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Research 721–750 of 1000+
- Stem cells and aberrant signaling of molecular systems in skin aging
- The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)
- Genomic and transcriptomic landscape to decipher the genetic basis of hyperpigmentation in Lanping black-boned sheep (Ovis aries)
- Infertility: Evaluation and Initial Management
- Neuroendocrine Controls of Keratin Expression in Human Skin
- Abstracts Pt.30
- Follikelhormone
- Dutasteride Micro-Injections in Androgenetic Alopecia
- Efectos de la disminución de los depósitos tisulares de hierro sobre los factores de riesgo cardiovascular en pacientes con hiperandrogenismo ovárico funcional
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Hair cross-sectioning in uncombable hair syndrome: An easy tool for complex diagnosis
- Establishment of Tsc2-deficient rat embryonic stem cells
- Clinico-epidemiology of Keratosis Pilaris with Histopathologic and Dermoscopic Evaluation – A Cross-sectional Study in a Rural Tertiary Hospital
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Compound glycyrrhizin promotes hair growth in C57BL/6 mice by regulating the Wnt/β-catenin pathway
- Diagnosis and management of vascular Ehlers-Danlos syndrome: Experience of the UK national diagnostic service, Sheffield
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation
- A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders
- 50832 Confetti variant of Alopecia Areata: A Single Center Retrospective Study to Describe a Novel Entity
- Editorial: Mechanisms and novel treatments of pigmentary disorders and skin regeneration
- FLCN, a novel autophagy component, interacts with GABARAP and is regulated by ULK1 phosphorylation
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- Global hotspots and trends in Acanthosis nigricans research: A bibliometric and visualized analysis
- Fibrodysplasia Ossificans Progressiva (FOP): A Segmental Progeroid Syndrome
- Inherited ichthyoses/generalized Mendelian disorders of cornification