Detalhe da pesquisa
1.
Long-term outcomes of autologous skeletal myoblast cell-sheet transplantation for end-stage ischemic cardiomyopathy.
Mol Ther
; 29(4): 1425-1438, 2021 04 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33429079
2.
Cardiomyopathy and altered integrin-actin signaling in Fhl1 mutant female mice.
Hum Mol Genet
; 28(2): 209-219, 2019 01 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30260394
3.
Elevated dual specificity protein phosphatase 4 in cardiomyopathy caused by lamin A/C gene mutation is primarily ERK1/2-dependent and its depletion improves cardiac function and survival.
Hum Mol Genet
; 27(13): 2290-2305, 2018 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29668927
4.
Recovery From Exhaustion of the Frank-Starling Mechanism by Mechanical Unloading With a Continuous-Flow Ventricular Assist Device.
Circ J
; 84(7): 1124-1131, 2020 06 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-32461540
5.
Jarvik 2000 with postauricular cable as destination therapy: first clinical case in Japan.
J Artif Organs
; 23(1): 89-92, 2020 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-31515649
6.
Decreased WNT/ß-catenin signalling contributes to the pathogenesis of dilated cardiomyopathy caused by mutations in the lamin a/C gene.
Hum Mol Genet
; 26(2): 333-343, 2017 01 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28069793
7.
Old-Age Onset Progressive Cardiac Contractile Dysfunction in a Patient with Polycystic Kidney Disease Harboring a PKD1 Frameshift Mutation.
Int Heart J
; 60(1): 220-225, 2019 Jan 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-30464138
8.
ERK1/2 directly acts on CTGF/CCN2 expression to mediate myocardial fibrosis in cardiomyopathy caused by mutations in the lamin A/C gene.
Hum Mol Genet
; 25(11): 2220-2233, 2016 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27131347
9.
Refractory Ventricular Arrhythmias in a Patient With Dilated Cardiomyopathy Caused by a Nonsense Mutation in BAG5.
Circ J
; 86(12): 2043, 2022 11 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-36130910
10.
Macrocyclic MEK1/2 inhibitor with efficacy in a mouse model of cardiomyopathy caused by lamin A/C gene mutation.
Bioorg Med Chem
; 25(3): 1004-1013, 2017 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28011205
11.
Mitogen-activated protein kinase kinase 1/2 inhibition and angiotensin II converting inhibition in mice with cardiomyopathy caused by lamin A/C gene mutation.
Biochem Biophys Res Commun
; 452(4): 958-61, 2014 Oct 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-25218145
12.
Left ventricular longitudinal strain by speckle-tracking echocardiography is associated with treatment-requiring cardiac allograft rejection.
J Card Fail
; 20(5): 359-64, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24561182
13.
Novel indices representing heterogeneous distributions of myocardial perfusion imaging.
Ann Nucl Med
; 38(6): 468-474, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38502462
14.
Diverse distribution patterns of segmental longitudinal strain are associated with different clinical features and outcomes in dilated cardiomyopathy.
J Echocardiogr
; 2024 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38451414
15.
Switching from Beraprost to Selexipag in the Treatment of Pulmonary Arterial Hypertension: Insights from a Phase IV Study of the Japanese Registry (The EXCEL Study: EXChange from bEraprost to seLexipag Study).
Pharmaceuticals (Basel)
; 17(5)2024 Apr 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38794126
16.
Arterial repair 4 months after zotarolimus-eluting stent implantation observed on angioscopy.
Circ J
; 77(5): 1186-92, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23412803
17.
Impella 5.0 as a Bridge to Implantable Left Ventricular Assist Deviceã- First Clinical Case in Japan.
Circ J
; 82(11): 2923-2924, 2018 10 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-29780066
18.
Pulmonary hypertension with a precapillary component in heart failure with preserved ejection fraction.
Heart
; 109(8): 626-633, 2023 03 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-36543519
19.
End-stage Hypertrophic Cardiomyopathy with Advanced Heart Failure in Patients Carrying MYH7 R453 Variants: A Case Series.
Intern Med
; 62(21): 3167-3173, 2023 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36948619
20.
A spinal muscular atrophy modifier implicates the SMN protein in SNARE complex assembly at neuromuscular synapses.
Neuron
; 111(9): 1423-1439.e4, 2023 05 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36863345