ArticleAmerican journal of human genetics1997
Hemizygous deletion of the syntaxin 1A gene in individuals with Williams syndrome.
Article in American journal of human genetics, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.
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
13 citing papers in PubMed, 1 synthesis or guideline pooled it, 84 citations in OpenAlex.
- Oxytocin and Oxytocin Receptor Gene Regulation in Williams Syndrome: A Systematic Review.The Yale journal of biology and medicine · 2021Pooled it
- Functional regulation of syntaxin-1: An underlying mechanism mediating exocytosis in neuroendocrine cells.Frontiers in endocrinology · 2023Review
- Atypical deletion of Williams-Beuren syndrome reveals the mechanism of neurodevelopmental disorders.BMC medical genomics · 2022Article
- Impaired glucose metabolism in subjects with the Williams-Beuren syndrome: A five-year follow-up cohort study.PloS one · 2017Observational
- High prevalence of diabetes and pre-diabetes in adults with Williams syndrome.American journal of medical genetics. Part C, Seminars in medical genetics · 2010Article
- Imaging analysis reveals mechanistic differences between first- and second-phase insulin exocytosis.The Journal of cell biology · 2007Article
- Refinement of the genomic structure of STX1A and mutation analysis in nondeletion Williams syndrome patients.American journal of medical genetics · 2002Article
- Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome.Genome research · 2002Article
- Characterization and gene structure of a novel retinoblastoma-protein-associated protein similar to the transcription regulator TFII-I.The Biochemical journal · 2000Article
- A physical map, including a BAC/PAC clone contig, of the Williams-Beuren syndrome--deletion region at 7q11.23.American journal of human genetics · 2000Article
- Comparative mapping of the region of human chromosome 7 deleted in williams syndrome.Genome research · 1999Article
- Williams syndrome: use of chromosomal microdeletions as a tool to dissect cognitive and physical phenotypes.American journal of human genetics · 1999Article
- The Caenorhabditis elegans unc-64 locus encodes a syntaxin that interacts genetically with synaptobrevin.Molecular biology of the cell · 1998Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors at 2 institutions in 2 countries.
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.