Detalhe da pesquisa
1.
The c.1617del variant of TMEM260 is identified as the most frequent single gene determinant for Japanese patients with a specific type of congenital heart disease.
J Hum Genet
; 69(5): 215-222, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38409496
2.
Functional characterization of variants found in Japanese patients with hereditary hemorrhagic telangiectasia.
Clin Genet
; 105(5): 543-548, 2024 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38225712
3.
Novel pathogenic GATA6 variant associated with congenital heart disease, diabetes mellitus and necrotizing enterocolitis.
Pediatr Res
; 95(1): 146-155, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37700164
4.
Flow pattern analysis of right ventricular outflow tract in repaired tetralogy of Fallot through 4D flow MRI.
Heart Vessels
; 39(6): 556-562, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38368576
5.
Genetic and functional analyses of TBX4 reveal novel mechanisms underlying pulmonary arterial hypertension.
J Mol Cell Cardiol
; 171: 105-116, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35914404
6.
Risk Factors of Coronary Artery Aneurysms in Kawasaki Disease with a Low Risk of Intravenous Immunoglobulin Resistance: An Analysis of Post RAISE.
J Pediatr
; 240: 158-163.e4, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34461064
7.
Exercise Stress Electrocardiography Using the Two-Minute Jump Test in Children.
Pediatr Cardiol
; 2022 Nov 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-36436005
8.
Successful Preoperative Partial Splenic Artery and Aneurysm Embolization for Thrombocytopenia Associated with Failed Fontan Circulation.
Int Heart J
; 63(5): 984-988, 2022 Sep 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-36104230
9.
Inositol 1,4,5-trisphosphate receptor 2 as a novel marker of vasculature to delineate processes of cardiopulmonary development.
Dev Biol
; 458(2): 237-245, 2020 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31758944
10.
Evaluation of a Kawasaki Disease Risk Model for Predicting Coronary Artery Aneurysms in a Japanese Population: An Analysis of Post RAISE.
J Pediatr
; 237: 96-101.e3, 2021 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-34147499
11.
Echocardiographic Left Ventricular Z-Score Utility in Predicting Pulmonary-Systemic Flow Ratio in Children With Ventricular Septal Defect or Patent Ductus Arteriosus.
Circ J
; 86(1): 128-135, 2021 12 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-34657926
12.
Outcomes of idiopathic pulmonary arterial hypertension in Japanese children: a retrospective cohort study.
Heart Vessels
; 36(9): 1392-1399, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-33738606
13.
Pregnancy and Delivery in Patients With Repaired Congenital Heart Diseaseã- A Retrospective Japanese Multicenter Study.
Circ J
; 84(12): 2270-2274, 2020 11 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-33055459
14.
Histone H1 quantity determines the efficiency of chromatin condensation in both apoptotic and live cells.
Biochem Biophys Res Commun
; 512(2): 202-207, 2019 04 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-30879765
15.
Correction: The c.1617del variant of TMEM260 is identified as the most frequent single gene determinant for Japanese patients with a specific type of congenital heart disease.
J Hum Genet
; 69(5): 223, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38459226
16.
Polysplenia Syndrome as a Risk Factor for Early Progression of Pulmonary Hypertension.
Circ J
; 83(4): 831-836, 2019 03 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-30842375
17.
Chronotropic incompetence to exercise in anorexia nervosa patients during the body-weight recovery phase as an index of insufficient treatment.
Heart Vessels
; 34(4): 711-715, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-30341630
18.
Type 2 inositol 1,4,5-trisphosphate receptor inhibits the progression of pulmonary arterial hypertension via calcium signaling and apoptosis.
Heart Vessels
; 34(4): 724-734, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-30460575
19.
MiR-133 promotes cardiac reprogramming by directly repressing Snai1 and silencing fibroblast signatures.
EMBO J
; 33(14): 1565-81, 2014 Jul 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-24920580
20.
Successful management of living donor liver transplantation for biliary atresia with single ventricle physiology-from peri-transplant through total cavopulmonary connection: A case report.
Pediatr Transplant
; 22(3): e13118, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29457852