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PMID:23889750
| Citation |
Kim, J, Stirling, KJ, Cooper, ME, Ascoli, M, Momany, AM, McDonald, EL, Ryckman, KK, Rhea, L, Schaa, KL, Cosentino, V, Gadow, E, Saleme, C, Shi, M, Hallman, M, Plunkett, J, Teramo, KA, Muglia, LJ, Feenstra, B, Geller, F, Boyd, HA, Melbye, M, Marazita, ML, Dagle, JM and Murray, JC (2013) Sequence variants in oxytocin pathway genes and preterm birth: a candidate gene association study. BMC Med. Genet. 14:77 |
|---|---|
| Abstract |
Preterm birth (PTB) is a complex disorder associated with significant neonatal mortality and morbidity and long-term adverse health consequences. Multiple lines of evidence suggest that genetic factors play an important role in its etiology. This study was designed to identify genetic variation associated with PTB in oxytocin pathway genes whose role in parturition is well known. |
| Links |
PubMed PMC3737028 Online version:10.1186/1471-2350-14-77 |
| Keywords |
Alleles; Animals; Argentina; COS Cells; Case-Control Studies; Cercopithecus aethiops; Cystinyl Aminopeptidase/genetics; Cystinyl Aminopeptidase/metabolism; Denmark; Female; Finland; Genetic Association Studies; Genetic Predisposition to Disease; Genomic Structural Variation; Gestational Age; Haplotypes; Humans; Inheritance Patterns; Inositol Phosphates/metabolism; Mutation, Missense; Oxytocin/genetics; Oxytocin/metabolism; Polymorphism, Single Nucleotide; Pregnancy; Premature Birth/genetics; Protein Binding; Receptors, Oxytocin/genetics; Receptors, Oxytocin/metabolism; Risk Factors |
| edit table |
Significance
Annotations
| Gene product | Qualifier | GO Term | Evidence Code | with/from | Aspect | Extension | Notes | Status |
|---|---|---|---|---|---|---|---|---|
| GO:0065009: regulation of molecular function |
ECO:0000315: |
P |
Figure 5 |
complete | ||||
See also
References
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