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Research 601–630 of 1000+
- Síndrome postfinasterida y disfunción eréctil. Caso clínico y revisión de la literatura
- Australasian Society for Dermatology Research Meeting, May 2007
- Balding man.
- Hypersensitivity reactions to anticoagulant drugs: diagnosis and management options
- Learning from nudity: lessons from the nude phenotype
- Brg1 Governs a Positive Feedback Circuit in the Hair Follicle for Tissue Regeneration and Repair
- Hormonal and Surgical Treatment Options for Transgender Men (Female-to-Male)
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Low level of maternal biotin intake changes the expression of biotin transporter in dams and fetuses in mice
- Premature Hair Graying: Underlying Contributors and Management Approaches - An Updated Literature Review
- Adult epidermal Notch activity induces dermal accumulation of T cells and neural crest derivatives through upregulation of jagged 1
- Particularidades dermatológicas, fisiológicas e as dermatoses na pele negra
- Techniques d'épargne cutanée dans la chirurgie de la gynécomastie
- An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review
- Congenital Triangular Alopecia: A Case of Effective Response with 5% Topical Minoxidil in a Male Adolescent
- Ichthyosis with confetti: clinics, molecular genetics and management
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- Skin, Genetic Defects, and Aging
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- A Congenital Hair Defect: Trichoschisis With Alternating Birefringence and Low Sulfur Content
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Hypomorphic mutation in the hairless gene accelerates pruritic atopic skin caused by feeding a special diet to mice
- New developments in the molecular treatment of ichthyosis: review of the literature
- Congenital milia En plaque on scalp
- Alopecia and Thyroid Disease
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- Lateral plate mesoderm directs human amnion and ventral skin organoid formation
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- The Mechanism and Research Progress of Skin Microbiota in Pathogenesis of Acne