These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

234 related articles for article (PubMed ID: 21836138)

  • 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; 184(10):1164-70. PubMed ID: 21836138
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic predisposition to bronchopulmonary dysplasia.
    Lal CV; Ambalavanan N
    Semin Perinatol; 2015 Dec; 39(8):584-91. PubMed ID: 26471063
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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;
    Am J Physiol Lung Cell Mol Physiol; 2018 Nov; 315(5):L858-L869. PubMed ID: 30113228
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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. PubMed ID: 23897914
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Overexpression of
    Hadchouel A; Franco-Montoya ML; Guerin S; Do Cruzeiro M; Lhuillier M; Ribeiro Baptista B; Boyer L; Lanone S; Delacourt C
    Am J Physiol Lung Cell Mol Physiol; 2020 Jul; 319(1):L71-L81. PubMed ID: 32374670
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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. PubMed ID: 28689251
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 192(5):589-96. PubMed ID: 26030808
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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. PubMed ID: 26963946
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 307(3):L231-9. PubMed ID: 24907056
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 3(9):e3188. PubMed ID: 18784838
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 8(3):2971-8. PubMed ID: 26045806
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Progress in understanding the genetics of bronchopulmonary dysplasia.
    Shaw GM; O'Brodovich HM
    Semin Perinatol; 2013 Apr; 37(2):85-93. PubMed ID: 23582962
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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;
    BMC Med Genet; 2014 Nov; 15():120. PubMed ID: 25409741
    [TBL] [Abstract][Full Text] [Related]  

  • 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;
    J Pediatr; 2015 Mar; 166(3):531-7.e13. PubMed ID: 25449221
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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. PubMed ID: 22348075
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Newborn Mice Lacking the Gene for Cyp1a1 Are More Susceptible to Oxygen-Mediated Lung Injury, and Are Rescued by Postnatal β-Naphthoflavone Administration: Implications for Bronchopulmonary Dysplasia in Premature Infants.
    Maturu P; Wei-Liang Y; Jiang W; Wang L; Lingappan K; Barrios R; Liang Y; Moorthy B; Couroucli XI
    Toxicol Sci; 2017 May; 157(1):260-271. PubMed ID: 28201809
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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. PubMed ID: 24288432
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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. PubMed ID: 26067474
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Exome sequencing of extreme phenotypes in bronchopulmonary dysplasia.
    Hadchouel A; Decobert F; Besmond C; Delacourt C
    Eur J Pediatr; 2020 Apr; 179(4):579-586. PubMed ID: 31848748
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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. PubMed ID: 18762515
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.