Catechol-O-methyltransferase (COMT) activity has been reported to be higher in African Americans (AA) than Caucasians (Cau). COMT converts 2- and 4-hydroxy (OH) estrogens to 2- and 4-methoxyestrogens, respectively, and can increase estrogenic milieu locally in tissues. To assess whether the increased incidence of preterm birth (PTB) among AA women is associated with single-nucleotide polymorphism (SNP) in the COMT gene, we examined variations in maternal and fetal COMT genes and their association with pregnancy outcomes (term vs preterm pregnancies) using 4 functional SNPs: rs4633, rs4680, rs4818, and rs6269 in both AA and Cau. We analyzed samples from 267 AA women (191 term and 76 preterm pregnancies) and 339 Cau (194 term and 145 preterm ...
Objective To evaluate the role DNA methylation may play in genes associated with preterm birth for h...
The ratio of the lengths of an individual’s second to fourth digit (2D:4D) is commonly used as a non...
Abstract: This study aimed to evaluate the effects of β2-adrenergic receptor (ADRB2) gene polymorphi...
Catechol-O-methyltransferase (COMT) activity has been reported to be higher in African Americans (AA...
OBJECTIVE: Preterm birth (PTB) is a multifactorial complication in which genetic and environmental f...
Abstract: Variations in genes involved in DNA repair systems have been proposed as risk factors for ...
Vitamin (vit) D deficiency and preterm birth (PTB) are more prevalent among African American (AA) wo...
Objective: Genetic polymorphisms associated with breast cancer risk are likely to differ among ethni...
The functional interaction of progesterone receptor (PR) isoforms PRA and PRB regulates myometrial t...
BACKGROUND : The causes of many cases of preterm birth (PTB) remain enigmatic. Increased understandi...
The primary risk factor for neonatal Group B streptococcus (GBS) infection, which is the leading cau...
An overrepresentation of adverse pregnancy outcomes has been observed in pregnancies associated with...
Contains fulltext : 53015.pdf (publisher's version ) (Closed access)BACKGROUND/AIM...
Background: Preterm delivery is the leading cause of neonatal morbidity and mortality. Two-thirds of...
In this study, we assessed the feasibility of fe-tal RhD genotyping by analysis of cell-free fetal D...
Objective To evaluate the role DNA methylation may play in genes associated with preterm birth for h...
The ratio of the lengths of an individual’s second to fourth digit (2D:4D) is commonly used as a non...
Abstract: This study aimed to evaluate the effects of β2-adrenergic receptor (ADRB2) gene polymorphi...
Catechol-O-methyltransferase (COMT) activity has been reported to be higher in African Americans (AA...
OBJECTIVE: Preterm birth (PTB) is a multifactorial complication in which genetic and environmental f...
Abstract: Variations in genes involved in DNA repair systems have been proposed as risk factors for ...
Vitamin (vit) D deficiency and preterm birth (PTB) are more prevalent among African American (AA) wo...
Objective: Genetic polymorphisms associated with breast cancer risk are likely to differ among ethni...
The functional interaction of progesterone receptor (PR) isoforms PRA and PRB regulates myometrial t...
BACKGROUND : The causes of many cases of preterm birth (PTB) remain enigmatic. Increased understandi...
The primary risk factor for neonatal Group B streptococcus (GBS) infection, which is the leading cau...
An overrepresentation of adverse pregnancy outcomes has been observed in pregnancies associated with...
Contains fulltext : 53015.pdf (publisher's version ) (Closed access)BACKGROUND/AIM...
Background: Preterm delivery is the leading cause of neonatal morbidity and mortality. Two-thirds of...
In this study, we assessed the feasibility of fe-tal RhD genotyping by analysis of cell-free fetal D...
Objective To evaluate the role DNA methylation may play in genes associated with preterm birth for h...
The ratio of the lengths of an individual’s second to fourth digit (2D:4D) is commonly used as a non...
Abstract: This study aimed to evaluate the effects of β2-adrenergic receptor (ADRB2) gene polymorphi...