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Research 571–600 of 1000+
- p75 Neurotrophin Receptor Antagonist Retards Apoptosis-driven Hair Follicle Involution (Catagen)
- A systematic simulation-based meta-analytical framework for prediction of physiological biomarkers in alopecia
- The nude gene and the skin
- Identification of a preferred substrate peptide for transglutaminase 3 and detection of <i>in situ</i> activity in skin and hair follicles
- The pioneer factor SOX9 competes for epigenetic factors to switch stem cell fates
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Recent advances in the molecular mechanisms determining tissue sensitivity to glucocorticoids: novel mutations, circadian rhythm and ligand-induced repression of the human glucocorticoid receptor
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- Hairless is a nuclear receptor corepressor essential for skin function
- Defining the identity of mouse embryonic dermal fibroblasts
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Updates in the understanding and treatments of skin & hair disorders in women of color
- Probing the Effects of Stress Mediators on the Human Hair Follicle
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Infrared and Raman Diagnostic Modeling of Phosphate Adsorption on Ceria Nanoparticles
- Smad4-dependent desmoglein-4 expression contributes to hair follicle integrity
- ER-located Ca2+ ATPase ACA2 regulates Ca2+ cytoplasmic pool linked to root hair growth in Arabidopsis thaliana
- MIM and Cortactin Antagonism Regulates Ciliogenesis and Hedgehog Signaling
- Physical and Functional Interaction between the Vitamin D Receptor and Hairless Corepressor, Two Proteins Required for Hair Cycling
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Mettl3-catalyzed m <sup>6</sup> A regulates histone modifier and modification expression in self-renewing somatic tissue
- Protein degradation: expanding the toolbox to restrain cancer drug resistance
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- PIEZO1-mediated calcium signaling reinforces mechanical properties of hair follicle stem cells to promote quiescence
- Male pattern hair loss: Can developmental origins explain the pattern?
- Genetic association of wool quality characteristics in United States Rambouillet sheep
- The atypical ‘hippocampal’ glutamate receptor coupled to phospholipase D that controls stretch‐sensitivity in primary mechanosensory nerve endings is homomeric purely metabotropic GluK2
- Temporal Layering of Signaling Effectors Drives Chromatin Remodeling during Hair Follicle Stem Cell Lineage Progression
- Amino acid–derived defense metabolites from plants: A potential source to facilitate novel antimicrobial development