Integrated genomic analyses in bronchopulmonary dysplasia.
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S. Bhattacharya | W. Carlo | T. Mariani | G. Page | R. Higgins | N. Ambalavanan | J. Murray | D. Kelly | O. Faye-Petersen | A. Cuna | C. Cotten | Waldemar A. Carlo | S. Bhattacharya | Jeffrey C. Murray | Thomas J. Mariani | C. Cotten | Grier P. Page | Alain C. Cuna | Waldemar A Carlo
[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.