Follow
Naomasa Makita
Naomasa Makita
National Cerebral and Cardiovascular Center
Verified email at ncvc.go.jp
Title
Cited by
Cited by
Year
Heart disease and stroke statistics—2017 update: a report from the American Heart Association
EJ Benjamin, MJ Blaha, SE Chiuve, M Cushman, SR Das, R Deo, ...
circulation 135 (10), e146-e603, 2017
170072017
Molecular mechanism for an inherited cardiac arrhythmia
PB Bennett, K Yazawa, N Makita, AL George Jr
Nature 376 (6542), 683-685, 1995
11331995
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
CR Bezzina, J Barc, Y Mizusawa, CA Remme, JB Gourraud, F Simonet, ...
Nature genetics 45 (9), 1044-1049, 2013
5402013
Fibrosis, connexin-43, and conduction abnormalities in the Brugada syndrome
K Nademanee, H Raju, SV De Noronha, M Papadakis, L Robinson, ...
Journal of the American College of Cardiology 66 (18), 1976-1986, 2015
3622015
Evidence for the existence of F2-isoprostane receptors on rat vascular smooth muscle cells
M Fukunaga, N Makita, LJ Roberts 2nd, JD Morrow, K Takahashi, KF Badr
American Journal of Physiology-Cell Physiology 264 (6), C1619-C1624, 1993
2981993
The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome
N Makita, E Behr, W Shimizu, M Horie, A Sunami, L Crotti, E Schulze-Bahr, ...
The Journal of clinical investigation 118 (6), 2219-2229, 2008
2682008
A nonsense mutation of the sodium channel gene SCN2A in a patient with intractable epilepsy and mental decline
K Kamiya, M Kaneda, T Sugawara, E Mazaki, N Okamura, M Montal, ...
Journal of Neuroscience 24 (11), 2690-2698, 2004
2672004
Drug-Induced Long-QT Syndrome Associated With a Subclinical SCN5A Mutation
N Makita, M Horie, T Nakamura, T Ai, K Sasaki, H Yokoi, M Sakurai, ...
Circulation 106 (10), 1269-1274, 2002
2492002
Enhanced Na+ Channel Intermediate Inactivation in Brugada Syndrome
DW Wang, N Makita, A Kitabatake, JR Balser, AL George Jr
Circulation research 87 (8), e37-e43, 2000
2192000
Electrocardiographic Characteristics and SCN5A Mutations in Idiopathic Ventricular Fibrillation Associated With Early Repolarization
H Watanabe, A Nogami, K Ohkubo, H Kawata, Y Hayashi, T Ishikawa, ...
Circulation: Arrhythmia and Electrophysiology 4 (6), 874-881, 2011
2112011
Novel calmodulin mutations associated with congenital arrhythmia susceptibility
N Makita, N Yagihara, L Crotti, CN Johnson, BM Beckmann, MS Roh, ...
Circulation: Cardiovascular Genetics 7 (4), 466-474, 2014
2102014
European heart rhythm association (EHRA)/heart rhythm society (HRS)/Asia pacific heart rhythm society (APHRS)/latin American heart rhythm society (LAHRS) expert consensus …
AAM Wilde, C Semsarian, MF Márquez, AS Shamloo, MJ Ackerman, ...
Europace 24 (8), 1307-1367, 2022
206*2022
Disease characterization using LQTS-specific induced pluripotent stem cells
T Egashira, S Yuasa, T Suzuki, Y Aizawa, H Yamakawa, T Matsuhashi, ...
Cardiovascular research 95 (4), 419-429, 2012
2042012
Voltage-gated Na+ channel beta 1 subunit mRNA expressed in adult human skeletal muscle, heart, and brain is encoded by a single gene.
N Makita, PB Bennett Jr, AL George Jr
Journal of Biological Chemistry 269 (10), 7571-7578, 1994
2031994
Pharmacological targeting of long QT mutant sodium channels.
DW Wang, K Yazawa, N Makita, AL George, PB Bennett
The Journal of clinical investigation 99 (7), 1714-1720, 1997
1981997
A novel SCN5A mutation associated with idiopathic ventricular fibrillation without typical ECG findings of Brugada syndrome
J Akai, N Makita, H Sakurada, N Shirai, K Ueda, A Kitabatake, ...
FEBS letters 479 (1-2), 29-34, 2000
1932000
High Risk for Bradyarrhythmic Complications in Patients With Brugada Syndrome Caused by SCN5AGene Mutations
T Makiyama, M Akao, K Tsuji, T Doi, S Ohno, K Takenaka, A Kobori, ...
Journal of the American College of Cardiology 46 (11), 2100-2106, 2005
1702005
Genotype-Phenotype Correlation of SCN5A Mutation for the Clinical and Electrocardiographic Characteristics of Probands With Brugada Syndrome: A Japanese …
K Yamagata, M Horie, T Aiba, S Ogawa, Y Aizawa, T Ohe, M Yamagishi, ...
Circulation 135 (23), 2255-2270, 2017
1622017
Molecular determinants of β1 subunit-induced gating modulation in voltage-dependent Na+ channels
N Makita, PB Bennett, AL George Jr
Journal of Neuroscience 16 (22), 7117-7127, 1996
1501996
A cardiac sodium channel mutation identified in Brugada syndrome associated with atrial standstill
N Takehara, N Makita, J Kawabe, N Sato, Y Kawamura, A Kitabatake, ...
Journal of internal medicine 255 (1), 137-142, 2004
1382004
The system can't perform the operation now. Try again later.
Articles 1–20