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- Filaggrin mutations as an archetype for understanding the pathophysiology of atopic dermatitis
- Skin diseases associated with atopic dermatitis
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Overlapping features of atopic dermatitis and alopecia areata: from pathogenesis to treatment
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- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Cutaneous gain-of-function mutation of LRIG3 leads to alopecia by upregulation of ERBB, PI3K/AKT, NOTCH1 signaling pathways
- Potential genetic associations of acne scar phenotypes: IL1A in fibrotic scarring and CYB5R1 in atrophic scarring
- 9. Immunology and Genetics
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- Careless talk costs lives: fibroblast growth factor receptor signalling and the consequences of pathway malfunction
- The Genetics of Human Skin Disease
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Transcriptomics analysis reveals molecular alterations underpinning spaceflight dermatology
- The genetic basis of dermatophytosis skin infection susceptibility
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Genomic and phenotypic characterization of Investigator Global Assessment (IGA) scale-based endotypes in atopic dermatitis
- Support for dermatological research in Sub‐Saharan Africa: insights from African hair and skin research programs
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Severe Hypernatremia as Presentation of Netherton Syndrome
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- LEKTI: Netherton Syndrome and Atopic Dermatitis
- Pleiotropic Role of Notch Signaling in Human Skin Diseases
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Frontal fibrosing alopecia