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Research 121–150 of 1000+
- Deep Hair Phenomics: Implications in Endocrinology, Development, and Aging
- A missense mutation in Lama3 causes androgen alopecia
- The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata
- MTHFR C677T Polymorphism and Serum Homocysteine Level as Risk Factors of Coronary Heart Disease in Patients with Androgenetic Alopecia: A Case Control Study
- Do Alopecia Areata and Hair Colour Have a Shared Genetic Component?
- Forensic DNA Phenotyping: Male Pattern Baldness: Traditional Review
- Hair Follicle-Related MicroRNA-34a Serum Expression and rs2666433A/G Variant in Patients with Alopecia: A Cross-Sectional Analysis
- Hormonal Control of Cardiac Action Potential Phase 1 Currents in the Brugada Syndrome
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- 46,XY DSD due to impaired androgen production
- High-throughput phenotyping methods for quantifying hair fiber morphology
- Phenotypic profiling of parents with cryptic nonclassic congenital adrenal hyperplasia: findings in 145 unrelated families
- <i>WNT10A</i> , dermatology and dentistry
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Is polycystic ovary syndrome a sexual conflict? A review
- Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?
- Abstracts
- Association of eNOS and STAT6 Gene Polymorphisms with the Susceptibility of Polycystic Ovary Syndrome in South Indian Women
- Aromatase deficiency in a male patient - Case report and review of the literature.
- Stem cell quiescence acts as a tumour suppressor in squamous tumours
- Steroid 5α-reductase 2 deficiency leads to reduced dominance-related and impulse-control behaviors
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk
- No Evidence that 2D:4D is Related to the Number of CAG Repeats in the Androgen Receptor Gene
- Identification and expression of the target gene SLC24A2 of oar-miR-377 and its novel SNPs effects on wool traits in sheep
- Main Plenary Sessions: Summaries of Papers
- Paraoxonase Enzyme Activity and Determination of Phenotypic Polymorphism in Patients with Acne Vulgaris