Masako Yoshida
Overview
Explore the profile of Masako Yoshida including associated specialties, affiliations and a list of published articles.
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Articles
7
Citations
81
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Recent Articles
1.
Yoshida M, Seiyama A
PLoS One
. 2022 Dec;
17(12):e0278682.
PMID: 36516162
The causes of reading difficulties in people with peripheral visual field loss are not fully understood. We conducted a two-dimensional gaze analysis on eye movements during reading in patients with...
2.
Yoshida M, Origuchi M, Urayama S, Takatsuki A, Kan S, Aso T, et al.
Neuroimage Clin
. 2014 Jul;
5:161-8.
PMID: 25068106
To evaluate changes in the visual processing of patients with progressive retinitis pigmentosa (RP) who acquired improved reading capability by eye-movement training (EMT), we performed functional magnetic resonance imaging (fMRI)...
3.
Wada Y, Harayama Y, Kamimura D, Yoshida M, Shibata T, Fujiwara K, et al.
Org Biomol Chem
. 2011 May;
9(13):4959-76.
PMID: 21597627
Various analogues of the marine alkaloids, discorhabdins, have been synthesized. The strategy contains spirocyclization with phenyliodine(III) bis(trifluoroacetate) (PIFA), oxidative fragmentation of the β-amino alcohols with the hypervalent iodine reagent C(6)F(5)I(OCOCF(3))(2),...
4.
Wada Y, Otani K, Endo N, Harayama Y, Kamimura D, Yoshida M, et al.
Org Lett
. 2009 Aug;
11(18):4048-50.
PMID: 19678676
Discorhabdin A (1) exhibits a strong cytotoxic activity in vitro, but it is difficult to synthesize and handle due to the instability of its highly strained N,S-acetal structure. We then...
5.
Harayama Y, Yoshida M, Kamimura D, Wada Y, Kita Y
Chemistry
. 2006 Apr;
12(18):4893-9.
PMID: 16604566
Hypervalent iodine(III) reagents are readily available, easy to handle, and have a low toxicity and similar reactivities to those of heavy metal reagents, and hence they are used for various...
6.
Harayama Y, Yoshida M, Kamimura D, Kita Y
Chem Commun (Camb)
. 2005 Mar;
(13):1764-6.
PMID: 15791325
The use of hypervalent iodine(III) reagents allowed us to develop the novel and efficient direct synthesis of N,O-acetal compounds via the oxidative fragmentation reaction of alpha-amino acids or alpha-amino alcohols;...
7.
Yoshida M, Xia Y
J Biol Chem
. 2003 Jul;
278(38):36953-8.
PMID: 12855682
Nitric oxide (NO) generated by inducible NO synthase (iNOS) plays crucial roles in inflammation and host defense. With an intrinsically bound calmodulin, iNOS is fully active once expressed in cells....