ReviewThe Ulster medical journal2007
Disorders of keratinisation: from rare to common genetic diseases of skin and other epithelial tissues.
Review in The Ulster medical journal, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
17 citing papers in PubMed.
- Hair keratin mutations in tooth enamel increase dental decay risk.The Journal of clinical investigation · 2014Trial
- Core Differentially Expressed Genes in Psoriasis Lesions: An Integrated Analysis of Four GEO Datasets.Psoriasis (Auckland, N.Z.) · 2026Article
- Article
- Transgradient Variant of Mal De Meleda Presenting As Palmoplantar Keratoderma: A Case Report.Cureus · 2024Article
- Retinoid-induced skeletal hyperostosis in disorders of keratinization.Clinical and experimental dermatology · 2022Article
- Genetic prescreening of a candidate for laser refractive surgery identifies risk for inadequate tissue response: a case report.Journal of medical case reports · 2022Article
- Dynamic Expression of Transient Receptor Potential Vanilloid-3 and Integrated Signaling with Growth Factor Pathways during Lung Epithelial Wound Repair following Wood Smoke Particle and Other Forms of Lung Cell Injury.Molecular pharmacology · 2021Article
- In vivo histology and p.L132V mutation in KRT12 gene in Japanese patients with Meesmann corneal dystrophy.Japanese journal of ophthalmology · 2019Article
- Article
- Orchestrated control of filaggrin-actin scaffolds underpins cornification.Cell death & disease · 2018Article
- Ichthyosis with confetti: clinics, molecular genetics and management.Orphanet journal of rare diseases · 2015Review
- Keratin 9 is required for the structural integrity and terminal differentiation of the palmoplantar epidermis.The Journal of investigative dermatology · 2014Article
- A mutation in the FAM83G gene in dogs with hereditary footpad hyperkeratosis (HFH).PLoS genetics · 2014Article
- Novel molecular therapies for heritable skin disorders.The Journal of investigative dermatology · 2012Review
- Genetics of Meesmann corneal dystrophy: a novel mutation in the keratin 3 gene in an asymptomatic family suggests genotype-phenotype correlation.Molecular vision · 2008Article
- The human keratins: biology and pathology.Histochemistry and cell biology · 2008Review
- Bioinspired Provisional Matrix Stimulates Regenerative Healing of Diabetic Wounds.Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair SocietyArticle
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
17476820PMC2001132What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.