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Research 391–420 of 1000+
- Anatomy and Physiology of the Skin
- Prevalence of androgenetic alopecia in China: a community-based study in six cities
- Biology of the wool follicle: an excursion into a unique tissue interaction system waiting to be re‐discovered
- THE PATHOGENESIS OF ALOPECIA AREATA
- Ferreting out stem cells from their niches
- Hair Follicle: A Novel Source of Multipotent Stem Cells for Tissue Engineering and Regenerative Medicine
- Normal Hair Growth in Children
- How to diagnose a lipodystrophy syndrome
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- One of These Things Is Not Like the Others: The Idea of Precedence in Health Technology Assessment and Coverage Decisions
- Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology
- Scalp whorls
- Advanced therapies of skin injuries
- The VEGF +405 G>C 5' untranslated region polymorphism and risk of PCOS: a study in the South Indian Women
- Androgen receptor genetic variant predicts COVID‐19 disease severity: a prospective longitudinal study of hospitalized COVID‐19 male patients
- Lifestyle and Physiological Factors Associated with Facial Wrinkling in Men and Women
- The Genetics of Human Skin Disease
- HAIR MATRIX CELL KINETICS: A SELECTIVE REVIEW
- A non-invasive study of alopecia in Japanese macaques Macaca fuscata
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Alopecias - Practical Evaluation and Management
- Atopic dermatitis and risk of autoimmune diseases: a systematic review and meta-analysis
- What’s New in the Histologic Evaluation of Alopecia and Hair-Related Disorders?
- Evaluation of Animal Models Suitable for Hair Research and Regeneration
- Analogs of human genetic skin disease in domesticated animals
- RETRACTED: Explore the genetic exposure to alopecia areata
- Current Genetics in Hair Diseases
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia