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- Biology of the wool follicle: an excursion into a unique tissue interaction system waiting to be re‐discovered
- Integument pattern formation involves genetic and epigenetic controls: feather arrays simulated by digital hormone models.
- Genetic basis of skin appendage development
- [Genetic expression and morphogenesis of the skin in vertebrates].
- HLA‐B alleles associated with frontal fibrosing alopecia in Brazil may share similar peptide presentation and T‐cell interaction profiles
- TMT-based quantitative proteomics reveals the genetic mechanisms of secondary hair follicle development in fine-wool sheep
- Risk factors for prostate cancer: a case-control study investigating selected key exposures and their interactions with predisposition genes
- Dual‐flow‐RootChip reveals local adaptations of roots towards environmental asymmetry at the physiological and genetic levels
- Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5
- LSD1 is Required for Hair Cell Regeneration in Zebrafish
- Hairless Up‐Regulates <i>Tgf‐β2</i> Expression via Down‐Regulation of miR‐31 in the Skin of “Hairpoor” (<i>Hr</i><sup><i>Hp</i></sup>) Mice
- Molecular Mechanisms Regulating Hair Follicle Development
- Modulating the stem cell niche for tissue regeneration
- Basal cell carcinoma — molecular biology and potential new therapies
- The population dynamics of cancer: a Darwinian perspective
- Distinct mechanisms underlie pattern formation in the skin and skin appendages
- From hair colour to diagnosis
- Acne Vulgaris
- Challenges and Strategies for Improving the Regenerative Effects of Mesenchymal Stromal Cell-Based Therapies
- Understanding the Molecular Landscape of Alopecia Areata: Key Genes, Regulatory Networks, and Therapeutic Targets
- [Hormonal interaction and hair growth].
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- Molecular Genetic and Endocrine Mechanisms of Hair Growth
- Gene-Environment Interaction Between <i>CYP1B1</i> and Oral Contraception on Frontal Fibrosing Alopecia
- A new mutation resulting in the truncation of the TRAF6-interacting domain of XEDAR: a possible novel cause of hypohidrotic ectodermal dysplasia: Figure 1
- Emerging interactions between skin stem cells and their niches
- Genetic Analysis of Androgen Receptors in Development and Disease
- Genetics of Vitiligo: A Review
- Hormonal and Genetic Controls of Hirsutism: Link Between hyperprolactinemia, Polycystic ovary syndrome and Hirsutism
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness