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Research 181–210 of 199
- Role of <i>foxn1</i> in <i>Xenopus laevis</i> thymopoiesis.
- Metabolic Regulation of Hematopoietic Stem Cells in the Hypoxic Niche
- CRISPR/Cas9‐mediated loss of FGF5 function increases wool staple length in sheep
- Recent advances on skin‐resident stem/progenitor cell functions in skin regeneration, aging and cancers and novel anti‐aging and cancer therapies
- High-coverage genome of the Tyrolean Iceman reveals unusually high Anatolian farmer ancestry
- CXXC5: A novel regulator and coordinator of TGF-β, BMP and Wnt signaling
- HPV8 Field Cancerization in a Transgenic Mouse Model Is due to Lrig1+ Keratinocyte Stem Cell Expansion
- PTEN Mediates Activation of Core Clock Protein BMAL1 and Accumulation of Epidermal Stem Cells
- The Pressurized Skin: A Review on the Pathological Effect of Mechanical Pressure on the Skin from the Cellular Perspective
- Longitudinal Assessment of the Prevalence of Actinic Keratosis and Extensive Risk Factor Evaluation: An Update from the Rotterdam Study
- Primary TSC2-/meth Cells Induce Follicular Neogenesis in an Innovative TSC Mouse Model
- iPSC-based approach for human hair follicle regeneration
- Safety and Efficacy of Nutrition-Based Interventions for Hair
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- Using WGCNA (weighted gene co-expression network analysis) to identify the hub genes of skin hair follicle development in fetus stage of Inner Mongolia cashmere goat
- Targeting the Hippo/YAP/TAZ signalling pathway: Novel opportunities for therapeutic interventions into skin cancers
- Hormonal profile and androgen receptor study in prepubertal girls with hypertrichosis
- ILC3s as central regulators of mucosal homeostasis and disease pathogenesis (Review)
- Dermal Microvascular Responses of Human Induced Pluripotent Stem Cell–Derived Skin Organoids to Inflammation and Injury
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Short anagen hair syndrome: association with mono- and biallelic variants in <i>WNT10A</i> and a genetic overlap with male pattern hair loss
- 092 Novel biallelic RIPK4 mutations cause ectodermal dysplasia with cutaneous syndactyly
- <i>WNT10A</i> , dermatology and dentistry
- 236 Wnt/planar cell polarity impairment and the genetics of yellow nail syndrome
- Abstracts
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Alopecia areata susceptibility variant identified by MHC risk haplotype sequencing reproduces symptomatic patched hair loss in mice