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Research 391–420 of 1000+
- Sex-limited chromosomes and non-reproductive traits
- Epigenetic Effects of Gender-Affirming Hormone Treatment: A Pilot Study of the ESR2 Promoter’s Methylation in AFAB People
- Drivers of plateau adaptability in cashmere goats revealed by genomic and transcriptomic analyses
- The coenzyme A precursor pantethine enhances antitumor immunity in sarcoma
- Unusual symptoms of iron deficiency anemia (2 clinical observations)
- Modern Polycystic Ovary Syndrome (PCOS) Management: Intelligent Drug Delivery and Metabolic Reprogramming for Ovarian Restoration and Fertility Optimization
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology
- Effects of lifelong testosterone exposure on health and disease using Mendelian randomization
- Data-driven analysis to understand long COVID using electronic health records from the RECOVER initiative
- Giant axonal neuropathy alters the structure of keratin intermediate filaments in human hair
- RETRACTED: Genetic association between asthma and alopecia areata: A two‐sample Mendelian randomization study
- Author response: Effects of lifelong testosterone exposure on health and disease using Mendelian randomization
- In Silico Promoter Motif Analysis of Human Fertility-Related Genes
- Integrin signalling regulates YAP/TAZ to control skin homeostasis
- Cell-Type-Specific Chromatin States Differentially Prime Squamous Cell Carcinoma Tumor-Initiating Cells for Epithelial to Mesenchymal Transition
- Bioactive inorganic particles‐based biomaterials for skin tissue engineering
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Frizzled Receptors in Development and Disease
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Production-scale fibronectin nanofibers promote wound closure and tissue repair in a dermal mouse model
- The <i>IRE</i> gene encodes a protein kinase homologue and modulates root hair growth in <i>Arabidopsis</i>
- Integrated analysis of long non-coding RNA and mRNA expression in different colored skin of koi carp
- Conserved γδ T cell selection by BTNL proteins limits progression of human inflammatory bowel disease
- A global analysis of CNVs in Chinese indigenous fine-wool sheep populations using whole-genome resequencing
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- CRISPR/Cas9‐mediated loss of FGF5 function increases wool staple length in sheep
- GLI2-specific Transcriptional Activation of the Bone Morphogenetic Protein/Activin Antagonist Follistatin in Human Epidermal Cells