# Skin and Cellular Biology Research **Type:** Topics **Canonical URL:** https://scholariq.org/topics/skin-and-cellular-biology-research/ ## Facts | Field | Value | | --- | --- | | Description | This cluster of papers explores the biology, pathology, and molecular mechanisms related to keratins, intermediate filaments, and associated disorders such as epidermolysis bullosa, Netherton syndrome, and ichthyoses. It covers topics including keratin expression in human tissues, mutations in genes encoding serine protease inhibitors, the role of vimentin in cell adhesion and migration, and the structure and functions of keratin proteins in various epithelia. | | Domain | Life Sciences | | Field | Biochemistry, Genetics and Molecular Biology | | OpenAlex ID | t11650 | | Works | 85 | ## Topic papers all Showing 15 of 85. - [Patisiran, an RNAi Therapeutic, for Hereditary Transthyretin Amyloidosis](https://scholariq.org/papers/patisiran-an-rnai-therapeutic-for-hereditary-transthyretin-amyloidosis/) - [Transglutaminases: crosslinking enzymes with pleiotropic functions](https://scholariq.org/papers/transglutaminases-crosslinking-enzymes-with-pleiotropic-functions/) - [Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris](https://scholariq.org/papers/loss-of-function-mutations-in-the-gene-encoding-filaggrin-cause-ichthyosis/) - [Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome](https://scholariq.org/papers/mutations-in-spink5-encoding-a-serine-protease-inhibitor-cause-netherton/) - [Revised nomenclature and classification of inherited ichthyoses: Results of the First Ichthyosis Consensus Conference in Sorèze 2009](https://scholariq.org/papers/revised-nomenclature-and-classification-of-inherited-ichthyoses-results-of-the/) - [Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility](https://scholariq.org/papers/consensus-reclassification-of-inherited-epidermolysis-bullosa-and-other/) - [Diagnostic Value of Cerebrospinal Fluid Neurofilament Light Protein in Neurology](https://scholariq.org/papers/diagnostic-value-of-cerebrospinal-fluid-neurofilament-light-protein-in-neurology/) - [Loss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizations](https://scholariq.org/papers/loss-of-function-variations-within-the-filaggrin-gene-predispose-for-atopic/) - [Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis](https://scholariq.org/papers/deletion-of-the-late-cornified-envelope-lce3b-and-lce3c-genes-as-a/) - [Gene therapy by skeletal muscle expression of decorin prevents fibrotic disease in rat kidney](https://scholariq.org/papers/gene-therapy-by-skeletal-muscle-expression-of-decorin-prevents-fibrotic-disease/) - [The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy](https://scholariq.org/papers/the-gene-encoding-gigaxonin-a-new-member-of-the-cytoskeletal-btb-kelch-repeat/) - [Plectin deficiency results in muscular dystrophy with epidermolysis bullosa](https://scholariq.org/papers/plectin-deficiency-results-in-muscular-dystrophy-with-epidermolysis-bullosa/) - [Mutations in ABCA12 Underlie the Severe Congenital Skin Disease Harlequin Ichthyosis](https://scholariq.org/papers/mutations-in-abca12-underlie-the-severe-congenital-skin-disease-harlequin/) - [Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wasting](https://scholariq.org/papers/desmoglein-1-deficiency-results-in-severe-dermatitis-multiple-allergies-and/) - [Mitochondrial Reactive Oxygen Species Promote Epidermal Differentiation and Hair Follicle Development](https://scholariq.org/papers/mitochondrial-reactive-oxygen-species-promote-epidermal-differentiation-and-hair/) ## Topic primary papers Showing 15 of 27. - [Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris](https://scholariq.org/papers/loss-of-function-mutations-in-the-gene-encoding-filaggrin-cause-ichthyosis/) - [Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome](https://scholariq.org/papers/mutations-in-spink5-encoding-a-serine-protease-inhibitor-cause-netherton/) - [Revised nomenclature and classification of inherited ichthyoses: Results of the First Ichthyosis Consensus Conference in Sorèze 2009](https://scholariq.org/papers/revised-nomenclature-and-classification-of-inherited-ichthyoses-results-of-the/) - [Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility](https://scholariq.org/papers/consensus-reclassification-of-inherited-epidermolysis-bullosa-and-other/) - [Gene therapy by skeletal muscle expression of decorin prevents fibrotic disease in rat kidney](https://scholariq.org/papers/gene-therapy-by-skeletal-muscle-expression-of-decorin-prevents-fibrotic-disease/) - [The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy](https://scholariq.org/papers/the-gene-encoding-gigaxonin-a-new-member-of-the-cytoskeletal-btb-kelch-repeat/) - [Plectin deficiency results in muscular dystrophy with epidermolysis bullosa](https://scholariq.org/papers/plectin-deficiency-results-in-muscular-dystrophy-with-epidermolysis-bullosa/) - [Mutations in ABCA12 Underlie the Severe Congenital Skin Disease Harlequin Ichthyosis](https://scholariq.org/papers/mutations-in-abca12-underlie-the-severe-congenital-skin-disease-harlequin/) - [Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organization.](https://scholariq.org/papers/loss-of-plectin-causes-epidermolysis-bullosa-with-muscular-dystrophy-cdna/) - [A synonymous SNP of the corneodesmosin gene leads to increased mRNA stability and demonstrates association with psoriasis across diverse ethnic groups](https://scholariq.org/papers/a-synonymous-snp-of-the-corneodesmosin-gene-leads-to-increased-mrna-stability/) - [Monoclonal cytokeratin antibodies that distinguish simple from stratified squamous epithelia: characterization on human tissues.](https://scholariq.org/papers/monoclonal-cytokeratin-antibodies-that-distinguish-simple-from-stratified/) - [A dermal HOX transcriptional program regulates site-specific epidermal fate](https://scholariq.org/papers/a-dermal-i-hox-i-transcriptional-program-regulates-site-specific-epidermal-fate/) - [Full-length cytokeratin-19 is released by human tumor cells: a potential role in metastatic progression of breast cancer](https://scholariq.org/papers/full-length-cytokeratin-19-is-released-by-human-tumor-cells-a-potential-role-in/) - [Dynamic JUNQ inclusion bodies are asymmetrically inherited in mammalian cell lines through the asymmetric partitioning of vimentin](https://scholariq.org/papers/dynamic-junq-inclusion-bodies-are-asymmetrically-inherited-in-mammalian-cell/) - [Social/economic costs and health-related quality of life in patients with epidermolysis bullosa in Europe](https://scholariq.org/papers/social-economic-costs-and-health-related-quality-of-life-in-patients-with/) --- Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.