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Research 181–210 of 387
- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- 889 Trpv3 gain-of-function mutation impairs differentiation of hair follicle inner root sheath
- Keratosis follicularis spinulosa decalvans in a family
- Stanozolol in the Treatment of Pityriasis Rubra Pilaris
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Trachyonychia with juvenile pityriasis rubra pilaris
- Hypotrichosis in a child with olmsted syndrome
- Activation of TRPV3 Regulates Inflammatory Actions of Human Epidermal Keratinocytes
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Poster Presentations
- Circle hairs are not rolled hairs
- Molecular Genetics of Keratinization Disorders – What’s New About Ichthyosis
- Pachyonychia Congenita-Associated Alopecia. A Microscopic Analysis Using Transverse Section Technique
- Dermatosis associated with menopause
- Promotion effect of Schisandra nigra on the growth of hair
- Frontal fibrosing alopecia: a review of eleven patients
- Substance P in keratosis follicularis spinulosa decalvans
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- A polarizing light microscopy can be an easy and reliable diagnostic tool of congenital keratinizing disorders including Netherton syndrome
- Molecular Genetics of Human Hair Diseases
- Clinical Snippets
- Dermoscopy in General Dermatology: A Practical Overview
- The epidermis: rising to the surface
- Keratin gene mutations in disorders of human skin and its appendages
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation