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Research 511–540 of 1000+
- Vitamin D: More Than a “Bone-a-Fide” Hormone
- Polycystic Ovary Syndrome, Insulin Resistance, and Obesity: Navigating the Pathophysiologic Labyrinth
- The Biological Actions of Dehydroepiandrosterone Involves Multiple Receptors
- The 5 Alpha-Reductase Isozyme Family: A Review of Basic Biology and Their Role in Human Diseases
- Chemistry42: An AI-Driven Platform for Molecular Design and Optimization
- Fundamental hair follicle biology and fine fibre production in animals
- K6irs1, K6irs2, K6irs3, and K6irs4 Represent the Inner-Root-Sheath-Specific Type II Epithelial Keratins of the Human Hair Follicle1
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Regulatory T Cells: the Many Faces of Foxp3
- Androgen sensitivity gateway to COVID‐19 disease severity
- Molecular evolution of the keratin associated protein gene family in mammals, role in the evolution of mammalian hair
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- PCOS and Depression: Common Links and Potential Targets
- Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
- The RpoS Gatekeeper in Borrelia burgdorferi: An Invariant Regulatory Scheme That Promotes Spirochete Persistence in Reservoir Hosts and Niche Diversity
- In Vitro Assembly and Structure of Trichocyte Keratin Intermediate Filaments
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Physiopathology of polycystic ovary syndrome in endocrinology, metabolism and inflammation
- 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.
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
- Metal-Chelation-Assisted Deposition of Polydopamine on Human Hair: A Ready-to-Use Eumelanin-Based Hair Dyeing Methodology
- COVID-19: Understanding Inter-Individual Variability and Implications for Precision Medicine
- The Impact of Angiotensin-Converting Enzyme 2 (ACE2) Expression Levels in Patients with Comorbidities on COVID-19 Severity: A Comprehensive Review
- Human hair keratin-associated proteins: Sequence regularities and structural implications
- Newly Developed Targeted Therapies Against the Androgen Receptor in Triple-Negative Breast Cancer: A Review
- The Pharmacology of Regenerative Medicine
- 5α-Reduced glucocorticoids: a story of natural selection