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Research 661–690 of 1000+
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- State-dependent signaling by Ca<sub>v</sub>1.2 regulates hair follicle stem cell function
- A rational approach to the diagnosis of polycystic ovarian syndrome during adolescence
- The Genetics of Human Skin Disease
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- Cytokine loaded layer-by-layer ultrathin matrices to deliver single dermal papilla cells for spot-by-spot hair follicle regeneration
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- 3D co-culture model of endothelial colony-forming cells (ECFCs) reverses late passage adipose-derived stem cell senescence for wound healing
- ADM Scaffolds Generate a Pro-regenerative Microenvironment During Full-Thickness Cutaneous Wound Healing Through M2 Macrophage Polarization via Lamtor1
- rPanglaoDB: an R package to download and merge labeled single-cell RNA-seq data from the PanglaoDB database
- Treatment of Cystathionine β-Synthase Deficiency in Mice Using a Minicircle-Based Naked DNA Vector
- The effect of dietary modulation of sulfur amino acids on cystathionine β synthase–deficient mice
- A second <i>KRT</i>71 allele in curly coated dogs
- Hair Loss in Autoimmune Cutaneous Bullous Disorders
- Scd1 ab-Xyk : a new asebia allele characterized by a CCC trinucleotide insertion in exon 5 of the stearoyl-CoA desaturase 1 gene in mouse
- The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis
- 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
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Solitary fixed drug eruption caused by finasteride
- Celsr1 and Celsr2 exhibit distinct adhesive interactions and contributions to planar cell polarity
- Harnessing the Biomimetic Effect of Macromolecular Crowding in the Cell-Derived Model of Clubfoot Fibrosis
- Triglycerides, independent of Ferriman Gallwey Score, is a main determinant of free testosterone index in PCOS
- Runx Family Genes in Tissue Stem Cell Dynamics
- Increased 25(OH)D3 level in redheaded people: Could redheadedness be an adaptation to temperate climate?
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Mimicking Hair Disorders by Genetic Manipulation of Organ-Cultured Human Hair Follicles
- Anterior neck fat deposition in lipodystrophy syndrome; a new variant on a theme?
- Heat Preconditioning of Nanofat Does Not Improve Its Vascularization Properties