Mikiharu Yoshida
Overview
Explore the profile of Mikiharu Yoshida including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
6
Citations
617
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Sekiguchi M, Zushida K, Yoshida M, Maekawa M, Kamichi S, Yoshida M, et al.
Brain
. 2008 Oct;
132(Pt 1):124-35.
PMID: 18927146
Duchenne muscular dystrophy (DMD) is accompanied by cognitive deficits and psychiatric symptoms. In the brain, dystrophin, the protein responsible for DMD, is localized to a subset of GABAergic synapses, but...
2.
3-Mercaptopyruvate sulfurtransferase produces hydrogen sulfide and bound sulfane sulfur in the brain
Shibuya N, Tanaka M, Yoshida M, Ogasawara Y, Togawa T, Ishii K, et al.
Antioxid Redox Signal
. 2008 Oct;
11(4):703-14.
PMID: 18855522
Hydrogen sulfide (H(2)S) is a synaptic modulator as well as a neuroprotectant. Currently, pyridoxal-5'-phosphate (PLP)-dependent cystathionine beta-synthase (CBS) is thought to be the major H(2)S-producing enzyme in the brain. We...
3.
Ampong B, Imamura M, Matsumiya T, Yoshida M, Takeda S
Acta Myol
. 2006 Mar;
24(2):134-44.
PMID: 16550931
Mutations in the dysferlin gene underlie two phenotypically distinct muscular dystrophies: Miyoshi myopathy and limb-girdle muscular dystrophy 2B. Dysferlin was proposed to have a putative functional role in mediating the...
4.
Ozawa E, Mizuno Y, Hagiwara Y, Sasaoka T, Yoshida M
Muscle Nerve
. 2005 Jun;
32(5):563-76.
PMID: 15937871
The original sarcoglycan (SG) complex has four subunits and comprises a subcomplex of the dystrophin-dystrophin-associated protein complex. Each SG gene has been shown to be responsible for limb-girdle muscular dystrophy,...
5.
Ishikawa-Sakurai M, Yoshida M, Imamura M, Davies K, Ozawa E
Hum Mol Genet
. 2004 Feb;
13(7):693-702.
PMID: 14962982
An intracellular protein, dystrophin, plays an important role in keeping muscle fibers intact by binding at its N-terminal end to the subsarcolemmal cytoskeletal actin network and via its C-terminal end...
6.
Sasaoka T, Imamura M, Araishi K, Noguchi S, Mizuno Y, Takagoshi N, et al.
Neuromuscul Disord
. 2003 Mar;
13(3):193-206.
PMID: 12609501
While calf muscle hypertrophy is a striking diagnostic finding in sarcoglycanopathy, as it is in Duchenne and Becker muscular dystrophies, its pathogenetic mechanism remains unknown. gamma-Sarcoglycan, one of the subunits...