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Research 361–390 of 1000+
- Андрогенетическая алопеция: патогенетические механизмы и подходы к лечению
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- Bachmann–Bupp syndrome and treatment
- Identification and characterization of genes for skin and hair disorders
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- Pvalb8, a Type of Oncomodulin, Regulates Neuromast Development and Auditory Function in Zebrafish
- FOXN1 deficient nude severe combined immunodeficiency
- Fibrodysplasia Ossificans Progressiva (FOP): A Segmental Progeroid Syndrome
- Establishment of Tsc2-deficient rat embryonic stem cells
- Keratins and disease at a glance
- Acne-Associated Syndromes
- Role of FGFR2-signaling in the pathogenesis of acne
- When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- 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
- 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
- Clinical Snippets
- 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
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Mechanism of JmjC-containing protein Hairless in the regulation of vitamin D receptor function
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- 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