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Research 541–570 of 1000+
- Relationship between the bacterial community structures on human hair and scalp
- GWASs Identify Genetic Loci Associated with Human Scalp Hair Whorl Direction
- Androgenic alopecia, premature graying, and hair thinning as independent predictors of coronary artery disease in young Asian males
- The Genetic Landscape of Androgenetic Alopecia: Current Knowledge and Future Perspectives
- The Transgender: Endocrinological Assessment
- Defining pseudofolliculitis barbae in 2001: A review of the literature and current trends
- Trichotillomania
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting
- A modified laparoscopic sleeve gastrectomy for the treatment of diabetes mellitus type 2 and metabolic syndrome in obesity
- Influence of knowledge and beliefs on consumption of performance enhancing agents in north-western Saudi Arabia
- 440 Charting the Spatially Resolved Hair Follicle Stem Cell Niche: A Multi-Omics Atlas of Healthy and Diseased Scalp
- Advantages of Incomplete Digestion in Human Hair Shaft Proteomics, a Focus on Cuticular Keratins
- The microbiome in patients with atopic dermatitis
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Trichoscopy in alopecias: Diagnosis simplified
- Gene expression profiling gets to the root of human hair follicle stem cells
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Sebaceous Gland Atrophy in Psoriasis: An Explanation for Psoriatic Alopecia?
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Association of Spironolactone Use With Risk of Cancer
- Prevalence of alopecia and its contributing factors among primary healthcare attendees in the Jazan region, Saudi Arabia
- Discovery of a sol–gel reinforcing the strength of hair structure: mechanisms of action and macroscopic effects on the hair
- Editorial: Advances and novel intervention in photodermatology
- Formulation characteristics, safety, and accessibility of conditioners for textured hair
- 26-SNP Panel Aids Guiding Androgenetic Alopecia Therapy and Provides Insight into Mechanisms of Action
- The effects of caffeine and adenosine on the microbiome and lipidome of the scalp
- Natural Asymmetry in Hair Growth Direction: Implications for Hairline Design in Male Patients