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Research 301–330 of 1000+
- Phytochemicals as emerging therapeutic agents for alopecia treatment
- Drug-Induced Skin, Nail and Hair Disorders
- Nutritional Clinical Studies in Dermatology
- To study the prevalence of cutaneous manifestationsin newborns and its correlation with defined maternal and neonatal factors
- The Basic Science of Hair Biology
- Expression of<i>Sfrp2</i>Is Increased in Catagen of Hair Follicles and Inhibits Keratinocyte Proliferation
- Vitamin D receptor-mediated control of Soggy, Wise, and Hairless gene expression in keratinocytes
- A spermidine-based nutritional supplement prolongs the anagen phase of hair follicles in humans: a randomized, placebo-controlled, double-blind study
- Disease causing homozygous variants in the human hairless gene
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- Follistatin and secreted frizzled-related protein 1, OVO homolog-like 1-regulated genes, are important for hair follicle neogenesis
- Development of squamous cell carcinoma from erythroplasia of Queyrat following photodynamic therapy
- The Role of Histone Demethylases in Disease
- Pediatric Radiation-Induced Alopecia Post Intracranial Vascular Malformation Embolization: A Case Report with Dermoscopic Findings
- Growth of the Hair
- CHRONIC TELOGEN EFFLUVIUM
- Normal Hair Growth in Children
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Computational derivation of a molecular framework for hair follicle biology from disease genes
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Moniletrix. Observación de esta infrecuente displasia pilosa en dos hermanos. Reporte clínico y dermatoscópico
- Disorders of the skin appendages
- 192 MicroRNAs and their regulatory interactions in the human hair follicle
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Do you know this syndrome? * Você conhece esta síndrome? *
- Diagnosis of hyperandrogenism: clinical criteria
- Endocrine Influences on Hair Growth
- Anagen effluvium