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Research 421–450 of 650
- Product Pharmacology and Medical Actives in Achieving Therapeutic Benefits
- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- The mouse keratin 6 isoforms are differentially expressed in the hair follicle, footpad, tongue and activated epidermis
- 889 Trpv3 gain-of-function mutation impairs differentiation of hair follicle inner root sheath
- Stanozolol in the Treatment of Pityriasis Rubra Pilaris
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Current Genetics in Hair Diseases
- 0847 The addition of collagen scaffolds to human cell therapy to modify skin identity
- Hypotrichosis in a child with olmsted syndrome
- Trachyonychia with juvenile pityriasis rubra pilaris
- Human Eccrine Sweat Gland Cells Can Reconstitute a Stratified Epidermis
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Activation of TRPV3 Regulates Inflammatory Actions of Human Epidermal Keratinocytes
- Epidermal and Hair Follicle Progenitor Cells Express Melanoma-Associated Chondroitin Sulfate Proteoglycan Core Protein
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Circle hairs are not rolled hairs
- Pachyonychia Congenita-Associated Alopecia. A Microscopic Analysis Using Transverse Section Technique
- Two Clinically Unusual Cases of Folliculotropic Mycosis Fungoides: One with and the Other without Syringotropism
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Adalimumab-induced psoriatic alopecia/alopecia areata-like reaction in a patient with Crohn's disease
- Frontal fibrosing alopecia: a review of eleven patients
- Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy
- Substance P in keratosis follicularis spinulosa decalvans
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- 1619 Spatial transcriptomic analysis of imiquimod-treated mouse skin reveals deregulation of lipid raft-associated markers which could be reversed by re-introduction of caveolin scaffolding domain peptide
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- Molecular Genetics of Human Hair Diseases