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Research 481–510 of 1000+
- Structure of human type II 5 alpha-reductase gene.
- Differential Auxin-Transporting Activities of PIN-FORMED Proteins in Arabidopsis Root Hair Cells
- Phospholipase A2 Is Required for PIN-FORMED Protein Trafficking to the Plasma Membrane in the<i>Arabidopsis</i>Root
- Fadrozole and finasteride exposures modulate sex steroid- and thyroid hormone-related gene expression in Silurana (Xenopus) tropicalis early larval development
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle
- Isolation and Characterization of a Novel Hair Follicle–Specific Gene, Hacl-1
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- RNA sequence analysis of dermal papilla cells’ regeneration in 3D culture
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Role of hair as Evidence in Investigation: A Forensic Approach
- Use of genetics in the prediction of success in male pattern hair loss therapy and mechanistic studies
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- Oral Presentations
- Developmental Mechanisms Controlling Cell Fate, Evolution of
- Functional identification of the phosphorylation sites of Arabidopsis PIN-FORMED3 for its subcellular localization and biological role
- Dietary glucoraphanin prevents the onset of psychosis in the adult offspring after maternal immune activation
- Functional analysis of the PIP5K1A gene in Liaoning Cashmere goats: an investigation based on bioinformatics, tissue localization, and biological functions
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Tracing the cellular origin of cancer
- Acne, the Skin Microbiome, and Antibiotic Treatment
- Identifying the Target Cells and Mechanisms of Merkel Cell Polyomavirus Infection
- Sex differences in SARS-CoV-2 infection rates and the potential link to prostate cancer
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Dissection of genetic variation and evidence for pleiotropy in male pattern baldness
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen