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Research 571–600 of 1000+
- Hypotrichosis in a child with olmsted syndrome
- Decision letter: NuMA-microtubule interactions are critical for spindle orientation and the morphogenesis of diverse epidermal structures
- Stem Cells and Peripheral Nerve
- Characterization of the Role of Transferrin receptor 1 (Tfr1) in the Intestinal Epithelium, Pancreas, and Skin
- The Roles of the Lrig1- and Lgr6-Positive Stem Cells in the Skin and the Functions of the Molecular Markers That Define Them
- The Roles of Smad2 and Smad3 in Mouse Skin Development
- Characterisation, genomic organisation, expression and function of the mEphA1 receptor Tyrosine Kinase
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Hairless Up‐Regulates <i>Tgf‐β2</i> Expression via Down‐Regulation of miR‐31 in the Skin of “Hairpoor” (<i>Hr</i><sup><i>Hp</i></sup>) Mice
- The Nuclear Vitamin D Receptor: Biological and Molecular Regulatory Properties Revealed
- Obesity resistance of the stearoyl-CoA desaturase-deficient (<i>scd1</i> <sup>-/-</sup>) mouse results from disruption of the epidermal lipid barrier and adaptive thermoregulation
- Multifunctional DNA Hydrogels with Hydrocolloid‐Cotton Structure for Regeneration of Diabetic Infectious Wounds
- Activin Controls Skin Morphogenesis and Wound Repair Predominantly via Stromal Cells and in a Concentration-Dependent Manner via Keratinocytes
- In vivo function of VDR in gene expression-VDR knock-out mice
- Clonal Growth of Dermal Papilla Cells in Hydrogels Reveals Intrinsic Differences between Sox2-Positive and -Negative Cells In Vitro and In Vivo
- Spontaneous Squamous Cell Carcinoma Induced by the Somatic Inactivation of <i>Retinoblastoma</i> and <i>Trp53</i> Tumor Suppressors
- Expression of <i>Foxi3</i> is regulated by ectodysplasin in skin appendage placodes
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- Insertional mutation of the hairless locus on mouse Chromosome 14
- Physical inactivity is a disease synonymous for a non-permissive brain disorder
- Cutaneous gene therapy
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Assessment of replication rates of human keratinocytes in engineered skin substitutes grafted to athymic mice
- Mesothelial Stem Cells and Stromal Vascular Fraction for Skin Rejuvenation
- The possible implication of the S250C variant of the autoimmune regulator protein in a patient with autoimmunity and immunodeficiency: in silico analysis suggests a molecular pathogenic mechanism for the variant
- Analysis of Copy Number Variation in the Whole Genome of Normal-Haired and Long-Haired Tianzhu White Yaks