ArticleMammalian genome : official journal of the International Mammalian Genome Society1995
Haplotype analysis of intra-specific backcross curly-tail mice confirms the localization of ct to chromosome 4.
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 5 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.
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Who cites it
5 citing papers in PubMed, 17 citations in OpenAlex.
- Mapping a chromosomal locus for valproic acid-induced exencephaly in mice.Mammalian genome : official journal of the International Mammalian Genome Society · 2004Article
- Effects of the curly tail genotype on neuroepithelial integrity and cell proliferation during late stages of primary neurulation.Journal of anatomy · 2001Article
- Curly tail: a 50-year history of the mouse spina bifida model.Anatomy and embryology · 2001Review
- The methylenetetrahydrofolate reductase (Mthfr) gene maps to distal mouse chromosome 4.Mammalian genome : official journal of the International Mammalian Genome Society · 1996Article
- Relationship between altered axial curvature and neural tube closure in normal and mutant (curly tail) mouse embryos.Anatomy and embryology · 1996Article
Corrections and comments
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
Abstract
We have determined the order of a number of SSR and SSC polymorphic markers that map to distal mouse Chromosome (Chr) 4 and have used analysis of these markers in backcrosses designed to test the localization of the curly-tail (ct) mutation. We have confirmed that ct maps to this region, close to the locus D4Mit69. Our results also support the hypothesis that ct is a semidominant, rather than a recessive, mutation, since we have identified abnormal-tailed mice that are likely to be heterozygous at the ct locus. Finally, we examined Pax7 as a candidate gene for the ct mutation and found no evidence of protein sequence differences in ct compared with wild-type mice.
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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.