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Research 751–780 of 1000+
- Cell death in skin function, inflammation, and disease
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Limb amputations; etiopathogenesis, diagnosis and the multidisciplinary therapeutic approach
- Mesenchymal Stem Cells With Modification of Junctional Adhesion Molecule A Induce Hair Formation
- Regulatory T cell dysfunction and immunotherapeutic breakthroughs in type 1 diabetes
- Effect of Fibroblast Growth Factor 10 and an Interacting Non-Coding RNA on Secondary Hair Follicle Dermal Papilla Cells in Cashmere Goats’ Follicle Development Assessed by Whole-Transcriptome Sequencing Technology
- Severe impact of late diagnosis of congenital adrenal hyperplasia on gender identity, sexual orientation and function: case report and review of the literature
- Role of Silver Nanoparticles in Wound Healing: Mechanisms, Efficacy, and Clinical Applications
- Integration of Point-of-Care Technology in the Decoding Process of Single Nucleotide Polymorphism for Healthcare Application †
- LHX2: a transcription factor in development, homeostasis, repair, and disease
- Therapeutic potential of <i>Asiaticoside</i> in wound healing after endoscopic submucosal dissection (ESD)
- RNA modifications: molecular orchestrators of wound healing
- Platelet-Rich Plasma (PRP): Molecular Mechanisms, Actions and Clinical Applications in Human Body
- Correlation Analysis of CXCL10, FOS, HOXC13, and WNT4 Gene Polymorphisms with Key Economic Traits—Initial Population Screening for Jiangnan Cashmere Goats
- From bench to babies – drug development for male subfertility
- Molecular Morbidity Score–Can MicroRNAs Assess the Burden of Disease?
- A guide to the use of bioassays in exploration of natural resources
- Transgenic mice display hair loss and regrowth overexpressing mutant <i>Hr</i> gene
- Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family
- Unravelling the molecular basis for symbiotic signal transduction in legumes
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Genetic targeting of lymphatic endothelial cells in mice: current strategies and future perspectives
- Discovery of Four New<em> FGF5</em> Variants Causing Long Hair in the Dog
- A group of type I keratin genes on human chromosome 17: characterization and expression.
- Characterization of a Cluster of Human High/Ultrahigh Sulfur Keratin-associated Protein Genes Embedded in the Type I Keratin Gene Domain on Chromosome 17q12-21
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.
- The Majority of Multipotent Epidermal Stem Cells Do Not Protect Their Genome by Asymmetrical Chromosome Segregation
- Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle