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Research 721–750 of 1000+
- Evolution, classification, structure, and functional diversification of steroid 5α-reductase family in eukaryotes
- Depletion of <i>Gsdma1/2/3</i> alleviates PMA-induced epidermal hyperplasia by inhibiting the EGFR–Stat3/Akt pathway
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Dermal lymphatic dilation in a mouse model of alopecia areata
- Impact of Combined Baricitinib and FTI Treatment on Adipogenesis in Hutchinson–Gilford Progeria Syndrome and Other Lipodystrophic Laminopathies
- Zinc and Zinc Transporters in Dermatology
- Advancing Regenerative Cellular Therapies in Non-Scarring Alopecia
- Cellular Senescence and Aging in Myotonic Dystrophy
- Prostaglandins: Key players in immunomodulation of the nervous system
- Skin regional specification and higher-order <i>HoxC</i> regulation
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Functional and long-lived melanocytes from human pluripotent stem cells with transient ectopic expression of JMJD3
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- PNKP is required for maintaining the integrity of progenitor cell populations in adult mice
- Tissue Regeneration, Stem Cells, and Wound Healing
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- Transcriptome analysis reveals the genetic basis underlying the development of skin appendages and immunity in hedgehog (Atelerix albiventris)
- Cyclin D3 deficiency inhibits skin tumor development, but does not affect normal keratinocyte proliferation
- Minoxidil restores thymic growth in 22q11.2 deletion syndrome by limiting Sox9+ chondrocyte expansion
- An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review
- The Multiple Consequences of Obesity
- Acne Syndromes and Mosaicism
- FLCN regulates transferrin receptor 1 transport and iron homeostasis
- Acne-Associated Syndromes
- Current Genetics in Hair Diseases
- H3K9me3 controls epidermis morphogenesis by regulating RNA Pol II dynamics at developmental promoters and enhancers
- The Genus Astragalus Species as an Emerging Source of Bioactive Phytochemicals: A Review of Dermatological and Cosmetic Applications
- Differential Expression of MITF, WNT3A, SLC7A11, and EDN3 in the Shoulder ‘Bider Marking’ of Dun Mongolian Horses
- Enhancing Cancer Therapy with Hyperthermia: Synergistic Effects with Natural Compounds and Conventional Treatments