Detalhe da pesquisa
1.
Degenerative mitral regurgitation due to flail leaflet: sex-related differences in presentation, management, and outcomes.
Eur Heart J
; 2024 May 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38751052
2.
Expanding the phenome and variome of the ROBO-SLIT pathway in congenital heart defects: toward improving the genetic testing yield of CHD.
J Transl Med
; 21(1): 160, 2023 02 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-36855159
3.
Calcium Handling in Inherited Cardiac Diseases: A Focus on Catecholaminergic Polymorphic Ventricular Tachycardia and Hypertrophic Cardiomyopathy.
Int J Mol Sci
; 24(4)2023 Feb 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36834774
4.
Transcriptome analysis of mouse and human sinoatrial node cells reveals a conserved genetic program.
Development
; 146(8)2019 04 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-30936179
5.
Identification of non-synonymous variations in ROBO1 and GATA5 genes in a family with bicuspid aortic valve disease.
J Hum Genet
; 67(9): 515-518, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-35534675
6.
Single Cell Approaches to Understand the Earliest Steps in Heart Development.
Curr Cardiol Rep
; 24(6): 611-621, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35384547
7.
Dilated-Left Ventricular Non-Compaction Cardiomyopathy in a Pediatric Case with SPEG Compound Heterozygous Variants.
Int J Mol Sci
; 23(9)2022 May 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35563595
8.
SCN5A Variants as Genetic Arrhythmias Triggers for Familial Bileaflet Mitral Valve Prolapse.
Int J Mol Sci
; 23(22)2022 Nov 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-36430924
9.
Msx1 haploinsufficiency modifies the Pax9-deficient cardiovascular phenotype.
BMC Dev Biol
; 21(1): 14, 2021 10 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34615475
10.
Bmp2 and Notch cooperate to pattern the embryonic endocardium.
Development
; 145(13)2018 07 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29853617
11.
Krox20 defines a subpopulation of cardiac neural crest cells contributing to arterial valves and bicuspid aortic valve.
Development
; 145(1)2018 01 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29158447
12.
Multiallelic rare variants support an oligogenic origin of sudden cardiac death in the young.
Herz
; 46(Suppl 1): 94-102, 2021 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-31970460
13.
Piezo1 is required for outflow tract and aortic valve development.
J Mol Cell Cardiol
; 143: 51-62, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32251670
14.
Identification of a peripheral blood gene signature predicting aortic valve calcification.
Physiol Genomics
; 52(12): 563-574, 2020 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33044885
15.
T-box genes and retinoic acid signaling regulate the segregation of arterial and venous pole progenitor cells in the murine second heart field.
Hum Mol Genet
; 27(21): 3747-3760, 2018 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30016433
16.
Asb2α-Filamin A Axis Is Essential for Actin Cytoskeleton Remodeling During Heart Development.
Circ Res
; 122(6): e34-e48, 2018 03 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-29374072
17.
Disruption of CXCR4 signaling in pharyngeal neural crest cells causes DiGeorge syndrome-like malformations.
Development
; 143(4): 582-8, 2016 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26755698
18.
A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide with RAF1 S259Y neomutation.
Genet Res (Camb)
; 101: e6, 2019 04 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-31030682
19.
The alternatively spliced LRRFIP1 Isoform-1 is a key regulator of the Wnt/ß-catenin transcription pathway.
Biochim Biophys Acta Mol Cell Res
; 1864(7): 1142-1152, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28322931
20.
Ectopic expression of Hoxb1 induces cardiac and craniofacial malformations.
Genesis
; 56(6-7): e23221, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30134070