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Research 121–150 of 1000+
- Development of Autoimmune Hair Loss Disease Alopecia Areata Is Associated with Cardiac Dysfunction in C3H/HeJ Mice
- Genetic basis of polycystic ovary syndrome
- CD133-positive dermal papilla-derived Wnt ligands regulate postnatal hair growth
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Grey, curly and short-haired Swiss Holstein cattle show genetic traces of the Simmental breed
- Association between DNA Methylation in the Core Promoter Region of the CUT-like Homeobox 1 (CUX1) Gene and Lambskin Pattern in Hu Sheep
- Genome-wide DNA methylation and transcriptome analyses reveal the key gene for wool type variation in sheep
- Nano-Enabled CRISPR-Cas Gene Editing for Cancer Therapeutics
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- SP1 and KROX20 Regulate the Proliferation of Dermal Papilla Cells and Target the CUX1 Gene
- The alopecia areata phenotype is induced by the water avoidance stress test in <i>cchcr1</i>-deficient mice
- Primary Generalized Glucocorticoid Resistance or Chrousos Syndrome: Allostasis Through a Mutated Glucocorticoid Receptor
- Australasian Society for Dermatology Research Meeting, May 2006
- Folliculin encoded by the <i>BHD</i> gene interacts with a binding protein, FNIP1, and AMPK, and is involved in AMPK and mTOR signaling
- Androgens and androgen receptor action in skin and hair follicles
- Interaction between stem cell factor and endothelin-1: effects on melanogenesis in human skin xenografts
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Apoptosis in human skin development: Morphogenesis, periderm, and stem cells
- Regulation of Involucrin Gene Expression
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- In vivo function of VDR in gene expression-VDR knock-out mice
- JMJD3 and NF-κB-dependent activation of Notch1 gene is required for keratinocyte migration during skin wound healing
- Idiopathic Hirsutism*
- Spinal and bulbar muscular atrophy: pathogenesis and clinical management
- CAG Repeat Testing of Androgen Receptor Polymorphism: Is This Necessary for the Best Clinical Management of Hypogonadism?
- Genetically separable determinants of hair keratin gene expression
- Epigenetic regulation in adult stem cells and cancers
- Novel anti-aging gene NM_026333 contributes to proton-induced aging via NCX1-pathway
- OVO Homolog-Like 1, a Target Gene of the Wnt/β-Catenin Pathway, Controls Hair Follicle Neogenesis