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Research 151–180 of 1000+
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Ectodysplasin Signaling in Cutaneous Appendage Development: Dose, Duration, and Diversity
- Dysfunction of keratinocyte adhesion
- Expression of COUP-TF-interacting protein 2 (CTIP2) in mouse skin during development and in adulthood
- Edar Signaling in the Control of Hair Follicle Development
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Platelet-rich plasma—an ‘Elixir’ for treatment of alopecia: personal experience on 117 patients with review of literature
- Role of β-Catenin Activation Levels and Fluctuations in Controlling Cell Fate
- Genetic Hair Disorders: A Review
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Transcriptional regulation of the thymus master regulator <i>Foxn1</i>
- P63 targeted deletion under the FOXN1 promoter disrupts pre-and post-natal thymus development, function and maintenance as well as induces severe hair loss
- Using High-Throughput Immunoblotting to Identify Proteins Involved in the Differentiation of ES Cells along the Hair Follicle Lineage in Vitro
- Recombinant Thrombomodulin Used to Successfully Treat Cronkhite-Canada Syndrome with Disseminated Intravascular Coagulation due to Sepsis in a Compromised Patient
- Retinoic Acid-Induced Epidermal Transdifferentiation in Skin
- Fully functional hair follicle organ regeneration using organ-inductive potential stem cells with an accessory mesenchymal cell population in an in vitro culture system
- DKK1 Mediated Inhibition of Wnt Signaling in Postnatal Mice Leads to Loss of TEC Progenitors and Thymic Degeneration
- Hair follicle and interfollicular epidermal stem cells make varying contributions to wound regeneration
- Keratin Expression Provides Novel Insight into the Morphogenesis and Function of the Companion Layer 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
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Small molecules facilitate single factor-mediated sweat gland cell reprogramming
- Analogs of human genetic skin disease in domesticated animals
- Understanding skin morphogenesis across developmental, regenerative and evolutionary levels
- The Roles of EDA2R in Ageing and Disease
- Introduction to JID Symposium Proceedings 52nd Annual Montagna Symposium on the Biology of Skin “Stem Cells in Skin” Held at Snowmass, Colorado, USA, June 13–17, 2003
- P311 induces the transdifferentiation of epidermal stem cells to myofibroblast-like cells by stimulating transforming growth factor β1 expression
- Expression Profiling Reveals Genes Involved in the Regulation of Wool Follicle Bulb Regression and Regeneration in Sheep
- Organogenesis From Dissociated Cells: Generation of Mature Cycling Hair Follicles From Skin-Derived Cells