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Research 331–360 of 1000+
- 924 Efficient genome editing using CRISPR/Cas9 ribonucleoprotein approach in iPS cells for recessive dystrophic epidermolysis bullosa
- Recent advances in the molecular mechanisms causing primary generalized glucocorticoid resistance
- Severe Acute Respiratory Syndrome (SARS)
- In vivo function of VDR in gene expression-VDR knock-out mice
- Long-COVID Clinical Features and Risk Factors: A Retrospective Analysis of Patients from the STOP-COVID Registry of the PoLoCOV Study
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- The Advances of Broad-Spectrum and Hot Anti-Coronavirus Drugs
- Antiandrogens as Therapies for COVID-19: A Systematic Review
- Interleukin gene polymorphisms and alopecia areata: A systematic review and meta-analysis
- Symptomatology of Long COVID Associated with Inherited and Acquired Thrombophilic Conditions: A Systematic Review
- Painful thickened skin on the soles of the feet
- Author response: Interplay of opposing fate choices stalls oncogenic growth in murine skin epithelium
- A Neonate with Blisters
- Subject Index
- Large Screening Identifies ACE2 Positively Correlates With NF-κB Signaling Activity and Targeting NF-κB Signaling Drugs Suppress ACE2 Levels
- A newborn presenting with congenital blistering
- Associations between clinical data, vaccination status, antibody responses, and post-COVID-19 symptoms in Thais infected with SARS-CoV-2 Delta and Omicron variants: a 1-year follow-up study
- Epstein-Barr virus associated with high-grade B-cell lymphoma in nude severe combined immunodeficiency
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
- Hidradenitis Suppurativa/Acne Inversa/Dissecting Terminal Hair Folliculitis
- Dermatologic Changes in Experimental Model of Long COVID
- A young male with kidney damage from genetic mitochondrial disease: case report and literature review
- Short-term Efficacy of Tofacitinib, a JAK Inhibitor, in IFIH1-related Aicardi-Goutières Syndrome
- Clinical analysis of 78 patients with non-classical 21-hydroxylase deficiency
- 269 Down-regulatory role of cholecystokinin on psoriatic epidermal inflammation
- 267 Deep phenotyping of patients with xeroderma pigmentosum and trichothiodystrophy
- Targeting of Skin Antigen-Presenting Cells
- Keratin disorders: from gene to therapy
- Learning from nudity: lessons from the nude phenotype
- Two Hydroxyproline Galactosyltransferases, GALT5 and GALT2, Function in Arabinogalactan-Protein Glycosylation, Growth and Development in Arabidopsis