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Research 331–360 of 1000+
- Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis
- Promotion of homology-directed DNA repair by polyamines
- CRISPR/Cas9‐mediated loss of FGF5 function increases wool staple length in sheep
- The Type I Keratin 19 Possesses Distinct and Context-dependent Assembly Properties
- Cell surface receptor kinase FERONIA linked to nutrient sensor TORC signaling controls root hair growth at low temperature linked to low nitrate in <i>Arabidopsis thaliana</i>
- Progress in studies of epidermal stem cells and their application in skin tissue engineering
- Down-regulation of Melanocortin Receptor Signaling Mediated by the Amino Terminus of Agouti Protein in XenopusMelanophores
- Genetic Basis of Alopecia Areata
- Distinct Phenotypic and Genomic Signatures Underlie Contrasting Pathogenic Potential of Staphylococcus epidermidis Clonal Lineages
- The human gut chemical landscape predicts microbe-mediated biotransformation of foods and drugs
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- S100A4/Nonmuscle Myosin IIA/p53 Axis Contributes to Aggressive Features in Ovarian High-Grade Serous Carcinoma
- Tyrosinase Depletion Prevents the Maturation of Melanosomes in the Mouse Hair Follicle
- Strategies for High-Efficiency Mutation Using the CRISPR/Cas System
- Combinatorial Biosynthesis of Sulfated Benzenediol Lactones with a Phenolic Sulfotransferase from Fusarium graminearum PH-1
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Infrared and Raman Diagnostic Modeling of Phosphate Adsorption on Ceria Nanoparticles
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Skin Development and Disease: A Molecular Perspective
- Epigallocatechin-3 Gallate Inhibits STAT-1/JAK2/IRF-1/HLA-DR/HLA-B and Reduces CD8 MKG2D Lymphocytes of Alopecia Areata Patients
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Identification of a Cyclosporine-Specific P450 Hydroxylase Gene through Targeted Cytochrome P450 Complement (CYPome) Disruption in Sebekia benihana
- Exact, time-independent estimation of clone size distributions in normal and mutated cells
- Transcriptome sequencing and identification of cytochrome P450 monooxygenases involved in the biosynthesis of maslinic acid and corosolic acid in <i>Avicennia marina</i>
- Dermo-Cosmetic Benefits of Marine Macroalgae-Derived Phenolic Compounds
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza