Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Shinichi Yamade"'
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 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
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f72393f9b27ed27c70763daed395cef
https://doi.org/10.1007/s10038-004-0189-5
https://doi.org/10.1007/s10038-004-0189-5
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1be15a5f7cf77ea5326c38228f05bc42
https://doi.org/10.1016/s0002-9394(03)00276-9
https://doi.org/10.1016/s0002-9394(03)00276-9
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cecfcaefa137052351919eae4111db9
Autor:
Kazumi Noguchi, Kiyono Miyazaki, Tomoko Ofuchi, Shinichi Yamade, Masue Noguchi, Taku Ito, Kazutaka Kani
Publikováno v:
JAPANESE ORTHOPTIC JOURNAL. 32:175-180
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9047c68b0d02c22c7116bf7d75abd74a
https://doi.org/10.4263/jorthoptic.32.175
https://doi.org/10.4263/jorthoptic.32.175
Publikováno v:
Journal of biochemistry. 158(3)
In 524 Japanese individuals with deutan colour vision defect, 76 had a normal-order pigment gene array, where the L gene is at the first position and the M gene(s) is located downstream. Of these 76 individuals, 69 had a -71A>C substitution in the M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23a2ea7e18b5693cfde50c0ebb34f572
https://pubmed.ncbi.nlm.nih.gov/25820227
https://pubmed.ncbi.nlm.nih.gov/25820227
Publikováno v:
Japanese Journal of Ophthalmology. 45:60-67
Purpose: We analyzed the red/green visual pigment genes in color-normal Japanese men to understand the relationship between color anomalies and genetic defects. Methods: DNA from 120 color-normal Japanese men was subjected to polymerase chain reactio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ecaa77aa5fed2c31bfcfb24894c641c
https://doi.org/10.1016/s0021-5155(00)00298-7
https://doi.org/10.1016/s0021-5155(00)00298-7
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8389f48b364c3b97e2ceaeaa5a112b3b
https://doi.org/10.1076/ceyr.21.4.767.5544
https://doi.org/10.1076/ceyr.21.4.767.5544