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Research 781–810 of 1000+
- Retinol dehydrogenase 12 (RDH12): Role in vision, retinal disease and future perspectives
- miR-370-3p Inhibited the Proliferation of Sheep Dermal Papilla Cells by Inhibiting the Expression of SMAD4
- Cultivation of Hair Matrix Cells from Cashmere Goat Skins and Exemplified Applications
- Zebrafish Model of Hereditary Pigmentary Disorders
- Identification of two additional novel mutations in the AR gene associated with severe forms of androgen insensitivity syndrome
- Identification of Epigenetic Regulator‐Associated Genes in Keloid Disease Through Integrated Bulk and Single‐Cell Transcriptomics With RT ‐ qPCR Validation
- CRISPR/Cas9-mediated Generation of<i>COL7A1</i>-deficient Keratinocyte Model of Recessive Dystrophic Epidermolysis Bullosa
- Genetic analysis of the role of androgen metabolism in the pathogenesis of prostate cancer
- Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene
- Essential resources and best practices for laboratory mouse research
- Cancer-Related Alopecia Risk and Treatment
- Genotypes of Single-nucleotide polymorphisms on DENND1A in an association with polycystic ovary syndrome among Saudi Arabian females
- Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient
- P78 Acrodermatitis enteropathica in children: clinical cases
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Regulatory pathway analysis of coat color genes in Mongolian horses
- Characterization of the Promoter Regions of Two Sheep Keratin-Associated Protein Genes for Hair Cortex-Specific Expression
- Comprehensive analysis of the expression profiles of mRNA, lncRNA, circRNA, and miRNA in primary hair follicles of coarse sheep fetal skin
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Clinically relevant aberrant Filip1l DNA methylation detected in a murine model of cutaneous squamous cell carcinoma
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- DNA Methylation Mediates lncRNA2919 Regulation of Hair Follicle Regeneration
- Epigenetics of Colorectal Cancer
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- <i>OsPHR2</i> Is Involved in Phosphate-Starvation Signaling and Excessive Phosphate Accumulation in Shoots of Plants
- Independent genomewide screens identify the tumor suppressor VTRNA2-1 as a human epiallele responsive to periconceptional environment
- Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development
- The Two Functional Keratin 6 Genes of Mouse Are Differentially Regulated and Evolved Independently from Their Human Orthologs