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Research 811–840 of 1000+
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Dermal papilla-induced hair differentiation of adult epithelial stem cells from human skin
- Evolution of hard proteins in the sauropsid integument in relation to the cornification of skin derivatives in amniotes
- Inducible deletion of epidermal <i>Dicer</i> and <i>Drosha</i> reveals multiple functions for miRNAs in postnatal skin
- Pharmacologic interventions in aging hair
- The molecular basis of human keratin disorders
- Aging of the hair follicle pigmentation system
- Trichoscopy in genetic hair shaft abnormalities
- Progressive Alopecia Reveals Decreasing Stem Cell Activation Probability during Aging of Mice with Epidermal Deletion of DNA Methyltransferase 1
- Viral-associated trichodysplasia spinulosa: a case with electron microscopic and molecular detection of the trichodysplasia spinulosa-associated human polyomavirus
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
- The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures
- Analyses of histological and transcriptome differences in the skin of short-hair and long-hair rabbits
- Comparative Anatomy of Mouse and Human Nail Units
- Studies on the Proteome of Human Hair - Identification of Histones and Deamidated Keratins
- Skin Structure, Physiology, and Pathology in Topical and Transdermal Drug Delivery
- S100A6: molecular function and biomarker role
- Conditional Activin Receptor Type 1B (Acvr1b) Knockout Mice Reveal Hair Loss Abnormality
- Essentials of hair care often neglected: Hair cleansing
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- The Cutaneous Epidermal Growth Factor Network: Can it be Translated Clinically to Stimulate Hair Growth?
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- Identification of a preferred substrate peptide for transglutaminase 3 and detection of <i>in situ</i> activity in skin and hair follicles
- SKIN AND HAIR COSMETIC ISSUES IN WOMEN OF COLOR
- Emerging roles of transit‐amplifying cells in tissue regeneration and cancer
- Black women’s hair: the main scalp dermatoses and aesthetic practices in women of African ethnicity
- Histopathology of aging of the hair follicle