Search
for
Sort by
Research 181–210 of 1000+
- DNA dioxygenases Tet2/3 regulate gene promoter accessibility and chromatin topology in lineage-specific loci to control epithelial differentiation
- Autotaxin–lysophosphatidic acid– LPA <sub>3</sub> signaling at the embryo‐epithelial boundary controls decidualization pathways
- Efficacy and Safety of Laser Therapy and Phototherapy in Cicatricial and NonCicatricial Alopecia: A Systematic Review Study
- Eyebrow and Eyelash Alopecia: A Clinical Review
- Wnt Signaling Across Adult Skin Mini-Organs: Interfollicular Epidermis, Hair Follicle, and Nail—Implications for Disease and Regeneration
- Hair & Cutaneous Development
- Oral Presentations
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Skin Development and Disease: A Molecular Perspective
- Ichthyosis with confetti: clinics, molecular genetics and management
- Intercellular junctions in normal epidermis
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- TMT-Based Quantitative Proteomic Analysis Reveals the Effect of Bone Marrow Derived Mesenchymal Stem Cell on Hair Follicle Regeneration
- Hair shaft disorders in children – An update
- Polymorphism of Keratin Gene KRT71 and Its Relationship with Wool Properties in Gansu Alpine Fine-Wool Sheep
- The Nutrient–Skin Connection: Diagnosing Eating Disorders Through Dermatologic Signs
- Beard Alopecia: An Updated and Comprehensive Review of Etiologies, Presentation and Treatment
- Nuclear Localization of STAT5A Modified with O-Linked N-Acetylglucosamine and Early Involution in the Mammary Gland of Hirosaki Hairless Rat
- Desmoglein 4 is regulated by transcription factors implicated in hair shaft differentiation
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- A missense mutation in Lama3 causes androgen alopecia
- Towards Defining the Pathogenesis of the Hairless Phenotype
- 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
- Analogs of human genetic skin disease in domesticated animals
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Proceedings of the Ninth World Congress for Hair Research (2015)