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Research 541–570 of 1000+
- Dermatologic Reactions to Targeted Therapy
- Australasian Society for Dermatology Research Meeting, May 2006
- Raman spectroscopy and electronic microscopy structural studies of Caucasian and Afro human hair
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Rapunzel! Rapunzel! How Strong Is Your Hair?
- WNT Signaling in Disease
- Overexpression of the calcium sensing receptor accelerates epidermal differentiation and permeability barrier formation in vivo
- Immunolocalization of junctional proteins in human hairs indicates that the membrane complex stabilizes the inner root sheath while desmosomes contact the companion layer through specific keratins
- The importance of basonuclin 2 in adult mice and its relation to basonuclin 1
- The New Keratin Nomenclature
- Hyaluronic Acid in Topical Applications: The Various Forms and Biological Effects of a Hero Molecule in the Cosmetics Industry
- In this Issue
- Utilizing functional genomics approaches to characterize risk genes in alopecia areata
- Hypotrichosis with juvenile macular dystrophy
- Augmenting Endogenous Wnt Signaling Improves Skin Wound Healing
- Autophagy-Mediated Cellular Remodeling during Terminal Differentiation of Keratinocytes in the Epidermis and Skin Appendages
- Floral attractants in the black orchid Brasiliorchis schunkeana (Orchidaceae, Maxillariinae): clues for presumed sapromyophily and potential antimicrobial activity
- Molecular Mechanisms and Targeted Therapeutics in Androgenetic Alopecia: From Signaling Pathways to Regenerative Approaches
- Identification of Differentially Expressed Genes During a Wool Follicle Growth Cycle Induced by Prolactin
- Existence of trichohyalin-keratohyalin hybrid granules: Co-localization of two major intermediate filament-associated proteins in non-follicular epithelia
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- ecancermedicalscience
- Investigation of the Morphologic and Scanned Electron Microscopic Properties of Wild Boar Bristles in the Balikesir Region
- Wool fiber curvature is correlated with abundance of K38 and specific keratin‐associated proteins
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- Repeatable Perming via Thiol–Michael Click Reaction: Using Amide Derived from Maleic Acid and Cystine
- Exosomes in trichology: A literature review
- Tissue Engineering in Cosmetics and Dermatology: A New Era of Innovation and Application