Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Kenichi Fukiage"'
Autor:
Kenichi Fukiage, Makoto Watanabe, Shiro Ikegawa, Zheng Wang, Cantas Alev, Yoshihiro Yamanaka, Jing-Yi Xue, Megumi Nishio, Yann Pretemer, Junya Toguchida, Shunsuke Kawai, Tohru Futami, Masako Tsukanaka, Sanae Nagata, Sakura Tamaki
Publikováno v:
Stem Cell Reports
Summary Chondrodysplasias are hereditary diseases caused by mutations in the components of growth cartilage. Although the unfolded protein response (UPR) has been identified as a key disease mechanism in mouse models, no suitable in vitro system has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::275bfd6280b1ee900d126311dd13e96e
https://doi.org/10.1016/j.stemcr.2021.01.014
https://doi.org/10.1016/j.stemcr.2021.01.014
Autor:
Yuko Koyama, Kazuya Sekiguchi, Makoto Ikeya, Sanae Nagata, Masataka Hada, Shuichi Matsuda, Kenichi Fukiage, Hirotsugu Maekawa, Yonghui Jin, Junko Sunaga, Cantas Alev, Taiji Adachi, Maya Uemura, Junya Toguchida, Sakura Tamaki, Yuki Harada, Megumi Nishio, Hiroyuki Yoshitomi, Shunsuke Kawai
Publikováno v:
Nature Biomedical Engineering. 3:558-570
The recapitulation of bone formation via the in vitro generation of bone-like nodules is frequently used to understand bone development. However, current bone-induction techniques are slow and difficult to reproduce. Here, we report the formation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc39d6574fb65623a845f07eb9017e76
https://doi.org/10.1038/s41551-019-0410-7
https://doi.org/10.1038/s41551-019-0410-7
Autor:
Kenichi Fukiage, Jing-Yi Xue, Masako Tsukanaka, Yann Pretemer, Tohru Futami, Junya Toguchida, Shunsuke Kawai, Zheng Wang, Megumi Nishio, Cantas Alev, Sanae Nagata, Makoto Watanabe, Shiro Ikegawa, Sakura Tamaki
SummaryChondrodysplasias are hereditary diseases caused by mutations in the components of growth cartilage. Although the unfolded protein response (UPR) has been identified as a key disease mechanism in mouse models, no suitablein vitrosystem has bee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91cc7c5b698493439987117a3bbeae9e
https://doi.org/10.1101/2020.05.19.103960
https://doi.org/10.1101/2020.05.19.103960
Publikováno v:
Journal of Pediatric Orthopaedics B. 26:519-525
The aim of this study is to evaluate the complications of humeral lengthening and their associated factors. Fifty-four achondroplastic patients were treated by bilateral humeral lengthening. Our original shoulder sling was sufficient to prevent shoul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::372f2dc50935f0ddcf97bc6e4ccdb836
https://doi.org/10.1097/bpb.0000000000000428
https://doi.org/10.1097/bpb.0000000000000428
Publikováno v:
Journal of Children's Orthopaedics
Purpose The aim of this study was to first develop and use 1.0 s ultrafast magnetic resonance imaging (MRI) to confirm the location of the femoral head in non-sedated infants with developmental dysplasia of the hip (DDH) after reduction with spica ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a7ad16e63737dce5d2ca588faecc6aa
https://doi.org/10.1007/s11832-016-0734-8
https://doi.org/10.1007/s11832-016-0734-8
Publikováno v:
Modern Rheumatology. 27:1098-1100
Chronic infantile neurological, cutaneous, and articular (CINCA) syndrome is a systemic autoinflammatory disease caused by increased production of interleukin (IL)-1β. We present a case of CINCA syndrome followed up to skeletal maturity. Joint contr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4011971fa685fb7399ec46c4f496904e
https://doi.org/10.3109/14397595.2015.1040609
https://doi.org/10.3109/14397595.2015.1040609
Autor:
Kenichi Fukiage, Tomitaka Nakayama, Tomoki Aoyama, K Ito, Yonghui Jin, Seiji Otsuka, Michiko Ueda, Takashi Nakamura, Takeshi Okamoto, Moritoshi Furu, Junya Toguchida, Satoshi Nagayama
Publikováno v:
Journal of Biological Chemistry. 285:29842-29850
Elucidating the regulatory mechanism for tissue-specific gene expression is key to understanding the differentiation process. The chondromodulin-I gene (ChM-I) is a cartilage-specific gene, the expression of which is regulated by the transcription fa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::923f2d64b61bd429d90d96ee9ef55a32
https://doi.org/10.1074/jbc.m110.116319
https://doi.org/10.1074/jbc.m110.116319
Autor:
Yasunari Kasai, Yonghui Jin, Hideo Niwa, Takanobu Otsuka, Junya Toguchida, Moritoshi Furu, Taira Maekawa, Michiko Ueda, Seiji Otsuka, Tomoki Aoyama, K Ito, Kenichi Fukiage, Takashi Nakamura, Eishi Ashihara, Shinya Yoshida, Akira Kobayashi, Akira Nasu, Shinya Kimura
Publikováno v:
Tissue Engineering Part C: Methods. 16:81-91
Bone marrow stromal cells (BMSCs) include cells with multidirectional differentiation potential described as mesenchymal stem cells. For clinical use, it is important to develop a way to isolate BMSCs from bone marrow in a closed system without centr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::967fc64cd34ea38767667bb6d8478cac
https://doi.org/10.1089/ten.tec.2008.0693
https://doi.org/10.1089/ten.tec.2008.0693
Autor:
Yonghui Jin, Yoshiki Kohno, Seiji Otsuka, Shunsuke Fujibayashi, K Ito, Tomitaka Nakayama, Tomoki Aoyama, Kotaro R. Shibata, Satoshi Fujita, Takashi Nakamura, Moritoshi Furu, Kenichi Fukiage, Masashi Neo, Junya Toguchida
Publikováno v:
Biochemical and Biophysical Research Communications. 365:406-412
Bone marrow stromal cells (BMSCs) are a mixture of cells differing in differentiation potential including mesenchymal stem cells, and so far no CD antigens were found to be predictable for the differentiation property of each BMSC. Here we attempted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c99db9463cb8413c90dd3807b694a281
https://doi.org/10.1016/j.bbrc.2007.10.149
https://doi.org/10.1016/j.bbrc.2007.10.149
Publikováno v:
Journal of pediatric orthopedics. Part B. 24(4)
The aims of this study were to quantify the femoral head volume (FHV) in developmental dysplasia of the hip (DDH) and to estimate its relation with the severity of the disease. Fifty-one patients (age range 2-11 months) with unilateral DDH were evalu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7da9ff378021c99f8980df3340aeec80
https://pubmed.ncbi.nlm.nih.gov/25812029
https://pubmed.ncbi.nlm.nih.gov/25812029