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Research 361–390 of 680
- <i>WNT10A</i> , dermatology and dentistry
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- What does acne genetics teach us about disease pathogenesis?
- Diagnostic approach to low‐renin hypertension
- Suppression of Wnt/β-catenin signaling by EGF receptor is required for hair follicle development
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
- Pathological findings in a case of stiff person syndrome with anti‐GAD antibodies
- Candidate SNP markers of reproductive potential are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters
- Androgenic Alopecia Is Associated with Less Dietary Soy, Higher Blood Vanadium and rs1160312 1 Polymorphism in Taiwanese Communities
- Clinical relevance of hair microscopy in alopecia
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Androgenetic Alopecia
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Concomitant presentation of alopecia areata in siblings: A rare occurrence
- Diseases of Periocular Hair
- Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice
- MOF-mediated histone H4 Lysine 16 acetylation governs mitochondrial and ciliary functions by controlling gene promoters
- A Brief Review on Acne Vulgaris: Chronic Inflammatory Disease
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Hepatitis C‐related mixed type vitiligo in a patient with Ivemark syndrome
- Cutaneous gain-of-function mutation of LRIG3 leads to alopecia by upregulation of ERBB, PI3K/AKT, NOTCH1 signaling pathways
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Sesamin alleviates androgenetic alopecia by targeting the AR MAPK Wnt axis
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures