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Research 151–180 of 702
- Mechanisms Involved in the Relationship between Vitamin D and Insulin Resistance: Impact on Clinical Practice
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Network Pharmacology Reveals Curcuma aeruginosa Roxb. Regulates MAPK and HIF-1 Pathways to Treat Androgenetic Alopecia
- 876 Imaging nanoscale changes in desmosome protein organization
- Prolactin and the Skin: A Dermatological Perspective on an Ancient Pleiotropic Peptide Hormone
- Menopause and hair loss in women: Exploring the hormonal transition
- Transforming growth factor-β in stem cells and tissue homeostasis
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- The Genetics of Human Skin Disease
- The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion
- Noval advance of histone modification in inflammatory skin diseases and related treatment methods
- Oestrogen functions in skin and skin appendages
- Friends Turned Foes: Angiogenic Growth Factors beyond Angiogenesis
- The Rotterdam Study: 2018 update on objectives, design and main results
- Biology and Genetics of Hair
- First Symposium of Ichthyosis Experts
- A review of hyperandrogenism state in polycystic ovarian syndrome
- LPA-producing enzyme PA-PLA<sub>1</sub>α regulates hair follicle development by modulating EGFR signalling
- Alopecia Areata: Pathogenesis, Diagnosis, and Therapies
- Alopecia areata: a comprehensive review of clinical, immunologic, and genetic perspectives
- Pseudo-Cushing Syndrome
- Pulmonary manifestations of Birt-Hogg-Dubé syndrome
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Polycystic ovary syndrome and iron overload: biochemical link and underlying mechanisms with potential novel therapeutic avenues
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Resistance to the Insulin and Elevated Level of Androgen: A Major Cause of Polycystic Ovary Syndrome
- Lifestyle Factors Involved in the Pathogenesis of Alopecia Areata