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Research 661–690 of 1000+
- Mucocutaneous reactions to chemotherapy
- Food Bioactive Compounds and Emerging Techniques for Their Extraction: Polyphenols as a Case Study
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Fibroblast growth factors: key players in regeneration and tissue repair
- Prevention and management of dermatological toxicities related to anticancer agents: ESMO Clinical Practice Guidelines☆
- The molecular basis of human keratin disorders
- Cutaneous Neuroimmune Interactions in Peripheral Neuropathic Pain States
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- A Clinical and Biological Guide for Understanding Chemotherapy-Induced Alopecia and Its Prevention
- Clinical and histological challenge in the differential diagnosis of diffuse alopecia: female androgenetic alopecia, telogen effluvium and alopecia areata – part II
- Stem cell-derived exosomes: emerging therapeutic opportunities for wound healing
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- A “hair‐raising” history of alopecia areata
- Alopecia areata – Current understanding and management
- Clinicopathologic Characteristics and Response to Treatment of Persistent Chemotherapy-Induced Alopecia in Breast Cancer Survivors
- Medical aesthetics – Current trends and a review of its applications
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Using qualitative methods to establish the clinically meaningful threshold for treatment success in alopecia areata
- Alopecia areata
- Prevention and Treatment of Chemotherapy-Induced Alopecia: What Is Available and What Is Coming?
- How Our Microbiome Influences the Pathogenesis of Alopecia Areata
- Platelet-rich plasma in interventional dermatology and trichology: How far have we come?
- Beard Alopecia: An Updated and Comprehensive Review of Etiologies, Presentation and Treatment
- Gene Expression of CD70 and CD27 Is Increased in Alopecia Areata Lesions and Associated with Disease Severity and Activity
- Biological Determinants of Hair Quality: An Integrated Review of Nutritional, Molecular, and Environmental Factors Supporting Hair Longevity