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Research 91–120 of 1000+
- Long-Term Bezafibrate Treatment Improves Skin and Spleen Phenotypes of the mtDNA Mutator Mouse
- CRISPR/Cas9-mediated Disruption of Fibroblast Growth Factor 5 in Rabbits Results in a Systemic Long Hair Phenotype by Prolonging Anagen
- Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Application of big data analytics in minoxidil drug development: a data-driven model for predicting efficacy and side effect risks
- Polycystic ovary syndrome: Criteria, phenotypes, race and ethnicity
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- Adaptive 3D Self‐Assembly of Colorectal Cancer Cells With Unchanged Tumor Phenotype and Drug Sensitivity
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Spatiotemporal regulation of acute wound healing by the NLRP3 inflammasome: dual roles in macrophage-fibroblast chemotaxis and phenotype during wound repair
- Forensic DNA phenotyping: a review on SNP panels, genotyping techniques, and prediction models
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Weakly supervised learning of biomedical information extraction from curated data
- Multi-scale modeling for cell fate specification during regeneration and development
- Phenotypic Characterization of Patients with Polycystic Ovary Syndrome in a Population from the Ecuadorian Andes: A Cross-Sectional Study
- A missense mutation in Lama3 causes androgen alopecia
- Macrophages in Skin Wounds: Functions and Therapeutic Potential
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- SNP variation in male pattern hair loss in Russians with different dihydrotestosterone levels
- Increased rate of hair keratin gene loss in the cetacean lineage
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Inflammatory memory-activated biomimetic nanovesicles regulate neutrophil plasticity and metabolic reprogramming for rapid diabetic wound healing via targeting miR-193a-5p/TLR4/JNK/P38 MAPK pathways
- Aqueous Dispersion of Unmodified Fullerene C60: Stimulation of Hair Growth and Study of a New Molecular Target for Interaction
- Deep Hair Phenomics: Implications in Endocrinology, Development, and Aging
- 26SCS-Loaded SilMA/Col Composite Sponge with Well-Arranged Layers Promotes Angiogenesis-Based Diabetic Wound Repair by Mediating Macrophage Inflammatory Response
- Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep
- Investigating the Relationship Between Androgenetic Alopecia and Hair Shape, Color, and Thickness: A Case‐Control Study
- Senotherapeutic Potential of Araliadiol in Senescent Human Dermal Fibroblasts: An In Vitro Study Using Three Senescence Models