Detalhe da pesquisa
1.
Human placental proteomics and exon variant studies link AAT/SERPINA1 with spontaneous preterm birth.
BMC Med
; 20(1): 141, 2022 04 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35477570
2.
Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2.
PLoS Genet
; 15(6): e1008107, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31194736
3.
Correction: Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth.
PLoS Genet
; 14(9): e1007673, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30212495
4.
Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth.
PLoS Genet
; 14(7): e1007394, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30001343
5.
Genetic Associations with Gestational Duration and Spontaneous Preterm Birth.
N Engl J Med
; 377(12): 1156-1167, 2017 09 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-28877031
6.
Spontaneous premature birth as a target of genomic research.
Pediatr Res
; 85(4): 422-431, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30353040
7.
CXCR3 Polymorphism and Expression Associate with Spontaneous Preterm Birth.
J Immunol
; 195(5): 2187-98, 2015 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26209629
8.
A study of genes encoding cytokines (IL6, IL10, TNF), cytokine receptors (IL6R, IL6ST), and glucocorticoid receptor (NR3C1) and susceptibility to bronchopulmonary dysplasia.
BMC Med Genet
; 15: 120, 2014 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25409741
9.
Allele-specific N-glycosylation delays human surfactant protein B secretion in vitro and associates with decreased protein levels in vivo.
Pediatr Res
; 74(6): 646-51, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24002332
10.
A study of collectin genes in spontaneous preterm birth reveals an association with a common surfactant protein D gene polymorphism.
Pediatr Res
; 71(1): 93-9, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22289856
11.
Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia.
Orphanet J Rare Dis
; 16(1): 412, 2021 10 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34627339
12.
Integrative genetic, genomic and transcriptomic analysis of heat shock protein and nuclear hormone receptor gene associations with spontaneous preterm birth.
Sci Rep
; 11(1): 17115, 2021 08 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-34429451
13.
Immature surfactant protein-B impairs the antioxidant capacity of HDL.
Int J Cardiol
; 285: 53-58, 2019 06 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30857841
14.
Correction to: Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia.
Orphanet J Rare Dis
; 17(1): 59, 2022 Feb 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-35177119
15.
Genome-wide association study of bronchopulmonary dysplasia: a potential role for variants near the CRP gene.
Sci Rep
; 7(1): 9271, 2017 08 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-28839172
16.
Cerebral Palsy and Polymorphism of the Chemokine CCL18 in Very Preterm Children.
Neonatology
; 108(2): 124-9, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26113374
17.
Genes Encoding Vascular Endothelial Growth Factor A (VEGF-A) and VEGF Receptor 2 (VEGFR-2) and Risk for Bronchopulmonary Dysplasia.
Neonatology
; 108(1): 53-9, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25998098
18.
Polymorphisms of the gene encoding Kit ligand are associated with bronchopulmonary dysplasia.
Pediatr Pulmonol
; 50(3): 260-270, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24610823
19.
A potential novel spontaneous preterm birth gene, AR, identified by linkage and association analysis of X chromosomal markers.
PLoS One
; 7(12): e51378, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23227263