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Results: 1 to 20 of 105

Similar articles for PubMed (Select 23582962)

1.

Progress in understanding the genetics of bronchopulmonary dysplasia.

Shaw GM, O'Brodovich HM.

Semin Perinatol. 2013 Apr;37(2):85-93. doi: 10.1053/j.semperi.2013.01.004. Review.

2.

A genome-wide association study (GWAS) for bronchopulmonary dysplasia.

Wang H, St Julien KR, Stevenson DK, Hoffmann TJ, Witte JS, Lazzeroni LC, Krasnow MA, Quaintance CC, Oehlert JW, Jelliffe-Pawlowski LL, Gould JB, Shaw GM, O'Brodovich HM.

Pediatrics. 2013 Aug;132(2):290-7. doi: 10.1542/peds.2013-0533. Epub 2013 Jul 29.

3.

Integrated genomic analyses in bronchopulmonary dysplasia.

Ambalavanan N, Cotten CM, Page GP, Carlo WA, Murray JC, Bhattacharya S, Mariani TJ, Cuna AC, Faye-Petersen OM, Kelly D, Higgins RD; Genomics and Cytokine Subcommittees of the Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network.

J Pediatr. 2015 Mar;166(3):531-7.e13. doi: 10.1016/j.jpeds.2014.09.052. Epub 2014 Nov 6.

PMID:
25449221
4.

Identification of SPOCK2 as a susceptibility gene for bronchopulmonary dysplasia.

Hadchouel A, Durrmeyer X, Bouzigon E, Incitti R, Huusko J, Jarreau PH, Lenclen R, Demenais F, Franco-Montoya ML, Layouni I, Patkai J, Bourbon J, Hallman M, Danan C, Delacourt C.

Am J Respir Crit Care Med. 2011 Nov 15;184(10):1164-70. doi: 10.1164/rccm.201103-0548OC. Epub 2011 Aug 11.

PMID:
21836138
5.

The genetics of bronchopulmonary dysplasia.

Bhandari V, Gruen JR.

Semin Perinatol. 2006 Aug;30(4):185-91. Review.

PMID:
16860158
6.

Association of a FGFR-4 gene polymorphism with bronchopulmonary dysplasia and neonatal respiratory distress.

Rezvani M, Wilde J, Vitt P, Mailaparambil B, Grychtol R, Krueger M, Heinzmann A.

Dis Markers. 2013;35(6):633-40. doi: 10.1155/2013/932356. Epub 2013 Oct 31.

7.

A TLR5 (g.1174C > T) variant that encodes a stop codon (R392X) is associated with bronchopulmonary dysplasia.

Sampath V, Garland JS, Le M, Patel AL, Konduri GG, Cohen JD, Simpson PM, Hines RN.

Pediatr Pulmonol. 2012 May;47(5):460-8. doi: 10.1002/ppul.21568. Epub 2011 Nov 4.

PMID:
22058078
8.

TNF-238 polymorphism may predict bronchopulmonary dysplasia among preterm infants in the Egyptian population.

Elhawary NA, Tayeb MT, Abdel-Ghafar S, Rashad M, Alkhotani AA.

Pediatr Pulmonol. 2013 Jul;48(7):699-706. doi: 10.1002/ppul.22748. Epub 2013 Jan 28.

PMID:
23359489
9.
10.

Single nucleotide polymorphisms of tumor necrosis factor-alpha and the susceptibility to bronchopulmonary dysplasia.

Strassberg SS, Cristea IA, Qian D, Parton LA.

Pediatr Pulmonol. 2007 Jan;42(1):29-36.

PMID:
17123322
11.

Influence of common non-synonymous Toll-like receptor 4 polymorphisms on bronchopulmonary dysplasia and prematurity in human infants.

Lavoie PM, Ladd M, Hirschfeld AF, Huusko J, Mahlman M, Speert DP, Hallman M, Lacaze-Masmonteil T, Turvey SE.

PLoS One. 2012;7(2):e31351. doi: 10.1371/journal.pone.0031351. Epub 2012 Feb 14.

12.

No association of urokinase gene 3'-UTR polymorphism with bronchopulmonary dysplasia for ventilated preterm infants.

Lin HC, Su BH, Lin TW, Hsu CM, Wan L, Tsai CH, Tsai FJ.

Acta Paediatr Taiwan. 2004 Nov-Dec;45(6):315-9.

PMID:
15868845
13.

Interleukin-10 -1082 G/A polymorphism and risk of death or bronchopulmonary dysplasia in ventilated very low birth weight infants.

Yanamandra K, Boggs P, Loggins J, Baier RJ.

Pediatr Pulmonol. 2005 May;39(5):426-32.

PMID:
15678510
14.

Genetic predisposing factors to bronchopulmonary dysplasia: preliminary data from a multicentre study.

Somaschini M, Castiglioni E, Volonteri C, Cursi M, Ferrari M, Carrera P.

J Matern Fetal Neonatal Med. 2012 Oct;25 Suppl 4:127-30. doi: 10.3109/14767058.2012.714995.

PMID:
22958043
15.

Tumour necrosis factor (--308A) polymorphism in very preterm infants with bronchopulmonary dysplasia: a meta-analysis.

Chauhan M, Bombell S, McGuire W.

Arch Dis Child Fetal Neonatal Ed. 2009 Jul;94(4):F257-9. doi: 10.1136/adc.2008.153122. Epub 2008 Dec 9. Review.

PMID:
19066187
16.

Dysplasia: a review.

Bokodi G, Treszl A, Kovács L, Tulassay T, Vásárhelyi B.

Pediatr Pulmonol. 2007 Oct;42(10):952-61. Review.

PMID:
17726703
17.

The genetic basis for bronchopulmonary dysplasia.

Parton LA, Strassberg SS, Qian D, Galvin-Parton PA, Cristea IA.

Front Biosci. 2006 May 1;11:1854-60.

PMID:
16368561
18.

Polymorphisms of interleukin 18 in the genetics of preterm birth and bronchopulmonary dysplasia.

Krueger M, Heinzmann A, Mailaparambil B, Härtel C, Göpel W.

Arch Dis Child Fetal Neonatal Ed. 2011 Jul;96(4):F299-300. doi: 10.1136/adc.2009.174862. Epub 2010 Oct 21.

PMID:
20971720
19.

Polymorphisms of surfactant protein A genes and the risk of bronchopulmonary dysplasia in preterm infants.

Weber B, Borkhardt A, Stoll-Becker S, Reiss I, Gortner L.

Turk J Pediatr. 2000 Jul-Sep;42(3):181-5.

PMID:
11105614
20.

IL-18R1 and IL-18RAP SNPs may be associated with bronchopulmonary dysplasia in African-American infants.

Floros J, Londono D, Gordon D, Silveyra P, Diangelo SL, Viscardi RM, Worthen GS, Shenberger J, Wang G, Lin Z, Thomas NJ.

Pediatr Res. 2012 Jan;71(1):107-14. doi: 10.1038/pr.2011.14.

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