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Research 301–330 of 1000+
- Pili Annulati
- Monilethrix in three generations
- DNA dioxygenases Tet2/3 regulate gene promoter accessibility and chromatin topology in lineage-specific loci to control epithelial differentiation
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- 574 A deep learning classifier for the analysis of tiger tail banding in trichothiodystrophy
- Trichoscopy in alopecias: Diagnosis simplified
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- The nude gene and the skin
- Revisiting the role of melatonin in human melanocyte physiology: A skin context perspective
- Marine Health-Promoting Compounds: Recent Trends for Their Characterization and Human Applications
- Dermatological problems of the puberty
- Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant
- Alopecia Areata: Updates from the Mouse Perspective
- Trichoscopic Findings in Androgenetic Alopecia
- Correlation of trichoscopic findings with clinico-epidemiological factors in male pattern&nbsp;<span style="font-size: 1rem;">hairloss: A cross-sectional study from a tertiary care center in Chengalpattu</span>
- Optimizing Scalp Cooling: (Ultra)Structural Follicular Characteristic and Restorative Advances
- Umbilical Cord Mesenchymal Stem Cell–Derived Exosomes Preserve Melanocyte Stem Cell Integrity Under Acute Neurogenic Oxidative Stress via Activation of the Nrf2– ARE Pathway in C57BL / 6J Mice
- Plica polonica: Trichoscopic findings with a brief literature review
- Congenital atrichia associated with nevus flammeus: A rare association
- SkIndia Quiz 24: Itchy papules over face
- Dermatologic Effects of Selumetinib in Pediatric Patients with Neurofibromatosis Type 1: Clinical Challenges and Therapeutic Management
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Alopecia in Epidermolysis Bullosa
- Zinc-responsive Acral Hyperkeratosis as a Sequele of Acrodermatitis Enteropathica
- Hair Bundle Defects and Loss of Function in the Vestibular End Organs of Mice Lacking the Receptor-Like Inositol Lipid Phosphatase PTPRQ
- Keep quiet—how stress regulates hair follicle stem cells
- Hair fragility (trichorrhexis nodosa) in alopecic Pomeranian dogs