Search
for
Sort by
Research 271–300 of 1000+
- Plasma Diaphanous Related Formin 1 Levels Are Associated with Altered Glucose Metabolism and Insulin Resistance in Patients with Polycystic Ovary Syndrome: A Case Control Study
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- Dermatologic Effects of Selumetinib in Pediatric Patients with Neurofibromatosis Type 1: Clinical Challenges and Therapeutic Management
- Effects of dietary camelina, flaxseed, and canola oil supplementation on inflammatory and oxidative markers, transepidermal water loss, and coat quality in healthy adult dogs
- Acetyl-CoA synthesis in the skin is a key determinant of systemic lipid homeostasis
- Prevalence, Phenotypes, and Comorbidities of Polycystic Ovary Syndrome Among Indian Women
- Beard Alopecia: An Updated and Comprehensive Review of Etiologies, Presentation and Treatment
- The Molecular Pathogenesis of Trichilemmal Carcinoma
- The Molecular Pathogenesis of Trichilemmal Carcinoma
- 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
- The mineralocorticoid receptor as a novel player in skin biology: beyond the renal horizon?
- UPDATE ON IDIOPATHIC HIRSUTISM: DIAGNOSIS AND TREATMENT
- The difficulty of finding ‘healthy’ volunteers
- Gonads
- The North American Menopause Society Recommendations for Clinical Care of Midlife Women
- <i>Polycystic Ovary Syndrome in Adolescence</i>
- Interventional studies for polycystic ovarian syndrome in children and adolescents
- Familial Androgenetic Alopecia in Siblings with Normal Endocrinological Status
- Molecular genetics of androgen insensitivity
- Sudden whitening of the hair in an 82-year-old woman: the ‘overnight greying’ phenomenon
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- PA15 Becker naevus syndrome associated with a mosaic pathogenic variant in <i>ACTB</i>
- The character “hairless” in the mouse
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- Physiological and retinoid-induced proliferations of epidermis basal keratinocytes are differently controlled
- Emerging medication for the treatment of male hypogonadism
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- The role of lymphocytes in the development and treatment of alopecia areata
- Rabson-Mendenhall syndrome: two case reports and a brief review of the literature
- Male fertility and skin diseases