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Research 571–600 of 1000+
- Single-Cell RNA Profiling of Human Skin Reveals Age-Related Loss of Dermal Sheath Cells and Their Contribution to a Juvenile Phenotype
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans
- Hair shaft structures in EDAR induced ectodermal dysplasia
- LncRNA H19 Overexpression Activates Wnt Signaling to Maintain the Hair Follicle Regeneration Potential of Dermal Papilla Cells
- The probable destructive mechanisms behind COVID-19 on male reproduction system and fertility
- CD34 defines melanocyte stem cell subpopulations with distinct regenerative properties
- Heterozygous <i>COL5A1</i> deletion in a cat with classical Ehlers–Danlos syndrome
- Use of pegvaliase in the management of phenylketonuria: Case series of early experience in US clinics
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Transcriptome Sequencing and Mass Spectrometry Reveal Genes Involved in the Non-mendelian Inheritance-Mediated Feather Growth Rate in Chicken
- Stretching the limits: from homeostasis to stem cell plasticity in wound healing and cancer
- Age-Related Changes in Hair Shaft Protein Profiling and Genetically Variant Peptides
- Assessing protein sequencing in human single hair shafts of decreasing lengths
- m6A Methylation Analysis of Differentially Expressed Genes in Skin Tissues of Coarse and Fine Type Liaoning Cashmere Goats
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Genome Report: chromosome-scale genome assembly of the African spiny mouse (<i>Acomys cahirinus</i>)
- Comprehensive Analysis of LncRNA AC010789.1 Delays Androgenic Alopecia Progression by Targeting MicroRNA-21 and the Wnt/β-Catenin Signaling Pathway in Hair Follicle Stem Cells
- Severe impact of late diagnosis of congenital adrenal hyperplasia on gender identity, sexual orientation and function: case report and review of the literature
- Repurposing With Purpose: Treatment of Bachmann–Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies
- Short-term Efficacy of Tofacitinib, a JAK Inhibitor, in IFIH1-related Aicardi-Goutières Syndrome
- Research on Mental Stress Recognition of Depressive Disorders in Patients With Androgenic Alopecia Based on Machine Learning and Fuzzy K-Means Clustering
- Effect of Sun exposure-induced ferroptosis mechanisms on pathology and potential biological processes of primary melanoma by microarray data analysis
- Melatonin Regulates the Periodic Growth of Cashmere by Upregulating the Expression of Wnt10b and β-catenin in Inner Mongolia Cashmere Goats
- STAT3 Partly Inhibits Cell Proliferation via Direct Negative Regulation of FST Gene Expression
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- An integrative analysis of the lncRNA-miRNA-mRNA competitive endogenous RNA network reveals potential mechanisms in the murine hair follicle cycle
- Editorial: Machine Learning Techniques on Gene Function Prediction Volume II