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Research 361–390 of 1000+
- Human Regulatory T Cells: Understanding the Role of Tregs in Select Autoimmune Skin Diseases and Post-Transplant Nonmelanoma Skin Cancers
- LEKTI: Netherton Syndrome and Atopic Dermatitis
- Clinical Snippets
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- Successful topical minoxidil treatment for hair density and length in trichorhinophalangeal syndrome type 1
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- In This Issue
- Two years of SARS-CoV-2 infection (2019–2021): structural biology, vaccination, and current global situation
- Generalised Glucocorticoid Resistance
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- Ichthyosis with confetti: clinics, molecular genetics and management
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Mechanism of JmjC-containing protein Hairless in the regulation of vitamin D receptor function
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Writer’s Cramp Presentation of Woodhouse–Sakati Syndrome – “Out of the Woods”
- The resistance mechanisms of bacteria against ciprofloxacin and new approaches for enhancing the efficacy of this antibiotic
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Keratin 17 in disease pathogenesis: from cancer to dermatoses
- Pleiotropic Role of Notch Signaling in Human Skin Diseases
- Skin Development and Disease: A Molecular Perspective
- Converging physiological roles of the anthrax toxin receptors
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Exploring the clinical implications of novel SRD5A2 variants in 46,XY disorders of sex development
- Ruxolitinib Rescues Multiorgan Clinical Autoimmunity in Patients with APS-1
- Inflammatory auxo-action in the stem cell division theory of cancer
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- JAK1 gain-of-function variant causes alopecia areata, atopic dermatitis, and autoimmune thyroid disease
- The interplay of oxidative stress and immune dysfunction in Hashimoto’s thyroiditis and polycystic ovary syndrome: a comprehensive review