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Research 571–600 of 1000+
- Unraveling Evolutionary Insights into AVT Peptide Conservation and Antimicrobial Motif Prediction Across Taxa
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Structural Stability of Wild Type and Mutated α-Keratin Fragments: Molecular Dynamics and Free Energy Calculations
- Role of Csdc2 in Regulating Secondary Hair Follicle Growth in Cashmere Goats
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- The function of TRPS1 in the development and differentiation of bone, kidney, and hair follicles.
- Quantification of the Vitamin D Receptor−Coregulator Interaction
- Sexually dimorphic sail feathers in the Mandarin duck as a model for lifelong developmental modulation
- Prostaglandin D2-Mediated DP2 and AKT Signal Regulate the Activation of Androgen Receptors in Human Dermal Papilla Cells
- Human hair keratin-associated proteins: Sequence regularities and structural implications
- HOXC13 Is Involved in the Regulation of Human Hair Keratin Gene Expression
- Release systems based on self-assembling RADA16-I hydrogels with a signal sequence which improves wound healing processes
- 3a-Phenylhexahydropentalene-1,6-dione
- Pmg-1 and Pmg-2 constitute a novel family of KAP genes differentially expressed during skin and mammary gland development
- Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix
- <i>De novo</i> mutations in monilethrix
- Arabidopsis ZINC FINGER PROTEIN1 Acts Downstream of GL2 to Repress Root Hair Initiation and Elongation by Directly Suppressing bHLH Genes
- Identification of differentially expressed genes affecting hair and cashmere growth in the Laiwu black goat by microarray
- Infrared and Raman Diagnostic Modeling of Phosphate Adsorption on Ceria Nanoparticles
- 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
- Hairless is a nuclear receptor corepressor essential for skin function
- Updates in the understanding and treatments of skin & hair disorders in women of color
- Expression of an Olfactomedin-Related Gene in Rat Hair Follicular Papilla Cells
- Primary Generalized Glucocorticoid Resistance or Chrousos Syndrome: Allostasis Through a Mutated Glucocorticoid Receptor
- 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
- Defining the identity of mouse embryonic dermal fibroblasts
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Probing the Effects of Stress Mediators on the Human Hair Follicle