ArticleMammalian genome : official journal of the International Mammalian Genome Society1995
Mapping the Bst mutation on mouse chromosome 16: a model for human optic atrophy.
Article in Mammalian genome : official journal of the International Mammalian Genome Society, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 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
9 citing papers in PubMed, 26 citations in OpenAlex.
- Phenotypic and functional characterization of Bst+/- mouse retina.Disease models & mechanisms · 2015Article
- Ribosomal protein L24 defect in belly spot and tail (Bst), a mouse Minute.Development (Cambridge, England) · 2004Article
- Three novel pigmentation mutants generated by genome-wide random ENU mutagenesis in the mouse.Comparative and functional genomics · 2004Article
- Gene structure and chromosomal localization of mouse Opa1 : its exclusion from the Bst locus.BMC genetics · 2003Article
- A review of primary hereditary optic neuropathies.Journal of inherited metabolic disease · 2003Review
- The bst locus on mouse chromosome 16 is associated with age-related subretinal neovascularization.Proceedings of the National Academy of Sciences of the United States of America · 2000Article
- Clinical features, molecular genetics, and pathophysiology of dominant optic atrophy.Journal of medical genetics · 1998Review
- Natural variation in neuron number in mice is linked to a major quantitative trait locus on Chr 11.The Journal of neuroscience : the official journal of the Society for Neuroscience · 1998Article
- Genetic and environmental control of variation in retinal ganglion cell number in mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 1996Article
Corrections and comments
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Authors and funding
7 authors at 2 institutions in 1 country.
Funding
Abstract
PubMed holds no abstract for this paper.
Indexed as
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.