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Research 601–630 of 1000+
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Hair Care and Dyeing
- Pharmacologic interventions in aging hair
- A powerful method for pleiotropic analysis under composite null hypothesis identifies novel shared loci between Type 2 Diabetes and Prostate Cancer
- <i>NUDT15</i>,<i>FTO</i>, and<i>RUNX1</i>genetic variants and thiopurine intolerance among Japanese patients with inflammatory bowel diseases
- Human Hair Graying Revisited: Principles, Misconceptions, and Key Research Frontiers
- Alopecia Areata
- Alopecias - Practical Evaluation and Management
- The exposome impact on hair health: etiology, pathogenesis and clinical features ‒ Part I
- Trichonodosis: a case report and literature review
- Genome-wide association study in frontal fibrosing alopecia identifies four susceptibility loci including HLA-B*07:02
- Assessment of the usefulness of dihydrotestosterone in the diagnostics of patients with androgenetic alopecia
- Predicting hair cortisol levels with hair pigmentation genes: a possible hair pigmentation bias
- A Genome-Wide Association Study and Machine-Learning Algorithm Analysis on the Prediction of Facial Phenotypes by Genotypes in Korean Women
- Exploring the Relationship Between Immune Cells and Non-Scarring Hair Loss: A Mendelian Randomization Study
- Assessing Causality Between Androgenetic Alopecia with Depression: A Bidirectional Mendelian Randomization Study
- Fundamental hair follicle biology and fine fibre production in animals
- 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.
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- Lineage Analysis of Epidermal Stem Cells
- A review of cutaneous lupus erythematosus: improving outcomes with a multidisciplinary approach
- Molecular characterization of HOXC8 gene and methylation status analysis of its exon 1 associated with the length of cashmere fiber in Liaoning cashmere goat
- Association of epidemiological and biochemical factors with premature graying of hair: A case–control study
- DNA phenotyping: current application in forensic science
- Understanding Pattern Hair Loss—Hair Biology Impacted by Genes, Androgens, Prostaglandins and Epigenetic Factors
- Spontaneous Quick Resolution of Uncombable Hair Syndrome-Like Disease
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- Pediatric adrenocortical carcinoma complicated by uric acid nephrolithiasis: a unique case report
- REVIEW ON SEASONAL INCIDENCE OF PSORIASIS EXACERBATIONS DURING WINTER IN INDIA: CLINICAL INSIGHTS AND OBSERVATIONS
- From the Microscopic Sweat Gland to Large Datasets: The Power of Quantitative Traits in Dermatology