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Items: 1 to 20 of 105

1.

Genome-wide transcriptional profiling reveals connective tissue mast cell accumulation in bronchopulmonary dysplasia.

Bhattacharya S, Go D, Krenitsky DL, Huyck HL, Solleti SK, Lunger VA, Metlay L, Srisuma S, Wert SE, Mariani TJ, Pryhuber GS.

Am J Respir Crit Care Med. 2012 Aug 15;186(4):349-58. doi: 10.1164/rccm.201203-0406OC. Epub 2012 Jun 21.

2.

Gene expression profile in newborn rat lungs after two days of recovery of mechanical ventilation.

Dénervaud V, Gremlich S, Trummer-Menzi E, Schittny JC, Roth-Kleiner M.

Pediatr Res. 2015 Dec;78(6):641-9. doi: 10.1038/pr.2015.155. Epub 2015 Sep 9.

PMID:
26353077
3.

The genome-wide transcriptional response to neonatal hyperoxia identifies Ahr as a key regulator.

Bhattacharya S, Zhou Z, Yee M, Chu CY, Lopez AM, Lunger VA, Solleti SK, Resseguie E, Buczynski B, Mariani TJ, O'Reilly MA.

Am J Physiol Lung Cell Mol Physiol. 2014 Oct 1;307(7):L516-23. doi: 10.1152/ajplung.00200.2014. Epub 2014 Aug 22.

4.

Differential expression of long non-coding RNAs in hyperoxia-induced bronchopulmonary dysplasia.

Bao TP, Wu R, Cheng HP, Cui XW, Tian ZF.

Cell Biochem Funct. 2016 Jul;34(5):299-309. doi: 10.1002/cbf.3190. Epub 2016 May 3.

PMID:
27137150
5.

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.

6.

Lysyl oxidase activity is dysregulated during impaired alveolarization of mouse and human lungs.

Kumarasamy A, Schmitt I, Nave AH, Reiss I, van der Horst I, Dony E, Roberts JD Jr, de Krijger RR, Tibboel D, Seeger W, Schermuly RT, Eickelberg O, Morty RE.

Am J Respir Crit Care Med. 2009 Dec 15;180(12):1239-52. doi: 10.1164/rccm.200902-0215OC. Epub 2009 Sep 24.

8.

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.

9.

Astragalus polysaccharides exert protective effects in newborn rats with bronchopulmonary dysplasia by upregulating the expression of EGFL7 in lung tissue.

Wang XH, Huang WM.

Int J Mol Med. 2014 Dec;34(6):1529-36. doi: 10.3892/ijmm.2014.1951. Epub 2014 Sep 30.

PMID:
25270395
10.

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.

11.

Gene expression profiling in preterm infants: new aspects of bronchopulmonary dysplasia development.

Pietrzyk JJ, Kwinta P, Wollen EJ, Bik-Multanowski M, Madetko-Talowska A, Günther CC, Jagła M, Tomasik T, Saugstad OD.

PLoS One. 2013 Oct 23;8(10):e78585. doi: 10.1371/journal.pone.0078585. eCollection 2013.

12.

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.

13.

Endothelin-1 signaling promotes fibrosis in vitro in a bronchopulmonary dysplasia model by activating the extrinsic coagulation cascade.

Kambas K, Chrysanthopoulou A, Kourtzelis I, Skordala M, Mitroulis I, Rafail S, Vradelis S, Sigalas I, Wu YQ, Speletas M, Kolios G, Ritis K.

J Immunol. 2011 Jun 1;186(11):6568-75. doi: 10.4049/jimmunol.1003756. Epub 2011 Apr 29.

14.

Human umbilical cord blood mononuclear cells in a double-hit model of bronchopulmonary dysplasia in neonatal mice.

Monz D, Tutdibi E, Mildau C, Shen J, Kasoha M, Laschke MW, Roolfs T, Schmiedl A, Tschernig T, Bieback K, Gortner L.

PLoS One. 2013 Sep 19;8(9):e74740. doi: 10.1371/journal.pone.0074740. eCollection 2013.

15.

MicroRNA expression profiling studies on bronchopulmonary dysplasia: a systematic review and meta-analysis.

Yang Y, Qiu J, Kan Q, Zhou XG, Zhou XY.

Genet Mol Res. 2013 Oct 30;12(4):5195-206. doi: 10.4238/2013.October.30.4. Review.

16.

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.

17.

Developmental regulation of p66Shc is altered by bronchopulmonary dysplasia in baboons and humans.

Lee MK, Pryhuber GS, Schwarz MA, Smith SM, Pavlova Z, Sunday ME.

Am J Respir Crit Care Med. 2005 Jun 15;171(12):1384-94. Epub 2005 Mar 18.

18.

MicroRNA expression aberration associated with bronchopulmonary dysplasia in preterm infants: a preliminary study.

Wu YT, Chen WJ, Hsieh WS, Tsao PN, Yu SL, Lai CY, Lee WC, Jeng SF.

Respir Care. 2013 Sep;58(9):1527-35. doi: 10.4187/respcare.02166. Epub 2013 Mar 12.

19.

SERPINB1 upregulation is associated with in vivo complex formation with neutrophil elastase and cathepsin G in a baboon model of bronchopulmonary dysplasia.

Yasumatsu R, Altiok O, Benarafa C, Yasumatsu C, Bingol-Karakoc G, Remold-O'Donnell E, Cataltepe S.

Am J Physiol Lung Cell Mol Physiol. 2006 Oct;291(4):L619-27. Epub 2006 Apr 14.

20.

Deregulation of the lysyl hydroxylase matrix cross-linking system in experimental and clinical bronchopulmonary dysplasia.

Witsch TJ, Turowski P, Sakkas E, Niess G, Becker S, Herold S, Mayer K, Vadász I, Roberts JD Jr, Seeger W, Morty RE.

Am J Physiol Lung Cell Mol Physiol. 2014 Feb;306(3):L246-59. doi: 10.1152/ajplung.00109.2013. Epub 2013 Nov 27.

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