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Research 211–240 of 1000+
- Enhancing Quercetin Bioavailability Attenuates Aging Phenotypes via the Gut Microbiota–Intestinal Barrier Axis in Aged Mice
- Normal Fur Development and Sebum Production Depends on Fatty Acid 2-Hydroxylase Expression in Sebaceous Glands
- Advanced glycation end-products inhibit mesenchymal-epidermal interaction by up-regulating proinflammatory cytokines in hair follicles
- Oral Centella asiatica Extract Attenuates UVB-Induced Skin Photoaging via Antioxidant, Anti-Inflammatory, and Extracellular Matrix-Preserving Effects in Hairless Mice
- Cutaneous disorders related to obesity
- Hair organ regeneration via the bioengineered hair follicular unit transplantation
- Deciphering the Complex Immunopathogenesis of Alopecia Areata
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- IL-15 in alopecia areata: the immune tolerance mechanistic insights and translational perspectives
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- S124 Variants of myxoid cysts: Diagnosis and treatment
- The function of TRPS1 in the development and differentiation of bone, kidney, and hair follicles.
- Combined effect of high-dose vitamin A, vitamin E supplementation, and zinc on adult patients with diabetes: A randomized trial
- Effect of a transcriptional inactive or absent vitamin D receptor on beta-cell function and glucose homeostasis in mice
- Lactate in skin homeostasis: metabolism, skin barrier, and immunomodulation
- Exome analysis for Cronkhite-Canada syndrome: A case report
- Quality of Life in Slovak Breast Cancer Survivors: A Cross-Sectional Study Using EORTC QLQ-C30 and BR23
- Loss of ERBB2 and ERBB3 Receptors Impacts Epidermal Differentiation in Mice
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Zinc transporter ZIP13 G289R variant from Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS) is associated with abnormal hair quality
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Prolactin and the Skin: A Dermatological Perspective on an Ancient Pleiotropic Peptide Hormone
- Skin ageing
- The Paradox of p53: What, How, and Why?
- What does acne genetics teach us about disease pathogenesis?
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Growth Hormone and the Human Hair Follicle
- Thyroxin Levels and Haematological changes in Dogs with Sarcoptic Mange
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Australasian Society for Dermatology Research Meeting, May 2006