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Items: 1 to 20 of 143

1.

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.

2.

Genetic predisposition to bronchopulmonary dysplasia.

Lal CV, Ambalavanan N.

Semin Perinatol. 2015 Dec;39(8):584-91. doi: 10.1053/j.semperi.2015.09.004. Epub 2015 Oct 23. Review.

3.

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.

4.

Ancestry and genetic associations with bronchopulmonary dysplasia in preterm infants.

Torgerson DG, Ballard PL, Keller RL, Oh SS, Huntsman S, Hu D, Eng C, Burchard EG, Ballard RA; TOLSURF Study Group.

Am J Physiol Lung Cell Mol Physiol. 2018 Nov 1;315(5):L858-L869. doi: 10.1152/ajplung.00073.2018. Epub 2018 Aug 16.

PMID:
30113228
5.

Genome-Wide Analysis of DNA Methylation in Hyperoxia-Exposed Newborn Rat Lung.

Chen CM, Liu YC, Chen YJ, Chou HC.

Lung. 2017 Oct;195(5):661-669. doi: 10.1007/s00408-017-0036-z. Epub 2017 Jul 8.

PMID:
28689251
6.

Surfactant protein B gene polymorphisms is associated with risk of bronchopulmonary dysplasia in Chinese Han population.

Zhang S, Zhang X, Li Q, Kong X, Zhang Y, Wei X, Song J, Feng Z.

Int J Clin Exp Pathol. 2015 Mar 1;8(3):2971-8. eCollection 2015.

7.

Exome Sequencing of Neonatal Blood Spots and the Identification of Genes Implicated in Bronchopulmonary Dysplasia.

Li J, Yu KH, Oehlert J, Jeliffe-Pawlowski LL, Gould JB, Stevenson DK, Snyder M, Shaw GM, O'Brodovich HM.

Am J Respir Crit Care Med. 2015 Sep 1;192(5):589-96. doi: 10.1164/rccm.201501-0168OC.

8.

Matrix metalloproteinase gene polymorphisms and bronchopulmonary dysplasia: identification of MMP16 as a new player in lung development.

Hadchouel A, Decobert F, Franco-Montoya ML, Halphen I, Jarreau PH, Boucherat O, Martin E, Benachi A, Amselem S, Bourbon J, Danan C, Delacourt C.

PLoS One. 2008 Sep 11;3(9):e3188. doi: 10.1371/journal.pone.0003188.

9.

Reduced platelet-derived growth factor receptor expression is a primary feature of human bronchopulmonary dysplasia.

Popova AP, Bentley JK, Cui TX, Richardson MN, Linn MJ, Lei J, Chen Q, Goldsmith AM, Pryhuber GS, Hershenson MB.

Am J Physiol Lung Cell Mol Physiol. 2014 Aug 1;307(3):L231-9. doi: 10.1152/ajplung.00342.2013. Epub 2014 Jun 6.

10.

A study of genes encoding cytokines (IL6, IL10, TNF), cytokine receptors (IL6R, IL6ST), and glucocorticoid receptor (NR3C1) and susceptibility to bronchopulmonary dysplasia.

Huusko JM, Karjalainen MK, Mahlman M, Haataja R, Kari MA, Andersson S, Toldi G, Tammela O, Rämet M, Lavoie PM, Hallman M; Gen-BPD Study Group.

BMC Med Genet. 2014 Nov 1;15:120. doi: 10.1186/s12881-014-0120-7.

11.

The genetic predisposition to bronchopulmonary dysplasia.

Yu KH, Li J, Snyder M, Shaw GM, O'Brodovich HM.

Curr Opin Pediatr. 2016 Jun;28(3):318-23. doi: 10.1097/MOP.0000000000000344. Review.

12.

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.

13.

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.

14.

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.

15.

Association of vitamin D binding protein polymorphisms with bronchopulmonary dysplasia: a case-control study of gc globulin and bronchopulmonary dysplasia.

Serce Pehlevan O, Karatekin G, Koksal V, Benzer D, Gursoy T, Yavuz T, Ovali F.

J Perinatol. 2015 Sep;35(9):763-7. doi: 10.1038/jp.2015.58. Epub 2015 Jun 11.

PMID:
26067474
16.

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.

17.

Heritability of bronchopulmonary dysplasia, defined according to the consensus statement of the national institutes of health.

Lavoie PM, Pham C, Jang KL.

Pediatrics. 2008 Sep;122(3):479-85. doi: 10.1542/peds.2007-2313.

18.

Replication of lung cancer susceptibility loci at chromosomes 15q25, 5p15, and 6p21: a pooled analysis from the International Lung Cancer Consortium.

Truong T, Hung RJ, Amos CI, Wu X, Bickeböller H, Rosenberger A, Sauter W, Illig T, Wichmann HE, Risch A, Dienemann H, Kaaks R, Yang P, Jiang R, Wiencke JK, Wrensch M, Hansen H, Kelsey KT, Matsuo K, Tajima K, Schwartz AG, Wenzlaff A, Seow A, Ying C, Staratschek-Jox A, Nürnberg P, Stoelben E, Wolf J, Lazarus P, Muscat JE, Gallagher CJ, Zienolddiny S, Haugen A, van der Heijden HF, Kiemeney LA, Isla D, Mayordomo JI, Rafnar T, Stefansson K, Zhang ZF, Chang SC, Kim JH, Hong YC, Duell EJ, Andrew AS, Lejbkowicz F, Rennert G, Müller H, Brenner H, Le Marchand L, Benhamou S, Bouchardy C, Teare MD, Xue X, McLaughlin J, Liu G, McKay JD, Brennan P, Spitz MR.

J Natl Cancer Inst. 2010 Jul 7;102(13):959-71. doi: 10.1093/jnci/djq178. Epub 2010 Jun 14.

19.

Genome-wide association mapping of acute lung injury in neonatal inbred mice.

Nichols JL, Gladwell W, Verhein KC, Cho HY, Wess J, Suzuki O, Wiltshire T, Kleeberger SR.

FASEB J. 2014 Jun;28(6):2538-50. doi: 10.1096/fj.13-247221. Epub 2014 Feb 26.

20.

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

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