Hisakazu Ogita
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Explore the profile of Hisakazu Ogita including associated specialties, affiliations and a list of published articles.
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91
Citations
2206
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Recent Articles
11.
Komeno M, Pang X, Shimizu A, Molla M, Yasuda-Yamahara M, Kume S, et al.
J Biol Chem
. 2021 May;
296:100761.
PMID: 33971198
Diabetes mellitus (DM) causes injury to tissues and organs, including to the heart and kidney, resulting in increased morbidity and mortality. Thus, novel potential therapeutics are continuously required to minimize...
12.
Rahman N, Sato A, Tsevelnorov K, Shimizu A, Komeno M, Ahmat Amin M, et al.
Cancer Res
. 2021 Mar;
81(9):2318-2331.
PMID: 33757977
The growth and progression of cancers are crucially regulated by the tumor microenvironment where tumor cells and stromal cells are mutually associated. In this study, we found that stomatin expression...
13.
Suzuki T, Ogita H, Sato A, Minamidate N, Hachiro K
Int Heart J
. 2021 Mar;
62(2):390-395.
PMID: 33731531
Perivascular adipose tissue (PVAT) secretes large amounts of inflammatory mediators and plays a certain role in atherosclerosis formation from the exterior of the vessel. In the present study, we examined...
14.
Tomita I, Kume S, Sugahara S, Osawa N, Yamahara K, Yasuda-Yamahara M, et al.
Cell Metab
. 2020 Jul;
32(3):404-419.e6.
PMID: 32726607
SGLT2 inhibitors offer strong renoprotection in subjects with diabetic kidney disease (DKD). But the mechanism for such protection is not clear. Here, we report that in damaged proximal tubules of...
15.
Shimizu A, Zankov D, Sato A, Komeno M, Toyoda F, Yamazaki S, et al.
FASEB J
. 2020 Mar;
34(5):6399-6417.
PMID: 32175648
Brugada syndrome (BrS) is an inherited channelopathy responsible for almost 20% of sudden cardiac deaths in patients with nonstructural cardiac diseases. Approximately 70% of BrS patients, the causative gene mutation(s)...
16.
Matsushima S, Shimizu A, Kondo M, Asano H, Ueno N, Nakayama H, et al.
Sci Rep
. 2020 Jan;
10(1):188.
PMID: 31932617
Anosmin-1 is a secreted glycoprotein encoded by the ANOS1 gene, and its loss of function causes Kallmann syndrome (KS), which is characterized by anosmia and hypogonadism due to olfactory bulb...
17.
Ahmat Amin M, Shimizu A, Ogita H
Cancers (Basel)
. 2019 Oct;
11(11).
PMID: 31652725
The members of the family of epithelial membrane proteins (EMPs), EMP1, EMP2, and EMP3, possess four putative transmembrane domain structures and are composed of approximately 160 amino acid residues. EMPs...
18.
Yamada N, Asano Y, Fujita M, Yamazaki S, Inanobe A, Matsuura N, et al.
Circulation
. 2019 Feb;
139(18):2157-2169.
PMID: 30764634
Background: Bradyarrhythmia is a common clinical manifestation. Although the majority of cases are acquired, genetic analysis of families with bradyarrhythmia has identified a growing number of causative gene mutations. Because...
19.
Katagiri S, Iwasa M, Hayashi T, Hosono K, Yamashita T, Kuniyoshi K, et al.
Sci Rep
. 2018 Aug;
8(1):11507.
PMID: 30065301
Blue cone monochromacy (BCM) is characterized by loss of function of both OPN1LW (the first) and OPN1MW (the downstream) genes on the X chromosome. The purpose of this study was...
20.
Ahmat Amin M, Shimizu A, Zankov D, Sato A, Kurita S, Ito M, et al.
Oncogene
. 2018 Jun;
37(40):5416-5434.
PMID: 29867202
Tumor metastasis is the most common cause of cancer death. Elucidation of the mechanism of tumor metastasis is therefore important in the development of novel, effective anti-cancer therapies to reduce...