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Research 451–480 of 1000+
- Proteins in Scalp Hair of Preschool Children
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- Hair Follicle Stem Cells and Hair Regeneration
- Aging of the hair follicle pigmentation system
- Ligand‐Independent Actions of the Vitamin D Receptor: More Questions Than Answers
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- miR-129-5p Participates in Hair Follicle Growth by Targeting HOXC13 in Rabbit
- Identification of key pathways and genes that regulate cashmere development in cashmere goats mediated by exogenous melatonin
- Identification of lncRNAs involved in the hair follicle cycle transition of cashmere goats in response to photoperiod change
- Melatonin promotes the development of the secondary hair follicles by regulating circMPP5
- Molecular Targets in Modern Cosmetic Science
- Unraveling the Molecular Mechanism of Bider Marking Formation in Dun Mongolian Horses Through Transcriptome Sequencing
- Research progress in the treatment of non-scarring alopecia: mechanism and treatment
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Bioactive Compound-Loaded Nanocarriers for Hair Growth Promotion: Current Status and Future Perspectives
- Identification of Key Pathways and Genes Related to the Development of Hair Follicle Cycle in Cashmere Goats
- Comprehensive analysis of the expression profiles of mRNA, lncRNA, circRNA, and miRNA in primary hair follicles of coarse sheep fetal skin
- A decade of neglecting sublingual mass: A case report of epidermoid cyst
- Characterization of Human Keratin-Associated Protein 1 Family Members
- Genetics of Structural Hair Disorders
- GWAS Identifies Three Susceptibility Loci for Trichilemmal Cysts
- Keratin K6irs is specific to the inner root sheath of hair follicles in mice and humans
- Mutation analysis of type II hair keratin gene in a pedigree with monilethrix
- Monilethrix in monozygotic twins with very rare mutation in KRT 86 gene
- Monilethrix
- Monilethrix: Beaded hair and hypotrichosis in a child
- Monilethrix
- A nonsense variant in <i>KRT31</i> is associated with autosomal-dominant monilethrix
- Solitary Nodular Lesion Over Face
- <i>Hoxc13</i> and the development of hair follicle