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Research 61–90 of 130
- Alopecia Areata: A Review of the Role of Oxidative Stress, Possible Biomarkers, and Potential Novel Therapeutic Approaches
- Episodic Bilateral Corneal Edema Caused by Hair Groom Gel
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Systemic Lupus Erythematosus
- Long-Term Intravital Imaging of the Cornea, Skin, and Hair Follicle by Multiphoton Microscope
- Saponins of Korean Red Ginseng May Protect Human Skin from Adipokine-Associated Inflammation and Pigmentation Resulting from Particulate Matter Exposure
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Uveodermatological syndrome associated with alopecia areata in a one‐year‐old female spayed Cavalier King Charles Spaniel dog
- Surgical Correction of cicatricial Entropion in cattle: Two cases
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- Ischemic Vaso-occlusive Retinopathy as Initial Presentation in Pediatric Systemic Lupus Erythematosus: A Case Report
- Biological Function of Long Non-coding RNA (LncRNA) Xist
- Targeting integrin pathways: mechanisms and advances in therapy
- Basement Membrane Zone Remodeling During Appendageal Development in Human Fetal Skin. The Absence of Type VII Collagen is Associated with Gelatinase-A (MMP2) Activity
- Madarosis: A marker of many Maladies
- Endocrine disorders in Woodhouse-Sakati syndrome: a systematic review of the literature
- Immediate Effect in the Retina and Choroid after 650 nm Low-Level Red Light Therapy in Children
- Co-factors of LIM domains (Clims/Ldb/Nli) regulate corneal homeostasis and maintenance of hair follicle stem cells
- S100A6 Protein—Expression and Function in Norm and Pathology
- Transcriptional profiling of putative human epithelial stem cells
- 3D printing sequentially strengthening high-strength natural polymer hydrogel bilayer scaffold for cornea regeneration
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Immunological and Histological Studies of Different Concentrations of Rosmarinus officinalis and Thymus vulgaris Extracts on Thymus Gland of Chick Embryos
- Mining and analysis of adverse event signals of isotretinoin based on the real-world data of FAERS database
- Transforming By-Products into Functional Resources: The Potential of Cucurbitaceae Family Seeds in Cosmetics
- Ocular comorbidities and its relation to clinical and dermoscopic features in patients with alopecia areata: a case-control study
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Diagnosis and management of vascular Ehlers-Danlos syndrome: Experience of the UK national diagnostic service, Sheffield