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Research 691–720 of 1000+
- Organoids and organ chips in ophthalmology
- Finasteride is effective for the treatment of central serous chorioretinopathy
- Microscopic polyangiitis secondary to Mycobacterium abscessus in a patient with bronchiectasis: a case report
- Clinical Case Notes. Optical coherence tomography of adult-onset foveomacular vitelliform dystrophy
- Organ Regeneration
- LHX2: a transcription factor in development, homeostasis, repair, and disease
- The Double-Edged Sword of Vitamin A: Function and Toxicity
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Is Hair Transplantation Indicated in Frontal Fibrosing Alopecia? The Results of Test Grafting in Three Patients
- Clinical Case Notes. Tamoxifen optic neuropathy
- Clinical Case Notes. Intraorbital ophthalmic artery aneurysms
- Clinical Case Notes. Lipoid proteinosis: a rare disorder with pathognomonic lid lesions
- CUTANEOUS T-CELL LYMPHOMA
- Clinical Case Notes. Castleman's disease of the lacrimal gland
- Clinical Case Notes. Malignant melanoma in eviscerated eyeball
- Hair removal by lasers and intense pulsed light sources
- TGF-β Family Signaling in Epithelial Differentiation and Epithelial–Mesenchymal Transition
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Sjogren-Larsson syndrome
- SOX9 in organogenesis: shared and unique transcriptional functions
- Vogt-Koyanagi-Harada Disease: A Narrative Review
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Identification of functional circRNAs regulating ovarian follicle development in goats
- Role of EZH2 in Uterine Gland Development
- An Australian family with macular dystrophy linked to autosomal recessive alopecia universalis
- Stem cells, organoids and their applications for human diseases: Special issue of BMB Reports in 2023
- Optical Coherence Tomography Angiography Findings in Polycystic Ovary Syndrome
- Abstracts
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy