Detalhe da pesquisa
1.
Paracrine signalling by cardiac calcitonin controls atrial fibrogenesis and arrhythmia.
Nature
; 587(7834): 460-465, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33149301
2.
Evasins: Tick Salivary Proteins that Inhibit Mammalian Chemokines.
Trends Biochem Sci
; 45(2): 108-122, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31679840
3.
Engineered anti-inflammatory peptides inspired by mapping an evasin-chemokine interaction.
J Biol Chem
; 295(32): 10926-10939, 2020 08 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32471866
4.
Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot.
Circ Res
; 124(4): 553-563, 2019 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30582441
5.
A knottin scaffold directs the CXC-chemokine-binding specificity of tick evasins.
J Biol Chem
; 294(29): 11199-11212, 2019 07 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-31167786
6.
The N-terminal domain of a tick evasin is critical for chemokine binding and neutralization and confers specific binding activity to other evasins.
J Biol Chem
; 293(16): 6134-6146, 2018 04 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-29487134
7.
Functional analysis of AEBP2, a PRC2 Polycomb protein, reveals a Trithorax phenotype in embryonic development and in ESCs.
Development
; 143(15): 2716-23, 2016 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27317809
8.
A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20.
Hum Mol Genet
; 25(11): 2331-2341, 2016 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26965164
9.
Pcsk5 is required in the early cranio-cardiac mesoderm for heart development.
BMC Dev Biol
; 17(1): 6, 2017 04 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-28446132
10.
Rare variants in NR2F2 cause congenital heart defects in humans.
Am J Hum Genet
; 94(4): 574-85, 2014 04 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-24702954
11.
The Retinoid Agonist Tazarotene Promotes Angiogenesis and Wound Healing.
Mol Ther
; 24(10): 1745-1759, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27480772
12.
Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defect.
Genet Med
; 18(2): 189-98, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25996639
13.
HIC2 is a novel dosage-dependent regulator of cardiac development located within the distal 22q11 deletion syndrome region.
Circ Res
; 115(1): 23-31, 2014 Jun 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-24748541
14.
Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability.
Hum Mutat
; 36(12): 1197-204, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26350204
15.
Glucocorticoid receptor is required for foetal heart maturation.
Hum Mol Genet
; 22(16): 3269-82, 2013 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23595884
16.
Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot.
Hum Mol Genet
; 22(7): 1473-81, 2013 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23297363
17.
Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease.
Am J Hum Genet
; 91(3): 489-501, 2012 Sep 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-22939634
18.
A pivotal role for tryptophan 447 in enzymatic coupling of human endothelial nitric oxide synthase (eNOS): effects on tetrahydrobiopterin-dependent catalysis and eNOS dimerization.
J Biol Chem
; 288(41): 29836-45, 2013 Oct 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-23965989
19.
Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls.
Hum Mol Genet
; 21(7): 1513-20, 2012 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22199024
20.
Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans.
Am J Hum Genet
; 98(3): 592, 2016 Mar 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28863274