Search
for
Sort by
Research 331–360 of 679
- The Genetics of Acne
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- The Roles of Keratinocytes in the Initiation, Progression and Maintenance of Hidradenitis Suppurativa
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- The Genetic Architecture of Alopecia Areata
- Homozygous whole body <i>Cbs</i> knockout in adult mice features minimal pathology during ageing despite severe homocysteinemia
- Applications of Antioxidant Nanoparticles in Immune-Mediated Inflammatory Diseases
- Reply
- Editorial: Treatment and prognostic assessment of liver cirrhosis and its complications, volume II
- Depressive and Anxiety Symptoms in Women with Polycystic Ovary Syndrome: A Meta-Analysis
- The brain–gut–skin axis in inflammatory and disfiguring skin diseases: mechanistic insights, clinical correlations, and therapeutic strategies
- Tissue-Specific Multi-Omics Integration Demonstrates Molecular Signatures Connecting Obesity to Immune Vulnerability
- Advancements in Bioactive Compounds and Therapeutic Agents for Alopecia: Trends and Future Perspectives
- Evaluation of Anthropometric Measurements, Arterial Stiffness and ECG Parameters in Alopecia Areata Patients
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- The Current and Emerging Role of Statins in the Treatment of PCOS: The Evidence to Date
- FGF5 is a crucial regulator of hair length in humans
- Managing the adverse effects of cytotoxic chemotherapy at the level of primary healthcare
- Drug Repurposing for Rare Diseases
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- Hair follicles modulate skin barrier function
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- The Rotterdam Study: 2010 objectives and design update
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects
- The Role of Nutrition on Thyroid Function
- Targeting the Complexity of In Vitro Skin Models: A Review of Cutting-Edge Developments