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Research 811–840 of 1000+
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Ectodysplasin Signaling in Cutaneous Appendage Development: Dose, Duration, and Diversity
- Cuprorivaite/hardystonite/alginate composite hydrogel with thermionic effect for the treatment of peri-implant lesion
- A Gender Hypothesis of sex disparities in adverse drug events
- Menopause, skin and common dermatoses. Part 4: oral disorders
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Promoting effect of type 17 collagen production by chlorogenic acid using PLGA nanoparticles in the human epidermal keratinocyte cell
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Rejuvenation of Aged Pig Facial Skin by Transplanting Allogeneic Granulocyte Colony-Stimulating Factor-Induced Peripheral Blood Stem Cells from a Young Pig
- Making the head: Caspases in life and death
- Identification of key genes and signaling pathways related to Hetian sheep wool density by RNA-seq technology
- Preparation and Optimization of Garlic Oil/Apple Cider Vinegar Nanoemulsion Loaded with Minoxidil to Treat Alopecia
- Transcriptome analyses of reprogrammed feather / scale chimeric explants revealed co-expressed epithelial gene networks during organ specification
- Three-Dimensional Organoid System Transplantation Technologies in Future Treatment of Central Nervous System Diseases
- The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome
- Oral Lichen Planus
- Cultivation of Human Hair Follicle Cells
- From Sea to Therapy: Marine Biomaterials for Drug Delivery and Wound Healing
- Advances in 3D printing for the repair of tympanic membrane perforation: a comprehensive review
- Is Satoyoshi syndrome an autoimmune disease? A systematic review
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Analysis of the expression pattern of the carrier protein transthyretin and its receptor megalin in the human scalp skin and hair follicles: hair cycle-associated changes
- Associations among hair loss, oral sulfur-containing gases, and gastrointestinal and metabolic linked diseases in Japanese elderly men: pilot study
- The Endocrine Control of the Hair Follicle
- Runx1 transcription factor is involved in the regulation of KAP5 gene expression in human hair follicles
- Management of Serious Adverse Events Following Deoxycholic Acid Injection for Submental and Jowl Fat Reduction: A Systematic Review and Management Recommendations
- Dermatological concerns for women and girls with turner syndrome
- Developmentally regulated expression of integrin alpha-6 distinguishes neural crest derivatives in the skin
- Nanoemulgel: For Promising Topical and Systemic Delivery