Lista de obras - John M Dagle - Dominio Público Uruguay

A Potential Role for the NOD1 Variant (rs6958571) in Gram-Positive Blood Stream Infection in ELBW Infants.

artículo científico publicado en 2017

A functional ATG16L1 (T300A) variant is associated with necrotizing enterocolitis in premature infants

artículo científico publicado en 2016

Antenatal Determinants of Bronchopulmonary Dysplasia and Late Respiratory Disease in Preterm Infants.

artículo científico publicado en 2017

Antioxidant response genes sequence variants and BPD susceptibility in VLBW infants.

artículo científico publicado en 2014

Antisense inhibition of epidermal growth factor receptor decreases expression of human surfactant protein A.

artículo científico

Application of kinetic polymerase chain reaction and molecular beacon assays to pooled analyses and high-throughput genotyping for candidate genes.

artículo científico publicado en 2004

Applying deep DNA sequencing to common, complex pediatric traits.

artículo científico publicado en 2012

Association of amino acids with common complications of prematurity

artículo científico publicado en 2013

Candidate gene linkage approach to identify DNA variants that predispose to preterm birth

artículo científico publicado en 2012

Characterization of modified antisense oligonucleotides in Xenopus laevis embryos

scientific article published on 01 January 2006

Chromosome targeting at short polypurine sites by cationic triplex-forming oligonucleotides.

artículo científico

Cytochrome P450 (CYP2D6) genotype is associated with elevated systolic blood pressure in preterm infants after discharge from the neonatal intensive care unit.

artículo científico publicado en 2011

Determination of genetic predisposition to patent ductus arteriosus in preterm infants

artículo científico publicado en 2009

Double paternal nondisjunction in an infant with transient neonatal diabetes mellitus and Klinefelter syndrome

artículo científico publicado en 2007

Effects of Advancing Gestation and Non-Caucasian Race on Ductus Arteriosus Gene Expression

artículo científico publicado en 2015

Efficacy of pharmacologic closure of patent ductus arteriosus in small-for-gestational-age extremely preterm infants

artículo científico publicado en 2017

Free solution mobility of DNA molecules containing variable numbers of cationic phosphoramidate internucleoside linkages

artículo científico publicado en 2000

Genetic Modifiers of Patent Ductus Arteriosus in Term Infants

artículo científico publicado en 2016

Genetic associations of surfactant protein D and angiotensin-converting enzyme with lung disease in preterm neonates.

artículo científico publicado en 2011

Genetic contributions to the development of retinopathy of prematurity

artículo científico publicado en 2009

Genetic variants associated with severe retinopathy of prematurity in extremely low birth weight infants

artículo científico publicado en 2014

Genetic variation in CYB5R3 is associated with methemoglobin levels in preterm infants receiving nitric oxide therapy

artículo científico publicado en 2014

Genetics of patent ductus arteriosus susceptibility and treatment

artículo científico

Hyperglycemia as a risk factor for the development of retinopathy of prematurity

artículo científico publicado en 2013

Improving survival of extremely preterm infants born between 22 and 25 weeks of gestation.

artículo científico publicado en 2012

Individual and center-level factors affecting mortality among extremely low birth weight infants

artículo científico publicado en 2013

Maternal and fetal variation in genes of cholesterol metabolism is associated with preterm delivery.

artículo científico publicado en 2007

Maternal factors and complications of preterm birth associated with neonatal thyroid stimulating hormone

artículo científico publicado en 2014

Necrotizing Enterocolitis Is Not Associated With Sequence Variants in Antioxidant Response Genes in Premature Infants

artículo científico publicado en 2016

Oligonucleotide-based strategies to reduce gene expression.

artículo científico publicado en 2001

Pathways of degradation and mechanism of action of antisense oligonucleotides in Xenopus laevis embryos

scientific article published on 01 January 1991

Patterns of gene expression in the ductus arteriosus are related to environmental and genetic risk factors for persistent ductus patency

artículo científico publicado en 2010

Peripherally inserted central catheters optimize nutrient intake in moderately preterm infants

artículo científico publicado en 2016

Peritoneal dialysis in an extremely low-birth-weight infant with acute kidney injury.

artículo científico publicado en 2014

Physiological Approach to Sodium Supplementation in Preterm Infants.

artículo científico publicado en 2018

Pitx2c attenuation results in cardiac defects and abnormalities of intestinal orientation in developing Xenopus laevis

artículo científico publicado en 2003

Polymorphisms in CYP2C9 are associated with response to indomethacin among neonates with patent ductus arteriosus

artículo científico publicado en 2017

Polymorphisms in NR5A2, gene encoding liver receptor homolog-1 are associated with preterm birth

artículo científico publicado en 2016

Polymorphisms in urea cycle enzyme genes are associated with persistent pulmonary hypertension of the newborn

artículo científico publicado en 2017

Positively charged oligonucleotides overcome potassium-mediated inhibition of triplex DNA formation.

artículo científico publicado en 1996

Possible roles of bilirubin and breast milk in protection against retinopathy of prematurity.

artículo científico publicado en 2010

Predicting gestational age using neonatal metabolic markers

artículo científico publicado en 2015

Quality of EHR data extractions for studies of preterm birth in a tertiary care center: guidelines for obtaining reliable data

artículo científico publicado en 2016

Replication of a genome-wide association study of birth weight in preterm neonates

artículo científico publicado en 2011

Replication of clinical associations with 17-hydroxyprogesterone in preterm newborns.

artículo científico publicado en 2012

Replication of genetic associations in the inflammation, complement, and coagulation pathways with intraventricular hemorrhage in LBW preterm neonates.

artículo científico publicado en 2011

Selective degradation of targeted mRNAs using partially modified oligonucleotides.

artículo científico publicado en 2000

Sequence variants in oxytocin pathway genes and preterm birth: a candidate gene association study

artículo científico publicado en 2013

Single mutations in ABCA3 increase the risk for neonatal respiratory distress syndrome in late preterm infants (gestational age 34-36 weeks).

artículo científico publicado en 2014

Single-Nucleotide Polymorphisms in the KCNN3 Gene Associate With Preterm Birth ⬇️

artículo científico publicado el 25 de enero de 2011

Substrate Specificity and Kinetics of Degradation of Antisense Oligonucleotides by a 3′ Exonuclease in Plasma ⬇️

artículo científico publicado el 1 de enero de 1991

Survivin mRNA is down-regulated during early Xenopus laevis embryogenesis

artículo científico publicado en 2002

Targeted degradation of mRNA inXenopusoocytes and embryos directed by modified oligonucleotides: studies of An2 and cyclin in embryogenesis ⬇️

artículo científico publicado el 25 de agosto de 1990

Utilization of antisense oligodeoxynucleotides with embryonic tissues in culture

artículo científico publicado en 1999

Lista de obras de John M Dagle

A Potential Role for the NOD1 Variant (rs6958571) in Gram-Positive Blood Stream Infection in ELBW Infants.

A functional ATG16L1 (T300A) variant is associated with necrotizing enterocolitis in premature infants

Antenatal Determinants of Bronchopulmonary Dysplasia and Late Respiratory Disease in Preterm Infants.

Antioxidant response genes sequence variants and BPD susceptibility in VLBW infants.

Antisense inhibition of epidermal growth factor receptor decreases expression of human surfactant protein A.

Application of kinetic polymerase chain reaction and molecular beacon assays to pooled analyses and high-throughput genotyping for candidate genes.

Applying deep DNA sequencing to common, complex pediatric traits.

Association of amino acids with common complications of prematurity

Candidate gene linkage approach to identify DNA variants that predispose to preterm birth

Characterization of modified antisense oligonucleotides in Xenopus laevis embryos

Chromosome targeting at short polypurine sites by cationic triplex-forming oligonucleotides.

Cytochrome P450 (CYP2D6) genotype is associated with elevated systolic blood pressure in preterm infants after discharge from the neonatal intensive care unit.

Determination of genetic predisposition to patent ductus arteriosus in preterm infants

Double paternal nondisjunction in an infant with transient neonatal diabetes mellitus and Klinefelter syndrome

Effects of Advancing Gestation and Non-Caucasian Race on Ductus Arteriosus Gene Expression

Efficacy of pharmacologic closure of patent ductus arteriosus in small-for-gestational-age extremely preterm infants

Free solution mobility of DNA molecules containing variable numbers of cationic phosphoramidate internucleoside linkages

Genetic Modifiers of Patent Ductus Arteriosus in Term Infants

Genetic associations of surfactant protein D and angiotensin-converting enzyme with lung disease in preterm neonates.

Genetic contributions to the development of retinopathy of prematurity

Genetic variants associated with severe retinopathy of prematurity in extremely low birth weight infants

Genetic variation in CYB5R3 is associated with methemoglobin levels in preterm infants receiving nitric oxide therapy

Genetics of patent ductus arteriosus susceptibility and treatment

Hyperglycemia as a risk factor for the development of retinopathy of prematurity

Improving survival of extremely preterm infants born between 22 and 25 weeks of gestation.

Individual and center-level factors affecting mortality among extremely low birth weight infants

Maternal and fetal variation in genes of cholesterol metabolism is associated with preterm delivery.

Maternal factors and complications of preterm birth associated with neonatal thyroid stimulating hormone

Necrotizing Enterocolitis Is Not Associated With Sequence Variants in Antioxidant Response Genes in Premature Infants

Oligonucleotide-based strategies to reduce gene expression.

Pathways of degradation and mechanism of action of antisense oligonucleotides in Xenopus laevis embryos

Patterns of gene expression in the ductus arteriosus are related to environmental and genetic risk factors for persistent ductus patency

Peripherally inserted central catheters optimize nutrient intake in moderately preterm infants

Peritoneal dialysis in an extremely low-birth-weight infant with acute kidney injury.

Physiological Approach to Sodium Supplementation in Preterm Infants.

Pitx2c attenuation results in cardiac defects and abnormalities of intestinal orientation in developing Xenopus laevis

Polymorphisms in CYP2C9 are associated with response to indomethacin among neonates with patent ductus arteriosus

Polymorphisms in NR5A2, gene encoding liver receptor homolog-1 are associated with preterm birth

Polymorphisms in urea cycle enzyme genes are associated with persistent pulmonary hypertension of the newborn

Positively charged oligonucleotides overcome potassium-mediated inhibition of triplex DNA formation.

Possible roles of bilirubin and breast milk in protection against retinopathy of prematurity.

Predicting gestational age using neonatal metabolic markers

Quality of EHR data extractions for studies of preterm birth in a tertiary care center: guidelines for obtaining reliable data

Replication of a genome-wide association study of birth weight in preterm neonates

Replication of clinical associations with 17-hydroxyprogesterone in preterm newborns.

Replication of genetic associations in the inflammation, complement, and coagulation pathways with intraventricular hemorrhage in LBW preterm neonates.

Selective degradation of targeted mRNAs using partially modified oligonucleotides.

Sequence variants in oxytocin pathway genes and preterm birth: a candidate gene association study

Single mutations in ABCA3 increase the risk for neonatal respiratory distress syndrome in late preterm infants (gestational age 34-36 weeks).

Single-Nucleotide Polymorphisms in the KCNN3 Gene Associate With Preterm Birth ⬇️

Substrate Specificity and Kinetics of Degradation of Antisense Oligonucleotides by a 3′ Exonuclease in Plasma ⬇️

Survivin mRNA is down-regulated during early Xenopus laevis embryogenesis

Targeted degradation of mRNA inXenopusoocytes and embryos directed by modified oligonucleotides: studies of An2 and cyclin in embryogenesis ⬇️

Utilization of antisense oligodeoxynucleotides with embryonic tissues in culture