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Research 271–300 of 1000+
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Translational perspectives in HTRA1-associated disorders: biomarkers, gene therapy, and future directions
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- Combined drug triads for synergic neuroprotection in retinal degeneration
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
- A Case Report and a Review of TRAPPC4‐Related TRAPPopathy
- N‑K GM SERIES: THE COMPLETE GEOMETRIC MEDICINE LIBRARY — From Discovery to Deployment: SELECTIVE‑ANTI‑BACTERIAL‑GM2, SELECTIVE‑ANTI‑PATHOGENIC‑FUNGI‑GM2, and the CMC Pocket Delivery System A Comprehensive Framework for Precision Antimicrobials — 1,000,000,000:1 Selectivity, Zero Ecological Harm, Free for Humanity
- Profibrotic Molecules Are Reduced in CRISPR-Edited Emery–Dreifuss Muscular Dystrophy Fibroblasts
- Short-term Efficacy of Tofacitinib, a JAK Inhibitor, in IFIH1-related Aicardi-Goutières Syndrome
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Alopecia areata in a patient with WNT10A heterozygous ectodermal dysplasia
- Therapeutics for COVID-19 and post COVID-19 complications: An update
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Deciphering the microbiology of hidradenitis suppurativa: a step forward towards understanding an enigmatic inflammatory skin disease
- A young male with kidney damage from genetic mitochondrial disease: case report and literature review
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings
- The Advances of Broad-Spectrum and Hot Anti-Coronavirus Drugs
- Forme létale de syndrome de Netherton au sein d’une famille multiplex consanguine
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Structural perspectives on the androgen receptor, the elusive shape-shifter
- Netherton Syndrome in a 9-Month-Old Child: Unraveling a Complex Dermatologic Disorder
- Ultraviolet Radiation in Wound Care: Sterilization and Stimulation
- Hidradenitis Suppurativa and Comorbid Disorder Biomarkers, Druggable Genes, New Drugs and Drug Repurposing—A Molecular Meta-Analysis
- CtBP1 Overexpression in Keratinocytes Perturbs Skin Homeostasis