Search
for
Sort by
Research 721–750 of 1000+
- Abstracts
- Hair shaft disorders
- A Rare Presentation of Biotinidase Deficiency Mimicking Acrodermatitis Enteropathica in a Toddler
- Epicardial fat thickness in children with classic congenital adrenal hyperplasia
- Why are men with premature alopecia at higher risk of benign prostatic hyperplasia? And what about prostate cancer?
- Surgical approach of ectropion in lamellar ichthyosis
- Ischemic onycholysis of the hands
- Melanocyte stem cells: a melanocyte reservoir in hair follicles for hair and skin pigmentation
- The Harmonies Played by TGF-β in Stem Cell Biology
- Laminin-511 is an epithelial message promoting dermal papilla development and function during early hair morphogenesis
- Extracellular vesicle-based drug overview: research landscape, quality control and nonclinical evaluation strategies
- The Majority of Multipotent Epidermal Stem Cells Do Not Protect Their Genome by Asymmetrical Chromosome Segregation
- The Inflammatory Caspases-1 and -11 Mediate the Pathogenesis of Dermatitis in Sharpin-Deficient Mice
- Cicatricial (Scarring) Alopecias
- Fluoroquinolone-induced serious, persistent, multisymptom adverse effects
- The Biology of Hair Growth
- An updated review of the sebaceous gland and its role in health and diseases Part 2: Pathophysiological clinical disorders of sebaceous glands
- Enhanced Insights into Frontal Fibrosing Alopecia: Advancements in Pathogenesis Understanding and Management Strategies
- B‐ RAF , naevi and melanoma: a complex relationship
- Hair diameter vs. hair density in male androgenetic alopecia
- Hair and Scalp Changes in Cutaneous and Systemic Lupus Erythematosus
- Alopecia Areata
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Molecular mechanisms of androgenetic alopecia
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Dermatologic manifestations of endocrine disorders
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Oral Manifestations of Hematologic and Nutritional Diseases
- Premature graying of hair
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT