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Research 121–150 of 1000+
- Ornithine decarboxylase transgenic mice as a model for human atrichia with papular lesions
- The Roles of EDA2R in Ageing and Disease
- Mediator 1 ablation induces enamel-to-hair lineage conversion in mice through enhancer dynamics
- Current Genetics in Hair Diseases
- A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders
- MICRO-MORPHOMETRIC STUDY OF SKIN IN DEVELOPING HUMAN FETUSES AND ITS CLINICAL RELEVANCE
- Keratin Expression Provides Novel Insight into the Morphogenesis and Function of the Companion Layer in Hair Follicles
- The promising prospect of human hair follicle regeneration in the shadow of new tissue engineering strategies
- Expression of COUP-TF-interacting protein 2 (CTIP2) in mouse skin during development and in adulthood
- Expression Profiling Reveals Genes Involved in the Regulation of Wool Follicle Bulb Regression and Regeneration in Sheep
- Novel recombinant R-spondin1 promotes hair regeneration by targeting the Wnt/β-catenin signaling pathway
- Developmental and evolutionary comparative analysis of a regulatory landscape in mouse and chicken
- Hair Loss in Children, Etiologies, and Treatment
- Identification of Stem Cell Populations in Sweat Glands and Ducts Reveals Roles in Homeostasis and Wound Repair
- Organogenesis From Dissociated Cells: Generation of Mature Cycling Hair Follicles From Skin-Derived Cells
- Edar Signaling in the Control of Hair Follicle Development
- Platelet-rich plasma—an ‘Elixir’ for treatment of alopecia: personal experience on 117 patients with review of literature
- Development and Maintenance of Epidermal Stem Cells in Skin Adnexa
- Use of Induced Pluripotent Stem Cells in Dermatological Research
- Analogs of human genetic skin disease in domesticated animals
- Intercellular junctions in normal epidermis
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- Editor's evaluation: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Molecular Mechanisms Regulating Hair Follicle Development
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Ichthyosis with confetti: clinics, molecular genetics and management
- Multipotent Nestin-Positive Stem Cells Reside in the Stroma of Human Eccrine and Apocrine Sweat Glands and Can Be Propagated Robustly In Vitro
- Induced pluripotent stem cell line MUSIi006-A derived from hair follicle keratinocytes as a non-invasive somatic cell source
- Approach to Alopecia in Dogs in Clinical Practice
- Organoid technology for tissue engineering