|
rs1042689672
|
|
|
0.030 |
GeneticVariation |
BEFREE |
The main SP-A haplotype, interactively with SP-B Ile131Thr polymorphism and with constitutional and environmental factors, influences the risk of RDS.
|
17142161 |
2006 |
|
rs1130866
|
|
|
0.030 |
GeneticVariation |
BEFREE |
The main SP-A haplotype, interactively with SP-B Ile131Thr polymorphism and with constitutional and environmental factors, influences the risk of RDS.
|
17142161 |
2006 |
|
rs1322403577
|
|
|
0.030 |
GeneticVariation |
BEFREE |
The main SP-A haplotype, interactively with SP-B Ile131Thr polymorphism and with constitutional and environmental factors, influences the risk of RDS.
|
17142161 |
2006 |
|
rs1042689672
|
|
|
0.030 |
GeneticVariation |
BEFREE |
An association between the SP-B Ile131Thr polymorphism and RDS was found.
|
12483294 |
2003 |
|
rs1130866
|
|
|
0.030 |
GeneticVariation |
BEFREE |
An association between the SP-B Ile131Thr polymorphism and RDS was found.
|
12483294 |
2003 |
|
rs1322403577
|
|
|
0.030 |
GeneticVariation |
BEFREE |
An association between the SP-B Ile131Thr polymorphism and RDS was found.
|
12483294 |
2003 |
|
rs1042689672
|
|
|
0.030 |
GeneticVariation |
BEFREE |
We propose that the SP-B Ile131Thr polymorphism is a determinant for certain SP-A alleles as factors causing genetic susceptibility to RDS (6A(2), 1A(0)) or protection against it (6A(3), 1A(2)).
|
11063734 |
2000 |
|
rs1130866
|
|
|
0.030 |
GeneticVariation |
BEFREE |
We propose that the SP-B Ile131Thr polymorphism is a determinant for certain SP-A alleles as factors causing genetic susceptibility to RDS (6A(2), 1A(0)) or protection against it (6A(3), 1A(2)).
|
11063734 |
2000 |
|
rs1322403577
|
|
|
0.030 |
GeneticVariation |
BEFREE |
We propose that the SP-B Ile131Thr polymorphism is a determinant for certain SP-A alleles as factors causing genetic susceptibility to RDS (6A(2), 1A(0)) or protection against it (6A(3), 1A(2)).
|
11063734 |
2000 |
|
rs13332514
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Using a tagging SNP (tSNP) strategy and real-time polymerase chain reaction, we genotyped four tSNPs (i.e., rs150929, rs4787273, rs11867129, and rs17135889) and one coding SNP (p.F353F) of the ABCA3 gene in preterm infants with RDS (n = 83) and without RDS (n = 83).We predicted the haplotypes.
|
26522252 |
2016 |
|
rs1799983
|
|
|
0.020 |
GeneticVariation |
BEFREE |
However, when the preterm infants were divided into two and three groups based on gestational age and birth weight, a study of the SNP rs1799983 of the NOS3 gene showed that the GG genotype and G allele frequencies were significantly increased in the RDS groups, the GT genotype and A allele were less frequent among the RDS groups in 26-32.9 weeks of gestational age and in a birth weight subgroup of <1.5 Kg.
|
24602444 |
2014 |
|
rs1799983
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Therefore, RDS seems to develop with alterations in eNOS Glu298Asp genotype frequencies in the Turkish population.
|
23359565 |
2013 |
|
rs149989682
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Term infants carrying the E292V missense mutation of the gene encoding ABCA3 are likely to develop respiratory distress syndrome, and the mutation has also been linked to interstitial lung disease in paediatric patients.
|
22145626 |
2012 |
|
rs1923537
|
|
|
0.020 |
GeneticVariation |
BEFREE |
We replicated a previous finding that rs1923537, a marker downstream of surfactant protein D (SFTPD) is associated with RDS in VPTB infants in that the T allele was overtransmitted from parents to offspring with RDS (P=8.4 × 10(-3)).
|
21960125 |
2012 |
|
rs1923537
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Four validated SNPs were genotyped with sequence-specific probes (TaqMan 7000) in 284 newborn infants below 32 weeks of GA. An association between the SNP rs1923537 and the development of respiratory distress syndrome (RDS) in the study population was found with a lower prevalence of RDS in infants having homozygous a minor allele genotype (odds ratio = 1.733, 95% confidence interval 1.139-2.636, adjusted p = 0.0408).
|
18785967 |
2009 |
|
rs13332514
|
|
|
0.020 |
GeneticVariation |
BEFREE |
The fourth common haplotype was overrepresented in very premature infants with RDS, being accounted for by SNP rs13332514 (F353F), with an increased minor allele frequency in RDS.
|
18246475 |
2008 |
|
rs149989682
|
|
|
0.020 |
GeneticVariation |
BEFREE |
E292V was over-represented in newborns with RD</span>S suggesting that E292V or its unique haplotype impart increased genetic risk for RDS.
|
18317237 |
2008 |
|
rs7316
|
|
|
0.010 |
GeneticVariation |
BEFREE |
This is the first report of association of SFTPB rs7316 polymorphism with RDS development in Iranian newborns.
|
28738720 |
2018 |
|
rs10178332
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We observed that ROCK1 gene rs2271255 (Lys222Glu) and rs35996865 polymorphisms, and ROCK2 gene rs726843, rs2290156, rs10178332, and rs35768389 (Asp601Val) polymorphisms were associated with RDS.
|
27269648 |
2017 |
|
rs1124
|
|
|
0.010 |
GeneticVariation |
BEFREE |
This is the first report of association of SFTPC rs1124 polymorphism with RDS development in Iranian newborns.
|
27884070 |
2017 |
|
rs2271255
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We observed that ROCK1 gene rs2271255 (Lys222Glu) and rs35996865 polymorphisms, and ROCK2 gene rs726843, rs2290156, rs10178332, and rs35768389 (Asp601Val) polymorphisms were associated with RDS.
|
27269648 |
2017 |
|
rs35768389
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We observed that ROCK1 gene rs2271255 (Lys222Glu) and rs35996865 polymorphisms, and ROCK2 gene rs726843, rs2290156, rs10178332, and rs35768389 (Asp601Val) polymorphisms were associated with RDS.
|
27269648 |
2017 |
|
rs35768389
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We observed that ROCK1 gene rs2271255 (Lys222Glu) and rs35996865 polymorphisms, and ROCK2 gene rs726843, rs2290156, rs10178332, and rs35768389 (Asp601Val) polymorphisms were associated with RDS.
|
27269648 |
2017 |
|
rs35996865
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We observed that ROCK1 gene rs2271255 (Lys222Glu) and rs35996865 polymorphisms, and ROCK2 gene rs726843, rs2290156, rs10178332, and rs35768389 (Asp601Val) polymorphisms were associated with RDS.
|
27269648 |
2017 |
|
rs370068089
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We previously identified the c.435G>C variant in the SFTPC gene associated with fatal neonatal respiratory distress syndrome in an infant girl.
|
28295039 |
2017 |