Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Hisao Ueyama"'
Autor:
Satoshi Katagiri, Maki Iwasa, Takaaki Hayashi, Katsuhiro Hosono, Takahiro Yamashita, Kazuki Kuniyoshi, Shinji Ueno, Mineo Kondo, Hisao Ueyama, Hisakazu Ogita, Yoshinori Shichida, Hidehito Inagaki, Hiroki Kurahashi, Hiroyuki Kondo, Masahito Ohji, Yoshihiro Hotta, Tadashi Nakano
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-10 (2018)
Abstract Blue cone monochromacy (BCM) is characterized by loss of function of both OPN1LW (the first) and OPN1MW (the downstream) genes on the X chromosome. The purpose of this study was to investigate the first and downstream genes in the OPN1LW/OPN
Externí odkaz:
https://doaj.org/article/d2b4e4b53c8d4f56bc9d219b8c1394a3
Autor:
Hisakazu Ogita, Kazushige Tsunoda, Futoshi Toyoda, Masahito Ohji, Akira Nakao, Kazuki Kuniyoshi, Hiroyuki Sakuramoto, Takeshi Iwata, Shuji Yamamoto, Yoshikazu Shimomura, Sanae Muraki-Oda, Hisao Ueyama, Motohiro Irifune
Publikováno v:
Japanese Journal of Ophthalmology. 60:187-197
To present the characteristics and pathology of a patient with congenital achromatopsia. The patient was a 22-year-old Japanese woman who was 8 years old when she first visited our clinic. Comprehensive ophthalmic examinations including visual acuity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e57b45a474a725d9260f2c979b11d297
https://doi.org/10.1007/s10384-016-0424-6
https://doi.org/10.1007/s10384-016-0424-6
Autor:
Hisao Ueyama1 datt@belle.shiga-med.ad.jp, Sanae Muraki2, Shoko Tanabe3, Shinichi Yamade2, Hisakazu Ogita1
Publikováno v:
Journal of Biochemistry. Sep2015, Vol. 158 Issue 3, p197-204. 8p.
Autor:
Tadashi Nakano, Hidehito Inagaki, Kazuki Kuniyoshi, Hiroki Kurahashi, Takahiro Yamashita, Masahito Ohji, Maki Iwasa, Hisakazu Ogita, Katsuhiro Hosono, Hisao Ueyama, Yoshihiro Hotta, Satoshi Katagiri, Hiroyuki Kondo, Takaaki Hayashi, Yoshinori Shichida, Mineo Kondo, Shinji Ueno
Publikováno v:
Scientific Reports
Scientific Reports, Vol 8, Iss 1, Pp 1-10 (2018)
Scientific Reports, Vol 8, Iss 1, Pp 1-10 (2018)
Blue cone monochromacy (BCM) is characterized by loss of function of both OPN1LW (the first) and OPN1MW (the downstream) genes on the X chromosome. The purpose of this study was to investigate the first and downstream genes in the OPN1LW/OPN1MW array
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e58e67b326e474fe946cc0aa531f1906
http://hdl.handle.net/2433/235730
http://hdl.handle.net/2433/235730
Novel mutations in the L visual pigment gene found in Japanese men with protan color-vision defect having a normal order L/M gene array
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::584c1afa881b7c3d2caecfab38c0b7ad
Autor:
Sanae Muraki-Oda, Hisao Ueyama, Shoko Tanabe, Shinichi Yamade, Hisakazu Ogita, Takahiro Yamashita, Yoshinori Shichida
Publikováno v:
Biochemical and Biophysical Research Communications. 424:152-157
We have analyzed L/M visual pigment gene arrays in 119 Japanese men with protanopia color vision defect and found that five had a normal gene order of L-M. Among the five men, two (identified as A376 and A642) had apparently normal L genes. To clarif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0eaae93036b86b85b88b4dfe95123bd8
https://doi.org/10.1016/j.bbrc.2012.06.094
https://doi.org/10.1016/j.bbrc.2012.06.094
Publikováno v:
Journal of Molecular and Cellular Cardiology. 50:58-65
Lysophosphatidylcholine (LPC) is a bioactive phospholipid that accumulates rapidly in the ischemic myocardium. In recent years, it has been shown that some of the actions of LPC are mediated through the activation of the membrane G proteins. However,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f10f1ec97558d21f20374d3c8b86411c
https://doi.org/10.1016/j.yjmcc.2010.10.006
https://doi.org/10.1016/j.yjmcc.2010.10.006
Autor:
Suguru Shioji, Eiji Isoya, Yoshitaka Matsusue, Shinji Imai, Hisao Ueyama, Tomohiro Mimura, Mitsuhiko Kubo, Kosei Ando
Publikováno v:
Acta Orthopaedica
Background and purpose Three-dimensionally (3D-) embedded chondrocytes have been suggested to maintain the chondrocytic phenotype. Furthermore, mechanical stress and growth factors have been found to be capable of enhancing cell proliferation and ECM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::baf1a36dbf21a4aeb250e7d81a124a1e
https://doi.org/10.3109/17453670903413111
https://doi.org/10.3109/17453670903413111
Autor:
Toru Kita, Keiko Tsuji, Takeru Makiyama, Hidetada Yoshida, Kazuhiko Obayashi, Hiroshi Matsuura, Shiro Kamakura, Wataru Shimizu, Futoshi Toyoda, Toshihiro Honda, Minoru Horie, Hisao Ueyama, Yoshihiro Miyamoto, Dimitar P. Zankov, Seiko Ohno
Publikováno v:
Human Mutation. 30:557-563
Long QT syndrome (LQTS) is an inherited disease involving mutations in the genes encoding a number of cardiac ion channels and a membrane adaptor protein. Among the genes that are responsible for LQTS, KCNE1 and KCNE2 are members of the KCNE family o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::478fdee2866b14ba9ded8324d1859f2c
https://doi.org/10.1002/humu.20834
https://doi.org/10.1002/humu.20834
Publikováno v:
Journal of Human Genetics. 51:686-694
Normal visual pigment gene arrays on the human X chromosome have a red gene at the first and a green gene at the second positions. More than half of the arrays have additional green genes downstream, but only the first two genes of the array are like
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58b0f26b89022a4253c52acfc775db03
https://doi.org/10.1007/s10038-006-0008-2
https://doi.org/10.1007/s10038-006-0008-2