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Research 631–660 of 1000+
- E-Poster
- Clinical guidelines of ukrainian hair research society. diagnosis and treatment of alopecia areata
- Status of research on the development and regeneration of hair follicles
- Nanotechnology-based techniques for hair follicle regeneration
- Proceedings of the Ninth World Congress for Hair Research (2015)
- Hair & Cutaneous Development
- TONGUE, RED
- Subject Index
- FGF5 is a crucial regulator of hair length in humans
- Management of Skin Toxicities in Cancer Treatment: An Australian/New Zealand Perspective
- Ovarian Hyperthecosis Presenting as Polycythemia
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- Treatments for alopecia areata: a network meta-analysis
- Alopecia areata: a review of diagnosis, pathogenesis and the therapeutic landscape
- The Effect of Drugs on Hair
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Trichoscopy pattern in alopecia areata: A systematic review and meta‐analysis
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- The molecular basis of human keratin disorders
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Desmoglein 4 is regulated by transcription factors implicated in hair shaft differentiation
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- Monilethrix – Case report of a rare disease
- Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
- Shh maintains dermal papilla identity and hair morphogenesis via a Noggin–Shh regulatory loop
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Inherited ichthyoses/generalized Mendelian disorders of cornification