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Research 721–750 of 1000+
- Use of Induced Pluripotent Stem Cells in Dermatological Research
- The Complexity of the Ovine and Caprine Keratin-Associated Protein Genes
- Identification of the Ovine Keratin-Associated Protein 21-1 Gene and Its Association with Variation in Wool Traits
- Candidate Gene Analysis Of Alopecia Areata In Jordanian Population Of Arab Descent: A Case–Control Study
- A homozygous missense mutation in the fibroblast growth factor 5 gene is associated with the long-hair trait in Angora rabbits
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- How Our Microbiome Influences the Pathogenesis of Alopecia Areata
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Sequence Variation in Caprine KRTAP6-2 Affects Cashmere Fiber Diameter
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- Hair India 2010
- Characterisation of Ovine KRTAP19-3 and Its Impact on Wool Traits in Chinese Tan Sheep
- The Menopausal Transition: Is the Hair Follicle “Going through Menopause”?
- Symptom Trajectories and Long-Term Sequelae of COVID-19: A Matched Case–Control Study with Population-Based Controls
- 5α-Reductase Isoenzymes: From Neurosteroid Biosynthesis to Neuropsychiatric Outcomes
- Paradoxical reactions in the era of modern biological therapy of psoriasis — a comprehensive analysis of pathomechanisms and clinical guidelines
- Androgenetic Alopecia and Risks of Overall and Aggressive Prostate Cancer: An Updated Systematic Review and Meta-Analysis
- 26-SNP Panel Aids Guiding Androgenetic Alopecia Therapy and Provides Insight into Mechanisms of Action
- 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
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Alopecia universalis with IL-12-RB1 and STAT4 mutations effectively treated with upadacitinib
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Insulin resistance as risk factor for the development of type 2 diabetes mellitus: a systematic approach
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology
- Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
- Epidemiology, management and the associated burden of mental health illness, atopic and autoimmune conditions, and common infections in alopecia areata: protocol for an observational study series
- Metabolic syndrome and dermatological diseases: association and treatment
- Cardiodermatology: the heart of the connection between the skin and cardiovascular disease