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Research 571–600 of 903
- Ageing processes influence keratin and KAP expression in human hair follicles
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- New oral anticoagulants and their reversal agents
- Protective effect of conditioning agents on Afro‐ethnic hair chemically treated with thioglycolate‐based straightening emulsion
- Platelet Extracellular Vesicles Loaded Gelatine Hydrogels for Wound Care
- Efficacy assessment of mesenchymal stem cell transplantation for burn wounds in animals: a systematic review
- Dermatoporosis: a further step to recognition
- Age‐dependent changes in damage processes of hair cuticle
- The Overexpression of Tβ4 in the Hair Follicle Tissue of Alpas Cashmere Goats Increases Cashmere Yield and Promotes Hair Follicle Development
- [Hormone replacement treatment and skin aging].
- Effects of ultra violet radiation on the soluble proteins of human hair
- Hair Breakage in Patients of African Descent: Role of Dermoscopy
- AN UPDATE OF HAIR SHAFT DISORDERS
- High-sulfur protein deficient human hair: clinical aspects and biochemical study of two unreported cases of a variant type of trichothiodystrophy
- Unique Hair Properties that Emerge from Combinations of Multiple Races
- Effects of dipotassium glycyrrhizinate on wound healing
- [Translated article] Trichoscopy: An Update
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Polymer- and Lipid-Based Nanostructures for Wound Healing with Barrier-Resolved Design
- A Novel Device to Insert FU Grafts into Premade Sites
- Whisker hair (acquired progressive kinking of the hair): An indication for finasteride 1 mg?
- Folliculitis decalvans managed with adalimumab: A case report
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Characterization of Bsk mice: I. The Bsk mutation does not involve a recombination of cornea-specific keratin 12 and skin-specific hair keratin genes.
- Kerion Celsi in a Nepalese Boy: An Underdiagnosed Cause of Scalp Swelling
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- [Genetic counseling in a case of neuro-ectodermosis: Vera Price trichothiodystrophy. Brittle hair with reduced sulfur content].
- Technical feasibility and economic benefit of combined shallot seedlings techniques in Indonesia
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil