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PTER gene

Known as: PHOSPHOTRIESTERASE-RELATED PROTEIN, PTER, phosphotriesterase related 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Abstract 1605: Pterostilbene, a natural phytoalexin, effectively protects against UVB-induced skin carcinogenesis by increasing antioxidant cellular defenses and preventing mutagenesis
Clinical and laboratory studies have demonstrated that skin exposure to ultraviolet radiation (UV) is the main cause of non… 
2007
2007
Saethre-Chotzen syndrome with severe developmental delay associated with deletion of chromosomic region 7p15 --> pter.
Saethre-Chotzen syndrome represents one of the most common types of craniosynostosis inherited as an autosomal dominant disorder… 
2006
2006
Breakpoint mapping in a case of mosaicism with partial monosomy 9p23 → pter and partial trisomy 1q41 → qter suggests neo‐telomere formation in stabilizing the deleted chromosome
We report on a clinical and molecular cytogenetic study of a patient who presents a complex chromosomal rearrangement with two… 
2006
2006
Vergleichsuntersuchung der spezifischen IgE-Messung (Allergenteststreifen Allergodip Mites and More®) mit dem Hautpricktest und der nasalen Provokation bei Hausstaub- und Vorratsmilbenallergikern
There have only been very limited published data dealing with correlations between skin prick test (SPT), in vitro diagnosis (IVD… 
2005
2005
Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 → pter) and partial monosomy 9p (9p22 → pter)
A 31-year-old, primigravid woman had received obstetric care in a private clinic. The pregnancy was uneventful until 34 weeks… 
2004
2004
Duplication 15q14 → pter: a rare chromosomal abnormality underlying bipolar affective disorder
2000
2000
Mild phenotype in two siblings with distal monosomy 12p13.31→pter
We report two sibs with trisomy for the region 2p25.1→pter and monosomy for the region 12p13.31→pter, due to adjacent‐1… 
1998
1998
Reproducibility of skin prick test results in epidemiologic studies: a comparison of two devices
The reproducibility of skin prick tests under field conditions is essential for comparing prevalences between centers in… 
1997
1997
Familial four breakpoint complex chromosomal rearrangement as a cause of monosomy 9p22-->pter and trisomy 10p11.2-->pter and 11q21 analysed by dual and triple colour FISH.
A familial four breakpoint complex chromosomal rearrangement involving chromosomes 9, 10, and 11 was ascertained through a child… 
1982
1982
Regional mapping of the gene coding for enolase-2 on human chromosome 12.
Enolase-2 (ENO2), previously termed 14-3-2 protein, is an isozyme of enolase that is enriched in neuronal tissue. The gene coding… 
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