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Research 211–240 of 1000+
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Experimental Induction of Alopecia Areata-Like Hair Loss in C3H/HeJ Mice Using Full-Thickness Skin Grafts
- Mutations in AEC syndrome skin reveal a role for p63 in basement membrane adhesion, skin barrier integrity and hair follicle biology
- Retinoic Acid and Mouse Skin Morphogenesis. II. Role of Epidermal Competence in Hair Glandular Metaplasia
- Mesothelial Stem Cells and Stromal Vascular Fraction for Skin Rejuvenation
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- [Proteomics-based screening of differentially expressed proteins in skin of Chinese merino fine sheep (JunKen type) of different gender].
- Skin as a Window to Endocrine Dysfunction: Dermatological and Metabolic Interactions in Polycystic Ovary Syndrome
- Skin fragility in the wild-derived, inbred mouse strain Mus pahari/EiJ
- 1344 Novel human 3D skin model for skin aging research
- Thymic epithelial cells : relatives of multipotent stem cells of the skin
- Phenotypic characterization of non-dermatophyte moulds from companion animals with mycotic dermatitis
- Forensic DNA phenotyping: the need for proportionate regulation and judicial clarity in law enforcement
- The role of activins and follistatins in skin and hair follicle development and function
- Aging skin and non-surgical procedures: a basic science overview
- Ultrastructural skin changes in Egyptian mandibuloacral dysplasia patients with p.Arg527Leu <i>LMNA</i> mutation and in their asymptomatic heterozygotic mothers
- Global Landscapes of Human Phenotypic Variation in Inherited Traits
- Human Skin is a Steroidogenic Tissue: Steroidogenic Enzymes and Cofactors Are Expressed in Epidermis, Normal Sebocytes, and an Immortalized Sebocyte Cell Line (SEB-1)
- Expression of <i>Foxi3</i> is regulated by ectodysplasin in skin appendage placodes
- Multiple skin tumours in a Doberman Pinscher with colour dilution alopecia
- Phenotypic Heterogeneity in 5 Japanese Patients with an Identical Point Mutation in the Vitamin D Receptor Gene
- 328 The transcription factor CEBPB is a novel hub gene and multi-functional disease driver in Psoriatic skin inflammation
- Genetic basis of skin appendage development
- Animal models of human skin disease
- Cyclin D3 deficiency inhibits skin tumor development, but does not affect normal keratinocyte proliferation
- 3D organotypic skin models recapitulate autoantibody-driven pemphigus pathomechanisms and targeted therapeutic response
- Epithelial Fibronectin meshwork controls skin regeneration
- 1350 The role of mitochondria in skin aging
- The Roles of the Lrig1- and Lgr6-Positive Stem Cells in the Skin and the Functions of the Molecular Markers That Define Them
- Activin Controls Skin Morphogenesis and Wound Repair Predominantly via Stromal Cells and in a Concentration-Dependent Manner via Keratinocytes