Evaluation of fetal and maternal genetic variation in the progesterone receptor gene for contributions to preterm birth.
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Determination of genetic predisposition to patent ductus arteriosus in preterm infantsPrevention of preterm delivery with 17-hydroxyprogesterone caproate: pharmacologic considerationsSpontaneous preterm birth and single nucleotide gene polymorphisms: a recent updateThe genetics of preterm birth: using what we know to design better association studiesDevelopmental origins of health and disease: environmental exposures.MI-GWAS: a SAS platform for the analysis of inherited and maternal genetic effects in genome-wide association studies using log-linear models.An evolutionary genomic approach to identify genes involved in human birth timingIdentification of fetal and maternal single nucleotide polymorphisms in candidate genes that predispose to spontaneous preterm labor with intact membranes.Patterns of gene expression in the ductus arteriosus are related to environmental and genetic risk factors for persistent ductus patency.Variations in CRHR1 are associated with persistent pulmonary hypertension of the newborn.Maternal factors and complications of preterm birth associated with neonatal thyroid stimulating hormonePharmacogenomics of 17-alpha hydroxyprogesterone caproate for recurrent preterm birth prevention.Sequence variants in oxytocin pathway genes and preterm birth: a candidate gene association studyAssociation between male infertility and either the +331G/A or the progins polymorphism of the progesterone receptor gene in a Chinese population.Genomics of preterm birth.Cytochrome P450 (CYP2D6) genotype is associated with elevated systolic blood pressure in preterm infants after discharge from the neonatal intensive care unit.Replication of genetic associations in the inflammation, complement, and coagulation pathways with intraventricular hemorrhage in LBW preterm neonates.MTHFR (C677T) polymorphism and PR (PROGINS) mutation as genetic factors for preterm delivery, fetal death and low birth weight: A Northeast Indian population based studyProgesterone receptor polymorphisms and clinical response to 17-alpha-hydroxyprogesterone caproateReplication of a genome-wide association study of birth weight in preterm neonatesProgesterone Receptor (PGR) gene polymorphism is associated with susceptibility to preterm birth.Genetic variation in CYB5R3 is associated with methemoglobin levels in preterm infants receiving nitric oxide therapy.Genetic associations of surfactant protein D and angiotensin-converting enzyme with lung disease in preterm neonates.DNA methylation provides insight into intergenerational risk for preterm birth in African Americans.Effects of Advancing Gestation and Non-Caucasian Race on Ductus Arteriosus Gene Expression.Replication of clinical associations with 17-hydroxyprogesterone in preterm newborns.Association of amino acids with common complications of prematurity.The role of glucocorticoids and progestins in inflammatory, autoimmune, and infectious disease.Polymorphisms in the fetal progesterone receptor and a calcium-activated potassium channel isoform are associated with preterm birth in an Argentinian population.Candidate gene linkage approach to identify DNA variants that predispose to preterm birth.The influence of maternal disease on metabolites measured as part of newborn screening.Genetic contributions to the development of retinopathy of prematurityPGRMC1 and PGRMC2 in uterine physiology and diseaseLocalization of a major susceptibility locus influencing preterm birthInvestigation of genetic risk factors for chronic adult diseases for association with preterm birth.Environmental risk factors and perinatal outcomes in preterm newborns, according to family recurrence of prematurity.Conditional Ablation of Progesterone Receptor Membrane Component 1 Results in Subfertility in the Female and Development of Endometrial Cysts.Bitter taste receptors as targets for tocolytics in preterm labor therapy.The association among cytochrome P450 3A, progesterone receptor polymorphisms, plasma 17-alpha hydroxyprogesterone caproate concentrations, and spontaneous preterm birth.Progesterone receptor gene polymorphisms are not associated with preterm birth in a Hispanic population.
P2860
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P2860
Evaluation of fetal and maternal genetic variation in the progesterone receptor gene for contributions to preterm birth.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年学术文章
@wuu
2007年学术文章
@zh-cn
2007年学术文章
@zh-hans
2007年学术文章
@zh-my
2007年学术文章
@zh-sg
2007年學術文章
@yue
2007年學術文章
@zh
2007年學術文章
@zh-hant
name
Evaluation of fetal and matern ...... ontributions to preterm birth.
@en
Evaluation of fetal and matern ...... ontributions to preterm birth.
@nl
type
label
Evaluation of fetal and matern ...... ontributions to preterm birth.
@en
Evaluation of fetal and matern ...... ontributions to preterm birth.
@nl
prefLabel
Evaluation of fetal and matern ...... ontributions to preterm birth.
@en
Evaluation of fetal and matern ...... ontributions to preterm birth.
@nl
P2093
P2860
P1433
P1476
Evaluation of fetal and matern ...... ontributions to preterm birth.
@en
P2093
David Merrill
Diana Caprau
Jeffrey C Murray
John Dagle
Karen Johnson
Katherine Steffen
Kristin Orr
Margaret E Cooper
Marla K Johnson
Mary L Marazita
P2860
P2888
P304
P356
10.1203/PDR.0B013E3181567BFC
P407
P577
2007-11-01T00:00:00Z
P5875
P6179
1010523385