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Research 61–90 of 788
- Comparison of Effects on Gene Expression Activity of Low-Molecular-Weight Lychee Fruit Polyphenol (Oligonol®), Adenosine, and Minoxidil in Human Dermal Papilla Cells
- Inherited Disorders of the Hair
- Current Genetics in Hair Diseases
- <i>WNT10A</i> gene variants at the root of short anagen hair syndrome
- Advances in the genetic understanding of hypohidrotic ectodermal dysplasia
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Hair growth-promoting effects of Stellera chamaejasme L. extract on C57BL/6 mice via induction of anagen phase genes
- Evolution of long scalp hair in humans
- Novel variant in <i>WNT10A</i> caused short anagen hair syndrome in a Chinese pedigree
- The Pathogenesis and Treatment Progress of Androgenic Alopecia
- Exploring links with rare variants, COVID-19 and short anagen hair syndrome
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Short anagen hair syndrome: association with mono- and biallelic variants in <i>WNT10A</i> and a genetic overlap with male pattern hair loss
- Integrated single-cell chromatin and transcriptomic analyses of human scalp reveal etiological insights into genetic risk for hair and skin disease
- Integrated Analysis of miRNAs and mRNA Profiling Reveals the Potential Role of miRNAs in Sheep Hair Follicle Development
- Gene Network Analysis Reveals Candidate Genes Related with the Hair Follicle Development in Sheep
- LB821 Human hair follicle dermal papilla as an in vitro model to study stress-induced hair growth arrest
- 415 IL-17C: Checkpoint in innate skin immunology
- 413 DC-HIL+ myeloid-derived suppressor cells are elevated in the peripheral blood and lesional skin of cutaneous lupus patients
- Montagna Symposium 2015: Harnessing Stem Cells to Reveal Novel Skin Biology and Disease Treatments
- Short anagen hair syndrome is caused by mutations in the <i>WNT10A</i> gene and has a genetic overlap with male pattern hair loss
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology
- 303 The role of rare variants in male-pattern hair loss: Analysis of whole exome sequencing data in the UK Biobank
- Androgenetic alopecia: Identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology
- Molecular biology of hair morphogenesis: Development and cycling
- Modulating hair follicle size with <i>Wnt10b/DKK1</i> during hair regeneration
- Activation of Wnt Signaling in Hematopoietic Regeneration
- Androgens modify Wnt agonists/antagonists expression balance in dermal papilla cells preventing hair follicle stem cell differentiation in androgenetic alopecia
- Wnt/β-catenin signaling pathway activates melanocyte stem cells in vitro and in vivo