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Research 301–330 of 1000+
- Tumor Necrosis Factor-Alpha and Polycystic Ovarian Syndrome: A Clinical, Biochemical, and Molecular Genetic Study
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Scarring Alopecia in Localized Dystrophic Epidermolysis Bullosa: A Case Report and a Scoping Review
- Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings
- Oral Presentations
- Anti-TNF antibody-induced psoriasiform skin lesions in patients with inflammatory bowel disease are characterised by interferon-γ-expressing Th1 cells and IL-17A/IL-22-expressing Th17 cells and respond to anti-IL-12/IL-23 antibody treatment
- Autoimmunity and autoimmune co-morbidities in psoriasis
- Nonclassic congenital adrenal hyperplasia
- Assessment of the impact of VDR polymorphisms on selected hormonal, metabolic and mineral balance markers in young women with hyperandrogenism
- Follikelhormone
- Fertility and Sterility Vol 101 No 4, April 2014
- Leucine-Rich Repeat-Containing G-Protein-Coupled Receptors as Markers of Adult Stem Cells
- ATP-dependent chromatin remodeling during mammalian development
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- Obesity and the skin
- Keratin disorders: from gene to therapy
- Disruption of FGF5 in Cashmere Goats Using CRISPR/Cas9 Results in More Secondary Hair Follicles and Longer Fibers
- A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females
- Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- Biology and Genetics of Hair
- Physiologic functions of PP2A: Lessons from genetically modified mice
- Reversing wrinkled skin and hair loss in mice by restoring mitochondrial function
- Beyond Expectations
- The Paradox of p53: What, How, and Why?
- Recent advances in the molecular mechanisms determining tissue sensitivity to glucocorticoids: novel mutations, circadian rhythm and ligand-induced repression of the human glucocorticoid receptor
- The Inflammatory Caspases-1 and -11 Mediate the Pathogenesis of Dermatitis in Sharpin-Deficient Mice
- Defects in mitochondrial DNA replication and oxidative damage in muscle of mtDNA mutator mice
- Genetic Defects in Human Pericentrin Are Associated With Severe Insulin Resistance and Diabetes