ArticleThe Journal of investigative dermatology2004
A recurrent intragenic deletion mutation in DSG4 gene in three Pakistani families with autosomal recessive hypotrichosis.
Article in The Journal of investigative dermatology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
What it found
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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
12 citing papers in PubMed, 45 citations in OpenAlex.
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia.Archives of dermatological research · 2024Article
- Autosomal recessive monilethrix: Novel variants of the DSG4 gene in three Chinese families.Molecular genetics & genomic medicine · 2022Article
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy.Molecular genetics and genomics : MGG · 2022Article
- An autosomal recessive mutation of DSG4 causes monilethrix through the ER stress response.The Journal of investigative dermatology · 2015Article
- Genetic mapping of a novel hypotrichosis locus to chromosome 7p21.3-p22.3 in a Pakistani family and screening of the candidate genes.Human genetics · 2010Article
- Mapping of a novel autosomal recessive hypotrichosis locus on chromosome 10q11.23–22.3.Human genetics · 2010Article
- A homozygous nonsense mutation in the human desmocollin-3 (DSC3) gene underlies hereditary hypotrichosis and recurrent skin vesicles.American journal of human genetics · 2009Article
- Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3).Human genetics · 2008Article
- Mapping of a gene for alopecia with mental retardation syndrome (APMR3) on chromosome 18q11.2-q12.2.Annals of human genetics · 2007Article
- A mutation in the lipase H (LIPH) gene underlie autosomal recessive hypotrichosis.Human genetics · 2007Article
- Defining the pathogenic involvement of desmoglein 4 in pemphigus and staphylococcal scalded skin syndrome.The Journal of clinical investigation · 2004Article
- Desmosomes: just cell adhesion or is there more?Cell adhesion & migrationReview
Corrections and comments
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Authors and funding
7 authors at 3 institutions in 3 countries.
Funding
Abstract
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Identifiers
What 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.