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Research 361–390 of 967
- Analysis of histology and long noncoding RNAs involved in the rabbit hair follicle density using RNA sequencing
- The alopecia areata phenotype is induced by the water avoidance stress test in <i>cchcr1</i>-deficient mice
- Inherited Epidermolysis Bullosa: A Clinical Case
- 600 Differential Molecular Signature of Dermal Papilla Cells (DPCs) from Balding and Non balding Scalp in 2D, 3D culture and Co-culture with Adipose-derived stem cells (ASCs)
- Two females with hair loss
- Pathogenesis and clinical features of alopecia in epidermolysis bullosa: A systematic review
- 943 Temporal-spatial activation of Wnt-signaling within Type1 / Type 2 immunity during wound healing
- Dermal niche signaling and epidermal stem cells
- An Investigation of Hair and its Keratin Associated Proteins using Advanced Light Microscopy
- Neuroendocrine Controls of Keratin Expression in Human Skin
- Regenerative Medicine Approaches for Engineering a Human Hair Follicle
- Influence of donor sources and culture media on the histo-morphological quality of human artificial skin models
- 855 Targeted deletion of crif1 in mouse skin epidermis impairs skin homeostasis
- 856 Topical application of newly developed pseudoceramide improved both skin and hair barrier functions
- 859 Building a functional niche for hair follicle stem cells
- 441 RPGRIP1L facilitates desmosomal adhesion through suppressing PKCβII-mediated desmoglein endocytosis: Implication in pemphigus
- Proteomics Characterization of Primary Human Oral Epithelial Cells Using a Novel Culture Technique for Use in Tissue Regeneration
- Hair Growth Defects of Diabetic and Hypercholesterolemic Wistar Albino Rats and Amelioration of Fish Oil-Treatment
- Epidermal Notch1 recruits innate lymphoid cells to orchestrate normal skin repair
- Modelling androgen synthesis and action during human sexual differentiation
- 9. Immunology and Genetics
- Australasian Society for Dermatology Research Meeting, May 2007
- Bald scalp in men with androgenetic alopecia retains hair follicle stem cells but lacks CD200-rich and CD34-positive hair follicle progenitor cells
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- A novel point mutation of keratin 17 (<i>KRT17</i>) in a Japanese family with pachyonychia congenita type 2: an RNA-based genetic analysis using a single hair bulb
- Exosomes derived from dermal papilla cells mediate hair follicle stem cells proliferation through the Wnt3a/β-catenin signaling pathway
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle
- Transcriptome Profile at Different Physiological Stages Reveals Potential Mode for Curly Fleece in Chinese Tan Sheep
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules