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Research 751–780 of 1000+
- The Use of Imaging Techniques in the Diagnosis of Dermatoses of the Scalp
- Exploring Hormone Therapy Effects on Reproduction and Health in Transgender Individuals
- Association between DNA Methylation in the Core Promoter Region of the CUT-like Homeobox 1 (CUX1) Gene and Lambskin Pattern in Hu Sheep
- Pharmacological Strategies for Mitigating Cytarabine-Induced Multi-Organ Toxicity: A Scoping Review on Mechanisms, Efficacy and Clinical Implications
- Parry–Romberg Syndrome: Radioclinical Dissociation in a Paucisymptomatic Form and a Proposed Diagnostic Framework
- Unraveling Translational Insights into Systemic Multi-Organ Toxicity of Cytosine Arabinoside (Ara-C): A Systematic Review of Preclinical Animal Evidence
- Ophthalmologic Comorbidities in Alopecia Areata
- Locally Synthetized 17-β-Estradiol Reverses Amyloid-β-42-Induced Hippocampal Long-Term Potentiation Deficits
- Helical twist direction in the macrofibrils of keratin fibres is left handed
- Zfp462 deficiency causes anxiety‐like behaviors with excessive self‐grooming in mice
- Moisture sorption/desorption of protein fibres
- Identification of an Intronic Regulatory Element Necessary for Tissue-Specific Expression of <i>Foxn1</i> in Thymic Epithelial Cells
- Enhanced Sensitivity to Ethanol-Induced Inhibition of LTP in CA1 Pyramidal Neurons of Socially Isolated C57BL/6J Mice: Role of Neurosteroids
- Polycystic Ovary Syndrome in the Context of Pituitary Adenomas: Prevalence, Pathophysiology and Clinical Management
- An N-Ethyl-N-Nitrosourea Induced Corticotropin-Releasing Hormone Promoter Mutation Provides a Mouse Model for Endogenous Glucocorticoid Excess
- Neurosteroids Involved in Regulating Inhibition in the Inferior Colliculus
- Molecular mechanism for transcriptional regulation of the parathyroid hormone gene by Epiprofin
- A small multigene hydroxyproline-O-galactosyltransferase family functions in arabinogalactan-protein glycosylation, growth and development in Arabidopsis
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Impact of Hydroxyapatite on Gelatin/Oxidized Alginate 3D-Printed Cryogel Scaffolds
- Keratins of the Human Hair Follicle
- Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix
- Neurosteroid-sensitive δ-GABA<sub>A</sub>receptors: A role in epileptogenesis?
- Characterization of the mechanical properties of the cortex region of human hair fibers by multiparametric Atomic Force Microscopy mapping
- Enzymatic Crosslinking of Amino Acids Improves the Repair Effect of Keratin on Hair Fibre
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- Regulatory T cells in dominant immunologic tolerance
- Hair shaft disorders in children – An update
- Analysis of Bimatoprost-Induced changes on Rabbits eyelash Follicle: Clinical and Electron microscopic study
- Analysis of Bimatoprost-Induced changes on Rabbits eyelash Follicle: Clinical and Electron microscopic study