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Research 511–540 of 1000+
- Dermatological problems of the puberty
- Overexpression of Nanog in amniotic fluid–derived mesenchymal stem cells accelerates dermal papilla cell activity and promotes hair follicle regeneration
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Alopecia Feminina De Origem Endócrina: Abordagem Integrativa
- Keratosis Follicularis Spinulosa Decalvans Associated with Acne Keloidalis Nuchae and Tufted Hair Folliculitis
- The mediation role of sleep on the relationship between drinks behavior and female androgenetic alopecia
- Analyse de la régulation du gène Hairless et identification des voies de signalisation affectées chez les mutants «bald Mill Hill».
- Current Genetics in Hair Diseases
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- The disruption of Sox21-mediated hair shaft cuticle differentiation causes cyclic alopecia in mice
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- Lifestyle and Physiological Factors Associated with Facial Wrinkling in Men and Women
- Insertional mutation of the hairless locus on mouse Chromosome 14
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- A systematic simulation-based meta-analytical framework for prediction of physiological biomarkers in alopecia
- Hair follicles modulate skin barrier function
- Problems in pattern alopecia
- Spermine Lipid Assembled Nanoparticles for siRNA Delivery and Androgenetic Alopecia Therapy
- The Nutrient–Skin Connection: Diagnosing Eating Disorders Through Dermatologic Signs
- Direct cellular reprogramming enables development of viral T antigen–driven Merkel cell carcinoma in mice
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Efficient Silencing of Androgen Receptor Gene via UTR-Targeting siRNAs for Androgenetic Alopecia Therapy
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Gender differences in skin: A review of the literature
- Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- Endogenous retinoids in the hair follicle and sebaceous gland
- Flavonoid Silibinin Increases Hair-Inductive Property Via Akt and Wnt/��-Catenin Signaling Activation in 3-Dimensional-Spheroid Cultured Human Dermal Papilla Cells
- PKC downregulation upon rapamycin treatment attenuates mitochondrial disease