Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Masaji Tachikawa"'
Publikováno v:
Renal Replacement Therapy, Vol 8, Iss 1, Pp 1-5 (2022)
Abstract Background To prevent tunnel infection of indwelling catheters, impregnation with antiseptics or antibiotics is effective. However, 13 patients using chlorhexidine–silver sulfadiazine-impregnated catheters experienced serious anaphylactic
Externí odkaz:
https://doaj.org/article/05fd221944d540e5914cc5e75cdb0bb3
Autor:
Masaji Tachikawa, Hiroshi Yamaguchi, Hiroki Kurahashi, Kazumoto Iijima, Wataru Satake, Hisahide Nishio, Shuichi Tsuneishi, Yuya Ouchi, Naoya Morisada, Ichiro Morioka, Hidehito Inagaki, Yuichi Takami, Mariko Taniguchi-Ikeda, Tatsushi Toda, H. Wada, Kazuhiro Kobayashi, Kandai Nozu, Satoshi Takada, Hiroaki Nagase, Nobuhiko Okamoto
Publikováno v:
Clinical Genetics. 93:931-933
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::216adc8a550a2936f9289676cb0d3e34
https://doi.org/10.1111/cge.13106
https://doi.org/10.1111/cge.13106
Publikováno v:
Journal of Biological Chemistry. 287:8398-8406
Fukuyama-type congenital muscular dystrophy (FCMD), the second most common childhood muscular dystrophy in Japan, is caused by alterations in the fukutin gene. Mutations in fukutin cause abnormal glycosylation of α-dystroglycan, a cell surface lamin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8de27e494f75620f955e7dcb1f19b8b6
https://doi.org/10.1074/jbc.m111.300905
https://doi.org/10.1074/jbc.m111.300905
Autor:
Akemi Nishimoto, Zhongpeng Lu, Kazuhiro Kobayashi, Youichi Tajima, Fan Wang, Motoi Kanagawa, Fumi Tashiro, Shin'ichi Takeda, Nobuhiro Fujikake, Kevin P. Campbell, Tatsushi Toda, Yuko Miyagoe-Suzuki, Mariko Taniguchi, Yoshitaka Nagai, Tomohiro Chiyonobu, Tamao Endo, Jun-ichi Miyazaki, Masaji Tachikawa, Satoshi Takeda
Publikováno v:
Human Molecular Genetics
Hypoglycosylation and reduced laminin-binding activity of alpha-dystroglycan are common characteristics of dystroglycanopathy, which is a group of congenital and limb-girdle muscular dystrophies. Fukuyama-type congenital muscular dystrophy (FCMD), ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95bc4ca73c2e8620dacb3840dadf7e4c
https://doi.org/10.1093/hmg/ddn387
https://doi.org/10.1093/hmg/ddn387
Autor:
Motoi Kanagawa, Tamao Endo, Hui Xiong, Nobuhiro Fujikake, Hiroshi Manya, Masaji Tachikawa, Akemi Nishimoto, Fan Wang, Tatsushi Toda, Kazuhiro Kobayashi, Satoshi Takeda, Tomohiro Chiyonobu, Glenn E. Morris, Yoshitaka Nagai
Publikováno v:
Biochemical and Biophysical Research Communications. 350:935-941
The recent identification of mutations in genes encoding demonstrated or putative glycosyltransferases has revealed a novel mechanism for congenital muscular dystrophy. Hypoglycosylated alpha-dystroglycan (alpha-DG) is commonly seen in Fukuyama-type
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d98aa7a54cc76ae7e46ac743a678fc99
https://doi.org/10.1016/j.bbrc.2006.09.129
https://doi.org/10.1016/j.bbrc.2006.09.129
Autor:
Kazuhiro Kobayashi, Junko Sasaki, Kiyomi Taniguchi, Tamao Endo, Hiroki Kano, Hiroki Kurahashi, Fan Wang, Kiichiro Matsumura, Satoshi Takeda, Tatsushi Toda, Toshio Terashima, Mariko Taniguchi, Yoshitaka Nagai, Masaji Tachikawa, Yoshihide Sunada
Publikováno v:
Congenital Anomalies. 43:97-104
Fukuyama-type congenital muscular dystrophy (FCMD), Walker-Warburg syndrome (WWS), and muscle-eye-brain (MEB) disease are clinically similar autosomal recessive disorders characterized by congenital muscular dystrophy, lissencephaly, and eye anomalie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76d4878ff583daf1aa9910d1ad9f04a4
https://doi.org/10.1111/j.1741-4520.2003.tb01033.x
https://doi.org/10.1111/j.1741-4520.2003.tb01033.x
Autor:
Masaji Tachikawa, Tomoko Kuribayashi, Nao Morikawa, Masayo Ito, Asako G. Terasaki, Yousuke Hashimoto, Kazuyo Ohashi, Koji Oshima, Hajime Mori
Publikováno v:
Cell motility and the cytoskeleton. 61(4)
We determined the full cDNA sequences of chicken gizzard filamin and cgABP260 (chicken gizzard actin-binding protein 260). The primary and secondary structures predicted by these sequences were similar to those of chicken retina filamin and human fil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9c2890687196c7cc2874c6f82018fa4
https://pubmed.ncbi.nlm.nih.gov/15986405
https://pubmed.ncbi.nlm.nih.gov/15986405
Autor:
Toshifumi Tsukahara, Masaji Tachikawa, Ichizo Nishino, Rumi Kurokawa, Tatsushi Toda, Satoru Noguchi, Kiichi Arahata, Masako Fujita, Atsumi Tsujimoto
Publikováno v:
Human molecular genetics. 12(6)
We have developed a novel cDNA microarray encompassing 3500 genes expressed in skeletal muscle. With this system, we have performed the first study of gene expression in samples from individual patients. We analyzed muscle specimen from individuals w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c90fd81621ce003af0b1e77ac685621f
https://pubmed.ncbi.nlm.nih.gov/12620965
https://pubmed.ncbi.nlm.nih.gov/12620965
Autor:
Yuko Nakabayashi, Yaeko Ichikawa, Kazuhiro Kobayashi, Tsutomu Fujiwara, Yusuke Nakamura, Yoshitaka Nagai, Masaji Tachikawa, Tatsushi Toda, Jun Goto, Koichiro Nakamura, Ichiro Kanazawa, Hye-Jung Han
Publikováno v:
Journal of human genetics. 47(6)
To obtain novel candidate genes for autosomal dominant spinocerebellar ataxia and other neurodegenerative disorders in which gene mutations remain unidentified, we screened a human fetal brain cDNA library using (CAG)(10) repeat probes. Sixteen cDNAs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9226b4e619af8e2c0742028063220d2d
https://pubmed.ncbi.nlm.nih.gov/12111376
https://pubmed.ncbi.nlm.nih.gov/12111376
Autor:
Yuko Nakabayashi, Masaji Tachikawa, Miho Murata, Tatsushi Toda, Yoshio Momose, Ichiro Kanazawa, Kazuhiro Kobayashi
Publikováno v:
Annals of neurology. 51(1)
We studied 20 single nucleotide polymorphisms in 18 candidate genes for association with Parkinson's disease. We found that homozygosity for the V66M polymorphism of the brain-derived neurotrophic factor (BDNF) gene occurs more frequently in patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4cdf9abfc59170d028c5486ce8dfacc
https://pubmed.ncbi.nlm.nih.gov/12783434
https://pubmed.ncbi.nlm.nih.gov/12783434