Search
for
Sort by
Research 121–150 of 1000+
- Molecular Genetics of Human Hair Diseases
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- TONGUE, RED
- Steatocystoma Multiplex
- Molecular mechanism of ligand recognition and activation of lysophosphatidic acid receptor LPAR6
- Screening of Protein Related to Wool Development and Fineness in Gansu Alpine Fine-Wool Sheep
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Polymorphism of Keratin Gene KRT71 and Its Relationship with Wool Properties in Gansu Alpine Fine-Wool Sheep
- Congenital atrichia associated with nevus flammeus: A rare association
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- The molecular basis of human keratin disorders
- Focused Review on Metal Nanoparticles in Hair Regeneration and Alopecia: Insights into Mechanisms, Assessment Techniques, Toxicity, Regulatory and Intellectual Property Perspectives
- Oral Presentations
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- Identification of the Key Genes Associated with Different Hair Types in the Inner Mongolia Cashmere Goat
- Hair shaft disorders in children – An update
- Hirsutism-A Comprehensive Update of Embryology, Aetiopathogenesis and Therapeutic Approach
- Treatment options for androgenetic alopecia: Efficacy, side effects, compliance, financial considerations, and ethics
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Wnt Signaling Across Adult Skin Mini-Organs: Interfollicular Epidermis, Hair Follicle, and Nail—Implications for Disease and Regeneration
- Skin Development and Disease: A Molecular Perspective
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Lysophospholipid Mediators in Health and Disease