Zobrazeno 1 - 10
of 694
pro vyhledávání: '"S. Ishiura"'
Publikováno v:
Materials Science Forum. :1920-1924
Amorphous alloys have many superior properties such as high tensile strength,anticorrosion and easy soft-magnetism, but few amorphous alloys have been used as final productsbecause they lack plasticity at room temperature. Thus, we have developed a n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf9297ca1d20ea735e3f593d91aa678d
https://doi.org/10.4028/www.scientific.net/msf.783-786.1920
https://doi.org/10.4028/www.scientific.net/msf.783-786.1920
Autor:
H, Koike, Z, Kouchi, T, Kinouchi, T, Maeda, H, Sorimachi, T C, Saido, K, Maruyama, A, Okuyama, K, Suzuki, S, Ishiura
Publikováno v:
Cytotechnology. 33(1-3)
Thimet oligopeptidase (TOP) is a thiol- andmetallo-dependent peptidase and has been shown to beone of the beta-secretase candidates. TOPexpressed in COS cells cleaved amyloid precursorprotein (APP) at the beta-secretase site, and wefound a proteolyti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fc778901aaf4f36039c917c2a7e2d523
https://pubmed.ncbi.nlm.nih.gov/19002828
https://pubmed.ncbi.nlm.nih.gov/19002828
Publikováno v:
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology. 24(2)
Myotonic Dystrophy (DM), the most common form of adult-onset muscular dystrophy, comprises at least 2 subtypes, DM1 and DM2. DM1 is caused by the expansion of a CTG repeat located in the 3' untranslated region of the DM protein kinase (DMPK) gene. Re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::12eb7575e501d01ea478940068646d34
https://pubmed.ncbi.nlm.nih.gov/16550919
https://pubmed.ncbi.nlm.nih.gov/16550919
Autor:
S, Ishiura
Publikováno v:
Nihon shinkei seishin yakurigaku zasshi = Japanese journal of psychopharmacology. 19(5)
The neurotransmitter serotonin is known to play a key role in determining emotional state in higher animals, especially in humans. Pharmacological studies have highlighted a subset of serotonin receptor subtypes (1A, 2B and 2C) worthy of knockout ana
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::85d4e55adf823f9e2f849e6fbcad6d23
https://pubmed.ncbi.nlm.nih.gov/10803209
https://pubmed.ncbi.nlm.nih.gov/10803209
Autor:
N, Takahashi, S, Ishiura
Publikováno v:
Nihon rinsho. Japanese journal of clinical medicine. 57(4)
Although the expansion of an unstable CTG repeat is known to be responsible for myotonic dystrophy (DM), the mechanism by which this genetic defect induces the disease has not yet been elucidated. In patients with DM, low expression of total DM prote
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0eafa8930105cca510b35a7fe5d8d5f6
https://pubmed.ncbi.nlm.nih.gov/10222792
https://pubmed.ncbi.nlm.nih.gov/10222792
Publikováno v:
Biochemical pharmacology. 56(4)
Recent studies indicate that calpain, a cytosolic Ca2+-dependent protease, constitutes a large family comprising ubiquitous, tissue-specific, and atypical calpains. p94 is a homologue of the catalytic large subunit of calpain, expressed predominantly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bb368da4fe2d3458c8f3f47d6c1392a9
https://pubmed.ncbi.nlm.nih.gov/9763216
https://pubmed.ncbi.nlm.nih.gov/9763216
Autor:
H, Ueda, N, Kameda, T, Baba, N, Terada, M, Shimokawa, M, Yamamoto, S, Ishiura, T, Kobayashi, S, Ohno
Publikováno v:
The Histochemical journal. 30(4)
The subcellular localization of myotonic dystrophy protein kinase has been examined in human cardiac muscles with confocal laser-scanning microscopy and electron microscopy. A polyclonal antibody was produced against the synthesized peptide from a hu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ad27d6488f9451527e263e945d7a0b5b
https://pubmed.ncbi.nlm.nih.gov/9610815
https://pubmed.ncbi.nlm.nih.gov/9610815
Autor:
S, Ishiura
Publikováno v:
Nihon rinsho. Japanese journal of clinical medicine. 55(12)
The mutation underlying myotonic dystrophy is the expansion of polymorphic CTG repeat in the 3'-noncoding region of the myotonin protein kinase (MtPK) gene mapping to chromosome 19q13.3. A full-length cDNA of human MtPK was cloned and expressed in CO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7abee528c88543b7a8c4a4e60342d194
https://pubmed.ncbi.nlm.nih.gov/9436436
https://pubmed.ncbi.nlm.nih.gov/9436436
Publikováno v:
Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme. 42
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6a88f7ca9bdd32db0ccb521c76fb8c6b
https://pubmed.ncbi.nlm.nih.gov/9366193
https://pubmed.ncbi.nlm.nih.gov/9366193
Autor:
M, Shimokawa, S, Ishiura, N, Kameda, M, Yamamoto, N, Sasagawa, N, Saitoh, H, Sorimachi, H, Ueda, S, Ohno, K, Suzuki, T, Kobayashi
Publikováno v:
The American journal of pathology. 150(4)
It is quite important to know the exact localization and function of myotonin protein kinase (MtPK), identified as the gene product of myotonic dystrophy, the most prevalent disease with multisystem disorders among muscular dystrophies. To investigat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::afa5b53846ebcd1483069fef8108346f
https://pubmed.ncbi.nlm.nih.gov/9094985
https://pubmed.ncbi.nlm.nih.gov/9094985