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Research 61–90 of 261
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Molecular Dissection of Mesenchymal–Epithelial Interactions in the Hair Follicle
- Organogenesis From Dissociated Cells: Generation of Mature Cycling Hair Follicles From Skin-Derived Cells
- TGF-β family signaling in stem cells
- Biology of the wool follicle: an excursion into a unique tissue interaction system waiting to be re‐discovered
- Keratin K15 as a Biomarker of Epidermal Stem Cells
- Spontaneous tumour regression in keratoacanthomas is driven by Wnt/retinoic acid signalling cross-talk
- Exploring the Drug Repurposing Versatility of Valproic Acid as a Multifunctional Regulator of Innate and Adaptive Immune Cells
- Tissue resident and follicular Treg cell differentiation is regulated by CRAC channels
- Smad4-dependent desmoglein-4 expression contributes to hair follicle integrity
- A genomic approach to susceptibility and pathogenesis leads to identifying potential novel therapeutic targets in androgenetic alopecia
- The Biology of Hair Growth
- Differential impact of environmental factors on systemic and localized autoimmunity
- HuR ablation destabilizes Foxp3 mRNA and impairs regulatory T cell function, contributing to an autoimmune phenotype
- Androgenic Alopecia: Cross-Talk Between Cell Signal Transduction Pathways
- Deciphering the cellular landscape and genetic underpinnings of fiber diameter determined by dermal papilla cells in fine-wool sheep
- Molecular heterogeneity of quiescent melanocyte stem cells revealed by single-cell RNA-sequencing
- Posters Presented at the 19th Joint Meeting of the International Society of Dermatopathology, March 2–3, 2016, Hilton Crystal City at Washington Reagan National Airport, Arlington, Virginia, USA
- Adverse cutaneous reactions to soft tissue fillers – a review of the histological features
- Defective trophoblast function in mice with a targeted mutation of Ets2
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Dynamic expression of the zinc-finger transcription factor Trps1 during hair follicle morphogenesis and cycling
- TRPS1 haploinsufficiency results in increased STAT3 and SOX9 mRNA expression in hair follicles in trichorhinophalangeal syndrome
- Successful topical minoxidil treatment for hair density and length in trichorhinophalangeal syndrome type 1
- Identification and dissection of an enhancer controlling epithelial gene expression in skin
- Targeting cardiac hypertrophy through a nuclear co‐repressor
- Molecular mechanism for transcriptional regulation of the parathyroid hormone gene by Epiprofin
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- Epigenetics of Colorectal Cancer