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Research 181–210 of 1000+
- Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum
- Autoimmune thyroid disease and human health: a systematic review of Mendelian randomization studies
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Evidence for Masculinization of Adipokine Gene Expression in Visceral and Subcutaneous Adipose Tissue of Obese Women With Polycystic Ovary Syndrome (PCOS)
- Emerging concepts about prenatal genesis, aberrant metabolism and treatment paradigms in polycystic ovary syndrome
- Integral Roles of Specific Proteoglycans in Hair Growth and Hair Loss: Mechanisms behind the Bioactivity of Proteoglycan Replacement Therapy with Nourkrin® with Marilex® in Pattern Hair Loss and Telogen Effluvium
- Computational derivation of a molecular framework for hair follicle biology from disease genes
- Analysis of Vitamin D Receptor (VDR) Gene Polymorphisms in Alopecia Areata
- Vandetanib-associated alopecia areata in a patient with metastatic medullary thyroid cancer
- Overexpression of HE4/WFDC2 gene in mice leads to keratitis and corneal opacity
- From Surgery to Pharmacology to Gene Therapy
- Ageratum Conyzoides L. Extract Inhibits 5α-Reductase Gene Expression and Prostaglandin D2 Release in Human Hair Dermal Papilla Cells and Improves Symptoms of Hair Loss in Otherwise Healthy Males and Females in an Open Label Pilot Study
- Phenotypic Heterogeneity in 5 Japanese Patients with an Identical Point Mutation in the Vitamin D Receptor Gene
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Novel small molecules downregulate CDK1 expression and inhibit Wnt/β-catenin signaling in cutaneous squamous cell carcinoma by targeting its distinct tumor-specific cellular landscape
- Recent advances in the molecular mechanisms determining tissue sensitivity to glucocorticoids: novel mutations, circadian rhythm and ligand-induced repression of the human glucocorticoid receptor
- CAG Repeat Testing of Androgen Receptor Polymorphism: Is This Necessary for the Best Clinical Management of Hypogonadism?
- Skin diseases in consequence of endocrine alterations
- TR3 is preferentially expressed by bulge epithelial stem cells in human hair follicles
- SAT-210 When Acne, Hirsutism and Menstrual Irregularities Are More Than PCOS
- Iron deficiency and diffuse nonscarring scalp alopecia in women: More pieces to the puzzle
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- Alopecia
- Hair, Cutaneous Homeostasis and Stem Cell Functions
- Pathways to inflammation: acne pathophysiology
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Hair greying & its palliative management
- Associated comorbidities in pediatric patients with alopecia areata
- Main Plenary Sessions: Summaries of Papers