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Research 691–720 of 1000+
- Insulin Resistance and Skin Diseases
- Telogen Effluvium: A Review
- Beyond Expectations
- The role of nuclear hormone receptors in cutaneous wound repair
- Dermatoscopy of hair shaft disorders
- Non-Edg family LPA receptors: the cutting edge of LPA research
- Endocrine Influences on Hair Growth
- Approach to the adult female patient with diffuse nonscarring alopecia
- Systematic Review of Platelet-Rich Plasma Use in Androgenetic Alopecia Compared with Minoxidil®, Finasteride®, and Adult Stem Cell-Based Therapy
- Mechanical forces in skin disorders
- Perspectives of Kennedy's disease
- The Spectrum of Skin Disease Among Indian Children
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- Localisation of members of the notch system and the differentiation of vibrissa hair follicles: Receptors, ligands, and fringe modulators
- Anagen effluvium
- Delivery of Tissue-Targeted Scalpels: Opportunities and Challenges for <i>In Vivo</i> CRISPR/Cas-Based Genome Editing
- Functional complexity of hair follicle stem cell niche and therapeutic targeting of niche dysfunction for hair regeneration
- HAIR AND SYSTEMATIC DISEASE
- Normal Hair Growth in Children
- 46,XY DSD due to impaired androgen production
- A review of the treatment of male pattern hair loss
- Defects in mitochondrial DNA replication and oxidative damage in muscle of mtDNA mutator mice
- An Overview of Alopecias
- How to diagnose a lipodystrophy syndrome
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- Drug-induced acne
- Increasing tinea capitis prevalence in Stockholm reflects immigration
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Coat condition, housing condition and measurement of faecal cortisol metabolites - a non-invasive study about alopecia in captive rhesus macaques (Macaca mulatta)
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen