeat Testing of Androgen Receptor Polymorphism: Is This Necessary for the Best Clinical Management of Hypogonadism?
- Management of CAH during pregnancy
- Genetic Fate Mapping Using Site-Specific Recombinases
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Smad4-dependent desmoglein-4 expression contributes to hair follicle integrity