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Research 721–750 of 1000+
- Australasian Society for Dermatology Research Meeting, May 2006
- Main Plenary Sessions: Summaries of Papers
- A genetic test for androgenetic alopecia: polymorphisms in the androgen receptor gene provide a genetic screening test for androgenetic alopecia and earlier medical intervention
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Hairless triggers reactivation of hair growth by promoting Wnt signaling
- Comparative Transcriptome Analysis of Fetal Skin Reveals Key Genes Related to Hair Follicle Morphogenesis in Cashmere Goats
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- Human KAP Genes, Only the Half of it? Extensive Size Polymorphisms in Hair Keratin-Associated Protein Genes
- Preparation of hair beads and hair follicle germs for regenerative medicine
- Exploring the Drug Repurposing Versatility of Valproic Acid as a Multifunctional Regulator of Innate and Adaptive Immune Cells
- Gene trajectory inference for single-cell data by optimal transport metrics
- Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle
- TSA restores hair follicle-inductive capacity of skin-derived precursors
- Effect of the FA2H Gene on cashmere fineness of Jiangnan cashmere goats based on transcriptome sequencing
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)
- Using WGCNA (weighted gene co-expression network analysis) to identify the hub genes of skin hair follicle development in fetus stage of Inner Mongolia cashmere goat
- Skin regeneration with conical and hair follicle structure of deep second-degree scalding injuries via combined expression of the EPO receptor and beta common receptor by local subcutaneous injection of nanosized rhEPO
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- High incidence of severe hand–foot syndrome during capecitabine–docetaxel combination chemotherapy
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- The relationship among androgens, insulin resistanceand ghrelin polymorphisms in post-adolescent malepatients with severe acne vulgaris
- Protein Kinase C<i>ε</i>, Which Is Linked to Ultraviolet Radiation-Induced Development of Squamous Cell Carcinomas, Stimulates Rapid Turnover of Adult Hair Follicle Stem Cells
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- In Vivo Evaluation of<i>Eclipta alba</i>Extract as Anticancer and Multidrug Resistance Reversal Agent
- Shh Gene Regulates the Proliferation and Apoptosis of Dermal Papilla Cells to Affect Its Differential Expression in Secondary Hair Follicle Growth Cycle of Cashmere Goats
- Efficient Gene Editing for Heart Disease via ELIP-Based CRISPR Delivery System
- CTLA4 +49AG (rs231775) and CT60 (rs3087243) gene variants are not associated with alopecia areata in a Mexican population from Monterrey Mexico
- The seasonal development dynamics of the yak hair cycle transcriptome
- Effects of bright light exposure during daytime on peripheral clock gene expression in humans