ReviewJournal of medical genetics1992
Splotch locus mouse mutants: models for neural tube defects and Waardenburg syndrome type I in humans.
Review in Journal of medical genetics, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 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
13 citing papers in PubMed, 70 citations in OpenAlex.
- Stem Cell-Derived Models of Neural Crest Are Essential to Understand Melanoma Progression and Therapy Resistance.Frontiers in molecular neuroscience · 2019Review
- Review
- Stat3-targeted therapies overcome the acquired resistance to vemurafenib in melanomas.The Journal of investigative dermatology · 2013Article
- TBX2 expression is regulated by PAX3 in the melanocyte lineage.Pigment cell & melanoma research · 2013Article
- The negative influence of high-glucose ambience on neurogenesis in developing quail embryos.PloS one · 2013Article
- PAX genes and human neural tube defects: an amino acid substitution in PAX1 in a patient with spina bifida.Journal of medical genetics · 1996Article
- Analysis of the mouse Splotch-delayed mutation indicates that the Pax-3 paired domain can influence homeodomain DNA-binding activity.Proceedings of the National Academy of Sciences of the United States of America · 1995Article
- Absence of linkage between familial neural tube defects and PAX3 gene.Journal of medical genetics · 1995Article
- A frameshift mutation in the gene for PAX3 in a girl with spina bifida and mild signs of Waardenburg syndrome.Journal of medical genetics · 1995Article
- Isolation of two isoforms of the PAX3 gene transcripts and their tissue-specific alternative expression in human adult tissues.Human genetics · 1994Article
- A mutation within intron 3 of the Pax-3 gene produces aberrantly spliced mRNA transcripts in the splotch (Sp) mouse mutant.Proceedings of the National Academy of Sciences of the United States of America · 1993Article
- Waardenburg syndrome and myelomeningocele in a family.Journal of medical genetics · 1993Article
- Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2.Nature genetics · 1993Article
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 at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
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.