Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Yonghui Jin"'
Autor:
Megumi Yokomizo-Goto, Nana Takenaka-Ninagawa, Chengzhu Zhao, Clémence Kiho Bourgeois Yoshioka, Mayuho Miki, Souta Motoike, Yoshiko Inada, Denise Zujur, William Theoputra, Yonghui Jin, Junya Toguchida, Makoto Ikeya, Hidetoshi Sakurai
Publikováno v:
Stem Cell Research & Therapy, Vol 15, Iss 1, Pp 1-19 (2024)
Abstract Background Ullrich congenital muscular dystrophy (UCMD) is caused by a deficiency in type 6 collagen (COL6) due to mutations in COL6A1, COL6A2, or COL6A3. COL6 deficiency alters the extracellular matrix structure and biomechanical properties
Externí odkaz:
https://doaj.org/article/f340ceaf0581411496358769fb395f06
Autor:
Shunsuke Kawai, Junko Sunaga, Sanae Nagata, Megumi Nishio, Masayuki Fukuda, Takeshi Kamakura, Liping Sun, Yonghui Jin, Satoko Sakamoto, Akira Watanabe, Shuichi Matsuda, Taiji Adachi, Junya Toguchida
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-14 (2023)
Abstract Although the formation of bone-like nodules is regarded as the differentiation process from stem cells to osteogenic cells, including osteoblasts and osteocytes, the precise biological events during nodule formation are unknown. Here we perf
Externí odkaz:
https://doaj.org/article/dbb57962a6144ea8b83bc0dd40be197a
Autor:
Hirotsugu Maekawa, Yonghui Jin, Megumi Nishio, Shunsuke Kawai, Sanae Nagata, Takeshi Kamakura, Hiroyuki Yoshitomi, Akira Niwa, Megumu K. Saito, Shuichi Matsuda, Junya Toguchida
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-15 (2022)
Abstract Background Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disease characterized by progressive heterotopic ossification (HO) in soft tissues due to a heterozygous mutation of the ACVR1A gene (FOP-ACVR1A), which erroneously tra
Externí odkaz:
https://doaj.org/article/1a29b45a74264b83b9eb2587ec53abff
Autor:
Takeshi Kamakura, Yonghui Jin, Megumi Nishio, Sanae Nagata, Masayuki Fukuda, Liping Sun, Shunsuke Kawai, Junya Toguchida
Publikováno v:
JBMR Plus, Vol 7, Iss 5, Pp n/a-n/a (2023)
ABSTRACT Collagen X is a non‐fibril collagen produced by hypertrophic chondrocytes and was believed to associate with the calcification process of growth plate cartilage. The homozygous loss of Col10a1 gene in mice, however, demonstrated no remarka
Externí odkaz:
https://doaj.org/article/44b157d147da47c9aeba1708c52fff2d
Autor:
Hirotsugu Maekawa, Shunsuke Kawai, Megumi Nishio, Sanae Nagata, Yonghui Jin, Hiroyuki Yoshitomi, Shuichi Matsuda, Junya Toguchida
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-11 (2020)
Abstract Background Fibrodysplasia ossificans progressiva (FOP) is a rare autosomal-dominant disease characterized by heterotopic ossification (HO) in soft tissues and caused by a mutation of the ACVR1A/ALK2 gene. Activin-A is a key molecule for init
Externí odkaz:
https://doaj.org/article/ec452d0b9c2c4ed4a7d2c0f47ad7cdca
Autor:
Yonghui Jin, Qiuju Du, Yanhui Li, Yang Zhang, Bing Chen, Mingzhen Wang, Kewei Chen, Yaohui Sun, Shiyong Zhao, Zhenyu Jing
Publikováno v:
Nanomaterials, Vol 12, Iss 15, p 2659 (2022)
Egg white protein is a non-toxic and biodegradable biopolymer that forms a gel easily via simple thermal denaturation treatment. A novel aerogel on the basis of egg white protein crosslinked with graphene oxide was prepared via a facile freeze-drying
Externí odkaz:
https://doaj.org/article/60c666ca739443e6873eef5d928724c5
Autor:
Sakura Tamaki, Makoto Fukuta, Kazuya Sekiguchi, Yonghui Jin, Sanae Nagata, Kazuo Hayakawa, Sho Hineno, Takeshi Okamoto, Makoto Watanabe, Knut Woltjen, Makoto Ikeya, Tomohisa Kato, Junya Toguchida
Publikováno v:
PLoS ONE, Vol 10, Iss 11, p e0142991 (2015)
The prevalence and specificity of unique fusion oncogenes are high in a number of soft tissue sarcomas (STSs). The close relationship between fusion genes and clinicopathological features suggests that a correlation may exist between the function of
Externí odkaz:
https://doaj.org/article/d079498d1d5d4653885620816cdf494a
Autor:
Yonghui Jin, Hassan Elalaf, Makoto Watanabe, Sakura Tamaki, Sho Hineno, Kazuhito Matsunaga, Knut Woltjen, Yukiko Kobayashi, Sanae Nagata, Makoto Ikeya, Tomohisa Kato, Takeshi Okamoto, Shuichi Matsuda, Junya Toguchida
Publikováno v:
PLoS ONE, Vol 10, Iss 7, p e0131998 (2015)
Somatic mutations in the isocitrate dehydrogenase (IDH)1/2 genes endow encoding proteins with neomorphic activity to produce the potential oncometabolite, 2-hydroxyglutarate (2-HG), which induces the hypermethylation of histones and DNA. The incidenc
Externí odkaz:
https://doaj.org/article/b75f900f13a9428f857006f6edd72963
Autor:
Akira Nasu, Makoto Ikeya, Takuya Yamamoto, Akira Watanabe, Yonghui Jin, Yoshihisa Matsumoto, Kazuo Hayakawa, Naoki Amano, Shingo Sato, Kenji Osafune, Tomoki Aoyama, Takashi Nakamura, Tomohisa Kato, Junya Toguchida
Publikováno v:
PLoS ONE, Vol 8, Iss 1, p e53771 (2013)
BACKGROUND: For regenerative therapy using induced pluripotent stem cell (iPSC) technology, cell type of origin to be reprogrammed should be chosen based on accessibility and reprogramming efficiency. Some studies report that iPSCs exhibited a prefer
Externí odkaz:
https://doaj.org/article/df60f45ec31e4744a543588258eb64f3
Autor:
Liping Sun, Yonghui Jin, Megumi Nishio, Makoto Watanabe, Takeshi Kamakura, Sanae Nagata, Masayuki Fukuda, Hirotsugu Maekawa, Shunsuke Kawai, Takuya Yamamoto, Junya Toguchida
Publikováno v:
Life Science Alliance; May2024, Vol. 7 Issue 5, p1-17, 17p