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Research 121–150 of 1000+
- Heterozygous Variants of the SLC39A4 Gene and Possible Increased Risk for Developing Acrodermatitis Enteropathica with Kaposi’s Varicelliform Eruption
- Dermal Blimp1 Acts Downstream of Epidermal TGFβ and Wnt/β-Catenin to Regulate Hair Follicle Formation and Growth
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Outbreak of thallium poisoning among Iraqi patients
- Fetal milieu-simulating hyaluronic acid-dopamine-chondroitin sulfate hydrogel promoting angiogenesis and hair regeneration for wound healing
- Diffuse Alopecia and Thyroid Atrophy in Sheep
- Feeding the skin: The emerging role of nutritional intervention in dermatological disorders
- Elevated serum heat shock protein-70 and interleukin-15: prognostic biomarkers correlating with clinical severity and diagnostic efficacy in active alopecia areata
- Two novel MBTPS2 missense mutations impairing S2P proteolytic activity lead to IFAP syndrome with new phenotypic anomalies
- 448 Physiological function of krox20 (Egr2) in epithelial stem cells
- Overview of popular cosmeceuticals in dermatology
- Nanomaterials-Based Wound Dressing for Advanced Management of Infected Wound
- Electrospun Scaffold of Collagen and Polycaprolactone Containing ZnO Quantum Dots for Skin Wound Regeneration
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Mineral, trace element, and toxic metal concentration in hair from dogs with idiopathic epilepsy compared to healthy controls
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- Diagnosis and treatment of female alopecia: Focusing on the iron deficiency-related alopecia
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation
- Beyond Wavy Hairs
- Mineral Malnutrition Following Bariatric Surgery
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- Nanotechnology Approaches in Chronic Wound Healing
- Phospholipase C 1 is required for skin stem cell lineage commitment
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Role of the vitamin D receptor in hair follicle biology
- Overexpression of spermidine/spermine N1-acetyltransferase under the control of mouse metallothionein I promoter in transgenic mice: evidence for a striking post-transcriptional regulation of transgene expression by a polyamine analogue
- Using the zebrafish lateral line to uncover novel mechanisms of action and prevention in drug-induced hair cell death
- FOXP3 <sup>+</sup> regulatory T cells and age‐related diseases