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Research 241–270 of 1000+
- Regulatory T Cells: the Many Faces of Foxp3
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Keratin 17 modulates hair follicle cycling in a TN<i>Fα</i>-dependent fashion
- The pathophysiology of polycystic ovary syndrome: trying to understand PCOS and its endocrinology
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- 5-Alpha-Reductase Inhibitors and Combination Therapy
- Setting reference values in trichology
- ESGCT and FSGT Collaborative Congress Helsinki, Finland September 17–20, 2015 Abstracts
- 312 CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells
- 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy
- 316 Specialized ribosomes in human dermal fibroblast senescence
- 313 Different polyamine levels in the vertex and occipital hair of pattern hair loss patients
- SLE and Serum Complement: Causative, Concomitant or Coincidental?
- Evidence of a Causal Relationship Between Body Mass Index and Immune-Mediated and Inflammatory Skin Diseases and Biomarkers: A Mendelian Randomization Study
- Clinical Findings, Response to Steroid Treatment, and Recurrence Rate in Alopecia Areata Patients with or without a Nonsynonymous Variant of Coiled-Coil Alpha-Helical Rod Protein 1
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Congenital hair loss disorders: Rare, but not too rare
- Genetic basis of polycystic ovary syndrome
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta
- Oral Presentations
- Comparison of comedolytic effect of benzoyl peroxide and adapalene in rhino mice
- Nonclassic Congenital Adrenal Hyperplasia
- Prevalence of CYP21 mutations and IRS1 variant among women with polycystic ovary syndrome and adrenal androgen excess
- CYP21A2 Mutations in Women with Polycystic Ovary Syndrome (PCOS)
- DNA phenotyping: current application in forensic science
- Genetic prediction of male pattern baldness
- Nuclear Topology, Epigenetics, and Keratinocyte Differentiation
- Spinal and bulbar muscular atrophy: pathogenesis and clinical management
- Diagnostic approach to low‐renin hypertension