Y Okamura-Oho
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Explore the profile of Y Okamura-Oho including associated specialties, affiliations and a list of published articles.
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15
Citations
1983
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0
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Recent Articles
1.
Carninci P, Kasukawa T, Katayama S, Gough J, Frith M, Maeda N, et al.
Science
. 2005 Sep;
309(5740):1559-63.
PMID: 16141072
This study describes comprehensive polling of transcription start and termination sites and analysis of previously unidentified full-length complementary DNAs derived from the mouse genome. We identify the 5' and 3'...
2.
Okamura-Oho Y, Miyashita T, Yamada M
Biochem Biophys Res Commun
. 2001 Dec;
289(5):957-60.
PMID: 11741283
An insulin-receptor substrate of 53-kDa protein (IRSp53) is an adapter protein, which interacts with the Rho-family of GTPases and mediates neurite outgrowth. It also binds to DRPLA protein, a product...
3.
U M, Miyashita T, Ohtsuka Y, Okamura-Oho Y, Shikama Y, Yamada M
Cell Death Differ
. 2001 Sep;
8(4):377-86.
PMID: 11550089
A growing number of inherited neurodegenerative disorders, including Huntington's disease, have been shown to be caused by the expansion of CAG/polyglutamine repeats. The molecular mechanism underlying these disorders, however, has...
4.
Yanagisawa H, Bundo M, Miyashita T, Okamura-Oho Y, Tadokoro K, Tokunaga K, et al.
Hum Mol Genet
. 2000 May;
9(9):1433-42.
PMID: 10814707
Dentatorubral-pallidoluysian atrophy (DRPLA) is one of the hereditary neurodegenerative disorders caused by expansion of CAG/glutamine repeats. To investigate the normal function of the DRPLA gene and the pathogenic mechanism of...
5.
Okamura-Oho Y, Miyashita T, Ohmi K, Yamada M
Hum Mol Genet
. 1999 May;
8(6):947-57.
PMID: 10332026
Dentatorubral-pallidoluysian atrophy (DRPLA) is an autosomal dominant neuro degrees enerative disorder associated with CAG/glutamine repeat expansion. While the DRPLA gene is ubiquitously expressed, neuron death occurs in specific anatomical areas...
6.
Miyashita T, Matsui J, Ohtsuka Y, Mami U, Fujishima S, Okamura-Oho Y, et al.
Biochem Biophys Res Commun
. 1999 Apr;
257(3):724-30.
PMID: 10208851
To date, eight neurodegenerative disorders, including Huntington's disease and dentatorubral-pallidoluysian atrophy, have been identified to be caused by expansion of a CAG repeat coding for a polyglutamine (polyQ) stretch. It...
7.
Miyashita T, Nagao K, Ohmi K, Yanagisawa H, Okamura-Oho Y, Yamada M
Biochem Biophys Res Commun
. 1998 Aug;
249(1):96-102.
PMID: 9705838
Dentatorubral-pallidoluysian atrophy (DRPLA) is an autosomal dominant neurodegenerative disorder caused by the abnormal CAG triplet-repeat expansion resulting in an elongated polyglutamine (polyQ) stretch. We have recently showed that the DRPLA...
8.
Okamura-Oho Y, Zhang S, Callahan J, Murata M, Oshima A, Suzuki Y
FEBS Lett
. 1998 Jan;
419(2-3):231-4.
PMID: 9428640
Lysosomal beta-galactosidase precursor is processed to a mature form and associated with protective protein in lysosomes. In this study we used two cysteine protease proinhibitors, E64-d for cathepsins B, S,...
9.
Miyashita T, Okamura-Oho Y, Mito Y, Nagafuchi S, Yamada M
J Biol Chem
. 1997 Nov;
272(46):29238-42.
PMID: 9361003
Dentatorubral pallidoluysian atrophy (DRPLA) is an autosomal dominant neurodegenerative disorder. It is associated with an abnormal CAG repeat expansion resulting in formation of a protein with an elongated polyglutamine stretch....
10.
Okamura-Oho Y, Zhang S, Hilson W, Hinek A, Callahan J
Biochem J
. 1996 Feb;
313 ( Pt 3):787-94.
PMID: 8611156
Processing of human beta-galactosidase (beta-GAL) was studied in permanently transfected Chinese hamster ovary (CHO) cells and compared with that in normal cells and in cells from subjects with GM1-gangliosidosis, galactosialidosis...