His scientific interests lie mostly in Biochemistry, Molecular biology, Calpain, Cell biology and Skeletal muscle. The concepts of his Biochemistry study are interwoven with issues in P3 peptide and Amyloid precursor protein. His work deals with themes such as Immunostaining, Complementary DNA, Messenger RNA, COS cells and ITGA7, which intersect with Molecular biology.
Shoichi Ishiura combines subjects such as Cysteine protease, Protein subunit, Autolysis, Peptide sequence and Binding site with his study of Calpain. His Cell biology research incorporates themes from Proteolysis, Mutant, Immunoprecipitation and Transmembrane protein. His Skeletal muscle research is multidisciplinary, incorporating perspectives in Myocyte and Duchenne muscular dystrophy.
His main research concerns Biochemistry, Molecular biology, Cell biology, Amyloid precursor protein and Skeletal muscle. Enzyme, Protease, Proteases, Proteolysis and Intracellular are among the areas of Biochemistry where Shoichi Ishiura concentrates his study. The various areas that Shoichi Ishiura examines in his Molecular biology study include Protein subunit, Complementary DNA, Calpain, COS cells and Myotonic dystrophy.
His research in Calpain intersects with topics in Peptide sequence and Calcium. Cell biology is often connected to Cleavage in his work. His Amyloid precursor protein study combines topics from a wide range of disciplines, such as Peptide and Senile plaques.
His primary areas of study are Molecular biology, Cell biology, Genetics, Alternative splicing and Biochemistry. His studies deal with areas such as Protein subunit, HEK 293 cells, Enhancer, Presenilin and splice as well as Molecular biology. His Cell biology research includes elements of Oxidative stress, Internal medicine, Dopamine, Endocrinology and Programmed cell death.
His work on Gene, Variable number tandem repeat, genomic DNA and Intron as part of general Genetics study is frequently linked to Benign adult familial myoclonic epilepsy, therefore connecting diverse disciplines of science. His research on Alternative splicing also deals with topics like
Shoichi Ishiura mostly deals with Molecular biology, Gene, Genetics, Cell biology and Intron. By researching both Molecular biology and Small nuclear RNA, Shoichi Ishiura produces research that crosses academic boundaries. His studies in Gene integrate themes in fields like Myotonic dystrophy and Epilepsy.
When carried out as part of a general Genetics research project, his work on Cell cycle, Cell division and Cell cycle checkpoint is frequently linked to work in Topoisomerase inhibitor, therefore connecting diverse disciplines of study. His Cell biology research is multidisciplinary, incorporating perspectives in Endocrinology, Internal medicine and Metabolism. His Intron research is multidisciplinary, incorporating elements of genomic DNA, DNA Repeat Expansion, Trinucleotide repeat expansion and Sequence analysis.
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Structure and physiological function of calpains
Hiroyuki Sorimachi;Shoichi Ishiura;Koichi Suzuki.
Biochemical Journal (1997)
Immunostaining of skeletal and cardiac muscle surface membrane with antibody against Duchenne muscular dystrophy peptide.
K Arahata;S Ishiura;T Ishiguro;T Tsukahara.
The VNTR polymorphism of the human dopamine transporter (DAT1) gene affects gene expression.
S Fuke;S Suo;N Takahashi;H Koike.
Pharmacogenomics Journal (2001)
Muscle-specific Calpain, p94, Responsible for Limb Girdle Muscular Dystrophy Type 2A, Associates with Connectin through IS2, a p94-specific Sequence
Hiroyuki Sorimachi;Kayoko Kinbara;Sumiko Kimura;Miwako Takahashi.
Journal of Biological Chemistry (1995)
Membrane-anchored metalloprotease MDC9 has an alpha-secretase activity responsible for processing the amyloid precursor protein.
Hisashi Koike;Shigeo Tomioka;Hiroyuki Sorimachi;Takaomi C. Saido.
Biochemical Journal (1999)
Putative function of ADAM9, ADAM10, and ADAM17 as APP -secretase
Masashi Asai;Chinatsu Hattori;Beáta Szabó;Noboru Sasagawa.
Biochemical and Biophysical Research Communications (2003)
Familial distal myopathy with rimmed vacuole and lamellar (myeloid) body formation.
Ikuya Nonaka;Nobuhiko Sunohara;Shoichi Ishiura;Eijiro Satoyoshi.
Journal of the Neurological Sciences (1981)
Muscle-specific calpain, p94, is degraded by autolysis immediately after translation, resulting in disappearance from muscle.
H. Sorimachi;N. Toyama-Sorimachi;T. C. Saido;H. Kawasaki.
Journal of Biological Chemistry (1993)
Studies of a calcium-activated neutral protease from chicken skeletal muscle. I. Purification and characterization.
Shoichi Ishiura;Hiromu Murofushi;Koichi Suzuki;Kazutomo Imahori.
Journal of Biochemistry (1978)
Calpain: novel family members, activation, and physiologic function.
K Suzuki;H Sorimachi;T Yoshizawa;K Kinbara.
Biological chemistry Hoppe-Seyler (1995)
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