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Research 331–360 of 1000+
- Oxidative stress in ageing of hair
- Androgens and androgen receptor action in skin and hair follicles
- Aging of hair
- TGF-β Family Signaling in Epithelial Differentiation and Epithelial–Mesenchymal Transition
- Lichen Planopilaris and Frontal Fibrosing Alopecia as Model Epithelial Stem Cell Diseases
- Tumour regression predicts higher risk of sentinel node involvement in thin cutaneous melanomas
- Botulinum Toxin Off-Label Use in Dermatology: A Review
- Acquired scalp alopecia. Part I: A review
- Scalp Itch: A Systematic Review
- Updates in the understanding and treatments of skin & hair disorders in women of color
- Treatment of androgen excess in females: Yesterday, today and tomorrow
- Hair aging and anti-aging
- Platelet Immune Interactions, Lifespan, and Senescence
- Primary cicatricial alopecias
- Langerin+ Dendritic Cells in Cutaneous Fibrosis: The TGF-β1 Signaling Axis
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- Non-Neoplastic Disorders of Hair
- National scientific medical meeting 1996 abstracts
- Molecular genetics of androgen insensitivity
- Cardiometabolic and neuroimaging correlates of cognitive function in polycystic ovary syndrome
- Modelling androgen synthesis and action during human sexual differentiation
- The probable destructive mechanisms behind COVID-19 on male reproduction system and fertility
- Farmácia dos Clérigos - Porto e nos Serviços Farmacêuticos da University College Hospital - Londres, Reino Unido, ao abrigo do programa Erasmus+
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- 461 Identification of a Novel Pathogenic XPC:c.2420+1G>C Variant in a Patient with Xeroderma Pigmentosum
- Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development
- Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome
- Generalized atrophic benign epidermolysis bullosa.
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature