Integrated genomic analyses in bronchopulmonary dysplasia.

[1]  Benjamin M. Smith,et al.  Genome-wide study of percent emphysema on computed tomography in the general population. The Multi-Ethnic Study of Atherosclerosis Lung/SNP Health Association Resource Study. , 2014, American journal of respiratory and critical care medicine.

[2]  J. Witte,et al.  A Genome-Wide Association Study (GWAS) for Bronchopulmonary Dysplasia , 2013, Pediatrics.

[3]  N. Ambalavanan,et al.  VARA attenuates hyperoxia-induced impaired alveolar development and lung function in newborn mice. , 2013, American journal of physiology. Lung cellular and molecular physiology.

[4]  A. Tanswell,et al.  The IGF-I/IGF-R1 pathway regulates postnatal lung growth and is a nonspecific regulator of alveologenesis in the neonatal rat. , 2013, American journal of physiology. Lung cellular and molecular physiology.

[5]  David Levine,et al.  GWASTools: an R/Bioconductor package for quality control and analysis of genome-wide association studies , 2012, Bioinform..

[6]  Laura J. Bierut,et al.  Assessment of Genotype Imputation Performance Using 1000 Genomes in African American Studies , 2012, PloS one.

[7]  S. Bhattacharya,et al.  Genome-wide transcriptional profiling reveals connective tissue mast cell accumulation in bronchopulmonary dysplasia. , 2012, American journal of respiratory and critical care medicine.

[8]  L. Rodrigues,et al.  Genetic variation and the risk of asthma: does it drive the differences in asthma prevalence among ethnic groups in North America? , 2012, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

[9]  C. Delacourt,et al.  Identification of SPOCK2 as a susceptibility gene for bronchopulmonary dysplasia. , 2011, American journal of respiratory and critical care medicine.

[10]  E. B. Meltzer,et al.  Severe lung fibrosis requires an invasive fibroblast phenotype regulated by hyaluronan and CD44 , 2011, The Journal of experimental medicine.

[11]  T. van der Poll,et al.  CD44 is protective during hyperoxia-induced lung injury. , 2011, American journal of respiratory cell and molecular biology.

[12]  C. Serhan,et al.  MicroRNAs in resolution of acute inflammation: identification of novel resolvin Dl‐miRNA circuits , 2011, The FASEB Journal.

[13]  H. Hakonarson,et al.  Analysing biological pathways in genome-wide association studies , 2010, Nature Reviews Genetics.

[14]  H. Too,et al.  High-performance quantification of mature microRNAs by real-time RT-PCR using deoxyuridine-incorporated oligonucleotides and hemi-nested primers. , 2010, RNA.

[15]  S. Oparil,et al.  Loss of Thy-1 inhibits alveolar development in the newborn mouse lung. , 2009, American journal of physiology. Lung cellular and molecular physiology.

[16]  S. McGowan,et al.  Platelet‐Derived Growth Factor Receptor‐Alpha‐Expressing Cells Localize to the Alveolar Entry Ring and Have Characteristics of Myofibroblasts During Pulmonary Alveolar Septal Formation , 2008, Anatomical record.

[17]  Kai Wang,et al.  Pathway-based approaches for analysis of genomewide association studies. , 2007, American journal of human genetics.

[18]  Manuel A. R. Ferreira,et al.  PLINK: a tool set for whole-genome association and population-based linkage analyses. , 2007, American journal of human genetics.

[19]  L. Ment,et al.  Familial and Genetic Susceptibility to Major Neonatal Morbidities in Preterm Twins , 2006, Pediatrics.

[20]  F. Tsai,et al.  Nonassociation of Interleukin 4 Intron 3 and 590 Promoter Polymorphisms with Bronchopulmonary Dysplasia for Ventilated Preterm Infants , 2005, Neonatology.

[21]  P. Donnelly,et al.  Genome-wide strategies for detecting multiple loci that influence complex diseases , 2005, Nature Genetics.

[22]  V. Ollikainen,et al.  Data mining and multiparameter analysis of lung surfactant protein genes in bronchopulmonary dysplasia. , 2004, Human molecular genetics.

[23]  S. Andersson,et al.  Insulin‐like growth factor‐1 (IGF‐1) and IGF‐1 receptor (IGF‐1R) expression in human lung in RDS and BPD , 2004, Pediatric pulmonology.

[24]  M. Daly,et al.  PGC-1α-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes , 2003, Nature Genetics.

[25]  A. Borkhardt,et al.  Polymorphisms of surfactant protein A genes and the risk of bronchopulmonary dysplasia in preterm infants. , 2000, The Turkish journal of pediatrics.

[26]  S. Antonarakis,et al.  Localization of a novel human RNA-editing deaminase (hRED2 or ADARB2) to chromosome 10p15 , 1997, Human Genetics.

[27]  P. Seeburg,et al.  RED2, a Brain-specific Member of the RNA-specific Adenosine Deaminase Family* , 1996, The Journal of Biological Chemistry.

[28]  M. S. Nijjar,et al.  Role of cyclic AMP and related enzymes in rat lung growth and development. , 1979, Biochimica et biophysica acta.

[29]  J. Neu Cytokines and Neurodevelopmental Outcomes in Extremely Low Birth Weight Infants , 2012 .

[30]  J. Tamargo,et al.  Soluble guanylyl cyclase during postnatal porcine pulmonary maturation. , 2005, American journal of physiology. Lung cellular and molecular physiology.

[31]  L. Monte,et al.  [Bronchopulmonary dysplasia]. , 2005, Jornal de pediatria.

[32]  A. Franklin,et al.  University of Texas Health Science Center at Houston. , 1983, Cutis.