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Research 421–450 of 1000+
- Different gene expression profile observed in dermal papilla cells related to androgenic alopecia by DNA macroarray analysis
- Sex steroid synthesis in human skin in situ: The roles of aromatase and steroidogenic acute regulatory protein in the homeostasis of human skin
- A preliminary study of finasteride in Tourette syndrome
- Endocrine-skin interactions
- Acquired scalp alopecia. Part I: A review
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Role of Trichoscopy in Children's Scalp and Hair Disorders
- Malignancy and Cancer Treatment-Related Hair and Nail Changes
- Mood disorders and quality of life in polycystic ovary syndrome
- Congenital hair loss disorders: Rare, but not too rare
- A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents
- Woolly hair nevus
- Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up
- Morphological Approach to Hair Disorders
- Short anagen syndrome
- Acquired scalp alopecia. Part II: A review
- Assessment of the usefulness of dihydrotestosterone in the diagnostics of patients with androgenetic alopecia
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Epidermal Polarity Genes in Health and Disease
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Hairless is a nuclear receptor corepressor essential for skin function
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- What does acne genetics teach us about disease pathogenesis?
- Alopecia areata: A review
- Role of β-Catenin Activation Levels and Fluctuations in Controlling Cell Fate
- Scalp Itch: A Systematic Review
- MicroRNA in skin diseases
- Androgenetic Alopecia: In Vivo Models
- Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases?
- Analysis of hidradenitis suppurativa–linked mutations in four genes and the effects of PSEN1-P242LfsX11 on cytokine and chemokine expression in macrophages