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Research 721–750 of 1000+
- Expression and Analysis of TBX3 Gene in the Skin from Three Locations on Dun Mongolian Bider Horse
- Analysis of the Long Non-Coding and Messenger RNA Expression Profiles in the Skin Tissue of Super Merino and Small-Tailed Han Sheep
- Fractal Pattern in the Premature Graying of Hair: A Case Report
- AUTOLOGOUS FAT GRAFTING UPDATE. PRESENTATION OF OWN RESULTS IN FACIAL REGENERATION
- 4 Platelet-Rich Plasma for Alopecia and Hair Restoration
- Developmental Mechanisms Controlling Cell Fate, Evolution of
- A review on Hair Loss & Damage
- Hair Examination
- Polycystic Ovary Syndrome in Adolescents
- COMMENTARY
- PREFACE
- Donor Site Reharvesting in Patients Whose Donor Sites Appear Exhausted
- PREFACE
- Cutaneous signals of immune system disease
- A comparative analysis of three explanatory models of mental disorder and a preferred focus of explanation
- SELF-CARE OF MALE PATTERN HAIR LOSS – Selfcare Journal
- Decreased Serum Ferritin is Associated With Alopecia in Women
- Biochemical and trichological characterization of diffuse alopecia in women
- Evolution of hard proteins in the sauropsid integument in relation to the cornification of skin derivatives in amniotes
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- Hair analysis for veterinary drug monitoring in livestock production
- Epidemiological study of prostate cancer (EPICAP): a population-based case–control study in France
- Androgenetic alopecia; drug safety and therapeutic strategies
- Activated Hair Follicle Stem Cells and Wnt/β-catenin Signaling Involve in Pathnogenesis of Sebaceous Neoplasms
- Marine Health-Promoting Compounds: Recent Trends for Their Characterization and Human Applications
- A comparison of transcriptomic patterns measured in the skin of Chinese fine and coarse wool sheep breeds
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Cellulose-Based Nanofibers in Wound Dressing
- THE DEVELOPMENT OF EARLY MOUSE EMBRYOS IN THE EXTRAEMBRYONIC COELOM OF THE CHICK
- Mitochondrial DNA 10158T>C mutation in a patient with mitochondrial encephalomyopathy with lactic acidosis, and stroke-like episodes syndrome