Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Sanae Oda"'
Autor:
Ryo Suzuki, Daiki Omata, Yusuke Oda, Mutsumi Sugii, Hitoshi Uruga, Johan Unga, Yoichi Negishi, Sanae Oda, Kazuo Maruyama
Publikováno v:
Asian Journal of Pharmaceutical Sciences, Vol 11, Iss 1, Pp 162-163 (2016)
Externí odkaz:
https://doaj.org/article/a986bd0ff10849c5967468ab9bad2022
Autor:
Sanae Oda-Sheehan
Based on her professional and personal experiences in education as well as in business, Sanae Oda-Sheehan (PhD) came to realize that there may be several problematic gaps hindering learning effectiveness in the Japanese EFL context. In exploring poss
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e83584122a006163485b82956dc85978
https://doi.org/10.47908/21
https://doi.org/10.47908/21
Publikováno v:
Journal of Human Genetics. 49:548-557
TEX28 gene (fTEX) is present immediately downstream of the red/green visual pigment gene array on the human X chromosome. Its pseudogene (pTEX) that lacks exon 1 is present within the array between pigment genes. We found that both fTEX and pTEX gene
Autor:
Sanae Oda, Shinichi Yamade, Yoshiko Aoki, Yasuhiro Nishida, Jiro Nakamura, Kazutaka Kani, Osamu Hayashi
Publikováno v:
American Journal of Ophthalmology. 136:482-489
Purpose To investigate extraocular muscle (EOM) path shift and prolapse of posterior eyeball from muscle cone in acquired esotropia with high myopia (AEHM), using magnetic resonance imaging. Design A case-control study. Methods There were 16 eyes wit
Publikováno v:
Vision Research. 43(5):489-495
The L-cone/M-cone visual pigment gene arrays were analyzed in a group of 63 Japanese females consisting of 7 applicants for examination of their carrier status, 14 color-deficient females, 6 obligate carriers with no genotypic data available for affe
Detection of female carriers of congenital color-vision deficiencies by visual pigment gene analysis
Publikováno v:
Current Eye Research. 21:767-773
Congenital color-vision deficiencies are frequent among males, 4.7-8.0%, suggesting that female carriers are present at a frequency of 9-15%. The purpose of this study was to determine whether carriers could be detected by analysis of the visual pigm
Autor:
Yoshinori Shichida, Yasuhiro Nishida, Hisao Ueyama, Shinichi Yamade, Sanae Oda, Shigeki Kuwayama, Shoko Tanabe, Hiroo Imai
Publikováno v:
Vision research. 44(19)
The L-cone/M-cone visual pigment gene arrays were analyzed in 125 Japanese males with protan color-vision deficiency. Arrays were successfully determined in 62/65 subjects with protanopia and 57/60 protanomaly subjects. Among the 62 protanopia subjec
Autor:
Tatsuya Iwami, Kazutaka Kani, Akihiro Inatomi, Osamu Hayashi, Jiro Nakamura, Yoshiko Aoki, Sanae Oda, Yasuhiro Nishida
Publikováno v:
Japanese journal of ophthalmology. 47(3)
Purpose: To review the results of a muscle transposition procedure in which the halves of the vertical rectus muscle bellies are sutured onto the sclera, without tenotomy of vertical recti as in Hummelsheim's procedure or surgical treatment of the la
Autor:
Shoko Tanabe, Yao-Hua Li, Iwao Ohkubo, Gui-Lian Fu, Shinichi Yamade, La-ongsri Atchaneeyasakul, Yasuhiro Nishida, Hisao Ueyama, Patcharee Lertrit, Sanae Oda
We studied 247 Japanese males with congenital deutan color-vision deficiency and found that 37 subjects (15.0%) had a normal genotype of a single red gene followed by a green gene(s). Two of them had missense mutations in the green gene(s), but the o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d5ee9e9d58008334ad36f71ece84e62
https://europepmc.org/articles/PMC152297/
https://europepmc.org/articles/PMC152297/
Autor:
Shinichi Yamade, Hiroo Imai, Yoshinori Shichida, Shoko Tanabe, Shigeki Kuwayama, Sanae Oda, Yasuhiro Nishida, Hisao Ueyama, Akimori Wada
Publikováno v:
Biochemical and biophysical research communications. 294(2)
The DNAs from 217 Japanese males with congenital red/green color-vision deficiencies were analyzed. Twenty-three subjects had the normal genotype of a single red gene, followed by a green gene. Four of the 23 were from the 69 protan subject group and