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Research 901–930 of 1000+
- Oral Presentations
- A review on computer‐aided chemogenomics and drug repositioning for rationalCOVID‐19 drug discovery
- Scientific opinion on the tolerable upper intake level for selenium
- Laser-Assisted Drug Delivery: A Systematic Review of Safety and Adverse Events
- Polymorphism of CAG and GGN repeats of androgen receptor gene in women with polycystic ovary syndrome
- A Clinical Review of Trichorrhexis Nodosa
- Hypotrichosis in a child with olmsted syndrome
- Analysis of histology and long noncoding RNAs involved in the rabbit hair follicle density using RNA sequencing
- Mesenchymal Stem Cell-Derived Extracellular Vesicles for Therapeutic Use and in Bioengineering Applications
- Volatile organic compounds: A proinflammatory activator in autoimmune diseases
- Comprehensive analysis of the expression profiles of mRNA, lncRNA, circRNA, and miRNA in primary hair follicles of coarse sheep fetal skin
- Identification of Genes Related to Hair Follicle Cycle Development in Inner Mongolia Cashmere Goat by WGCNA
- Stem Cell Use to Treat Dermatological Disorders
- Eclipta prostrata (L.) L. (Asteraceae): Ethnomedicinal Uses, Chemical Constituents, and Biological Activities
- Gene Expression During Drosophila Wing Morphogenesis and Differentiation
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- Single-Cell RNA Profiling of Human Skin Reveals Age-Related Loss of Dermal Sheath Cells and Their Contribution to a Juvenile Phenotype
- A partially automated method for DNA extraction from marmoset hair follicles to avoid blood chimerism
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- Growth and viability of Liaoning Cashmere goat hair follicles during the annual hair follicle cycle
- Proteomic analysis identifies differentially expressed proteins participating in forming Type III brush hair in Yangtze River Delta white goat
- Protein and amino acid composition of hair from mice carrying the naked (<i>N</i>) gene
- BMP-FGF Signaling Axis Mediates Wnt-Induced Epidermal Stratification in Developing Mammalian Skin
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Skin and hair: models for exploring organ regeneration
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Hair shaft structures in EDAR induced ectodermal dysplasia