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Research 151–180 of 1000+
- Use of Induced Pluripotent Stem Cells in Dermatological Research
- Stabilization of epithelial β-catenin compromises mammary cell fate acquisition and branching morphogenesis
- Noggin overexpression inhibits eyelid opening by altering epidermal apoptosis and differentiation
- Highly Upregulated Lhx2 in the Foxn1−/− Nude Mouse Phenotype Reflects a Dysregulated and Expanded Epidermal Stem Cell Niche
- A 4kb Fragment of the Desmocollin 3 Promoter Directs Reporter Gene Expression to Parakeratotic Epidermis and Primary Hair Follicles
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- Cutaneous Retinoic Acid Levels Determine Hair Follicle Development and Downgrowth
- 1314 Advanced age impairs self-renewal and biases fate choice of hair follicle dermal stem cells
- 1311 Efficacy of topical tofacitinib in promoting hair growth in non-scarring alopecia
- Identifying novel strategies for treating human hair loss disorders: Cyclosporine A suppresses the Wnt inhibitor, SFRP1, in the dermal papilla of human scalp hair follicles
- Hair Growth Promoting Effect of 4HGF Encapsulated with PGA Nanoparticles (PGA-4HGF) by β-Catenin Activation and Its Related Cell Cycle Molecules
- Telogen Effluvium
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Hair shaft miniaturization causes stem cell depletion through mechanosensory signals mediated by a Piezo1-calcium-TNF-α axis
- Evaluation of Clinical and Oral Findings in Patients with Epidermolysis bullosa
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Ectodermal Dysplasia: Otolaryngologic Manifestations and Management
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- 092 Novel biallelic RIPK4 mutations cause ectodermal dysplasia with cutaneous syndactyly
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- A new mutation resulting in the truncation of the TRAF6-interacting domain of XEDAR: a possible novel cause of hypohidrotic ectodermal dysplasia: Figure 1
- Tissue expansion for correction of alopecia in a child with hypohidrotic ectodermal dysplasia
- Analogs of human genetic skin disease in domesticated animals
- Altered skin development and impaired proliferative and inflammatory responses in transgenic mice overexpressing the glucocorticoid receptor
- MICRO-MORPHOMETRIC STUDY OF SKIN IN DEVELOPING HUMAN FETUSES AND ITS CLINICAL RELEVANCE
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies
- 1426 Deletion of hoxc13 in frogs reveals key steps in the molecular evolution of cornified skin appendages
- Inherited disorders of the skin in human and mouse: from development to differentiation.
- Expression of <i>Foxi3</i> is regulated by ectodysplasin in skin appendage placodes