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Research 781–810 of 1000+
- Identification of a link between Wnt/β-catenin signalling and the cell fusion pathway
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Delineation of Matriptase Protein Expression by Enzymatic Gene Trapping Suggests Diverging Roles in Barrier Function, Hair Formation, and Squamous Cell Carcinogenesis
- PCOS and Depression: Common Links and Potential Targets
- Wnt/β‐catenin pathway in tissue injury: roles in pathology and therapeutic opportunities for regeneration
- Arabidopsis CNGC14 Mediates Calcium Influx Required for Tip Growth in Root Hairs
- Visualising Androgen Receptor Activity in Male and Female Mice
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Vitamin D and calcium regulation of epidermal wound healing
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Fibroblasts – the cellular choreographers of wound healing
- The disruption of Sox21-mediated hair shaft cuticle differentiation causes cyclic alopecia in mice
- Folliculin, the Product of the Birt-Hogg-Dube Tumor Suppressor Gene, Interacts with the Adherens Junction Protein p0071 to Regulate Cell-Cell Adhesion
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- A subpopulation of itch‐sensing neurons marked by Ret and somatostatin expression
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- The keratin 19 promoter is potent for cell-specific targeting of genes in transgenic mice
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Bone Morphogenetic Protein Signaling Regulates Postnatal Hair Follicle Differentiation and Cycling
- Notch Signaling Regulates Late-Stage Epidermal Differentiation and Maintains Postnatal Hair Cycle Homeostasis
- Analyses of histological and transcriptome differences in the skin of short-hair and long-hair rabbits
- Overexpression of mIGF-1 in Keratinocytes Improves Wound Healing and Accelerates Hair Follicle Formation and Cycling in Mice
- Embryonic hair follicle fate change by augmented β-catenin through Shh and Bmp signaling
- SARS-CoV-2 Spike Protein S1-Mediated Endothelial Injury and Pro-Inflammatory State Is Amplified by Dihydrotestosterone and Prevented by Mineralocorticoid Antagonism
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis
- Krtap16, Characterization of a New Hair Keratin-associated Protein (KAP) Gene Complex on Mouse Chromosome 16 and Evidence for Regulation by Hoxc13