Search
for
Sort by
Research 901–930 of 1000+
- A global analysis of CNVs in Chinese indigenous fine-wool sheep populations using whole-genome resequencing
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- The impact of a lifestyle promotion program on anthropometric and clinical manifestations in adolescents with polycystic ovarian syndrome: a randomized controlled trial
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- The exposome impact on hair health: etiology, pathogenesis and clinical features ‒ Part I
- Adult female acne: Clinical and therapeutic particularities (Review)
- Identification of Candidate Genes for Min Pig Villi Hair Traits by Genome-Wide Association of Copy Number Variation
- Harnessing Microbiome, Bacterial Extracellular Vesicle, and Artificial Intelligence for Polycystic Ovary Syndrome Diagnosis and Management
- Post-Treatment of Micro-Needling with a Dexpanthenol-Containing Ointment Accelerates Epidermal Wound Healing in Human 3D Skin Models
- Age-associated thin hair displays molecular, structural and mechanical characteristic changes
- Social Perception of Male Faces. Individuals, Clusters, Dimensions
- Mediator 1 ablation induces enamel-to-hair lineage conversion in mice through enhancer dynamics
- 74398 Oral Intake of Colostrum-Derived Bioactives for Hair and Skin: Integrating Mechanistic, Translational, and Clinical Evidence
- Artificial Intelligence in Dermatology: Assessing Predictability in Clinical Diagnosis
- Combination of oral minoxidil and bicalutamide for the treatment of female pattern hair loss in adolescents
- Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma
- Hair Disease Classification Using Convolutional Neural Network (CNN) Algorithm with VGG-16 Architecture
- Compound Heterozygous Mutations in <i>Forkhead Box N1</i> (<i>FOXN1</i>) Lead to a Severe Immunodeficiency but Normal Hair and Nail Development in Patients
- An induced pluripotent stem cell-based approach for hair follicle development and regeneration
- Nanotribological characterization of human hair and skin using atomic force microscopy
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Targeting Wnt/β-catenin signaling and its interplay with TGF-β and Notch signaling pathways for the treatment of chronic wounds
- Proinflammatory cytokines regulate epidermal stem cells in wound epithelialization
- Quantification of the Vitamin D Receptor−Coregulator Interaction
- Inhibition of JAK-STAT Signaling with Baricitinib Reduces Inflammation and Improves Cellular Homeostasis in Progeria Cells
- Current Advanced Therapies Based on Human Mesenchymal Stem Cells for Skin Diseases
- A powerful method for pleiotropic analysis under composite null hypothesis identifies novel shared loci between Type 2 Diabetes and Prostate Cancer
- Evaluating cepharanthine analogues as natural drugs against SARS‐CoV‐2
- Identification of Trichohyalin-Like 1, an S100 Fused-Type Protein Selectively Expressed in Hair Follicles
- Regionalisation of the skin