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Research 691–720 of 1000+
- Engineering Cell Surfaces with Polyelectrolyte Materials for Translational Applications
- Reduced plakoglobin increases the risk of sodium current defects and atrial conduction abnormalities in response to androgenic anabolic steroid abuse
- Genome-wide p63-Target Gene Analyses Reveal TAp63/NRF2-Dependent Oxidative Stress Responses
- Current Protocols: Alopecia Areata Mouse Models for Drug Efficacy and Mechanism Studies
- Proceedings of the Inaugural Pediatric Dermatology Research Alliance (PeDRA) Conference
- Volatile organic compounds: A proinflammatory activator in autoimmune diseases
- Identification of Genes Related to Hair Follicle Cycle Development in Inner Mongolia Cashmere Goat by WGCNA
- Hair loss in women
- Acne-Associated Syndromes
- Application of multi-omics techniques to androgenetic alopecia: Current status and perspectives
- Gene Expression During Drosophila Wing Morphogenesis and Differentiation
- Association Between Human Hair Loss and the Expression Levels of Nucleolin, Nucleophosmin, and<i>UBTF</i>Genes
- Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Systematic Analysis of Non-coding RNAs Involved in the Angora Rabbit (Oryctolagus cuniculus) Hair Follicle Cycle by RNA Sequencing
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- The probable destructive mechanisms behind COVID-19 on male reproduction system and fertility
- Safety and efficacy of advanced and targeted acid α-glucosidase (AT-GAA) (ATB200/AT2221) in ERT-switch nonambulatory patients with Pompe disease: preliminary results from the ATB200-02 trial
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix
- The molecular basis of human keratin disorders
- Post-transcriptional Regulation of Keratinocyte Progenitor Cell Expansion, Differentiation and Hair Follicle Regression by miR-22
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Transcriptome Sequencing and Mass Spectrometry Reveal Genes Involved in the Non-mendelian Inheritance-Mediated Feather Growth Rate in Chicken
- CD34 defines melanocyte stem cell subpopulations with distinct regenerative properties
- GRHL3 binding and enhancers rearrange as epidermal keratinocytes transition between functional states
- Novel anti-Mullerian hormone receptor 2 binding peptide prevents chemotherapy-related ovarian follicle loss in a mouse model
- Recent advances in Forensic DNA Phenotyping of appearance, ancestry and age