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Research 391–420 of 1000+
- Ichthyosis with confetti: clinics, molecular genetics and management
- 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
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- 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
- Large-Scale, Multicenter, Prospective Registry Study of Ripretinib in Advanced GIST: A Real-World Study from China
- Writer’s Cramp Presentation of Woodhouse–Sakati Syndrome – “Out of the Woods”
- Zebrafish Model of Hereditary Pigmentary Disorders
- Correlation Analysis of BLTP1 (KIAA1109) and KIF27 Gene Polymorphisms with Wool Traits in Subo Merino Sheep
- Efficacy and safety of the Exfoliate-Dissolve-Repair skin care approach in the treatment of keratosis pilaris: a randomized controlled clinical trial study protocol
- Beyond Coincidence in Neurofibromatosis Type 1: Becker Nevus Adjacent to Plexiform Neurofibroma with Brachial Plexus Involvement and Integrated Mechanistic Illustration
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- COVID-19: How Effective Are the Repurposed Drugs and Novel Agents in Treating the Infection?
- Congenital Adrenal Hyperplasia
- Genetics of Alopecia
- Le mélanome malin bilatéral de l'uvée
- The L412F variant of Toll-like receptor 3 (TLR3) is associated with cutaneous candidiasis, increased susceptibility to cytomegalovirus, and autoimmunity
- A temperature-sensitive <i>FERONIA</i> mutant allele that alters root hair growth
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Vitamina D y la piel. Una revisión para dermatólogos
- The Roles of Keratinocytes in the Initiation, Progression and Maintenance of Hidradenitis Suppurativa
- Carcinogenesis of the Human Scalp. An Immunometabolic Centered View