Genetic Polymorphisms of LPCAT1, CHPT1 and PCYT1B and Risk of Neonatal Respiratory Distress Syndrome among a Chinese Han Population
Tài liệu tham khảo
Hallman, 2002, Surfactant proteins and genetic predisposition to respiratory distress syndrome, Semin Perinatol, 26, 450, 10.1053/sper.2002.37314
Hallman, 2012, Premature birth and diseases in premature infants: common genetic background?, J Matern Fetal Neonatal Med, 25, 21, 10.3109/14767058.2012.667600
Jobe, 1993, Pulmonary surfactant therapy, N Engl J Med, 328, 861, 10.1056/NEJM199303253281208
Agassandian, 2013, Surfactant phospholipid metabolism, Biochim Biophys Acta, 1831, 612, 10.1016/j.bbalip.2012.09.010
Nakanishi, 2006, Cloning and characterization of mouse lung-type acyl-CoA:lysophosphatidylcholine acyltransferase 1 (LPCAT1). Expression in alveolar type II cells and possible involvement in surfactant production, J Biol Chem, 281, 20140, 10.1074/jbc.M600225200
Lin, 2015, Lysophosphatidylcholine acyltransferase 1 (LPCAT1) specifically interacts with phospholipid transfer protein starD10 to facilitate surfactant phospholipid trafficking in alveolar type II cells, J Biol Chem, 290, 18559, 10.1074/jbc.M115.666701
Chatterjee, 2009, Role of 5'- and 3'-untranslated regions of mRNAs in human diseases, Biol Cell, 101, 251, 10.1042/BC20080104
Kaya, 2017, Association of Rho-kinase gene polymorphisms with respiratory distress syndrome in preterm neonates, Pediatr Neonatol, 58, 36, 10.1016/j.pedneo.2015.12.006
Shen, 2014, Analysis of nitric oxide synthase gene polymorphisms in neonatal respiratory distress syndrome among the Chinese Han population, Ital J Pediatr, 40, 27, 10.1186/1824-7288-40-27
Gortner, 2018, Review demonstrates that less invasive surfactant administration in preterm neonates leads to fewer complications, Acta Paediatr, 107, 736, 10.1111/apa.14161
Rutkowska, 2019, Severe bronchopulmonary dysplasia - incidence and predictive factors in a prospective, multicenter study in very preterm infants with respiratory distress syndrome, J Matern Fetal Neonatal Med, 32, 1958, 10.1080/14767058.2017.1422711
Wambach, 2016, Functional characterization of ATP-binding cassette transporter A3 mutations from infants with respiratory distress syndrome, Am J Respir Cell Mol Biol, 55, 716, 10.1165/rcmb.2016-0008OC
Somaschini, 2018, Surfactant proteins gene variants in premature newborn infants with severe respiratory distress syndrome, J Perinatol, 38, 337, 10.1038/s41372-017-0018-2
Rämet, 2000, Association between the surfactant protein A (SP-A) gene locus and respiratory-distress syndrome in the Finnish population, Am J Hum Genet, 66, 1569, 10.1086/302906
Chang, 2016, Genetic polymorphisms of SP-A, SP-B, and SP-D and risk of respiratory distress syndrome in preterm neonates, Med Sci Monit, 22, 5091, 10.12659/MSM.898553
Fatahi, 2018, Association of SP-B gene 9306 A/G polymorphism (rs7316) and risk of RDS, J Matern Fetal Neonatal Med, 31, 2965, 10.1080/14767058.2017.1359829
Fatahi, 2017, Association of SP-C gene codon 186 polymorphism (rs1124) and risk of RDS, J Matern Fetal Neonatal Med, 30, 2585, 10.1080/14767058.2016.1256994
Karjalainen, 2008, Haplotype analysis of ABCA3: association with respiratory distress in very premature infants, Ann Med, 40, 56, 10.1080/07853890701611094
Tian, 2016, The haplotype TGGAG in the ABCA3 gene increases the risk of respiratory distress syndrome in preterm infants in southern China, Pediatr Neonatol, 57, 188, 10.1016/j.pedneo.2015.09.002
Lyra, 2011, Surfactant protein B gene polymorphism in preterm babies with respiratory distress syndrome, Braz J Med Biol Res, 44, 66, 10.1590/S0100-879X2010007500147
Harayama, 2009, Biosynthesis of phosphatidylcholine by human lysophosphatidylcholine acyltransferase 1, J Lipid Res, 50, 1824, 10.1194/jlr.M800500-JLR200
Moessinger, 2014, Two different pathways of phosphatidylcholine synthesis, the Kennedy Pathway and the Lands Cycle, differentially regulate cellular triacylglycerol storage, BMC Cell Biol, 15, 43, 10.1186/s12860-014-0043-3
Wambach, 2012, Single ABCA3 mutations increase risk for neonatal respiratory distress syndrome, Pediatrics, 130, e1575, 10.1542/peds.2012-0918
Bridges, 2010, LPCAT1 regulates surfactant phospholipid synthesis and is required for transitioning to air breathing in mice, J Clin Invest, 120, 1736, 10.1172/JCI38061
Wittke-Thompson, 2005, Rational inferences about departures from Hardy-Weinberg equilibrium, Am J Hum Genet, 76, 967, 10.1086/430507
Chen, 2006, Identification and characterization of a lysophosphatidylcholine acyltransferase in alveolar type II cells, Proc Natl Acad Sci USA, 103, 11724, 10.1073/pnas.0604946103
Welch, 2016, Amniotic fluid LPCAT1 mRNA correlates with the lamellar body count, J Perinat Med, 44, 531, 10.1515/jpm-2015-0008
Welch, 2018, Maternal plasma LPCAT 1 mRNA correlates with lamellar body count, J Perinat Med, 46, 429, 10.1515/jpm-2017-0057