Detalhe da pesquisa
1.
The origins of unpredictability in life outcome prediction tasks.
Proc Natl Acad Sci U S A
; 121(24): e2322973121, 2024 Jun 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38833466
2.
Identifying gaps in parental support for families of children with hypoplastic left heart syndrome.
Cardiol Young
; 32(2): 215-222, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-33966677
3.
Model system identification of novel congenital heart disease gene candidates: focus on RPL13.
Hum Mol Genet
; 28(23): 3954-3969, 2019 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31625562
4.
Natural underlying mtDNA heteroplasmy as a potential source of intra-person hiPSC variability.
EMBO J
; 35(18): 1979-90, 2016 09 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27436875
5.
Addressing Variability and Heterogeneity of Induced Pluripotent Stem Cell-Derived Cardiomyocytes.
Adv Exp Med Biol
; 1212: 1-29, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-30850960
6.
Loss of Ventricular Function After Bidirectional Cavopulmonary Connection: Who Is at Risk?
Pediatr Cardiol
; 41(8): 1714-1724, 2020 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-32780223
7.
Hypoplastic left heart syndrome: From bedside to bench and back.
J Mol Cell Cardiol
; 135: 109-118, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31419439
8.
Current Interventional and Surgical Management of Congenital Heart Disease: Specific Focus on Valvular Disease and Cardiac Arrhythmias.
Circ Res
; 120(6): 1027-1044, 2017 Mar 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-28302746
9.
KMT2D-NOTCH Mediates Coronary Abnormalities in Hypoplastic Left Heart Syndrome.
Circ Res
; 131(3): 280-282, 2022 07 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-35762338
10.
Modeling structural and functional deficiencies of RBM20 familial dilated cardiomyopathy using human induced pluripotent stem cells.
Hum Mol Genet
; 25(2): 254-65, 2016 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26604136
11.
NOTCH1-Dependent Nitric Oxide Signaling Deficiency in Hypoplastic Left Heart Syndrome Revealed Through Patient-Specific Phenotypes Detected in Bioengineered Cardiogenesis.
Stem Cells
; 35(4): 1106-1119, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28142228
12.
Fathers' Perceived Reasons for Their Underrepresentation in Child Health Research and Strategies to Increase Their Involvement.
Matern Child Health J
; 21(2): 267-274, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27473093
13.
Patient-Specific Induced Pluripotent Stem Cells Implicate Intrinsic Impaired Contractility in Hypoplastic Left Heart Syndrome.
Circulation
; 142(16): 1605-1608, 2020 10 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-33074758
14.
Rbm20-deficient cardiogenesis reveals early disruption of RNA processing and sarcomere remodeling establishing a developmental etiology for dilated cardiomyopathy.
Hum Mol Genet
; 23(14): 3779-91, 2014 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24584570
15.
Nos3-/- iPSCs model concordant signatures of in utero cardiac pathogenesis.
J Mol Cell Cardiol
; 87: 228-36, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26344701
16.
Compound heterozygous NOTCH1 mutations underlie impaired cardiogenesis in a patient with hypoplastic left heart syndrome.
Hum Genet
; 134(9): 1003-11, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26164125
17.
Selection via pluripotency-related transcriptional screen minimizes the influence of somatic origin on iPSC differentiation propensity.
Stem Cells
; 32(9): 2350-9, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24802033
18.
New and TALENted genome engineering toolbox.
Circ Res
; 113(5): 571-87, 2013 Aug 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-23948583
19.
Transcriptome from circulating cells suggests dysregulated pathways associated with long-term recurrent events following first-time myocardial infarction.
J Mol Cell Cardiol
; 74: 13-21, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24801707
20.
Transcriptional atlas of cardiogenesis maps congenital heart disease interactome.
Physiol Genomics
; 46(13): 482-95, 2014 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24803680