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Research 421–450 of 1000+
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Cutaneous manifestations of systemic infection in children
- Delayed Diagnosis of Ectopic Thyroid Due to Ignored Borderline Result of Newborn Screening for Congenital Hypothyroidism
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Genetics of Inherited Ichthyoses and Related Diseases
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- New developments in the molecular treatment of ichthyosis: review of the literature
- Efficacy of 0.1% adapalene in a non-inflammatory Kyoto Rhino Rat acne model
- Positive Impact of Fish Oil on Diabetic and Hypercholestrolemic Skin Disorders
- Potential of the Nano-Encapsulation of Antioxidant Molecules in Wound Healing Applications: An Innovative Strategy to Enhance the Bio-Profile
- Role of Stearoyl-CoA Desaturase-1 in Skin Integrity and Whole Body Energy Balance
- Transport of Biotin in Human Keratinocytes
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Phospholipase A2 in skin biology: new insights from gene-manipulated mice and lipidomics
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Murine Epidermal Ceramide Synthase 4 Is a Key Regulator of Skin Barrier Homeostasis
- Retinol dehydrogenase 12 (RDH12): Role in vision, retinal disease and future perspectives
- Ichthyosis with confetti: a rare diagnosis and treatment plan
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Ichthyosis follicularis alopecia and photophobia syndrome:Transient improvement with oral isotretinoin
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Current Genetics in Hair Diseases
- Pathophysiology of Androgenetic Alopecia and Implications for Treatment: An Overview of Current Literature
- Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1‐deficient Jack Russell Terriers and response to topical ceramide
- The expanding significance of keratin intermediate filaments in normal and diseased epithelia
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Health Risks Associated with Long-Term Finasteride and Dutasteride Use: It’s Time to Sound the Alarm
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review