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Research 61–90 of 1000+
- Perspectives of Kennedy's disease
- Skin features in myotonic dystrophy type 1: An observational study
- Transforming growth factor-β in stem cells and tissue homeostasis
- Careless talk costs lives: fibroblast growth factor receptor signalling and the consequences of pathway malfunction
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- Acne as a chronic systemic disease
- 46,XY DSD due to impaired androgen production
- Parathyroid Hormone Hormone-Related Protein and the PTH Receptor Regulate Angiogenesis of the Skin
- A Clinical Approach to Severe Insulin Resistance
- What does acne genetics teach us about disease pathogenesis?
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Characterization of Primary Cilia and Intraflagellar Transport 20 in the Epidermis
- An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- Modelling androgen synthesis and action during human sexual differentiation
- The human keratins: biology and pathology
- The Rotterdam Study: 2018 update on objectives, design and main results
- The North American Menopause Society Recommendations for Clinical Care of Midlife Women
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- Cartilage to bone transformation during fracture healing is coordinated by the invading vasculature and induction of the core pluripotency genes
- Targeting the Wnt pathways for therapies
- MicroRNA-214 controls skin and hair follicle development by modulating the activity of the Wnt pathway
- Congenital Adrenal Hyperplasia
- Wnt signaling in skin organogenesis
- Regeneration of skin appendages and nerves: current status and further challenges
- Management of congenital ichthyoses: European guidelines of care, part two
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- How to diagnose a lipodystrophy syndrome
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen