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Research 121–150 of 1000+
- Localisation and regulation of cholesterol transporters in the human hair follicle: mapping changes across the hair cycle
- Madarosis, milphosis, eyelash trichomegaly, and dermatochalasis
- Molecular Genetics of Alopecias
- Disease causing homozygous variants in the human hairless gene
- Secondary amenorrhea
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Decline of life’s energy theory of ageing 1. Revitalisation of energy metabolism and ageing mitochondria
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Role of DNA Methylation in the Pathogenesis of Skin Disorders: Mechanisms, Inhibitors of Methylation‐Related Enzyme, and Molecular Docking Studies
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Coexistence of Woolly Hair and Monilethrix: A Cases Study
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü
- 皮膚組織の再生に向けた皮膚由来幹細胞に関する研究
- Toxic and Metabolic Disorders of the Nervous System
- Hair and Scalp Variation Related to Gender
- Topische Immuntherapie mit Diphenylcyclopropenon bei verschiedenen Typen der Alpecia areata: Assoziation zu klinischen Parametern und einem funktionellen Genpolymorphismus des Interleukin-6-Promotors
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- Hoxc-Dependent Mesenchymal Niche Heterogeneity Drives Regional Hair Follicle Regeneration
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Alopecia in Children: The Most Common Causes
- Loss of the Y Chromosome: A Review of Molecular Mechanisms, Age Inference, and Implications for Men’s Health
- Computational derivation of a molecular framework for hair follicle biology from disease genes
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- The Who’s, What’s, and “Y”s: Y Sex Chromosome Loss and Methylation for Analysis in Male Aging and Mortality and Forensic Science Applications
- Sex-Chromosome-Related Dimorphism in Steroidogenic Enzymes and Androgen Receptor in Response to Testosterone Treatment: An In Vitro Study on Human Primary Skeletal Muscle Cells
- Learning from nudity: lessons from the nude phenotype
- Are the cutaneous manifestations during or due to SARS-CoV-2 infection/COVID-19 frequent or not? Revision of possible pathophysiologic mechanisms
- Common Skin Disorders in Pediatric Skin of Color
- Skin diseases in consequence of endocrine alterations