User profiles for HIROMI KIMURA

Hiromi Kimura

Verified email at aist.go.jp
Cited by 1173

Tetraspanins CD9 and CD81 function to prevent the fusion of mononuclear phagocytes

…, T Miyazaki, T Funakoshi, H Kimura… - The Journal of cell …, 2003 - rupress.org
Tetraspanins CD9 and CD81 facilitate the fusion between gametes, myoblasts, or virus-infected
cells. Here, we investigated the role of these tetraspanins in the fusion of mononuclear …

[HTML][HTML] Lipocalin-type prostaglandin D synthase (β-trace) is a newly recognized type of retinoid transporter

T Tanaka, Y Urade, H Kimura, N Eguchi… - Journal of Biological …, 1997 - ASBMB
Lipocalin-type prostaglandin D synthase is responsible for the biosynthesis of prostaglandin
D 2 in the central nervous system and the genital organs and is secreted into the …

Effects of a 12-month multicomponent exercise program on physical performance, daily physical activity, and quality of life in very elderly people with minor disabilities …

N Taguchi, Y Higaki, S Inoue, H Kimura… - Journal of …, 2010 - jstage.jst.go.jp
Background: Although studies suggest that exercise training improves physical performance
and health-related quality of life (HRQOL) among elderly people, most of these studies …

Gefitinib in patients with brain metastases from non–small-cell lung cancer: review of 15 clinical cases

…, S Kawamura, T Iwasaki, Y Takeda, H Kimura… - Clinical lung cancer, 2004 - Elsevier
The clinical efficacy of gefitinib, a tyrosine kinase inhibitor of epidermal growth factor
receptor (EGFR), on brain metastases (BMs) from non–small-cell lung cancer (NSCLC) was …

Phenotype Variability in Patients Carrying KCNJ2 Mutations

H Kimura, J Zhou, M Kawamura, H Itoh… - Circulation …, 2012 - Am Heart Assoc
Background— Mutations of KCNJ2, the gene encoding the human inward rectifier potassium
channel Kir2.1, cause Andersen-Tawil syndrome (ATS), a disease exhibiting ventricular …

Exon 3 deletion of RYR2 encoding cardiac ryanodine receptor is associated with left ventricular non-compaction

S Ohno, M Omura, M Kawamura, H Kimura, H Itoh… - Europace, 2014 - academic.oup.com
Aims Ryanodine receptor gene (RYR2) mutations are well known to cause catecholaminergic
polymorphic ventricular tachycardia (CPVT). Recently, RYR2 exon 3 deletion has been …

Long QT syndrome type 8: novel CACNA1C mutations causing QT prolongation and variant phenotypes

…, S Ohno, WG Ding, F Toyoda, H Itoh, H Kimura… - Europace, 2014 - academic.oup.com
Aims CACNA1C mutations have been reported to cause LQTS type 8 (LQT8; Timothy
syndrome), which exhibits severe phenotypes, although the frequency of patients with LQT8 …

[HTML][HTML] Rapid differentiation of human pluripotent stem cells into functional neurons by mRNAs encoding transcription factors

…, S Wakabayashi, M Matsushita, M Sakota, H Kimura… - Scientific reports, 2017 - nature.com
Efficient differentiation of human pluripotent stem cells (hPSCs) into neurons is paramount
for disease modeling, drug screening, and cell transplantation therapy in regenerative …

Expression of tetraspanins in human lung cancer cells: frequent downregulation of CD9 and its contribution to cell motility in small cell lung cancer

T Funakoshi, I Tachibana, Y Hoshida, H Kimura… - Oncogene, 2003 - nature.com
Small cell lung cancer (SCLC) invades locally and metastasizes distantly extremely early
when compared with nonsmall cell lung cancer (NSCLC). The underlying molecular …

Genetic background of catecholaminergic polymorphic ventricular tachycardia in Japan

…, K Dochi, Q Wang, K Hasegawa, H Kimura… - Circulation …, 2013 - jstage.jst.go.jp
Background: The genetic background of catecholaminergic polymorphic ventricular tachycardia
(CPVT) has been extensively investigated for the last decade in Western countries, but it …